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Daniah Beleford, MD, PhD

Title(s)Postdoctoral Scholar, HDF Comprehensive Cancer Ctr
SchoolSchool of Medicine
Address1450 Third St
San Francisco CA 94158
Phone--
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    Collapse Biography 
    Collapse Education and Training
    University of California, San FranciscoPost-Doctoral Research FellowshipHelen Diller Family Comprehensive Cancer Center
    University of California, San FranciscoClinical Fellowship2019Genetics and Genomics
    University of California, San FranciscoResidency2018Genetics and Genomics
    Mayo Clinic College of MedicineMD, PhD - Biochemistry and Molecular BiologyMedical Scientist Training Program
    Cornell UniversityBA (Daniah Thompson)Genetics and Development

    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 missense variant, p.(Ile269Asn), in MC4R as a secondary finding in a child with BCL11A-related intellectual disability. Eur J Med Genet. 2020 Jun 10; 103969. Beleford DT, Van Ziffle J, Hodoglugil U, Slavotinek AM. PMID: 32534219.
      View in: PubMed   Mentions:    Fields:    
    2. Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness. Hum Mol Genet. 2020 Jun 05. Slavotinek A, Misceo D, Htun S, Mathisen L, Frengen E, Foreman M, Hurtig JE, Enyenihi L, Sterrett MC, Leung SW, Schneidman-Duhovny D, Estrada-Veras J, Duncan JL, Haaxma CA, Kamsteeg EJ, Xia V, Beleford D, Si Y, Douglas G, Treidene HE, van Hoof A, Fasken MB, Corbett AH. PMID: 32504085.
      View in: PubMed   Mentions:    Fields:    
    3. A novel truncating variant in ring finger protein 113A (RNF113A) confirms the association of this gene with X-linked trichothiodystrophy. Am J Med Genet A. 2020 03; 182(3):513-520. Mendelsohn BA, Beleford DT, Abu-El-Haija A, Alsaleh NS, Rahbeeni Z, Martin PM, Rego S, Huang A, Capodanno G, Shieh JT, Van Ziffle J, Risch N, Alkuraya FS, Slavotinek AM. PMID: 31880405.
      View in: PubMed   Mentions:    Fields:    
    4. X-linked duplication copy number variation in a familial overgrowth condition. Am J Med Genet C Semin Med Genet. 2019 12; 181(4):644-649. Ha TK, Mardy AH, Beleford D, Spanier A, Wayman BV, Penon-Portmann M, Wiita AP, Shieh JT. PMID: 31762227.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    5. Schimke immunoosseous dysplasia and management considerations for vascular risks. Am J Med Genet A. 2019 07; 179(7):1246-1252. Beleford DT, Diab M, Qubty WF, Malloy MJ, Long RK, Shieh JT. PMID: 31039288.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    6. Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review. Am J Med Genet A. 2019 06; 179(6):966-977. Kumar A, Zastrow DB, Kravets EJ, Beleford D, Ruzhnikov MRZ, Grove ME, Dries AM, Kohler JN, Waggott DM, Yang Y, Huang Y, Mackenzie KM, Eng CM, Fisher PG, Ashley EA, Teng JM, Stevenson DA, Shieh JT, Wheeler MT, Bernstein JA. PMID: 30920161.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    7. Neuro-Oncology. PATH-07. FAMILIAL MELANOMA-ASTROCYTOMA SYNDROME: SYNCHRONOUS DIFFUSE ASTROCYTOMA AND PLEOMORPHIC XANTHOASTROCYTOMA IN A PATIENT WITH GERMLINE CDKN2A/B DELETION AND A SIGNIFICANT FAMILY HISTORY. 2017; 19(suppl_6):vi171–vi172. View Publication.
    8. Familial melanoma-astrocytoma syndrome: synchronous diffuse astrocytoma and pleomorphic xanthoastrocytoma in a patient with germline CDKN2A/B deletion and a significant family history. Clin Neuropathol. 2017 Sep/Oct; 36(5):213-221. Chan AK, Han SJ, Choy W, Beleford D, Aghi MK, Berger MS, Shieh JT, Bollen AW, Perry A, Phillips JJ, Butowski N, Solomon DA. PMID: 28699883.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    9. Role of heparan sulfatases in ovarian and breast cancer. Am J Cancer Res. 2013; 3(1):34-45. Khurana A, Beleford D, He X, Chien J, Shridhar V. PMID: 23359864.
      View in: PubMed   Mentions:
    10. Handbook of Proteolytic Enzymes. Chapter 572 - HtrA3 Peptidase. 2012; 3:2584-2590. View Publication.
    11. Cleavage of PGRP-LC receptor in the Drosophila IMD pathway in response to live bacterial infection in S2 cells. Self Nonself. 2011 Jul; 2(3):125-141. Schmidt RL, Rinaldo FM, Hesse SE, Hamada M, Ortiz Z, Beleford DT, Page-McCaw A, Platt JL, Tang AH. PMID: 22496930.
      View in: PubMed   Mentions:
    12. High temperature requirement A3 (HtrA3) promotes etoposide- and cisplatin-induced cytotoxicity in lung cancer cell lines. J Biol Chem. 2010 Apr 16; 285(16):12011-27. Beleford D, Rattan R, Chien J, Shridhar V. PMID: 20154083.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    13. Methylation induced gene silencing of HtrA3 in smoking-related lung cancer. Clin Cancer Res. 2010 Jan 15; 16(2):398-409. Beleford D, Liu Z, Rattan R, Quagliuolo L, Boccellino M, Baldi A, Maguire J, Staub J, Molina J, Shridhar V. PMID: 20068077.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansAnimalsCells
    14. Cell proliferation and epidermal growth factor signaling in non-small cell lung adenocarcinoma cell lines are dependent on Rin1. J Biol Chem. 2009 Sep 25; 284(39):26331-9. Tomshine JC, Severson SR, Wigle DA, Sun Z, Beleford DA, Shridhar V, Horazdovsky BF. PMID: 19570984.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    15. A role for candidate tumor-suppressor gene TCEAL7 in the regulation of c-Myc activity, cyclin D1 levels and cellular transformation. Oncogene. 2008 Dec 11; 27(58):7223-34. Chien J, Narita K, Rattan R, Giri S, Shridhar R, Staub J, Beleford D, Lai J, Roberts LR, Molina J, Kaufmann SH, Prendergast GC, Shridhar V. PMID: 18806825.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    16. Identification and characterization of the chromatin-binding domains of the HIV-1 integrase interactor LEDGF/p75. J Mol Biol. 2006 Jul 21; 360(4):760-73. Llano M, Vanegas M, Hutchins N, Thompson D, Delgado S, Poeschla EM. PMID: 16793062.
      View in: PubMed   Mentions: 87     Fields:    Translation:HumansCells
    17. Identification of the LEDGF/p75 HIV-1 integrase-interaction domain and NLS reveals NLS-independent chromatin tethering. J Cell Sci. 2005 Apr 15; 118(Pt 8):1733-43. Vanegas M, Llano M, Delgado S, Thompson D, Peretz M, Poeschla E. PMID: 15797927.
      View in: PubMed   Mentions: 87     Fields:    Translation:HumansAnimalsCells
    18. CCR5 and CXCR4 usage by non-clade B human immunodeficiency virus type 1 primary isolates. J Virol. 2002 Mar; 76(6):3059-64. Thompson DA, Cormier EG, Dragic T. PMID: 11861874.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    19. Human immunodeficiency virus type 1 entry inhibitors PRO 542 and T-20 are potently synergistic in blocking virus-cell and cell-cell fusion. J Infect Dis. 2001 Apr 01; 183(7):1121-5. Nagashima KA, Thompson DA, Rosenfield SI, Maddon PJ, Dragic T, Olson WC. PMID: 11237840.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansAnimalsCells
    20. Entry of R5X4 and X4 human immunodeficiency virus type 1 strains is mediated by negatively charged and tyrosine residues in the amino-terminal domain and the second extracellular loop of CXCR4. Virology. 2000 Jun 05; 271(2):240-7. Kajumo F, Thompson DA, Guo Y, Dragic T. PMID: 10860877.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansCells
    21. Specific interaction of CCR5 amino-terminal domain peptides containing sulfotyrosines with HIV-1 envelope glycoprotein gp120. Proc Natl Acad Sci U S A. 2000 May 23; 97(11):5762-7. Cormier EG, Persuh M, Thompson DA, Lin SW, Sakmar TP, Olson WC, Dragic T. PMID: 10823934.
      View in: PubMed   Mentions: 70     Fields:    Translation:HumansCells
    22. A binding pocket for a small molecule inhibitor of HIV-1 entry within the transmembrane helices of CCR5. Proc Natl Acad Sci U S A. 2000 May 09; 97(10):5639-44. Dragic T, Trkola A, Thompson DA, Cormier EG, Kajumo FA, Maxwell E, Lin SW, Ying W, Smith SO, Sakmar TP, Moore JP. PMID: 10779565.
      View in: PubMed   Mentions: 133     Fields:    Translation:HumansAnimalsCells
    23. Differential inhibition of human immunodeficiency virus type 1 fusion, gp120 binding, and CC-chemokine activity by monoclonal antibodies to CCR5. J Virol. 1999 May; 73(5):4145-55. Olson WC, Rabut GE, Nagashima KA, Tran DN, Anselma DJ, Monard SP, Segal JP, Thompson DA, Kajumo F, Guo Y, Moore JP, Maddon PJ, Dragic T. PMID: 10196311.
      View in: PubMed   Mentions: 76     Fields:    Translation:HumansCells
    24. CCR5-Mediated human immunodeficiency virus entry depends on an amino-terminal gp120-binding site and on the conformational integrity of all four extracellular domains. J Virol. 1999 Feb; 73(2):1645-8. Genoud S, Kajumo F, Guo Y, Thompson D, Dragic T. PMID: 9882373.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
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