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Results: 1-11 |
Results: 11
SEQUENCE-ANALYSIS OF THYROID TRANSCRIPTION FACTOR-I GENE REVEALS ABSENCE OF MUTATIONS IN PATIENTS WITH THYROID DYSGENESIS BUT PRESENCE OF POLYMORPHISMS IN THE 5'-FLANKING REGION AND INTRON
Authors: HISHINUMA A KURIBAYASHI T KANNO Y ONIGATA K NAGASHIMA K IEIRI T
Citation: A. Hishinuma et al., SEQUENCE-ANALYSIS OF THYROID TRANSCRIPTION FACTOR-I GENE REVEALS ABSENCE OF MUTATIONS IN PATIENTS WITH THYROID DYSGENESIS BUT PRESENCE OF POLYMORPHISMS IN THE 5'-FLANKING REGION AND INTRON, Endocrine journal, 45(4), 1998, pp. 563-567
A NEW COMPOUND HETEROZYGOUS MUTATION (W17X, 436-]T) IN THE CYTOCHROMEP450C17 GENE CAUSES 17-ALPHA-HYDROXYLASE(5G)17,20-LYASE DEFICIENCY/
Authors: SUZUKI Y NAGASHIMA T NOMURA Y ONIGATA K NAGASHIMA K MORIKAWA A
Citation: Y. Suzuki et al., A NEW COMPOUND HETEROZYGOUS MUTATION (W17X, 436-]T) IN THE CYTOCHROMEP450C17 GENE CAUSES 17-ALPHA-HYDROXYLASE(5G)17,20-LYASE DEFICIENCY/, The Journal of clinical endocrinology and metabolism, 83(1), 1998, pp. 199-202
A NOVEL POINT MUTATION OF THYROID-HORMONE RECEPTOR-BETA GENE IN A FAMILY WITH RESISTANCE TO THYROID-HORMONE
Authors: NAGASHIMA T YAGI H NAGASHIMA K SAKURAI A ONIGATA K NOMURA Y MORIKAWA A MATAZOW G COUCH RM WEISS RE REFETOFF S
Citation: T. Nagashima et al., A NOVEL POINT MUTATION OF THYROID-HORMONE RECEPTOR-BETA GENE IN A FAMILY WITH RESISTANCE TO THYROID-HORMONE, Thyroid, 7(5), 1997, pp. 771-773
DETECTION OF SKEWED X-INACTIVATION IN 2 FEMALE CARRIERS OF VASOPRESSIN TYPE-2 RECEPTOR GENE MUTATION
Authors: NOMURA Y ONIGATA K NAGASHIMA T YUTANI S MOCHIZUKI H NAGASHIMA K MORIKAWA A
Citation: Y. Nomura et al., DETECTION OF SKEWED X-INACTIVATION IN 2 FEMALE CARRIERS OF VASOPRESSIN TYPE-2 RECEPTOR GENE MUTATION, The Journal of clinical endocrinology and metabolism, 82(10), 1997, pp. 3434-3437
IDENTIFICATION OF MUTATIONS IN THE HEPATOCYTE NUCLEAR FACTOR (HNF)-1-ALPHA GENE IN JAPANESE SUBJECTS WITH IDDM
Authors: YAMADA S NISHIGORI H ONDA H UTSUGI T YANAGAWA T MARUYAMA T ONIGATA K NAGASHIMA K NAGAI R MORIKAWA A TAKEUCHI T TAKEDA J
Citation: S. Yamada et al., IDENTIFICATION OF MUTATIONS IN THE HEPATOCYTE NUCLEAR FACTOR (HNF)-1-ALPHA GENE IN JAPANESE SUBJECTS WITH IDDM, Diabetes, 46(10), 1997, pp. 1643-1647
A NOVEL POINT MUTATION (R243Q) IN EXON-7 OF THE C-ERBA-BETA THYROID-HORMONE RECEPTOR GENE IN A FAMILY WITH RESISTANCE TO THYROID-HORMONE (VOL 5, PG 355, 1995)
Authors: ONIGATA K YAGI H SAKURAI A NAGASHIMA T NOMURA Y NAGASHIMA K HASHIZUME K MORIKAWA A
Citation: K. Onigata et al., A NOVEL POINT MUTATION (R243Q) IN EXON-7 OF THE C-ERBA-BETA THYROID-HORMONE RECEPTOR GENE IN A FAMILY WITH RESISTANCE TO THYROID-HORMONE (VOL 5, PG 355, 1995), Thyroid, 5(6), 1995, pp. 508-508
A NOVEL POINT MUTATION (R243Q) IN EXON-7 OF THE C-ERBA-BETA THYROID-HORMONE RECEPTOR GENE IN A FAMILY WITH RESISTANCE TO THYROID-HORMONE
Authors: ONIGATA K YAGI H SAKURAI A NAGASHIMA T NOMURA Y NAGASHIMA K HASHIZUME K MORIKAWA A
Citation: K. Onigata et al., A NOVEL POINT MUTATION (R243Q) IN EXON-7 OF THE C-ERBA-BETA THYROID-HORMONE RECEPTOR GENE IN A FAMILY WITH RESISTANCE TO THYROID-HORMONE, Thyroid, 5(5), 1995, pp. 355-358
FAMILIAL CONGENITAL HYPOPITUITARISM WITH CENTRAL DIABETES-INSIPIDUS
Authors: YAGI H NAGASHIMA K MIYAKE H TAMAI S ONIGATA K YUTANI S KUROUME T
Citation: H. Yagi et al., FAMILIAL CONGENITAL HYPOPITUITARISM WITH CENTRAL DIABETES-INSIPIDUS, The Journal of clinical endocrinology and metabolism, 78(4), 1994, pp. 884-889
RELATIONSHIP BETWEEN SERUM LEVELS OF METHYLGUANIDINE AND GLYCEMIC CONTROL IN IDDM CHILDREN
Authors: NAGASHIMA K YAGI H YUTANI S MIYAKE H ONIGATA K KUROUME T
Citation: K. Nagashima et al., RELATIONSHIP BETWEEN SERUM LEVELS OF METHYLGUANIDINE AND GLYCEMIC CONTROL IN IDDM CHILDREN, Diabetes care, 16(8), 1993, pp. 1196-1198
LIPOPROTEIN(A) LEVELS IN JAPANESE CHILDREN WITH IDDM
Authors: NAGASHIMA K YUTANI S MIYAKE H ONIGATA K YAGI H KUROUME T
Citation: K. Nagashima et al., LIPOPROTEIN(A) LEVELS IN JAPANESE CHILDREN WITH IDDM, Diabetes care, 16(5), 1993, pp. 846-846
TRANSPORT OF TRIIODOTHYRONINE BY ERYTHROCYTES FROM PREMATURE AND TERMINFANTS
Authors: NAGASHIMA K ONIGATA K YAGI H KUROUME T
Citation: K. Nagashima et al., TRANSPORT OF TRIIODOTHYRONINE BY ERYTHROCYTES FROM PREMATURE AND TERMINFANTS, Biology of the neonate, 64(6), 1993, pp. 354-359
Risultati: 1-11 |