IP3receptor mutations and brain diseases in human and rodents-Reference-Cited by-同舟云学术

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IP3receptor mutations and brain diseases in human and rodents

Published:2017-03-21 Issue:6 Volume:141 Page:790-807
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J. Neurochem.

Author:

Hisatsune Chihiro¹,Mikoshiba Katsuhiko¹

Affiliation:

1. Laboratory for Developmental Neurobiology; Brain Science Institute; Institute of Physical and Chemical Research (RIKEN); Saitama Japan

Funder

Grant-in-Aid for Scientific Research (S)

Grant-in-Aid for Scientific Research (C)

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jnc.13991/fullpdf

Reference221 articles.

1. Enzymological analysis of mutant protein kinase C gamma causing spinocerebellar ataxia type 14 and dysfunction in Ca2+ homeostasis;Adachi;J. Biol. Chem.,2008

2. When, where and how? Focus on neuronal calcium dysfunctions in Alzheimer's Disease;Agostini;Cell Calcium,2016

3. Tissue transglutaminase inhibits autophagy in pancreatic cancer cells;Akar;Mol. Cancer Res.,2007

4. Amyloid beta oligomers induce Ca2+ dysregulation and neuronal death through activation of ionotropic glutamate receptors;Alberdi;Cell Calcium,2010

5. Postnatal-development of cerebellar cortex in Rat. 2. phases in maturation of purkinje-cells and of molecular layer;Altman;Journal of Comparative Neurology,1972

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