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    Ramon Birnbaum

    TitlePostdoctoral Scholar
    SchoolUCSF School of Pharmacy
    DepartmentBioengineering and Therapeutic Sciences
    Address1550 4th St., Rock Hall
    San Francisco CA 94143
    Phone415-476-5166

       Bibliographic 
       Publications
      Publications by year:
      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.
      1. Cohen I, Birnbaum RY, Leibson K, Taube R, Sivan S, Birk OS. ZNF750 is expressed in differentiated keratinocytes and regulates epidermal late differentiation genes. PLoS One. 2012; 7(8):e42628.
        View in: PubMed
      2. Birnbaum RY, Everman DB, Murphy KK, Gurrieri F, Schwartz CE, Ahituv N. Functional characterization of tissue-specific enhancers in the DLX5/6 locus. Hum Mol Genet. 2012 Nov 15; 21(22):4930-8.
        View in: PubMed
      3. Birnbaum RY, Clowney EJ, Agamy O, Kim MJ, Zhao J, Yamanaka T, Pappalardo Z, Clarke SL, Wenger AM, Nguyen L, Gurrieri F, Everman DB, Schwartz CE, Birk OS, Bejerano G, Lomvardas S, Ahituv N. Coding exons function as tissue-specific enhancers of nearby genes. Genome Res. 2012 Jun; 22(6):1059-68.
        View in: PubMed
      4. Birnbaum RY, Hayashi G, Cohen I, Poon A, Chen H, Lam ET, Kwok PY, Birk OS, Liao W. Association analysis identifies ZNF750 regulatory variants in psoriasis. BMC Med Genet. 2011; 12:167.
        View in: PubMed
      5. Birnbaum RY, Landau D, Elbedour K, Ofir R, Birk OS, Carmi R. Deletion of the first pair of fibronectin type III repeats of the integrin beta-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients. Am J Med Genet A. 2008 Apr 15; 146A(8):1063-6.
        View in: PubMed
      6. Birnbaum RY, Zvulunov A, Hallel-Halevy D, Cagnano E, Finer G, Ofir R, Geiger D, Silberstein E, Feferman Y, Birk OS. Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750, encoding a putative C2H2 zinc finger protein. Nat Genet. 2006 Jul; 38(7):749-51.
        View in: PubMed
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