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1. Clinical and genetic characteristics of patients with Doose syndrome. Issue 3 (23rd July 2020)

2. De novo mutations in the X-linked TFE3 gene cause intellectual disability with pigmentary mosaicism and storage disorder-like features. Issue 12 (14th May 2020)

3. Depositional facies and sequence of the latest Pleistocene to Holocene incised valley fill in Kushiro Plain, Hokkaido, northern Japan. (18th March 2016)

6. Genetic defects in peroxisome morphogenesis (Pex11β, dynamin‐like protein 1, and nucleoside diphosphate kinase 3) affect docosahexaenoic acid‐phospholipid metabolism. Issue 2 (23rd December 2022)

8. Maternal ω3 docosapentaenoic acid inhibits infant allergic dermatitis through TRAIL‐expressing plasmacytoid dendritic cells in mice. Issue 8 (4th March 2020)