Shima Eda相关文献与解析，生知库 | 链接生命科学的每一步

A Novel Constitutively Active c.98 G > C, p.(R33P) Variant in RAB11A Associated with Intellectual Disability Promotes Neuritogenesis and Affects Oligodendroglial Arborization

RAB11A基因中一种与智力障碍相关的新型组成型活性变异c.98 G > C, p.(R33P)促进神经突起生成并影响少突胶质细胞树突化

doi:10.1155/2023/8126544

Yumi Tsuneura,Taeko Kawai,Keitaro Yamada,Shintaro Aoki,Mitsuko Nakashima,Shima Eda,Tohru Matsuki,Masashi Nishikawa,Koh-Ichi Nagata,Yasushi Enokido,Hirotomo Saitsu,Atsuo Nakayama

Knockdown of Son, a mouse homologue of the ZTTK syndrome gene, causes neuronal migration defects and dendritic spine abnormalities

Son（ZTTK 综合征基因的小鼠同源物）的敲低会导致神经元迁移缺陷和树突棘异常

期刊:Molecular Brain

影响因子:3.3

doi:10.1186/s13041-020-00622-4

Masashi Ueda, Tohru Matsuki, Masahide Fukada, Shima Eda, Akie Toya, Akio Iio, Hidenori Tabata, Atsuo Nakayama

神经

发表日期：2020

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Identification of novel compound heterozygous mutations in ACO2 in a patient with progressive cerebral and cerebellar atrophy

在患有进行性大脑和小脑萎缩的患者中鉴定出 ACO2 中的新型复合杂合突变

期刊:Molecular Genetics & Genomic Medicine

影响因子:1.5

doi:10.1002/mgg3.698

Masahide Fukada, Keitaro Yamada, Shima Eda, Ken Inoue, Chihiro Ohba, Naomichi Matsumoto, Hirotomo Saitsu, Atsuo Nakayama

Generation of Bradyrhizobium japonicum mutants with increased N2O reductase activity by selection after introduction of a mutated dnaQ gene

通过导入突变的dnaQ基因并进行筛选，获得N2O还原酶活性增强的日本根瘤菌突变体

期刊:

影响因子:3.9

doi:10.1128/AEM.01850-08.

Manabu Itakura,Kazufumi Tabata, Shima Eda, Hisayuki Mitsui, Kiriko Murakami, Junichi Yasuda, Kiwamu Minamisawa

发表日期：2008

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The MCPH7 Gene Product STIL Is Essential for Dendritic Spine Formation

MCPH7基因产物STIL对树突棘的形成至关重要

The distribution of neuroligin4, an autism-related postsynaptic molecule, in the human brain

自闭症相关突触后分子神经连接素 4 在人类大脑中的分布

A Novel Constitutively Active c.98 G > C, p.(R33P) Variant in RAB11A Associated with Intellectual Disability Promotes Neuritogenesis and Affects Oligodendroglial Arborization

RAB11A基因中一种与智力障碍相关的新型组成型活性变异c.98 G > C, p.(R33P)促进神经突起生成并影响少突胶质细胞树突化

Knockdown of Son, a mouse homologue of the ZTTK syndrome gene, causes neuronal migration defects and dendritic spine abnormalities

Son（ZTTK 综合征基因的小鼠同源物）的敲低会导致神经元迁移缺陷和树突棘异常

Identification of novel compound heterozygous mutations in ACO2 in a patient with progressive cerebral and cerebellar atrophy

在患有进行性大脑和小脑萎缩的患者中鉴定出 ACO2 中的新型复合杂合突变

Generation of Bradyrhizobium japonicum mutants with increased N2O reductase activity by selection after introduction of a mutated dnaQ gene

通过导入突变的dnaQ基因并进行筛选，获得N2O还原酶活性增强的日本根瘤菌突变体