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    Divya Punwani, PhD

    SchoolUCSF School of Medicine
    Address555 Mission Bay Blvd South
    San Francisco CA 94158
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      Collapse Biography 
      Collapse Education and Training
      University of OxfordDPhilImmunology2010
      University of OxfordMScImmunology2006

      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. 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
      2. 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.
      3. 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.
      4. 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.
      5. 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.
      6. Punwani DV, 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
      7. Punwani DV, 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
      8. Kumta NB, Irani SF, Punwani DV. Infantile polymyoclonia. J Postgrad Med. 1976 Oct; 22(4):194-7. PMID: 1032835.
        View in: PubMed
      9. Kumta NB, Irani SF, Sekhri RR, Punwani DV. Congenital contractural arachnodactyly. J Postgrad Med. 1976 Oct; 22(4):191-3. PMID: 1032834.
        View in: PubMed
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