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Results: 1-15 |
Results: 15
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
CHANGES IN SERUM IGF-I AND IGFBP-3 CONCENTRATIONS DURING THE IGF-I GENERATION TEST PERFORMED PROSPECTIVELY IN CHILDREN WITH SHORT STATURE
Authors: COTTERILL AM CAMACHOHUBNER C DUQUESNOY P SAVAGE MO
Citation: Am. Cotterill et al., CHANGES IN SERUM IGF-I AND IGFBP-3 CONCENTRATIONS DURING THE IGF-I GENERATION TEST PERFORMED PROSPECTIVELY IN CHILDREN WITH SHORT STATURE, Clinical endocrinology, 48(6), 1998, pp. 719-724
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
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
A NEW C-KIT MUTATION IN A CASE OF AGGRESSIVE MAST-CELL DISEASE
Authors: PIGNON JM GIRAUDIER S DUQUESNOY P JOUAULT H IMBERT M VAINCHENKER W VERNANT JP TULLIEZ M
Citation: Jm. Pignon et al., A NEW C-KIT MUTATION IN A CASE OF AGGRESSIVE MAST-CELL DISEASE, British Journal of Haematology, 96(2), 1997, pp. 374-376
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
NEW C-KIT MUTATION IN A CASE OF AGGRESSIVE MAST-CELL DISEASE
Authors: PIGNON JM GIRAUDIER G DUQUESNOY P JOUAULT H IMBERT M VAINCHENKER W VERNANT JP TULLIEZ M
Citation: Jm. Pignon et al., NEW C-KIT MUTATION IN A CASE OF AGGRESSIVE MAST-CELL DISEASE, Blood, 88(10), 1996, pp. 381-381
THE INSULIN-LIKE GROWTH-FACTOR-I GENERATION TEST IN THE INVESTIGATIONOF SHORT STATURE
Authors: COTTERILL AM CAMACHOHUBNER C WOODS K MARTINELLI C DUQUESNOY P SAVAGE MO
Citation: Am. Cotterill et al., THE INSULIN-LIKE GROWTH-FACTOR-I GENERATION TEST IN THE INVESTIGATIONOF SHORT STATURE, Acta paediatrica, 83, 1994, pp. 128-130
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
ISOLATED GROWTH-HORMONE DEFICIENCY TYPE IA ASSOCIATED WITH A 45-KILOBASE GENE DELETION WITHIN THE HUMAN GROWTH-HORMONE GENE-CLUSTER IN AN ITALIAN FAMILY
Authors: GHIZZONI L DUQUESNOY P TORRESANI T VOTTERO A GOOSSENS M BERNASCONI S
Citation: L. Ghizzoni et al., ISOLATED GROWTH-HORMONE DEFICIENCY TYPE IA ASSOCIATED WITH A 45-KILOBASE GENE DELETION WITHIN THE HUMAN GROWTH-HORMONE GENE-CLUSTER IN AN ITALIAN FAMILY, Pediatric research, 36(5), 1994, pp. 654-659
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
A HOMOZYGOUS INSERTION-DELETION IN THE TYPE-VII COLLAGEN GENE (COL7A1) IN HALLOPEAU-SIEMENS DYSTROPHIC EPIDERMOLYSIS-BULLOSA
Authors: HILAL L ROCHAT A DUQUESNOY P BLANCHETBARDON C WECHSLER J MARTIN N CHRISTIANO AM BARRANDON Y UITTO J GOOSSENS M HOVNANIAN A
Citation: L. Hilal et al., A HOMOZYGOUS INSERTION-DELETION IN THE TYPE-VII COLLAGEN GENE (COL7A1) IN HALLOPEAU-SIEMENS DYSTROPHIC EPIDERMOLYSIS-BULLOSA, Nature genetics, 5(3), 1993, pp. 287-293
A NATURALLY-OCCURRING GROWTH-HORMONE RECEPTOR MUTATION - IN-VIVO AND IN-VITRO EVIDENCE FOR THE FUNCTIONAL IMPORTANCE OF THE WS MOTIF COMMONTO ALL MEMBERS OF THE CYTOKINE RECEPTOR SUPERFAMILY
Authors: DURIEZ B SOBRIER ML DUQUESNOY P TIXIERBOICHARD M DECUYPERE E COQUERELLE G ZEMAN M GOOSSENS M AMSELEM S
Citation: B. Duriez et al., A NATURALLY-OCCURRING GROWTH-HORMONE RECEPTOR MUTATION - IN-VIVO AND IN-VITRO EVIDENCE FOR THE FUNCTIONAL IMPORTANCE OF THE WS MOTIF COMMONTO ALL MEMBERS OF THE CYTOKINE RECEPTOR SUPERFAMILY, Molecular endocrinology, 7(6), 1993, pp. 806-814
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