Licia Selleri, PhD, MD

Title(s)Professor, Orofacial Sciences
SchoolSchool of Dentistry
AddressLocation Required, #001
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    Collapse Biography 
    Collapse Education and Training
    Ginnasio Ludovico MuratoriBaccalaureat1980
    University of ModenaM.D. 1985Medical School
    University of Modena, and Erasmus University (Advisors: Dr. Umberto Torelli & Dr. Gerard Grosveld)Ph.D. Molecular Biology1990Graduate School
    The Salk Institute for Biological Studies, Molecular Genetics Laboratory (Advisor: Dr. Glen Evans)“Fogarty” Postdoctoral Fellow1992

    Collapse Overview 
    Collapse Overview
    UCSF School of Medicine
    Department of Anatomy
    Institute of Human Genetics
    Eli and Edythe Broad Center of Regeneration Medicine & Stem Cell Research

    Genetic and regulatory control of morphogenesis in embryonic development, evolution, and disease

    The laboratory studies the genetic and regulatory basis of how elaborately patterned tissues form during embryonic development and evolution. The laboratory combines different genetic approaches, using the mouse as a model, to understand the mechanisms underpinning basic developmental processes related to cranial and appendicular morphogenesis. They discovered that homeodomain-containing transcription factors of the Pbx family, also known as Hox-cofactors, are critical developmental regulators through the transcriptional control of target genes within tissue-specific regulatory networks. The lab uses genetically-engineered and ethylnitrosourea (ENU)-mutagenized mouse lines. Recently they utilize additional animal models, such as jerboas and primates, with the ultimate goal to identify novel genes and regulatory networks underlying morphogenesis of embryonic structures, morphological variation, and evolution. Focus is also given to how perturbation of these regulatory networks can result in human congenital disease.

    Collapse Research 
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    Transcriptional regulatory landscapes underlying FEZ Formation
    NIH R01DE028324Mar 11, 2020 - Feb 28, 2025
    Role: Co-Principal Investigator
    Phenotype-driven approach to understanding the function of craniofacial regulators using IMPC-generated mouse strains
    NIH R01DE028753Apr 1, 2019 - Mar 31, 2024
    Role: Principal Investigator
    Pbx-Directed Control of Cellular Behaviors that Drive Midface Morphogenesis
    NIH R01DE024745Jul 1, 2015 - May 31, 2026
    Role: Principal Investigator
    Epigenetic landscapes and regulatory divergence of human craniofacial traits
    NIH U01DE024430May 22, 2014 - Apr 30, 2020
    Role: Co-Principal Investigator
    Genetic and Transcriptional Control of Spleen Development
    NIH R01HD061403Sep 15, 2010 - May 31, 2015
    Role: Principal Investigator
    NIH R21DE018031Apr 1, 2008 - Mar 31, 2011
    Role: Principal Investigator
    Mechanisms of Pbx-directed Genetic & Transcriptional Control of Limb Development
    NIH R01HD043997Apr 1, 2003 - Dec 31, 2017
    Role: Principal Investigator

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    Collapse Featured Publications

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. A common cis-regulatory variant impacts normal-range and disease-associated human facial shape through regulation of PKDCC during chondrogenesis. Elife. 2024 Mar 14; 13. Mohammed J, Arora N, Matthews HS, Hansen K, Bader M, Walsh S, Shaffer JR, Weinberg SM, Swigut T, Claes P, Selleri L, Wysocka J. PMID: 38483448; PMCID: PMC10939500.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimals
    2. Conserved enhancers control notochord expression of vertebrate Brachyury. Nat Commun. 2023 10 18; 14(1):6594. Kemmler CL, Smolikova J, Moran HR, Mannion BJ, Knapp D, Lim F, Czarkwiani A, Hermosilla Aguayo V, Rapp V, Fitch OE, Bötschi S, Selleri L, Farley E, Braasch I, Yun M, Visel A, Osterwalder M, Mosimann C, Kozmik Z, Burger A. PMID: 37852970; PMCID: PMC10584899.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimals
    3. ESCRT-dependent control of craniofacial morphogenesis with concomitant perturbation of NOTCH signaling. Dev Biol. 2023 11; 503:25-42. Hermosilla Aguayo V, Martin P, Tian N, Zheng J, Aho R, Losa M, Selleri L. PMID: 37573008.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    4. A spatio-temporally constrained gene regulatory network directed by PBX1/2 acquires limb patterning specificity via HAND2. Nat Commun. 2023 07 06; 14(1):3993. Losa M, Barozzi I, Osterwalder M, Hermosilla-Aguayo V, Morabito A, Chacón BH, Zarrineh P, Girdziusaite A, Benazet JD, Zhu J, Mackem S, Capellini TD, Dickel D, Bobola N, Zuniga A, Visel A, Zeller R, Selleri L. PMID: 37414772; PMCID: PMC10325989.
      View in: PubMed   Mentions: 1     Fields:    Translation:Animals
    5. Shaping faces: genetic and epigenetic control of craniofacial morphogenesis. Nat Rev Genet. 2023 09; 24(9):610-626. Selleri L, Rijli FM. PMID: 37095271.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    6. Conserved enhancer logic controls the notochord expression of vertebrate Brachyury. bioRxiv. 2023 Apr 20. Kemmler CL, Smolikova J, Moran HR, Mannion BJ, Knapp D, Lim F, Czarkwiani A, Hermosilla Aguayo V, Rapp V, Fitch OE, Bötschi S, Selleri L, Farley E, Braasch I, Yun M, Visel A, Osterwalder M, Mosimann C, Kozmik Z, Burger A. PMID: 37131681; PMCID: PMC10153258.
      View in: PubMed   Mentions:
    7. Generation of Schwann cell derived melanocytes from hPSCs identifies pro-metastatic factors in melanoma. bioRxiv. 2023 Mar 07. Samuel RM, Navickas A, Maynard A, Gaylord EA, Garcia K, Bhat S, Majd H, Richter MN, Elder N, Le D, Nguyen P, Shibata B, Llabata ML, Selleri L, Laird DJ, Darmanis S, Goodarzi H, Fattahi F. PMID: 36945537; PMCID: PMC10028814.
      View in: PubMed   Mentions:
    8. The hSSB1 orthologue Obfc2b is essential for skeletogenesis but dispensable for the DNA damage response in vivo. EMBO J. 2021 Jan 15; 40(2):e107130. Feldhahn N, Ferretti E, Robbiani DF, Callen E, Deroubaix S, Selleri L, Nussenzweig A, Nussenzweig MC. PMID: 33448440; PMCID: PMC7809697.
      View in: PubMed   Mentions:    Fields:    
    9. Loss of Extreme Long-Range Enhancers in Human Neural Crest Drives a Craniofacial Disorder. Cell Stem Cell. 2020 11 05; 27(5):765-783.e14. Long HK, Osterwalder M, Welsh IC, Hansen K, Davies JOJ, Liu YE, Koska M, Adams AT, Aho R, Arora N, Ikeda K, Williams RM, Sauka-Spengler T, Porteus MH, Mohun T, Dickel DE, Swigut T, Hughes JR, Higgs DR, Visel A, Selleri L, Wysocka J. PMID: 32991838; PMCID: PMC7655526.
      View in: PubMed   Mentions: 59     Fields:    Translation:HumansCells
    10. FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research. Development. 2020 09 21; 147(18). Samuels BD, Aho R, Brinkley JF, Bugacov A, Feingold E, Fisher S, Gonzalez-Reiche AS, Hacia JG, Hallgrimsson B, Hansen K, Harris MP, Ho TV, Holmes G, Hooper JE, Jabs EW, Jones KL, Kesselman C, Klein OD, Leslie EJ, Li H, Liao EC, Long H, Lu N, Maas RL, Marazita ML, Mohammed J, Prescott S, Schuler R, Selleri L, Spritz RA, Swigut T, van Bakel H, Visel A, Welsh I, Williams C, Williams TJ, Wysocka J, Yuan Y, Chai Y. PMID: 32958507; PMCID: PMC7522026.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansAnimals
    11. A Specialized Niche in the Pancreatic Microenvironment Promotes Endocrine Differentiation. Dev Cell. 2020 10 26; 55(2):150-162.e6. Cozzitorto C, Mueller L, Ruzittu S, Mah N, Willnow D, Darrigrand JF, Wilson H, Khosravinia D, Mahmoud AA, Risolino M, Selleri L, Spagnoli FM. PMID: 32857951; PMCID: PMC7720791.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansAnimalsCells
    12. Ubiquitous overexpression of CXCL12 confers radiation protection and enhances mobilization of hematopoietic stem and progenitor cells. Stem Cells. 2020 09; 38(9):1159-1174. Rajendiran S, Smith-Berdan S, Kunz L, Risolino M, Selleri L, Schroeder T, Forsberg EC. PMID: 32442338.
      View in: PubMed   Mentions: 7     Fields:    Translation:AnimalsCells
    13. Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease. Hum Mol Genet. 2020 05 08; 29(7):1068-1082. Alankarage D, Szot JO, Pachter N, Slavotinek A, Selleri L, Shieh JT, Winlaw D, Giannoulatou E, Chapman G, Dunwoodie SL. PMID: 31625560; PMCID: PMC7206850.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansAnimals
    14. Corrigendum: 'Building a perfect body': control of vertebrate organogenesis by PBX-dependent regulatory networks. Genes Dev. 2019 05 01; 33(9-10):590. Selleri L, Zappavigna V, Ferretti E. PMID: 31043493; PMCID: PMC6499327.
      View in: PubMed   Mentions:    Fields:    
    15. 'Building a perfect body': control of vertebrate organogenesis by PBX-dependent regulatory networks. Genes Dev. 2019 03 01; 33(5-6):258-275. Selleri L, Zappavigna V, Ferretti E. PMID: 30824532; PMCID: PMC6411007.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansAnimals
    16. Genetics of scapula and pelvis development: An evolutionary perspective. Curr Top Dev Biol. 2019; 132:311-349. Young M, Selleri L, Capellini TD. PMID: 30797513; PMCID: PMC6430119.
      View in: PubMed   Mentions: 6     Fields:    Translation:Animals
    17. Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons. Proc Natl Acad Sci U S A. 2018 08 21; 115(34):E8007-E8016. Bolze A, Boisson B, Bosch B, Antipenko A, Bouaziz M, Sackstein P, Chaker-Margot M, Barlogis V, Briggs T, Colino E, Elmore AC, Fischer A, Genel F, Hewlett A, Jedidi M, Kelecic J, Krüger R, Ku CL, Kumararatne D, Lefevre-Utile A, Loughlin S, Mahlaoui N, Markus S, Garcia JM, Nizon M, Oleastro M, Pac M, Picard C, Pollard AJ, Rodriguez-Gallego C, Thomas C, Von Bernuth H, Worth A, Meyts I, Risolino M, Selleri L, Puel A, Klinge S, Abel L, Casanova JL. PMID: 30072435; PMCID: PMC6112730.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansCells
    18. Pbx loss in cranial neural crest, unlike in epithelium, results in cleft palate only and a broader midface. J Anat. 2018 08; 233(2):222-242. Welsh IC, Hart J, Brown JM, Hansen K, Rocha Marques M, Aho RJ, Grishina I, Hurtado R, Herzlinger D, Ferretti E, Garcia-Garcia MJ, Selleri L. PMID: 29797482; PMCID: PMC6036936.
      View in: PubMed   Mentions: 12     Fields:    Translation:Animals
    19. Face morphogenesis is promoted by Pbx-dependent EMT via regulation of Snail1 during frontonasal prominence fusion. Development. 2018 03 01; 145(5). Losa M, Risolino M, Li B, Hart J, Quintana L, Grishina I, Yang H, Choi IF, Lewicki P, Khan S, Aho R, Feenstra J, Vincent CT, Brown AMC, Ferretti E, Williams T, Selleri L. PMID: 29437830; PMCID: PMC5868993.
      View in: PubMed   Mentions: 18     Fields:    Translation:AnimalsCells
    20. PBX transcription factors drive pulmonary vascular adaptation to birth. J Clin Invest. 2018 02 01; 128(2):655-667. McCulley DJ, Wienhold MD, Hines EA, Hacker TA, Rogers A, Pewowaruk RJ, Zewdu R, Chesler NC, Selleri L, Sun X. PMID: 29251627; PMCID: PMC5785269.
      View in: PubMed   Mentions: 14     Fields:    Translation:AnimalsCells
    21. De novo, deleterious sequence variants that alter the transcriptional activity of the homeoprotein PBX1 are associated with intellectual disability and pleiotropic developmental defects. Hum Mol Genet. 2017 12 15; 26(24):4849-4860. Slavotinek A, Risolino M, Losa M, Cho MT, Monaghan KG, Schneidman-Duhovny D, Parisotto S, Herkert JC, Stegmann APA, Miller K, Shur N, Chui J, Muller E, DeBrosse S, Szot JO, Chapman G, Pachter NS, Winlaw DS, Mendelsohn BA, Dalton J, Sarafoglou K, Karachunski PI, Lewis JM, Pedro H, Dunwoodie SL, Selleri L, Shieh J. PMID: 29036646; PMCID: PMC6455034.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansAnimalsCells
    22. Toward Microsurgical Correction of Cleft Lip Ex Utero through Restoration of Craniofacial Developmental Programs. Plast Reconstr Surg. 2017 Jul; 140(1):75-85. Dong X, Landford WN, Hart J, Risolino M, Kaymakcalan O, Jin J, Toyoda Y, Ferretti E, Selleri L, Spector JA. PMID: 28338586; PMCID: PMC5886781.
      View in: PubMed   Mentions: 2     Fields:    Translation:Animals
    23. A Hox-Embedded Long Noncoding RNA: Is It All Hot Air? PLoS Genet. 2016 Dec; 12(12):e1006485. Selleri L, Bartolomei MS, Bickmore WA, He L, Stubbs L, Reik W, Barsh GS. PMID: 27977680; PMCID: PMC5157941.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansAnimals
    24. Ovarian Cancer Chemoresistance Relies on the Stem Cell Reprogramming Factor PBX1. Cancer Res. 2016 11 01; 76(21):6351-6361. Jung JG, Shih IM, Park JT, Gerry E, Kim TH, Ayhan A, Handschuh K, Davidson B, Fader AN, Selleri L, Wang TL. PMID: 27590741; PMCID: PMC7375390.
      View in: PubMed   Mentions: 35     Fields:    Translation:HumansCells
    25. Parallel Pbx-Dependent Pathways Govern the Coalescence and Fate of Motor Columns. Neuron. 2016 Sep 07; 91(5):1005-1020. Hanley O, Zewdu R, Cohen LJ, Jung H, Lacombe J, Philippidou P, Lee DH, Selleri L, Dasen JS. PMID: 27568519; PMCID: PMC5017921.
      View in: PubMed   Mentions: 24     Fields:    Translation:AnimalsCells
    26. A PBX1 transcriptional network controls dopaminergic neuron development and is impaired in Parkinson's disease. EMBO J. 2016 09 15; 35(18):1963-78. Villaescusa JC, Li B, Toledo EM, Rivetti di Val Cervo P, Yang S, Stott SR, Kaiser K, Islam S, Gyllborg D, Laguna-Goya R, Landreh M, Lönnerberg P, Falk A, Bergman T, Barker RA, Linnarsson S, Selleri L, Arenas E. PMID: 27354364; PMCID: PMC5282836.
      View in: PubMed   Mentions: 51     Fields:    Translation:HumansCells
    27. The FaceBase Consortium: a comprehensive resource for craniofacial researchers. Development. 2016 07 15; 143(14):2677-88. Brinkley JF, Fisher S, Harris MP, Holmes G, Hooper JE, Jabs EW, Jones KL, Kesselman C, Klein OD, Maas RL, Marazita ML, Selleri L, Spritz RA, van Bakel H, Visel A, Williams TJ, Wysocka J, FaceBase Consortium, Chai Y. PMID: 27287806; PMCID: PMC4958338.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansAnimals
    28. Pbx1 is required for adult subventricular zone neurogenesis. Development. 2016 07 01; 143(13):2281-91. Grebbin BM, Hau AC, Groß A, Anders-Maurer M, Schramm J, Koss M, Wille C, Mittelbronn M, Selleri L, Schulte D. PMID: 27226325; PMCID: PMC4958316.
      View in: PubMed   Mentions: 26     Fields:    Translation:AnimalsCells
    29. Spleen hypoplasia leads to abnormal stress hematopoiesis in mice with loss of Pbx homeoproteins in splenic mesenchyme. J Anat. 2016 07; 229(1):153-69. Zewdu R, Risolino M, Barbulescu A, Ramalingam P, Butler JM, Selleri L. PMID: 27075259; PMCID: PMC5341595.
      View in: PubMed   Mentions: 5     Fields:    Translation:Animals
    30. Pbx Regulates Patterning of the Cerebral Cortex in Progenitors and Postmitotic Neurons. Neuron. 2015 Dec 16; 88(6):1192-1207. Golonzhka O, Nord A, Tang PLF, Lindtner S, Ypsilanti AR, Ferretti E, Visel A, Selleri L, Rubenstein JLR. PMID: 26671461; PMCID: PMC4688141.
      View in: PubMed   Mentions: 32     Fields:    Translation:AnimalsCells
    31. Enhancer divergence and cis-regulatory evolution in the human and chimp neural crest. Cell. 2015 Sep 24; 163(1):68-83. Prescott SL, Srinivasan R, Marchetto MC, Grishina I, Narvaiza I, Selleri L, Gage FH, Swigut T, Wysocka J. PMID: 26365491; PMCID: PMC4848043.
      View in: PubMed   Mentions: 172     Fields:    Translation:HumansAnimalsCells
    32. Pbx1-dependent control of VMC differentiation kinetics underlies gross renal vascular patterning. Development. 2015 Aug 01; 142(15):2653-64. Hurtado R, Zewdu R, Mtui J, Liang C, Aho R, Kurylo C, Selleri L, Herzlinger D. PMID: 26138478; PMCID: PMC4529034.
      View in: PubMed   Mentions: 28     Fields:    Translation:Animals
    33. An allelic series of miR-17 ∼ 92-mutant mice uncovers functional specialization and cooperation among members of a microRNA polycistron. Nat Genet. 2015 Jul; 47(7):766-75. Han YC, Vidigal JA, Mu P, Yao E, Singh I, González AJ, Concepcion CP, Bonetti C, Ogrodowski P, Carver B, Selleri L, Betel D, Leslie C, Ventura A. PMID: 26029871; PMCID: PMC4485521.
      View in: PubMed   Mentions: 66     Fields:    Translation:AnimalsCells
    34. Mouse regulatory DNA landscapes reveal global principles of cis-regulatory evolution. Science. 2014 Nov 21; 346(6212):1007-12. Vierstra J, Rynes E, Sandstrom R, Zhang M, Canfield T, Hansen RS, Stehling-Sun S, Sabo PJ, Byron R, Humbert R, Thurman RE, Johnson AK, Vong S, Lee K, Bates D, Neri F, Diegel M, Giste E, Haugen E, Dunn D, Wilken MS, Josefowicz S, Samstein R, Chang KH, Eichler EE, De Bruijn M, Reh TA, Skoultchi A, Rudensky A, Orkin SH, Papayannopoulou T, Treuting PM, Selleri L, Kaul R, Groudine M, Bender MA, Stamatoyannopoulos JA. PMID: 25411453; PMCID: PMC4337786.
      View in: PubMed   Mentions: 147     Fields:    Translation:HumansAnimalsCells
    35. A comparative encyclopedia of DNA elements in the mouse genome. Nature. 2014 Nov 20; 515(7527):355-64. Yue F, Cheng Y, Breschi A, Vierstra J, Wu W, Ryba T, Sandstrom R, Ma Z, Davis C, Pope BD, Shen Y, Pervouchine DD, Djebali S, Thurman RE, Kaul R, Rynes E, Kirilusha A, Marinov GK, Williams BA, Trout D, Amrhein H, Fisher-Aylor K, Antoshechkin I, DeSalvo G, See LH, Fastuca M, Drenkow J, Zaleski C, Dobin A, Prieto P, Lagarde J, Bussotti G, Tanzer A, Denas O, Li K, Bender MA, Zhang M, Byron R, Groudine MT, McCleary D, Pham L, Ye Z, Kuan S, Edsall L, Wu YC, Rasmussen MD, Bansal MS, Kellis M, Keller CA, Morrissey CS, Mishra T, Jain D, Dogan N, Harris RS, Cayting P, Kawli T, Boyle AP, Euskirchen G, Kundaje A, Lin S, Lin Y, Jansen C, Malladi VS, Cline MS, Erickson DT, Kirkup VM, Learned K, Sloan CA, Rosenbloom KR, Lacerda de Sousa B, Beal K, Pignatelli M, Flicek P, Lian J, Kahveci T, Lee D, Kent WJ, Ramalho Santos M, Herrero J, Notredame C, Johnson A, Vong S, Lee K, Bates D, Neri F, Diegel M, Canfield T, Sabo PJ, Wilken MS, Reh TA, Giste E, Shafer A, Kutyavin T, Haugen E, Dunn D, Reynolds AP, Neph S, Humbert R, Hansen RS, De Bruijn M, Selleri L, Rudensky A, Josefowicz S, Samstein R, Eichler EE, Orkin SH, Levasseur D, Papayannopoulou T, Chang KH, Skoultchi A, Gosh S, Disteche C, Treuting P, Wang Y, Weiss MJ, Blobel GA, Cao X, Zhong S, Wang T, Good PJ, Lowdon RF, Adams LB, Zhou XQ, Pazin MJ, Feingold EA, Wold B, Taylor J, Mortazavi A, Weissman SM, Stamatoyannopoulos JA, Snyder MP, Guigo R, Gingeras TR, Gilbert DM, Hardison RC, Beer MA, Ren B, Mouse ENCODE Consortium. PMID: 25409824; PMCID: PMC4266106.
      View in: PubMed   Mentions: 861     Fields:    Translation:HumansAnimalsCells
    36. Principles of regulatory information conservation between mouse and human. Nature. 2014 Nov 20; 515(7527):371-375. Cheng Y, Ma Z, Kim BH, Wu W, Cayting P, Boyle AP, Sundaram V, Xing X, Dogan N, Li J, Euskirchen G, Lin S, Lin Y, Visel A, Kawli T, Yang X, Patacsil D, Keller CA, Giardine B, mouse ENCODE Consortium, Kundaje A, Wang T, Pennacchio LA, Weng Z, Hardison RC, Snyder MP. PMID: 25409826; PMCID: PMC4343047.
      View in: PubMed   Mentions: 159     Fields:    Translation:HumansAnimalsCells
    37. ESCRT-II/Vps25 constrains digit number by endosome-mediated selective modulation of FGF-SHH signaling. Cell Rep. 2014 Oct 23; 9(2):674-87. Handschuh K, Feenstra J, Koss M, Ferretti E, Risolino M, Zewdu R, Sahai MA, Bénazet JD, Peng XP, Depew MJ, Quintana L, Sharpe J, Wang B, Alcorn H, Rivi R, Butcher S, Manak JR, Vaccari T, Weinstein H, Anderson KV, Lacy E, Selleri L. PMID: 25373905; PMCID: PMC4223648.
      View in: PubMed   Mentions: 5     Fields:    Translation:AnimalsCells
    38. Pbx1 activates Fgf10 in the mesenchyme of developing lungs. Genesis. 2014 May; 52(5):399-407. Li W, Lin CY, Shang C, Han P, Xiong Y, Lin CJ, Yang J, Selleri L, Chang CP. PMID: 24591256.
      View in: PubMed   Mentions: 6     Fields:    Translation:AnimalsCells
    39. ADAM17 controls endochondral ossification by regulating terminal differentiation of chondrocytes. Mol Cell Biol. 2013 Aug; 33(16):3077-90. Hall KC, Hill D, Otero M, Plumb DA, Froemel D, Dragomir CL, Maretzky T, Boskey A, Crawford HC, Selleri L, Goldring MB, Blobel CP. PMID: 23732913; PMCID: PMC3753912.
      View in: PubMed   Mentions: 25     Fields:    Translation:AnimalsCells
    40. Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia. Science. 2013 May 24; 340(6135):976-8. Bolze A, Mahlaoui N, Byun M, Turner B, Trede N, Ellis SR, Abhyankar A, Itan Y, Patin E, Brebner S, Sackstein P, Puel A, Picard C, Abel L, Quintana-Murci L, Faust SN, Williams AP, Baretto R, Duddridge M, Kini U, Pollard AJ, Gaud C, Frange P, Orbach D, Emile JF, Stephan JL, Sorensen R, Plebani A, Hammarstrom L, Conley ME, Selleri L, Casanova JL. PMID: 23579497; PMCID: PMC3677541.
      View in: PubMed   Mentions: 102     Fields:    Translation:Humans
    41. The hSSB1 orthologue Obfc2b is essential for skeletogenesis but dispensable for the DNA damage response in vivo. EMBO J. 2012 Oct 17; 31(20):4045-56. Feldhahn N, Ferretti E, Robbiani DF, Callen E, Deroubaix S, Selleri L, Nussenzweig A, Nussenzweig MC. PMID: 22940690; PMCID: PMC3474923.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansAnimalsCells
    42. Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module. Dev Cell. 2012 May 15; 22(5):913-26. Koss M, Bolze A, Brendolan A, Saggese M, Capellini TD, Bojilova E, Boisson B, Prall OW, Elliott DA, Solloway M, Lenti E, Hidaka C, Chang CP, Mahlaoui N, Harvey RP, Casanova JL, Selleri L. PMID: 22560297; PMCID: PMC3356505.
      View in: PubMed   Mentions: 37     Fields:    Translation:HumansAnimalsCells
    43. A conserved Pbx-Wnt-p63-Irf6 regulatory module controls face morphogenesis by promoting epithelial apoptosis. Dev Cell. 2011 Oct 18; 21(4):627-41. Ferretti E, Li B, Zewdu R, Wells V, Hebert JM, Karner C, Anderson MJ, Williams T, Dixon J, Dixon MJ, Depew MJ, Selleri L. PMID: 21982646; PMCID: PMC3199312.
      View in: PubMed   Mentions: 106     Fields:    Translation:HumansAnimalsCells
    44. Epigenetic regulation of early osteogenesis and mineralized tissue formation by a HOXA10-PBX1-associated complex. Cells Tissues Organs. 2011; 194(2-4):146-50. Gordon JA, Hassan MQ, Koss M, Montecino M, Selleri L, van Wijnen AJ, Stein JL, Stein GS, Lian JB. PMID: 21597276; PMCID: PMC3178072.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansAnimalsCells
    45. Hox and Pbx factors control retinoic acid synthesis during hindbrain segmentation. Dev Cell. 2011 Apr 19; 20(4):469-82. Vitobello A, Ferretti E, Lampe X, Vilain N, Ducret S, Ori M, Spetz JF, Selleri L, Rijli FM. PMID: 21497760; PMCID: PMC3677862.
      View in: PubMed   Mentions: 46     Fields:    Translation:Animals
    46. Control of pelvic girdle development by genes of the Pbx family and Emx2. Dev Dyn. 2011 May; 240(5):1173-89. Capellini TD, Handschuh K, Quintana L, Ferretti E, Di Giacomo G, Fantini S, Vaccari G, Clarke SL, Wenger AM, Bejerano G, Sharpe J, Zappavigna V, Selleri L. PMID: 21455939; PMCID: PMC3081414.
      View in: PubMed   Mentions: 10     Fields:    Translation:Animals
    47. Pbx homeodomain proteins: TALEnted regulators of limb patterning and outgrowth. Dev Dyn. 2011 May; 240(5):1063-86. Capellini TD, Zappavigna V, Selleri L. PMID: 21416555; PMCID: PMC3081394.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansAnimalsCells
    48. Scapula development is governed by genetic interactions of Pbx1 with its family members and with Emx2 via their cooperative control of Alx1. Development. 2010 Aug 01; 137(15):2559-69. Capellini TD, Vaccari G, Ferretti E, Fantini S, He M, Pellegrini M, Quintana L, Di Giacomo G, Sharpe J, Selleri L, Zappavigna V. PMID: 20627960; PMCID: PMC2927673.
      View in: PubMed   Mentions: 30     Fields:    Translation:AnimalsCells
    49. Ectopic Meis1 expression in the mouse limb bud alters P-D patterning in a Pbx1-independent manner. Int J Dev Biol. 2009; 53(8-10):1483-94. Mercader N, Selleri L, Criado LM, Pallares P, Parras C, Cleary ML, Torres M. PMID: 19247936.
      View in: PubMed   Mentions: 18     Fields:    Translation:Animals
    50. Conservation of notochord gene expression across chordates: insights from the Leprecan gene family. Genesis. 2008 Nov; 46(11):683-96. Capellini TD, Dunn MP, Passamaneck YJ, Selleri L, Di Gregorio A. PMID: 18798549; PMCID: PMC3065379.
      View in: PubMed   Mentions: 16     Fields:    Translation:Animals
    51. Pbx/Meis deficiencies demonstrate multigenetic origins of congenital heart disease. Circ Res. 2008 Sep 26; 103(7):702-9. Stankunas K, Shang C, Twu KY, Kao SC, Jenkins NA, Copeland NG, Sanyal M, Selleri L, Cleary ML, Chang CP. PMID: 18723445; PMCID: PMC2633052.
      View in: PubMed   Mentions: 79     Fields:    Translation:HumansAnimals
    52. Pbx1/Pbx2 govern axial skeletal development by controlling Polycomb and Hox in mesoderm and Pax1/Pax9 in sclerotome. Dev Biol. 2008 Sep 15; 321(2):500-14. Capellini TD, Zewdu R, Di Giacomo G, Asciutti S, Kugler JE, Di Gregorio A, Selleri L. PMID: 18691704; PMCID: PMC5918304.
      View in: PubMed   Mentions: 19     Fields:    Translation:Animals
    53. Interleukin-10 expression in macrophages during phagocytosis of apoptotic cells is mediated by homeodomain proteins Pbx1 and Prep-1. Immunity. 2007 Dec; 27(6):952-64. Chung EY, Liu J, Homma Y, Zhang Y, Brendolan A, Saggese M, Han J, Silverstein R, Selleri L, Ma X. PMID: 18093541; PMCID: PMC2194654.
      View in: PubMed   Mentions: 113     Fields:    Translation:HumansAnimalsCells
    54. Cooperation between p27 and p107 during endochondral ossification suggests a genetic pathway controlled by p27 and p130. Mol Cell Biol. 2007 Jul; 27(14):5161-71. Yeh N, Miller JP, Gaur T, Capellini TD, Nikolich-Zugich J, de la Hoz C, Selleri L, Bromage TG, van Wijnen AJ, Stein GS, Lian JB, Vidal A, Koff A. PMID: 17502351; PMCID: PMC1951950.
      View in: PubMed   Mentions: 10     Fields:    Translation:AnimalsCells
    55. Development and function of the mammalian spleen. Bioessays. 2007 Feb; 29(2):166-77. Brendolan A, Rosado MM, Carsetti R, Selleri L, Dear TN. PMID: 17226804.
      View in: PubMed   Mentions: 66     Fields:    Translation:HumansAnimals
    56. B-cell development fails in the absence of the Pbx1 proto-oncogene. Blood. 2007 May 15; 109(10):4191-9. Sanyal M, Tung JW, Karsunky H, Zeng H, Selleri L, Weissman IL, Herzenberg LA, Cleary ML. PMID: 17244677; PMCID: PMC1885499.
      View in: PubMed   Mentions: 37     Fields:    Translation:AnimalsCells
    57. Hypomorphic mutation of the TALE gene Prep1 (pKnox1) causes a major reduction of Pbx and Meis proteins and a pleiotropic embryonic phenotype. Mol Cell Biol. 2006 Aug; 26(15):5650-62. Ferretti E, Villaescusa JC, Di Rosa P, Fernandez-Diaz LC, Longobardi E, Mazzieri R, Miccio A, Micali N, Selleri L, Ferrari G, Blasi F. PMID: 16847320; PMCID: PMC1592771.
      View in: PubMed   Mentions: 57     Fields:    Translation:AnimalsCells
    58. Pax6 is regulated by Meis and Pbx homeoproteins during pancreatic development. Dev Biol. 2006 Dec 15; 300(2):748-57. Zhang X, Rowan S, Yue Y, Heaney S, Pan Y, Brendolan A, Selleri L, Maas RL. PMID: 17049510.
      View in: PubMed   Mentions: 35     Fields:    Translation:HumansAnimalsCells
    59. Pbx1/Pbx2 requirement for distal limb patterning is mediated by the hierarchical control of Hox gene spatial distribution and Shh expression. Development. 2006 Jun; 133(11):2263-73. Capellini TD, Di Giacomo G, Salsi V, Brendolan A, Ferretti E, Srivastava D, Zappavigna V, Selleri L. PMID: 16672333.
      View in: PubMed   Mentions: 87     Fields:    Translation:AnimalsCells
    60. Hox cofactors in vertebrate development. Dev Biol. 2006 Mar 15; 291(2):193-206. Moens CB, Selleri L. PMID: 16515781.
      View in: PubMed   Mentions: 240     Fields:    Translation:HumansAnimalsCells
    61. Spatio-temporal expression of Pbx3 during mouse organogenesis. Gene Expr Patterns. 2006 Oct; 6(7):747-57. Di Giacomo G, Koss M, Capellini TD, Brendolan A, Pöpperl H, Selleri L. PMID: 16434237.
      View in: PubMed   Mentions: 29     Fields:    Translation:Animals
    62. A Pbx1-dependent genetic and transcriptional network regulates spleen ontogeny. Development. 2005 Jul; 132(13):3113-26. Brendolan A, Ferretti E, Salsi V, Moses K, Quaggin S, Blasi F, Cleary ML, Selleri L. PMID: 15944191.
      View in: PubMed   Mentions: 65     Fields:    Translation:AnimalsCells
    63. Abnormalities of caudal pharyngeal pouch development in Pbx1 knockout mice mimic loss of Hox3 paralogs. Dev Biol. 2004 Dec 15; 276(2):301-12. Manley NR, Selleri L, Brendolan A, Gordon J, Cleary ML. PMID: 15581866.
      View in: PubMed   Mentions: 44     Fields:    Translation:Animals
    64. Pbx3 deficiency results in central hypoventilation. Am J Pathol. 2004 Oct; 165(4):1343-50. Rhee JW, Arata A, Selleri L, Jacobs Y, Arata S, Onimaru H, Cleary ML. PMID: 15466398; PMCID: PMC1618620.
      View in: PubMed   Mentions: 42     Fields:    Translation:AnimalsCells
    65. The TALE homeodomain protein Pbx2 is not essential for development and long-term survival. Mol Cell Biol. 2004 Jun; 24(12):5324-31. Selleri L, DiMartino J, van Deursen J, Brendolan A, Sanyal M, Boon E, Capellini T, Smith KS, Rhee J, Pöpperl H, Grosveld G, Cleary ML. PMID: 15169896; PMCID: PMC419882.
      View in: PubMed   Mentions: 42     Fields:    Translation:Animals
    66. Pbx1 is essential for adrenal development and urogenital differentiation. Genesis. 2003 Nov; 37(3):123-30. Schnabel CA, Selleri L, Cleary ML. PMID: 14595835.
      View in: PubMed   Mentions: 63     Fields:    Translation:Animals
    67. Pbx1 inactivation disrupts pancreas development and in Ipf1-deficient mice promotes diabetes mellitus. Nat Genet. 2002 Apr; 30(4):430-5. Kim SK, Selleri L, Lee JS, Zhang AY, Gu X, Jacobs Y, Cleary ML. PMID: 11912494.
      View in: PubMed   Mentions: 81     Fields:    Translation:AnimalsCells
    68. Requirement for Pbx1 in skeletal patterning and programming chondrocyte proliferation and differentiation. Development. 2001 Sep; 128(18):3543-57. Selleri L, Depew MJ, Jacobs Y, Chanda SK, Tsang KY, Cheah KS, Rubenstein JL, O'Gorman S, Cleary ML. PMID: 11566859.
      View in: PubMed   Mentions: 142     Fields:    Translation:AnimalsCells
    69. The Hox cofactor and proto-oncogene Pbx1 is required for maintenance of definitive hematopoiesis in the fetal liver. Blood. 2001 Aug 01; 98(3):618-26. DiMartino JF, Selleri L, Traver D, Firpo MT, Rhee J, Warnke R, O'Gorman S, Weissman IL, Cleary ML. PMID: 11468159.
      View in: PubMed   Mentions: 68     Fields:    Translation:AnimalsCells
    70. Expression of Pbx1b during mammalian organogenesis. Mech Dev. 2001 Jan; 100(1):131-5. Schnabel CA, Selleri L, Jacobs Y, Warnke R, Cleary ML. PMID: 11118899.
      View in: PubMed   Mentions: 34     Fields:    Translation:Animals
    71. Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation. Genes Chromosomes Cancer. 1999 Mar; 24(3):199-206. Wlodarska I, Selleri L, La Starza R, Paternotte C, Evans GA, Boogaerts M, Van den Berghe H, Mecucci C. PMID: 10451699.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    72. Organization and regulatory aspects of the human intestinal mucin gene (MUC2) locus. J Biol Chem. 1997 Mar 21; 272(12):7968-76. Velcich A, Palumbo L, Selleri L, Evans G, Augenlicht L. PMID: 9065467.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    73. De novo 46,XX, dir dup (11)(q133.3-->q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopenia. Clin Genet. 1996 Apr; 49(4):206-10. Legius E, Wlodarska I, Selleri L, Evans GA, Wu R, Smet G, Fryns JP. PMID: 8828987.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    74. An STS content map of human chromosome 11: localization of 910 YAC clones and 109 islands. Genomics. 1995 Sep 20; 29(2):512-25. Quackenbush J, Davies C, Bailis JM, Khristich JV, Diggle K, Marchuck Y, Tobin J, Clark SP, Rodkins A, Marcano S, et al. PMID: 8666402.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    75. A novel L23-related gene 40 kb downstream of the imprinted H19 gene is biallelically expressed in mid-fetal and adult human tissues. Hum Mol Genet. 1995 Sep; 4(9):1499-507. Tsang P, Gilles F, Yuan L, Kuo YH, Lupu F, Samara G, Moosikasuwan J, Goye A, Zelenetz AD, Selleri L, et al. PMID: 8541832.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    76. Translocation (11;15)(q23;q14) in three patients with acute non-lymphoblastic leukemia (ANLL): clinical, cytogenetic and molecular studies. Leukemia. 1995 Jul; 9(7):1162-6. Hernández JM, Mecucci C, Beverloo HB, Selleri L, Wlodarska I, Stul M, Michaux L, Verhoef G, Van Orshoven A, Cassiman JJ, et al. PMID: 7630191.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    77. High-resolution physical mapping of a 250-kb region of human chromosome 11q24 by genomic sequence sampling (GSS). Genomics. 1995 Apr 10; 26(3):489-501. Selleri L, Smith MW, Holmsen AL, Romo AJ, Thomas SD, Paternotte C, Romberg LC, Wei YH, Evans GA. PMID: 7607672.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    78. Spontaneous loss of Ph chromosome with maintenance of clonal hemopoiesis in an untreated patient with myeloproliferative disease and a long survival. Genes Chromosomes Cancer. 1995 Mar; 12(3):237-40. Luppi M, Morselli M, Emilia G, Temperani P, Marasca R, Barozzi P, Selleri L, Torelli G. PMID: 7536465.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    79. Yeast artificial chromosome cloning of 3.2 megabases within chromosomal band 11q24 closely linking c-ets 1 and Fli-1 and encompassing the Ewing sarcoma breakpoint. Genomics. 1994 Jul 01; 22(1):137-47. Selleri L, Giovannini M, Hermanson GG, Romo A, Quackenbush J, Penny L, Khristich JV, Evans GA. PMID: 7959760.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    80. Cloning of the entire FLI1 gene, disrupted by the Ewing's sarcoma translocation breakpoint on 11q24, in a yeast artificial chromosome. Cytogenet Cell Genet. 1994; 67(2):129-36. Selleri L, Giovannini M, Romo A, Zucman J, Delattre O, Thomas G, Evans GA. PMID: 8039423.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    81. A sequence-tagged site map of human chromosome 11. Genomics. 1993 Sep; 17(3):699-725. Smith MW, Clark SP, Hutchinson JS, Wei YH, Churukian AC, Daniels LB, Diggle KL, Gen MW, Romo AJ, Lin Y, et al. PMID: 8244387.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimalsCells
    82. A trithorax-like gene is interrupted by chromosome 11q23 translocations in acute leukaemias. Nat Genet. 1993 Aug; 4(4):431. Djabali M, Selleri L, Parry P, Bower M, Young B, Evans GA. PMID: 8401594.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansAnimalsCells
    83. Tandem linkage of genes coding for leukemia inhibitory factor (LIF) and oncostatin M (OSM) on human chromosome 22. Cytogenet Cell Genet. 1993; 64(3-4):240-4. Giovannini M, Djabali M, McElligott D, Selleri L, Evans GA. PMID: 8404048.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    84. Localization of the human oncostatin M gene (OSM) to chromosome 22q12, distal to the Ewing's sarcoma breakpoint. Cytogenet Cell Genet. 1993; 62(1):32-4. Giovannini M, Selleri L, Hermanson GG, Evans GA. PMID: 8422753.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    85. A novel zinc finger gene on human chromosome 1qter that is alternatively spliced in human tissues and cell lines. Am J Hum Genet. 1993 Jan; 52(1):192-203. Saleh M, Selleri L, Evans GA. PMID: 7916577; PMCID: PMC1682137.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    86. Isolation and expression of linked zinc finger gene clusters on human chromosome 11q. Genomics. 1992 Dec; 14(4):970-8. Saleh M, Selleri L, Little PF, Evans GA. PMID: 1339395.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    87. Structure and linkage of the D2 dopamine receptor and neural cell adhesion molecule genes on human chromosome 11q23. Genomics. 1992 Dec; 14(4):1010-8. Eubanks JH, Djabali M, Selleri L, Grandy DK, Civelli O, McElligott DL, Evans GA. PMID: 1478642.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    88. Interphase cytogenetics for the detection of the t(11;22)(q24;q12) in small round cell tumors. J Clin Invest. 1992 Nov; 90(5):1911-8. Giovannini M, Selleri L, Biegel JA, Scotlandi K, Emanuel BS, Evans GA. PMID: 1430213; PMCID: PMC443252.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    89. Detection and characterization of "chimeric" yeast artificial chromosome clones by fluorescent in situ suppression hybridization. Genomics. 1992 Oct; 14(2):536-41. Selleri L, Eubanks JH, Giovannini M, Hermanson GG, Romo A, Djabali M, Maurer S, McElligott DL, Smith MW, Evans GA. PMID: 1427876.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    90. A trithorax-like gene is interrupted by chromosome 11q23 translocations in acute leukaemias. Nat Genet. 1992 Oct; 2(2):113-8. Djabali M, Selleri L, Parry P, Bower M, Young BD, Evans GA. PMID: 1303259.
      View in: PubMed   Mentions: 122     Fields:    Translation:HumansAnimalsCells
    91. Serum autoantibodies and the diagnosis of type-1 autoimmune hepatitis in Italy: a reappraisal at the light of hepatitis C virus infection. Gut. 1992 Sep; 33(9):1260-3. Cassani F, Muratori L, Manotti P, Lenzi M, Fusconi M, Ballardini G, Selleri L, Volta U, Zauli D, Miniero R, et al. PMID: 1330845; PMCID: PMC1379498.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    92. Dek-can rearrangement in translocation (6;9)(p23;q34). Leukemia. 1992 Jun; 6(6):489-94. Soekarman D, von Lindern M, van der Plas DC, Selleri L, Bartram CR, Martiat P, Culligan D, Padua RA, Hasper-Voogt KP, Hagemeijer A, et al. PMID: 1602786.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    93. Cosmid linking clones localized to the long arm of human chromosome 11. Genomics. 1992 May; 13(1):134-43. Hermanson GG, Lichter P, Selleri L, Ward DC, Evans GA. PMID: 1577478.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    94. Isolation, localization, and physical mapping of a highly polymorphic locus on human chromosome 11q13. Genomics. 1991 Nov; 11(3):720-9. Eubanks JH, Selleri L, Hart R, Rosette C, Evans GA. PMID: 1685481.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    95. Human herpesvirus-6 in human lymphomas: identification of specific sequences in Hodgkin's lymphomas by polymerase chain reaction. Blood. 1991 May 15; 77(10):2251-8. Torelli G, Marasca R, Luppi M, Selleri L, Ferrari S, Narni F, Mariano MT, Federico M, Ceccherini-Nelli L, Bendinelli M, et al. PMID: 1674220.
      View in: PubMed   Mentions: 27     Fields:    Translation:HumansCells
    96. Chromosomal in situ hybridization using yeast artificial chromosomes. Genet Anal Tech Appl. 1991 Apr; 8(2):59-66. Selleri L, Hermanson GG, Eubanks JH, Evans GA. PMID: 2064820.
      View in: PubMed   Mentions: 8     Fields:    Translation:AnimalsCells
    97. Molecular localization of the t(11;22)(q24;q12) translocation of Ewing sarcoma by chromosomal in situ suppression hybridization. Proc Natl Acad Sci U S A. 1991 Feb 01; 88(3):887-91. Selleri L, Hermanson GG, Eubanks JH, Lewis KA, Evans GA. PMID: 1992479; PMCID: PMC50919.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    98. Sinus histiocytosis with massive lymphadenopathy: immunological, cytogenetic and molecular studies. Blut. 1990 Jun; 60(6):339-44. Sacchi S, Artusi T, Selleri L, Temperani P, Zucchini P, Vecchi A, Emilia G, Torelli U. PMID: 2375964.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    99. Ratios between the abundance of messenger RNA and the corresponding protein of two growth-related genes, c-myc and vimentin, in leukemia blast cells. Cancer Res. 1990 Apr 01; 50(7):1988-91. Ferrari S, Tagliafico E, D'Incá M, Ceccherelli G, Manfredini R, Selleri L, Donelli A, Sacchi S, Torelli G, Torelli U. PMID: 2180559.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    100. [Mitochondrial DNA deletion in a case of progressive ophthalmoplegia]. Medicina (Firenze). 1990 Apr-Jun; 10(2):166-8. Luppi M, Marasca R, Sola P, Corradi M, Fancinelli M, Montorsi M, Manfredini R, Selleri L. PMID: 2273955.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    101. Chronic myeloid leukemia may be associated with several bcr-abl transcripts including the acute lymphoid leukemia-type 7 kb transcript. Blood. 1990 Mar 01; 75(5):1146-53. Selleri L, von Lindern M, Hermans A, Meijer D, Torelli G, Grosveld G. PMID: 2407300.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    102. Chronic myelogenous leukemia with typical clinical and morphological features can be Philadelphia chromosome negative and "bcr negative". Hematol Pathol. 1990; 4(2):67-77. Selleri L, Emilia G, Luppi M, Temperani P, Zucchini P, Tagliafico E, Artusi T, Sarti M, Donelli A, Castoldi GL, et al. PMID: 2197265.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    103. [Identification of human herpesvirus HHV-6 sequence in a case of Hodgkin's disease by polymerase chain reaction]. Medicina (Firenze). 1990 Jan-Mar; 10(1):43-5. Marasca R, Luppi M, Montorsi M, Fancinelli M, Sabbatini R, Mariano MT, Selleri L. PMID: 2166207.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    104. Extramedullary pleural blast crisis in chronic myelogenous leukemia: cytogenetic and molecular study. Acta Haematol. 1990; 83(4):198-202. Sacchi S, Temperani P, Selleri L, Zucchini P, Morselli S, Vecchi A, Longo R, Torelli G, Emilia G, Torelli U. PMID: 2115717.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    105. Serum antibodies to thymus epithelial cells in non-A, non-B and cryptogenic chronic liver disease. Liver. 1989 Oct; 9(5):279-87. Cassani F, Tremolada F, Bianchi FB, Baffoni L, Selleri L, Benvegnu L, Craxi A, Realdi G, Zauli D, Pisi E. PMID: 2479804.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    106. Philadelphia-positive chronic myelogenous leukemia with typical bcr/abl molecular features and atypical, prolonged survival. Leukemia. 1989 Jul; 3(7):538-42. Selleri L, Emilia G, Temperani P, Grassilli E, Zucchini P, Tagliafico E, Bonati A, Venezia L, Ferrari S, Torelli U, et al. PMID: 2733455.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    107. Expression of the myeloperoxidase gene in acute and chronic myeloid leukemias: relationship to the expression of cell cycle-related genes. Leukemia. 1989 Jun; 3(6):423-30. Ferrari S, Tagliafico E, Ceccherelli G, Selleri L, Calabretta B, Donelli A, Temperani P, Sarti M, Sacchi S, Emilia G, et al. PMID: 2542700.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    108. Cytogenetic and molecular studies in primary myelofibrosis. Cancer Genet Cytogenet. 1989 Mar; 38(1):101-13. Emilia G, Temperani P, Ferrari S, Zucchini P, Tagliafico E, Selleri L, Torelli G, Artusi T, Torelli U. PMID: 2713806.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    109. [Polymerase chain reaction for the diagnostic identification of HIV infection]. Medicina (Firenze). 1989 Jan-Mar; 9(1):41-3. Selleri L, Grassilli E, Tagliafico E, Corradi M, Luppi M, Ceccherelli G, Borghi V. PMID: 2739527.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    110. Isodicentric X chromosome in myeloproliferative disorders. Acta Haematol. 1989; 81(3):152-4. Temperani P, Zucchini P, Emilia G, Sacchi S, Selleri L, Torelli U. PMID: 2496563.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    111. Absence of alternative splicing in bcr-abl mRNA in chronic myeloid leukemia cell lines. Blood. 1988 Dec; 72(6):2066-9. Hermans A, Selleri L, Gow J, Grosveld GC. PMID: 2848601.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    112. Expression of oncogenes and cell cycle related genes in acute and chronic leukemias. Leukemia. 1988 Dec; 2(12 Suppl):160S-166S. Ferrari S, Calabretta B, Selleri L, Ceccherelli G, Torelli G, Torelli U. PMID: 3199878.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    113. bcr-abl oncogene activation in Philadelphia chromosome-positive acute lymphoblastic leukemia. Leukemia. 1988 Oct; 2(10):628-33. Hermans A, Gow J, Selleri L, von Lindern M, Hagemeijer A, Wiedemann LM, Grosveld G. PMID: 3172839.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    114. [Possible correlations between proliferation and differentiation of blast cells in acute promyelocytic leukemia: a molecular study]. Medicina (Firenze). 1988 Oct-Dec; 8(4):425-8. Tagliafico E, Manfredini R, Selleri L, Zucchini P, Ceccherelli G. PMID: 2854184.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    115. Myeloperoxidase gene expression in blast cells with a lymphoid phenotype in cases of acute lymphoblastic leukemia. Blood. 1988 Sep; 72(3):873-6. Ferrari S, Mariano MT, Tagliafico E, Sarti M, Ceccherelli G, Selleri L, Merli F, Narni F, Donelli A, Torelli G, et al. PMID: 2458150.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    116. Prognostic significance of "short-term" effects of chemotherapy on MYC and histone H3 mRNA levels in acute leukemia patients. Proc Natl Acad Sci U S A. 1988 May; 85(10):3590-4. Venturelli D, Lange B, Narni F, Selleri L, Mariano MT, Torelli U, Gewirtz AM, Calabretta B. PMID: 3285345; PMCID: PMC280259.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    117. Philadelphia-positive chronic myeloid leukemia with a chromosome 22 breakpoint outside the breakpoint cluster region. Blood. 1987 Nov; 70(5):1659-64. Selleri L, Narni F, Emilia G, Colò A, Zucchini P, Venturelli D, Donelli A, Torelli U, Torelli G. PMID: 3478105.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    118. Expression of c-myb protooncogene and other cell cycle-related genes in normal and neoplastic human colonic mucosa. Cancer Res. 1987 Oct 15; 47(20):5266-9. Torelli G, Venturelli D, Coló A, Zanni C, Selleri L, Moretti L, Calabretta B, Torelli U. PMID: 3652034.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    119. Establishment and characterization of a human IgA-kappa-secreting plasma cell line (MT3). Int J Cancer. 1987 Sep 15; 40(3):383-8. Donelli A, Narni F, Tabilio A, Emilia G, Selleri L, Colo A, Zucchini P, Montagnani G, Torelli G, Torelli U. PMID: 3114153.
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    120. Immunoglobulin and T-cell receptor beta chain gene rearrangements as lineage markers in human leukemias: a study of 78 cases. Haematologica. 1987 Sep-Oct; 72(5):391-7. Narni F, Colò A, Venturelli D, Selleri L, Donelli A, Tabilio A, Artusi T, Di Prisco U, Torelli G, Torelli U. PMID: 3121460.
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    121. Promyelocytic crisis of chronic myeloid leukaemia. Br J Haematol. 1987 Jun; 66(2):276-7. Emilia G, Sacchi S, Selleri L, Zucchini P, Artusi T, Torelli U. PMID: 3475112.
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    122. Molecular study of the Philadelphia translocation in chronic myelogenous leukemia in different stages of disease. Haematologica. 1987 May-Jun; 72(3):201-8. Torelli G, Selleri L, Emilia G, Narni F, Colò A, Zucchini P, Donelli A, Venturelli D, Torelli U. PMID: 3040551.
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    123. Simultaneously increased expression of the c-myc and mu chain genes in the acute blastic transformation of a chronic lymphocytic leukaemia. Br J Haematol. 1987 Feb; 65(2):165-70. Torelli UL, Torelli GM, Emilia G, Selleri L, Venturelli D, Artusi T, Donelli A, Colò A, Fornieri C. PMID: 3103669.
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    124. Nuclear protrusions and marker chromosomes in lymphocytes of two patients with cutaneous T-cell lymphoma. Acta Haematol. 1987; 78(1):61-2. Emilia G, Torelli G, Sacchi S, Zucchini P, Selleri L, Temperani P, Torelli U. PMID: 3116814.
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    125. Clinical subsets of scleroderma: relevance of fluorescent and precipitating antinuclear antibodies. Clin Exp Rheumatol. 1987 Jan-Mar; 5(1):23-8. Cassani F, Tosti A, Bianchi FB, Fusconi M, Selleri L, Baffoni L, Veronesi S, Volta U, Lenzi M, Pisi E. PMID: 3109797.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    126. Growth-dependent expression of human Mr 53,000 tumor antigen messenger RNA in normal and neoplastic cells. Cancer Res. 1986 Nov; 46(11):5738-42. Calabretta B, Kaczmarek L, Selleri L, Torelli G, Ming PM, Ming SC, Mercer WE. PMID: 3019534.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    127. Cellular levels of mRNA from c-myc, c-myb and c-fes onc-genes in normal myeloid and erythroid precursors of human bone marrow: an in situ hybridization study. Br J Haematol. 1986 Feb; 62(2):287-92. Emilia G, Donelli A, Ferrari S, Torelli U, Selleri L, Zucchini P, Moretti L, Venturelli D, Ceccherelli G, Torelli G. PMID: 3947550.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    128. Differential patterns of expression of cell cycle-related genes in blast cells of acute myeloid leukemia. Leuk Res. 1986; 10(10):1249-54. Torelli U, Selleri L, Venturelli D, Donelli A, Emilia G, Ceccherelli G, Turchi L, Torelli G. PMID: 3464813.
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    129. Activation of c-myb expression by phytohemagglutinin stimulation in normal human T lymphocytes. Mol Cell Biol. 1985 Oct; 5(10):2874-7. Torelli G, Selleri L, Donelli A, Ferrari S, Emilia G, Venturelli D, Moretti L, Torelli U. PMID: 3915538; PMCID: PMC367031.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansCells
    130. Expression of human c-fes onc-gene occurs at detectable levels in myeloid but not in lymphoid cell populations. Br J Haematol. 1985 Jan; 59(1):21-5. Ferrari S, Torelli U, Selleri L, Donelli A, Venturelli D, Moretti L, Torelli G. PMID: 3855647.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    131. Study of the levels of expression of two oncogenes, c-myc and c-myb, in acute and chronic leukemias of both lymphoid and myeloid lineage. Leuk Res. 1985; 9(7):833-42. Ferrari S, Torelli U, Selleri L, Donelli A, Venturelli D, Narni F, Moretti L, Torelli G. PMID: 3860696.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    132. Low-dose intravenous pepsin-treated gammaglobulin for idiopathic thrombocytopenic purpura in adults. Br J Haematol. 1984 Dec; 58(4):761-2. Emilia G, Sacchi S, Torelli G, Selleri L, Torelli U. PMID: 6542801.
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