Role of a heterotrimeric G-protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability-Reference-Cited by-同舟云学术

Role of a heterotrimeric G-protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability

Published:2016-11-29 Issue:1 Volume:140 Page:82-95
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J. Neurochem.

Author:

Hamada Nanako¹²,Negishi Yutaka³,Mizuno Makoto¹,Miya Fuyuki⁴⁵,Hattori Ayako³,Okamoto Nobuhiko⁶,Kato Mitsuhiro⁷,Tsunoda Tatsuhiko⁴⁵,Yamasaki Mami⁸,Kanemura Yonehiro⁹¹⁰,Kosaki Kenjiro¹¹,Tabata Hidenori¹,Saitoh Shinji³,Nagata Koh-ichi¹¹²

Affiliation:

1. Department of Molecular Neurobiology; Institute for Developmental Research; Aichi Human Service Center; Kasugai Japan

2. Research Fellow of Japan Society for the Promotion of Science; Tokyo Japan

3. Department of Pediatrics and Neonatology; Nagoya City University Graduate School of Medical Sciences; Nagoya Japan

4. Department of Medical Science Mathematics; Medical Research Institute; Tokyo Medical and Dental University; Tokyo Japan

5. Laboratory for Medical Science Mathematics; RIKEN Center for Integrative Medical Sciences; Yokohama Japan

6. Department of Medical Genetics; Osaka Medical Center and Research Institute for Maternal and Child Health; Osaka Japan

7. Department of Pediatrics; Showa University School of Medicine; Tokyo Japan

8. Department of Neurosurgery; Takatsuki General Hospital; Osaka Japan

9. Division of Regenerative Medicine; Institute for Clinical Research; Osaka National Hospital; National Hospital Organization; Osaka Japan

10. Department of Neurosurgery; Institute for Clinical Research; Osaka National Hospital; National Hospital Organization; Osaka Japan

11. Center for Medical Genetics; Keio University School of Medicine; Tokyo Japan

12. Department of Neurochemistry; Nagoya University Graduate School of Medicine; Nagoya Japan

Funder

Japan Society for the Promotion of Science London

Practical Research Project for Rare/Intractable Diseases

Japan Agency for Medical Research and Development

Takeda Science Foundation

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jnc.13878/fullpdf

Reference47 articles.

1. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010

2. GPCR mediated regulation of synaptic transmission;Betke;Prog. Neurobiol.,2012

3. Receptor-effector coupling by G proteins;Birnbaumer;Biochim. Biophys. Acta,1990

4. Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia;Fox;Neuron,1998

5. Mutations in GNAL cause primary torsion dystonia;Fuchs;Nat. Genet.,2013

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A new variant confirms GNAI2 as a rare cause of periventricular nodular heterotopia;Neurological Sciences;2024-09-09

2. MiR-30c-5p-Targeted Regulation of GNAI2 Improves Neural Function Injury and Inflammation in Cerebral Ischemia-Reperfusion Injury;Applied Biochemistry and Biotechnology;2023-12-28

3. MED13L and its disease‐associated variants influence the dendritic development of cerebral cortical neurons in the mammalian brain;Journal of Neurochemistry;2023-02-28

4. Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes;Brain;2022-07-04

5. Investigating the effects of chronic perinatal alcohol and combined nicotine and alcohol exposure on dopaminergic and non-dopaminergic neurons in the VTA;Scientific Reports;2021-04-22