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Divya Punwani, PhD

TitleSpecialist
SchoolUCSF School of Medicine
DepartmentPediatrics
Address555 Mission Bay Blvd South
San Francisco CA 94158
Phone415-476-3674
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    Collapse Biography 
    Collapse Education and Training
    University of OxfordDPhil2010Immunology
    University of OxfordMSc2006Immunology

    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.
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    1. Punwani D, Zhang Y, Yu J, Cowan MJ, Rana S, Kwan A, Adhikari AN, Lizama CO, Mendelsohn BA, Fahl SP, Chellappan A, Srinivasan R, Brenner SE, Wiest DL, Puck JM. Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11B. N Engl J Med. 2016 Dec; 375(22):2165-2176. PMID: 27959755.
      View in: PubMed
    2. Punwani D, Kawahara M, Yu J, Sanford U, Roy S, Patel K, Carbonaro DA, Karlen AD, Khan S, Cornetta KG, Rothe M, Schambach A, Kohn DB, Malech HL, McIvor RS, Puck JM, Cowan MJ. Lentivirus Mediated Correction of Artemis-deficient Severe Combined Immunodeficiency. Hum Gene Ther. 2016 Sep 09. PMID: 27611239.
      View in: PubMed
    3. Chan AY, Punwani D, Kadlecek TA, Cowan MJ, Olson JL, Mathes EF, Sunderam U, Fu SM, Srinivasan R, Kuriyan J, Brenner SE, Weiss A, Puck JM. A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70. J Exp Med. 2016 Feb 8; 213(2):155-65. PMID: 26783323.
      View in: PubMed
    4. Punwani D, Wang H, Chan AY, Cowan MJ, Mallott J, Sunderam U, Mollenauer M, Srinivasan R, Brenner SE, Mulder A, Claas FH, Weiss A, Puck JM. Combined immunodeficiency due to MALT1 mutations, treated by hematopoietic cell transplantation. J Clin Immunol. 2015 Feb; 35(2):135-46. PMID: 25627829; PMCID: PMC4352191.
    5. Punwani D, Gonzalez-Espinosa D, Comeau AM, Dutra A, Pak E, Puck J. Cellular calibrators to quantitate T-cell receptor excision circles (TRECs) in clinical samples. Mol Genet Metab. 2012 Nov; 107(3):586-91. PMID: 23062576; PMCID: PMC3483425.
    6. Gregory AP, Dendrou CA, Attfield KE, Haghikia A, Xifara DK, Butter F, Poschmann G, Kaur G, Lambert L, Leach OA, Prömel S, Punwani D, Felce JH, Davis SJ, Gold R, Nielsen FC, Siegel RM, Mann M, Bell JI, McVean G, Fugger L. TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosis. Nature. 2012 Aug 23; 488(7412):508-11. PMID: 22801493; PMCID: PMC4268493.
    7. Punwani D, Simon K, Choi Y, Dutra A, Gonzalez-Espinosa D, Pak E, Naradikian M, Song CH, Zhang J, Bodine DM, Puck JM. Transcription factor zinc finger and BTB domain 1 is essential for lymphocyte development. J Immunol. 2012 Aug 1; 189(3):1253-64. PMID: 22753936; PMCID: PMC3401355.
    8. Punwani D, Purohit V, Irani SF, Kumta NB. Apert's syndrome--a type of acrocephalosyndactyly (a case report). J Postgrad Med. 1979 Apr; 25(2):109-11. PMID: 501671.
      View in: PubMed
    9. Punwani D, Naik G, Prabhu SV, Irani SF, Kumta NB. Screening for hemoglobinopathy using cellulose acetate electrophoresis in cases of hepatosplenomegaly with anaemia. Indian Pediatr. 1978 Nov; 15(11):905-8. PMID: 751923.
      View in: PubMed
    10. Kumta NB, Irani SF, Punwani D. Infantile polymyoclonia. J Postgrad Med. 1976 Oct; 22(4):194-7. PMID: 1032835.
      View in: PubMed
    11. Kumta NB, Irani SF, Sekhri RR, Punwani D. Congenital contractural arachnodactyly. J Postgrad Med. 1976 Oct; 22(4):191-3. PMID: 1032834.
      View in: PubMed
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