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Volumn 8, Issue 4, 1996, Pages 445-447

Genetic effects on immunity Inherited disorders of lymphocyte development and function. Editorial overview

Author keywords

[No Author keywords available]

Indexed keywords

AGAMMAGLOBULINEMIA; DNA REPAIR; DNA STRAND BREAKAGE; GENE MUTATION; HUMAN; IMMUNE DEFICIENCY; IMMUNE RESPONSE; IMMUNOGENETICS; IMMUNOPATHOLOGY; LYMPHOCYTE FUNCTION; NONHUMAN; SHORT SURVEY; WISKOTT ALDRICH SYNDROME; ANIMAL; CELL DIFFERENTIATION; EDITORIAL; GENETICS; IMMUNOLOGY; LYMPHOCYTE; PATHOLOGY;

EID: 0030204685     PISSN: 09527915     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0952-7915(96)80027-6     Document Type: Editorial
Times cited : (4)

References (15)
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  • 4
    • 0026047309 scopus 로고
    • Severe combined immunodeficiency (SCID) in man - B cell negative SCID patients exhibit an irregular recombination pattern at the JH locus
    • Schwarz K, Hansen-Hagge TE, Knobloch C, Friedrich W, Kleihauer E, Bartram C. Severe combined immunodeficiency (SCID) in man - B cell negative SCID patients exhibit an irregular recombination pattern at the JH locus. J Exp Med. 174:1991;1039-1048.
    • (1991) J Exp Med , vol.174 , pp. 1039-1048
    • Schwarz, K.1    Hansen-Hagge, T.E.2    Knobloch, C.3    Friedrich, W.4    Kleihauer, E.5    Bartram, C.6
  • 8
    • 0028292001 scopus 로고
    • Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase
    • Elder ME, Lin D, Clever J, Chan AC, Hope TJ, Weiss A, Parslow TG. Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase. Science. 264:1994;1596-1599.
    • (1994) Science , vol.264 , pp. 1596-1599
    • Elder, M.E.1    Lin, D.2    Clever, J.3    Chan, A.C.4    Hope, T.J.5    Weiss, A.6    Parslow, T.G.7
  • 10
    • 0028921573 scopus 로고
    • Jaks and Stats in signaling by the cytokine receptor superfamily
    • Ihle JN, Kerr IM. Jaks and Stats in signaling by the cytokine receptor superfamily. Trends Genet. 11:1995;69-74.
    • (1995) Trends Genet , vol.11 , pp. 69-74
    • Ihle, J.N.1    Kerr, I.M.2
  • 13
    • 0030006284 scopus 로고    scopus 로고
    • Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization
    • Symons M, Derry JMJ, Karlak B, Jiang S, Lemahiev V, McCormick F, Francke V, Abo A. Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization. Cell. 84:1996;723-734.
    • (1996) Cell , vol.84 , pp. 723-734
    • Symons, M.1    Derry, J.M.J.2    Karlak, B.3    Jiang, S.4    Lemahiev, V.5    McCormick, F.6    Francke, V.7    Abo, A.8
  • 14
    • 0029680639 scopus 로고    scopus 로고
    • Two GTPases, CDC42 and Rac, bind directly to a protein implicated in the immunodeficiency disorder Wiskott - Aldrich syndrome
    • Aspenstrom P, Lindberg U, Hall A. Two GTPases, CDC42 and Rac, bind directly to a protein implicated in the immunodeficiency disorder Wiskott - Aldrich syndrome. Curr Biol. 6:1996;70-75.
    • (1996) Curr Biol , vol.6 , pp. 70-75
    • Aspenstrom, P.1    Lindberg, U.2    Hall, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.