Literature DB >> 11384753

Pathogenesis of adult-onset type II citrullinemia caused by deficiency of citrin, a mitochondrial solute carrier protein: tissue and subcellular localization of citrin.

M Iijima1, A Jalil, L Begum, T Yasuda, N Yamaguchi, M Xian Li, N Kawada, H Endou, K Kobayashi, T Saheki.   

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Year:  2001        PMID： 11384753     DOI： 10.1016/s0065-2571(00)00022-4

Source DB:  PubMed          Journal:  Adv Enzyme Regul        ISSN： 0065-2571


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  18 in total

1.  Screening of SLC25A13 mutation in the Thai population.

Authors:  Parith Wongkittichote; Chonlaphat Sukasem; Atsuo Kikuchi; Wichai Aekplakorn; Laran T Jensen; Shigeo Kure; Duangrurdee Wattanasirichaigoon
Journal:  World J Gastroenterol       Date:  2013-11-21       Impact factor: 5.742

2.  Prediction of the functional effect of novel SLC25A13 variants using a S. cerevisiae model of AGC2 deficiency.

Authors:  Parith Wongkittichote; Sumalee Tungpradabkul; Duangrurdee Wattanasirichaigoon; Laran T Jensen
Journal:  J Inherit Metab Dis       Date:  2012-10-03       Impact factor: 4.982

3.  Citrulline and ammonia accumulating in citrullinemia reduces antioxidant capacity of rat brain in vitro.

Authors:  Cristina C Prestes; Angela M Sgaravatti; Carolina D Pederzolli; Mirian B Sgarbi; Giovanni K Zorzi; Clóvis M D Wannmacher; Moacir Wajner; Angela T S Wyse; Carlos Severo Dutra Filho
Journal:  Metab Brain Dis       Date:  2006-04-27       Impact factor: 3.584

4.  Novel variants of human SCaMC-3, an isoform of the ATP-Mg/P(i) mitochondrial carrier, generated by alternative splicing from 3'-flanking transposable elements.

Authors:  Araceli Del Arco
Journal:  Biochem J       Date:  2005-08-01       Impact factor: 3.857

5.  Citrin and aralar1 are Ca(2+)-stimulated aspartate/glutamate transporters in mitochondria.

Authors:  L Palmieri; B Pardo; F M Lasorsa; A del Arco; K Kobayashi; M Iijima; M J Runswick; J E Walker; T Saheki; J Satrústegui; F Palmieri
Journal:  EMBO J       Date:  2001-09-17       Impact factor: 11.598

6.  Blood glucose and insulin and correlation of SLC25A13 mutations with biochemical changes in NICCD patients.

Authors:  Chun-Ting Lu; Qi-Ping Shi; Ze-Jian Li; Jiong Li; Lie Feng
Journal:  Exp Biol Med (Maywood)       Date:  2017-05-18

7.  Role of the glutamate dehydrogenase reaction in furnishing aspartate nitrogen for urea synthesis: studies in perfused rat liver with 15N.

Authors:  Itzhak Nissim; Oksana Horyn; Bohdan Luhovyy; Adam Lazarow; Yevgeny Daikhin; Ilana Nissim; Marc Yudkoff
Journal:  Biochem J       Date:  2003-11-15       Impact factor: 3.857

8.  AGC1 Deficiency Causes Infantile Epilepsy, Abnormal Myelination, and Reduced N-Acetylaspartate.

Authors:  Marni J Falk; Dong Li; Xiaowu Gai; Elizabeth McCormick; Emily Place; Francesco M Lasorsa; Frederick G Otieno; Cuiping Hou; Cecilia E Kim; Nada Abdel-Magid; Lyam Vazquez; Frank D Mentch; Rosetta Chiavacci; Jinlong Liang; Xuanzhu Liu; Hui Jiang; Giulia Giannuzzi; Eric D Marsh; Guo Yiran; Lifeng Tian; Ferdinando Palmieri; Hakon Hakonarson
Journal:  JIMD Rep       Date:  2014-02-11

9.  Slc25a13-knockout mice harbor metabolic deficits but fail to display hallmarks of adult-onset type II citrullinemia.

Authors:  David S Sinasac; Mitsuaki Moriyama; M Abdul Jalil; Laila Begum; Meng Xian Li; Mikio Iijima; Masahisa Horiuchi; Brian H Robinson; Keiko Kobayashi; Takeyori Saheki; Lap-Chee Tsui
Journal:  Mol Cell Biol       Date:  2004-01       Impact factor: 4.272

10.  Overexpression of the peroxin Pex34p suppresses impaired acetate utilization in yeast lacking the mitochondrial aspartate/glutamate carrier Agc1p.

Authors:  Chalongchai Chalermwat; Thitipa Thosapornvichai; Parith Wongkittichote; John D Phillips; James E Cox; Amornrat N Jensen; Duangrurdee Wattanasirichaigoon; Laran T Jensen
Journal:  FEMS Yeast Res       Date:  2019-12-01       Impact factor: 2.796
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