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Results: 1-9 |
Results: 9
A DUPLICATED GENE IN THE BREAKPOINT REGIONS OF THE 7Q11.23 WILLIAMS-BEUREN-SYNDROME DELETION ENCODES THE INITIATOR BINDING-PROTEIN TFII-I AND BAP-135, A PHOSPHORYLATION TARGET OF BTK
Authors: JURADO LAP WANG YK PEOPLES R COLOMA A CRUCES J FRANCKE U
Citation: Lap. Jurado et al., A DUPLICATED GENE IN THE BREAKPOINT REGIONS OF THE 7Q11.23 WILLIAMS-BEUREN-SYNDROME DELETION ENCODES THE INITIATOR BINDING-PROTEIN TFII-I AND BAP-135, A PHOSPHORYLATION TARGET OF BTK, Human molecular genetics, 7(3), 1998, pp. 325-334
A NOVEL HUMAN HOMOLOG OF THE DROSOPHILA FRIZZLED WNT RECEPTOR GENE BINDS WINGLESS PROTEIN AND IS IN THE WILLIAMS-SYNDROME DELETION AT 7Q11.23
Authors: WANG YK SAMOS CH PEOPLES R PEREZJURADO LA NUSSE R FRANCKE U
Citation: Yk. Wang et al., A NOVEL HUMAN HOMOLOG OF THE DROSOPHILA FRIZZLED WNT RECEPTOR GENE BINDS WINGLESS PROTEIN AND IS IN THE WILLIAMS-SYNDROME DELETION AT 7Q11.23, Human molecular genetics, 6(3), 1997, pp. 465-472
LOCALIZATION OF THE HUMAN HIP1 GENE CLOSE TO THE ELASTIN (ELN) LOCUS ON 7Q11.23
Authors: WEDEMEYER N PEOPLES R HIMMELBAUER H LEHRACH H FRANCKE U WANKER EE
Citation: N. Wedemeyer et al., LOCALIZATION OF THE HUMAN HIP1 GENE CLOSE TO THE ELASTIN (ELN) LOCUS ON 7Q11.23, Genomics, 46(2), 1997, pp. 313-315
MOLECULAR DEFINITION OF THE CHROMOSOME-7 DELETION IN WILLIAMS-SYNDROME AND PARENT-OF-ORIGIN EFFECTS ON GROWTH
Authors: JURADO LAP PEOPLES R KAPLAN P HAMEL BCJ FRANCKE U
Citation: Lap. Jurado et al., MOLECULAR DEFINITION OF THE CHROMOSOME-7 DELETION IN WILLIAMS-SYNDROME AND PARENT-OF-ORIGIN EFFECTS ON GROWTH, American journal of human genetics, 59(4), 1996, pp. 781-792
THE GENE FOR REPLICATION FACTOR-C SUBUNIT-2 (RFC2) IS WITHIN THE 7Q11.23 WILLIAMS-SYNDROME DELETION
Authors: PEOPLES R PEREZJURADO L WANG YK KAPLAN P FRANCKE U
Citation: R. Peoples et al., THE GENE FOR REPLICATION FACTOR-C SUBUNIT-2 (RFC2) IS WITHIN THE 7Q11.23 WILLIAMS-SYNDROME DELETION, American journal of human genetics, 58(6), 1996, pp. 1370-1373
HEMIZYGOSITY AT THE INSULIN-LIKE GROWTH-FACTOR-I RECEPTOR (IGF1R) LOCUS AND GROWTH FAILURE IN THE RING CHROMOSOME-15 SYNDROME
Authors: PEOPLES R MILATOVICH A FRANCKE U
Citation: R. Peoples et al., HEMIZYGOSITY AT THE INSULIN-LIKE GROWTH-FACTOR-I RECEPTOR (IGF1R) LOCUS AND GROWTH FAILURE IN THE RING CHROMOSOME-15 SYNDROME, Cytogenetics and cell genetics, 70(3-4), 1995, pp. 228-234
GENETIC AND PHYSICAL MAPPING OF THE WILLIAMS-SYNDROME DELETION IN 57 PATIENTS DEFINES COMMON BREAKPOINTS
Authors: PEOPLES R JURADO LAP KAPLAN P FRANCKE U
Citation: R. Peoples et al., GENETIC AND PHYSICAL MAPPING OF THE WILLIAMS-SYNDROME DELETION IN 57 PATIENTS DEFINES COMMON BREAKPOINTS, American journal of human genetics, 57(4), 1995, pp. 1293-1293
RECEPTOR MUTATIONS AND HAPLOTYPES IN GROWTH-HORMONE RECEPTOR DEFICIENCY - A GLOBAL SURVEY AND IDENTIFICATION OF THE ECUADORIAN E180SPLICE MUTATION IN AN ORIENTAL JEWISH PATIENT
Authors: BERG MA PEOPLES R PEREZJURADO L GUEVARAAGUIRRE J ROSENBLOOM AL LARON Z MILNER RDG FRANCKE U
Citation: Ma. Berg et al., RECEPTOR MUTATIONS AND HAPLOTYPES IN GROWTH-HORMONE RECEPTOR DEFICIENCY - A GLOBAL SURVEY AND IDENTIFICATION OF THE ECUADORIAN E180SPLICE MUTATION IN AN ORIENTAL JEWISH PATIENT, Acta paediatrica, 83, 1994, pp. 112-114
ENDOR AND ESEEM INVESTIGATION OF AG-2(I)CU-2(II) BOVINE SUPEROXIDE-DISMUTASE
Authors: GURBIEL RJ PEOPLES R DOAN PE CLINE JF MCCRACKEN J PEISACH J HOFFMAN BM VALENTINE JS
Citation: Rj. Gurbiel et al., ENDOR AND ESEEM INVESTIGATION OF AG-2(I)CU-2(II) BOVINE SUPEROXIDE-DISMUTASE, Inorganic chemistry, 32(9), 1993, pp. 1813-1819
Risultati: 1-9 |