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Results:
1-12
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Results: 12
Authors:
KRUDE H
BIEBERMANN H
LUCK W
HORN R
BRABANT G
GRUTERS A
Citation: H. Krude et al., SEVERE EARLY-ONSET OBESITY, ADRENAL INSUFFICIENCY AND RED HAIR PIGMENTATION CAUSED BY POMC MUTATIONS IN HUMANS, Nature genetics, 19(2), 1998, pp. 155-157
Authors:
SCHONEBERG T
SCHULZ A
BIEBERMANN H
GRUTERS A
GRIMM T
HUBSCHMANN K
FILLER G
GUDERMANN T
SCHULTZ G
Citation: T. Schoneberg et al., V2 VASOPRESSIN RECEPTOR DYSFUNCTION IN NEPHROGENIC DIABETES-INSIPIDUSCAUSED BY DIFFERENT MOLECULAR MECHANISMS, Human mutation, 12(3), 1998, pp. 196-205
Authors:
BIEBERMANN H
SCHONEBERG T
SCHULZ A
KRAUSE G
GRUTERS A
SCHULTZ G
GUDERMANN T
Citation: H. Biebermann et al., A CONSERVED TYROSINE RESIDUE (Y601) IN TRANSMEMBRANE DOMAIN-5 OF THE HUMAN THYROTROPIN RECEPTOR SERVES AS A MOLECULAR SWITCH TO DETERMINE G-PROTEIN COUPLING, The FASEB journal, 12(14), 1998, pp. 1461-1471
Authors:
GUDERMANN T
BIEBERMANN H
SCHONEBERG T
SCHULZ A
KRAUSE G
GRUTERS A
SCHULTZ G
Citation: T. Gudermann et al., A CONSERVED TYROSINE RESIDUE (Y601) IN TRANSMEMBRANE DOMAIN-5 DETERMINES G-PROTEIN COUPLING OF THE HUMAN THYROTROPIN RECEPTOR, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 2113-2113
Authors:
GUDERMANN T
BIEBERMANN H
SCHONEBERG T
SCHULZ A
DRECHSLER K
KRAUSE G
GRUTERS A
SCHULTZ G
Citation: T. Gudermann et al., A CONSERVED TYROSINE RESIDUE (Y601) IN THE HUMAN THYROTROPIN RECEPTORIS ESSENTIAL FOR CONSTITUTIVE ACTIVITY AND DUAL COUPLING POTENTIAL, Naunyn-Schmiedeberg's archives of pharmacology, 357(4), 1998, pp. 201-201
Authors:
GRUTERS A
SCHONEBERG T
BIEBERMANN H
KRUDE H
KROHN HP
DRALLE K
GUDERMANN T
Citation: A. Gruters et al., SEVERE CONGENITAL HYPERTHYROIDISM CAUSED BY A GERM-LINE NEO MUTATION IN THE EXTRACELLULAR PORTION OF THE THYROTROPIN RECEPTOR, The Journal of clinical endocrinology and metabolism, 83(5), 1998, pp. 1431-1436
Authors:
KRUDE H
BIEBERMANN H
KROHN HP
DRALLE H
GRUTERS A
Citation: H. Krude et al., CONGENITAL HYPERTHYROIDISM, EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 105, 1997, pp. 6-11
Authors:
BIEBERMANN H
GRUTERS A
SCHONEBERG T
GUDERMANN T
Citation: H. Biebermann et al., CONGENITAL HYPOTHYROIDISM CAUSED BY MUTATIONS IN THE THYROTROPIN-RECEPTOR GENE, The New England journal of medicine, 336(19), 1997, pp. 1390-1391
Authors:
BIEBERMANN H
SCHONEBERG T
KRUDE H
SCHULTZ G
GUDERMANN T
GRUTERS A
Citation: H. Biebermann et al., MUTATIONS OF THE HUMAN THYROTROPIN RECEPTOR GENE CAUSING THYROID HYPOPLASIA AND PERSISTENT CONGENITAL HYPOTHYROIDISM, The Journal of clinical endocrinology and metabolism, 82(10), 1997, pp. 3471-3480
Authors:
KRUDE H
BIEBERMANN H
GOPEL W
GRUTERS A
Citation: H. Krude et al., THE GENE FOR THE THYROTROPIN RECEPTOR (TSHR) AS A CANDIDATE GENE FOR CONGENITAL HYPOTHYROIDISM WITH THYROID DYSGENESIS, EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 104, 1996, pp. 117-120
Authors:
GRUTERS A
KOHLER B
WOLF A
SOLING A
DEVIJLDER L
KRUDE H
BIEBERMANN H
Citation: A. Gruters et al., SCREENING FOR MUTATIONS OF THE HUMAN THYROID PEROXIDASE GENE IN PATIENTS WITH CONGENITAL HYPOTHYROIDISM, EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES, 104, 1996, pp. 121-123
Authors:
KOHLER B
SCHNABEL D
BIEBERMANN H
GRUTERS A
Citation: B. Kohler et al., TRANSIENT CONGENITAL HYPOTHYROIDISM AND HYPERTHYROTROPINEMIA - NORMALTHYROID-FUNCTION AND PHYSICAL DEVELOPMENT AT THE AGES OF 6-14 YEARS, The Journal of clinical endocrinology and metabolism, 81(4), 1996, pp. 1563-1567
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