Citrin/Mitochondrial Glycerol-3-phosphate Dehydrogenase Double Knock-out Mice Recapitulate Features of Human Citrin Deficiency-Reference-Cited by-同舟云学术

Citrin/Mitochondrial Glycerol-3-phosphate Dehydrogenase Double Knock-out Mice Recapitulate Features of Human Citrin Deficiency

Published:2007-08 Issue:34 Volume:282 Page:25041-25052
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Saheki Takeyori,Iijima Mikio,Li Meng Xian,Kobayashi Keiko,Horiuchi Masahisa,Ushikai Miharu,Okumura Fumihiko,Meng Xiao Jian,Inoue Ituro,Tajima Atsushi,Moriyama Mitsuaki,Eto Kazuhiro,Kadowaki Takashi,Sinasac David S.,Tsui Lap-Chee,Tsuji Mihoko,Okano Akira,Kobayashi Tsuyoshi

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference63 articles.

1. Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD)

2. The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein

3. Molecular Cloning of Aralar, a New Member of the Mitochondrial Carrier Superfamily That Binds Calcium and Is Present in Human Muscle and Brain

4. Citrin and aralar1 are Ca2+-stimulated aspartate/glutamate transporters in mitochondria

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