スポンサーリンク
Department of Pediatrics, Yamagata University School of Medicine | 論文
- Changes in physicochemical properties of microtubules lead to the formation of a single spherical structure of mitochondrial assembly enveloping nuclear chromatins
- Role of mitochondria in the switch mechanism of the cell death mode from apoptosis to necrosis-Studies on ρ^0 cells
- Crystal Structures of Sulochrin Derivatives
- Three patients with different phenotypes in a family with chromosome 22q11.2 deletions
- Abnormal glucose metabolism in aromatic L-amino acid decarboxylase deficiency
- A case of Baraitser-Winter syndrome with unusual brain MRI findings : Pachygyria, subcortical-band heterotopia, and periventricular heterotopia
- Combination effect of a TGF-β receptor kinase inhibitor with 5-FU analog S1 on lymph node metastasis of scirrhous gastric cancer in mice
- Terminal deletion of chromosome 10q : Clinical features and literature review
- Angiographic Determination of Left and Right Ventricular Volumes and Left Ventricular Mass in Normal Infants and Children
- Lipoblastoma with aberration in the long arm of chromosome 8
- The Jeune syndrome in a sister and younger brother
- Clinical Evaluation of Recombinant Human Growth Hormone in Noonan Syndrome
- A case of progressive familial intrahepatic cholestasis type 1 with compound heterozygous mutations of ATP8B1
- Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome
- Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan
- Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease : nonsense mutation probably causes a recessive phenotype
- Phenotypic variability in a family with Townes-Brocks syndrome
- Compound heterozygous PMP22 deletion mutations causing severe Charcot-Marie-Tooth disease type 1
- Association of vitamin D-related gene polymorphisms with manifestation of vitamin D deficiency in children
- Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms : 211G>A (G71R) mutation becomes a risk factor under inadequate feeding