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Results: 1-10 |
Results: 10
MOLECULAR CHARACTERIZATION OF THE HUMAN INTERLEUKIN (IL)-17 RECEPTOR
Authors: YAO ZB SPRIGGS MK DERRY JMJ STROCKBINE L PARK LS VANDENBOS T ZAPPONE J PAINTER SL ARMITAGE RJ
Citation: Zb. Yao et al., MOLECULAR CHARACTERIZATION OF THE HUMAN INTERLEUKIN (IL)-17 RECEPTOR, Cytokine, 9(11), 1997, pp. 794-800
WISKOTT-ALDRICH SYNDROME PROTEIN, A NOVEL EFFECTOR FOR THE GTPASE CDC42HS, IS IMPLICATED IN ACTIN POLYMERIZATION
Authors: SYMONS M DERRY JMJ KARLAK B JIANG S LEMAHIEU V MCCORMICK F FRANCKE U ABO A
Citation: M. Symons et al., WISKOTT-ALDRICH SYNDROME PROTEIN, A NOVEL EFFECTOR FOR THE GTPASE CDC42HS, IS IMPLICATED IN ACTIN POLYMERIZATION, Cell, 84(5), 1996, pp. 723-734
WASP GENE-MUTATIONS IN WISKOTT-ALDRICH SYNDROME AND X-LINKED THROMBOCYTOPENIA
Authors: DERRY JMJ KERNS JA WEINBERG KI OCHS HD VOLPINI V ESTIVILL X WALKER AP FRANCKE U
Citation: Jmj. Derry et al., WASP GENE-MUTATIONS IN WISKOTT-ALDRICH SYNDROME AND X-LINKED THROMBOCYTOPENIA, Human molecular genetics, 4(7), 1995, pp. 1127-1135
RBM3, A NOVEL HUMAN GENE IN XP11.23 WITH A PUTATIVE RNA-BINDING DOMAIN
Authors: DERRY JMJ KERNS JA FRANCKE U
Citation: Jmj. Derry et al., RBM3, A NOVEL HUMAN GENE IN XP11.23 WITH A PUTATIVE RNA-BINDING DOMAIN, Human molecular genetics, 4(12), 1995, pp. 2307-2311
MUTATION ANALYSIS OF THE WISKOTT-ALDRICH SYNDROME GENE
Authors: ZHU Q ZHANG M BLASE RM DERRY JMJ CHEN SH FRANCKE U OCHS HD
Citation: Q. Zhu et al., MUTATION ANALYSIS OF THE WISKOTT-ALDRICH SYNDROME GENE, The FASEB journal, 9(4), 1995, pp. 780-780
CLONING AND CHARACTERIZATION OF A NOVEL ZINC-FINGER GENE IN XP11.2
Authors: DERRY JMJ JESS U FRANCKE U
Citation: Jmj. Derry et al., CLONING AND CHARACTERIZATION OF A NOVEL ZINC-FINGER GENE IN XP11.2, Genomics, 30(2), 1995, pp. 361-365
THE MOUSE HOMOLOG OF THE WISKOTT-ALDRICH SYNDROME PROTEIN (WASP) GENEIS HIGHLY CONSERVED AND MAPS NEAR THE SCURFY (SF) MUTATION ON THE X-CHROMOSOME
Authors: DERRY JMJ WIEDEMANN P BLAIR P WANG Y KERNS JA LEMAHIEU V GODFREY VL WILKINSON JE FRANCKE U
Citation: Jmj. Derry et al., THE MOUSE HOMOLOG OF THE WISKOTT-ALDRICH SYNDROME PROTEIN (WASP) GENEIS HIGHLY CONSERVED AND MAPS NEAR THE SCURFY (SF) MUTATION ON THE X-CHROMOSOME, Genomics, 29(2), 1995, pp. 471-477
THE WISKOTT-ALDRICH SYNDROME AND X-LINKED CONGENITAL THROMBOCYTOPENIAARE CAUSED BY MUTATIONS OF THE SAME GENE
Authors: ZHU QL ZHANG M BLAESE RM DERRY JMJ JUNKER A FRANCKE U CHEN SH OCHS HD
Citation: Ql. Zhu et al., THE WISKOTT-ALDRICH SYNDROME AND X-LINKED CONGENITAL THROMBOCYTOPENIAARE CAUSED BY MUTATIONS OF THE SAME GENE, Blood, 86(10), 1995, pp. 3797-3804
DYSTROGLYCAN - BRAIN LOCALIZATION AND CHROMOSOME MAPPING IN THE MOUSE
Authors: GORECKI DC DERRY JMJ BARNARD EA
Citation: Dc. Gorecki et al., DYSTROGLYCAN - BRAIN LOCALIZATION AND CHROMOSOME MAPPING IN THE MOUSE, Human molecular genetics, 3(9), 1994, pp. 1589-1597
ISOLATION OF A NOVEL GENE MUTATED IN WISKOTT-ALDRICH SYNDROME
Authors: DERRY JMJ OCHS HD FRANCKE U
Citation: Jmj. Derry et al., ISOLATION OF A NOVEL GENE MUTATED IN WISKOTT-ALDRICH SYNDROME, Cell, 78(4), 1994, pp. 635-644
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