50 ASSOCIATION STUDY OF HUMAN MUT T HOMOLOGUE 1 GENE VAL83MET POLYMORPHISM WITH TYPE 1 DIABETES MELLrrus.
スポンサーリンク
概要
著者
-
Matsuura N
Department Of Life Science Okayama University Of Science
-
Kohno H
Department Of Endocrinology And Metabolism Fukuoka Children's Hospital
-
Ihara K
Department Of Pediatrics Graduate School Of Medical Sciences Kyushu University
-
Hara T
Department Of Anatomy Tokyo Dental College
-
Kuromaru R
Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University
-
Kuromaru R
Department Of Pediatrics Graduate School Of Medical Sciences Kyushu University
-
Miyak K
Department of Endocrinology and Metabolism, Fukuoka children's Hospital
-
Miyak K
Department Of Endocrinology And Metabolism Fukuoka Children's Hospital:department Of Pediatrics
関連論文
- インスリン微量変動法の血糖コントロールに対する有効性の検討
- Hyaline vascular-type Castleman's disease in the hepatoduodenal ligament : Report of a case
- Indocarbazostatins C and D, New Inhibitors of NGF-induced Neuronal Differentiation in PC12 Cells
- Synthesis and Activity of Pyrimidinylpropenamide Antibiotics : The Alkyl Analogues of Sparsomycin(Organic Chemistry)
- Indocarbazostatin and Indocarbazostatin B, Novel Inhibitors of NGF-induced Neuronal Differentiation in PC12 Cells : II. Isolation, Physicochemical Properties and Structural Elucidation
- Indocarbazostatin and Indocarbazostatin B, Novel Inhibitors of NGF-induced Neuronal Differentiation in PC12 Cells : I. Screening, Taxonomy, Fermentation and Biological Activities
- Indocardazostatin, a Novel Inhibitor of NGF-induced Neurite Outgrowth from Rat Pheochromocytoma PC12 Cells
- Inducible and endothelial constitutive nitric oxide synthase gene polymorphisms in Kawasaki disease
- Novel polymorphism in the 5'-untranslated region of the interleukin-4 gene
- A Case of Growth Hormone and Gonadotropin Deficiency Associated with Unilateral Anophthalmia, Microphallus, Cryptorchidism, and Mental Retardation
- Long-Term Effect of Growth hormone (GH) Treatment on Body Composition in Children with GH Deficiency
- Cloning of the Gene Cluster Responsible for the Biosynthesis of Brasilicardin A, a Unique Diterpenoid
- Presence of Copalyl Diphosphate Synthase Gene in an Actinomycete Possessing the Mevalonate Pathway
- Molecular epidemiology of C9 deficiency heterozygotes with an Arg95Stop mutation of the C9 gene in Japan
- Primary Adult T-Cell Leukemia/Lymphoma of Bone
- A Morphological Study of the Apical Third of the Root Canal in the Maxillary First Premolar using Micro-CT
- Vitamin D deficiency rickets caused by improper lifestyle in Japanese children
- Two Cases of Allgrove Syndrome with Mutations in the AAAS Gene
- 34 THIAMAZOL OR PROPILTHIOURACIL AND L-T4 COMBINATION THERAPY FOR INFANTS BORN TO MOTHER WITH GRAVES' DISEASE
- 46 GENETIC ANALYSIS IN PATIENTS WITH CONGENITAL NEPHROGENIC DIABETES INSIPIDUS
- 48 DIAGNOSIS OF MILD CONGENIAL HYPOTHYROIDISM ETIOLOGY OF THE DISEASE AND CONFIRMATORY TEST PERFORMED BY COUNCIL MEMBERS OF THE JSPE FOR DIAGNOSIS OF THE DISEASE
- 54 TWO PUBERTAL BOYS WITH IMPAIRED GLUCOSE TOLERANCE AND THRIFTY PHENOTYPE
- 145 PROSECTIVE STUDY OF BODY COMPOSITION AND LIPID PROFILES DURING GROWTH HORMONE TREATMENT IN CHILDREN WITE TURNER SYNDROME
- 37 2 CACES OF ALLGROVE SYNDROME WITH A MUTATION IN THE AAAS GENE
- 85 POSTPRANDIAL INJECTION OF A RAPID-ACTING INSULIN ANALOG IN 'CLOSE ADJUSTMENT SLIDING SCALE'
- 50 ASSOCIATION STUDY OF HUMAN MUT T HOMOLOGUE 1 GENE VAL83MET POLYMORPHISM WITH TYPE 1 DIABETES MELLrrus.
- 179 α-TUBULIN GENE EXPRESSION IN THE BRAIN OF rdw RATS WITH CONGENITAL HYPOTHYROIDISM