16 results on '"Yamasaki, Mami"'
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2. Novel MCA/ID syndrome with ASH1L mutation
3. Role of a heterotrimeric G-protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability
4. Novel splicing mutation in theASXL3gene causing Bainbridge-Ropers syndrome
5. Prenatal molecular diagnosis of X-linked hydrocephalus via a silent C924T mutation in theL1CAMgene
6. Brain malformation with loss of normal FGFR3 expression in thanatophoric dysplasia type I
7. Phenotypic Spectrum ofCOL4A1Mutations: Porencephaly to Schizencephaly
8. Hydrocephalus with Hirschsprung disease: Severe end of X-linked hydrocephalus spectrum
9. ABCB1 is predominantly expressed in human fetal neural stem/progenitor cells at an early development stage
10. Two new cases of pure 1q terminal deletion presenting with brain malformations
11. Effect of neurosphere size on the growth rate of human neural stem/progenitor cells
12. First case of L1CAM gene mutation identified in MASA syndrome in Asia
13. Characterization of ABC transporter ABCB1 expressed in human neural stem/progenitor cells
14. Human neural stem/progenitor cells, expanded in long‐term neurosphere culture, promote functional recovery after focal ischemia in Mongolian gerbils
15. Evaluation of in vitro proliferative activity of human fetal neural stem/progenitor cells using indirect measurements of viable cells based on cellular metabolic activity
16. Isolation and expression analysis of a novel human homologue of theDrosophila glial cells missing(gcm) gene
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