16 results on '"Morisaki, Hiroko"'
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2. Mutation of ACTA2 Gene as an Important Cause of Familial and Nonfamilial Nonsyndromatic Thoracic Aortic Aneurysm and/or Dissection (TAAD)
3. Mutations of the TGF-β Type II Receptor BMPR2 in Pulmonary Arterial Hypertension
4. A mutation update on the LDS-associated genesTGFB2/3andSMAD2/3
5. CDH13 gene coding t-cadherin influences variations in plasma adiponectin levels in the Japanese population
6. Mutation ofACTA2gene as an important cause of familial and nonfamilial nonsyndromatic thoracic aortic aneurysm and/or dissection (TAAD)
7. Mutations of the TGF-β type II receptorBMPR2 in pulmonary arterial hypertension
8. BMPR2 mutations found in Japanese patients with familial and sporadic primary pulmonary hypertension
9. Erratum:BMPR2 mutations found in Japanese patients with familial and sporadic primary pulmonary hypertension
10. Two novel polymorphisms g.1715G>A (A496T) and g.1838G>A (3?UTR), and the g.1548G>A (E469K) variant in the intercellular adhesion molecule 1 (ICAM1) gene: Distribution in the Japanese and European American populations
11. Population analysis of g.2488delG and three novel polymorphisms (g.4497G>A, g.4503G>A and g.2319G>A) in the plasminogen activator inhibitor 1 (PAI-1) gene
12. First missense mutations (R388W and R425H) of AMPD1 accompanied with myopathy found in a Japanese patient
13. Eight novel mutations of theFBN1 gene found in Japanese patients with Marfan syndrome
14. Eight novel mutations of the FBN1 gene found in Japanese patients with Marfan syndrome.
15. Erratum: BMPR2 mutations found in Japanese patients with familial and sporadic primary pulmonary hypertension.
16. Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertension.
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