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Results: 1-13 |
Results: 13
HETEROZYGOUS MUTATION IN THE WSXWS EQUIVALENT MOTIF OF THE GROWTH-HORMONE RECEPTOR IN A CHILD WITH POOR RESPONSE TO GROWTH-HORMONE THERAPY
Authors: TAUBER MT PORRA V DASTOT F MOLINAS C AMSELEM S CHOLIN S ROCHICCIOLI P BIETH E
Citation: Mt. Tauber et al., HETEROZYGOUS MUTATION IN THE WSXWS EQUIVALENT MOTIF OF THE GROWTH-HORMONE RECEPTOR IN A CHILD WITH POOR RESPONSE TO GROWTH-HORMONE THERAPY, Growth hormone & IGF research, 8(3), 1998, pp. 211-216
EVOLUTIONARY DIVERGENCE OF THE TRUNCATED GROWTH-HORMONE (GH) RECEPTORISOFORM IN ITS ABILITY TO GENERATE A SOLUBLE GH BINDING-PROTEIN (VOL 137, PG 79, 1998)
Authors: DASTOT F DUQUESNOY P SOBRIER ML GOOSSENS M AMELEM S
Citation: F. Dastot et al., EVOLUTIONARY DIVERGENCE OF THE TRUNCATED GROWTH-HORMONE (GH) RECEPTORISOFORM IN ITS ABILITY TO GENERATE A SOLUBLE GH BINDING-PROTEIN (VOL 137, PG 79, 1998), Molecular and cellular endocrinology, 141(1-2), 1998, pp. 195-195
EVOLUTIONARY DIVERGENCE OF THE TRUNCATED GROWTH-HORMONE RECEPTOR ISOFORM IN ITS ABILITY TO GENERATE A SOLUBLE GROWTH-HORMONE BINDING-PROTEIN
Authors: DASTOT F DUQUESNOY P SOBRIER ML GOOSSENS M AMSELEM S
Citation: F. Dastot et al., EVOLUTIONARY DIVERGENCE OF THE TRUNCATED GROWTH-HORMONE RECEPTOR ISOFORM IN ITS ABILITY TO GENERATE A SOLUBLE GROWTH-HORMONE BINDING-PROTEIN, Molecular and cellular endocrinology, 137(1), 1998, pp. 79-84
EXTENSIVE PHENOTYPIC ANALYSIS OF A FAMILY WITH GROWTH-HORMONE (GH) DEFICIENCY CAUSED BY A MUTATION IN THE GH-RELEASING HORMONE-RECEPTOR GENE
Authors: NETCHINE I TALON P DASTOT F VITAUX F GOOSSENS M AMSELEM S
Citation: I. Netchine et al., EXTENSIVE PHENOTYPIC ANALYSIS OF A FAMILY WITH GROWTH-HORMONE (GH) DEFICIENCY CAUSED BY A MUTATION IN THE GH-RELEASING HORMONE-RECEPTOR GENE, The Journal of clinical endocrinology and metabolism, 83(2), 1998, pp. 432-436
HUMAN PROP-1 - CLONING, MAPPING, GENOMIC STRUCTURE - MUTATIONS IN FAMILIAL COMBINED PITUITARY-HORMONE DEFICIENCY
Authors: DUQUESNOY P ROY A DASTOT F GHALI I TEINTURIER C NETCHINE Z CACHEUX V HAFEZ M SALAH N CHAUSSAIN JL GOOSSENS M BOUGNERES P AMSELEM S
Citation: P. Duquesnoy et al., HUMAN PROP-1 - CLONING, MAPPING, GENOMIC STRUCTURE - MUTATIONS IN FAMILIAL COMBINED PITUITARY-HORMONE DEFICIENCY, FEBS letters, 437(3), 1998, pp. 216-220
INTRONIC MUTATION IN THE GROWTH-HORMONE (GH) RECEPTOR GENE FROM A GIRL WITH LARON-SYNDROME AND EXTREMELY HIGH SERUM GH BINDING-PROTEIN - EXTENDED PHENOTYPIC STUDY IN A VERY LARGE PEDIGREE
Authors: SILBERGELD A DASTOT F KLINGER B KANETY H ESHET R AMSELEM S LARON Z
Citation: A. Silbergeld et al., INTRONIC MUTATION IN THE GROWTH-HORMONE (GH) RECEPTOR GENE FROM A GIRL WITH LARON-SYNDROME AND EXTREMELY HIGH SERUM GH BINDING-PROTEIN - EXTENDED PHENOTYPIC STUDY IN A VERY LARGE PEDIGREE, Journal of pediatric endocrinology & metabolism, 10(3), 1997, pp. 265-274
9 NOVEL GROWTH-HORMONE RECEPTOR GENE-MUTATIONS IN PATIENTS WITH LARONSYNDROME
Authors: SOBRIER ML DASTOT F DUQUESNOY P KANDEMIR N YORDAM N GOOSSENS M AMSELEM S
Citation: Ml. Sobrier et al., 9 NOVEL GROWTH-HORMONE RECEPTOR GENE-MUTATIONS IN PATIENTS WITH LARONSYNDROME, The Journal of clinical endocrinology and metabolism, 82(2), 1997, pp. 435-437
PHENOTYPE - GENOTYPE RELATIONSHIPS IN GROWTH-HORMONE INSENSITIVITY SYNDROME
Authors: WOODS KA DASTOT F PREECE MA CLARK AJL POSTELVINAY MC CHATELAIN PG RANKE MB ROSENFELD RG AMSELEM S SAVAGE MO
Citation: Ka. Woods et al., PHENOTYPE - GENOTYPE RELATIONSHIPS IN GROWTH-HORMONE INSENSITIVITY SYNDROME, The Journal of clinical endocrinology and metabolism, 82(11), 1997, pp. 3529-3535
A MEMBRANE-FIXED, TRUNCATED ISOFORM OF THE HUMAN GROWTH-HORMONE RECEPTOR
Authors: AMIT T BERGMAN T DASTOT F YOUDIM MBH AMSELEM S HOCHBERG Z
Citation: T. Amit et al., A MEMBRANE-FIXED, TRUNCATED ISOFORM OF THE HUMAN GROWTH-HORMONE RECEPTOR, The Journal of clinical endocrinology and metabolism, 82(11), 1997, pp. 3813-3817
MOLECULAR-BASIS OF INHERITED GROWTH-HORMONE RESISTANCE IN CHILDHOOD
Authors: AMSELEM S SOBRIER ML DASTOT F DUQUESNOY P DURIEZ B GOOSSENS M
Citation: S. Amselem et al., MOLECULAR-BASIS OF INHERITED GROWTH-HORMONE RESISTANCE IN CHILDHOOD, Bailliere's clinical endocrinology and metabolism, 10(3), 1996, pp. 353-369
ALTERNATIVELY SPLICED FORMS IN THE CYTOPLASMIC DOMAIN OF THE HUMAN GROWTH-HORMONE (GH) RECEPTOR REGULATE ITS ABILITY TO GENERATE A SOLUBLE GH-BINDING PROTEIN
Authors: DASTOT F SOBRIER ML DUQUESNOY P DURIEZ B GOOSSENS M AMSELEM S
Citation: F. Dastot et al., ALTERNATIVELY SPLICED FORMS IN THE CYTOPLASMIC DOMAIN OF THE HUMAN GROWTH-HORMONE (GH) RECEPTOR REGULATE ITS ABILITY TO GENERATE A SOLUBLE GH-BINDING PROTEIN, Proceedings of the National Academy of Sciences of the United Statesof America, 93(20), 1996, pp. 10723-10728
A SINGLE AMINO-ACID SUBSTITUTION IN THE EXOPLASMIC DOMAIN OF THE HUMAN GROWTH-HORMONE (GH) RECEPTOR CONFERS FAMILIAL GH RESISTANCE (LARON-SYNDROME) WITH POSITIVE GH-BINDING ACTIVITY BY ABOLISHING RECEPTOR HOMODIMERIZATION
Authors: DUQUESNOY P SOBRIER ML DURIEZ B DASTOT F BUCHANAN CR SAVAGE MO PREECE MA CRAESCU CT BLOUQUIT Y GOOSSENS M AMSELEM S
Citation: P. Duquesnoy et al., A SINGLE AMINO-ACID SUBSTITUTION IN THE EXOPLASMIC DOMAIN OF THE HUMAN GROWTH-HORMONE (GH) RECEPTOR CONFERS FAMILIAL GH RESISTANCE (LARON-SYNDROME) WITH POSITIVE GH-BINDING ACTIVITY BY ABOLISHING RECEPTOR HOMODIMERIZATION, EMBO journal, 13(6), 1994, pp. 1386-1395
AN EXON-SKIPPING MUTATION IN THE BTK GENE OF A PATIENT WITH X-LINKED AGAMMAGLOBULINEMIA AND ISOLATED GROWTH-HORMONE DEFICIENCY
Authors: DURIEZ B DUQUESNOY P DASTOT F BOUGNERES P AMSELEM S GOOSSENS M
Citation: B. Duriez et al., AN EXON-SKIPPING MUTATION IN THE BTK GENE OF A PATIENT WITH X-LINKED AGAMMAGLOBULINEMIA AND ISOLATED GROWTH-HORMONE DEFICIENCY, FEBS letters, 346(2-3), 1994, pp. 165-170
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