スポンサーリンク
Department of Medical Genetics, Tohoku University School of Medicine | 論文
- Stable Expression of the Motor Protein Prestin in Chinese Hamster Ovary Cells(Bioengineering)
- Anaplastic ganglioglioma with sarcomatous component : An immunohistochemical study and molecular analysis of p53 tumor suppressor gene
- Hypercalcemia due to all-trans retinoic acid therapy for acute promyelocytic leukemia : A case report of effective treatment with bisphosphonate
- Association of the RIP2 Gene with Childhood Atopic Asthma
- Association between genetic variation in the gene for death-associated protein-3 (DAP3) and adult asthma
- Hypospadias in a Male Patient with 21-hydroxylase Deficiency
- Neonatal-Onset Brainstem Reticular Reflex Myoclonus Following a Prenatal Brain Insult : Generalized Myoclonic Jerk and a Brainstem Lesion
- An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway
- Serum Nutritional Status of Tocopherol and Retinol Normalized to Lipids of Persons Living in the Southern Rural Terai Region in Nepal
- Clinical characterization of familial dilated cardiomyopathy with conduction defect caused by a novel lamin A/C gene mutation
- Proteolytic Activation of Single-chain Tissue-type Plasminogen Activator by Protease/α_2-Macroglobulin Complex Isolated from Human Ovarian Follicular Fluid(Endocrinology)
- Rapid Multiplexing and Simultaneous Detection of Human Spermatogenetic Failure with a 12 Lane Microchip Electrophoresis System(Analytical Biochemistry)
- A Case of Basal Cell Adenocarcinoma of the Parotid Gland
- A Case of Leiomyosarcoma of the Sphenoid Sinus
- Artificial Neural Network Predictive Model for Allergic Disease Using Single Nucleotide Polymorphisms Data
- Ultrasonographic Findings in Neonates Screened for Congenital Hypothyroidism
- A possible mechanism of neonatal intrahepatic cholestasis caused by citrin deficiency
- Novel missense mutation (R94S) in the TAZ (G4.5) gene in a Japanese patient with Barth syndrome
- Spermatogenic ability is different among males in different Y chromosome lineage
- B-56. Clinical Significance of Early Epilepsy