(Q38300554)

1 September 2017

title

Citrin/mitochondrial glycerol-3-phosphate dehydrogenase double knock-out mice recapitulate features of human citrin deficiency (English)

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1 September 2017

Takeyori Saheki

1

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1 September 2017

Mikio Iijima

2

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1 September 2017

Meng Xian Li

3

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1 September 2017

Keiko Kobayashi

4

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1 September 2017

Masahisa Horiuchi

5

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1 September 2017

Miharu Ushikai

6

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1 September 2017

Fumihiko Okumura

7

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1 September 2017

Xiao Jian Meng

8

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1 September 2017

Ituro Inoue

9

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1 September 2017

Atsushi Tajima

10

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1 September 2017

Mitsuaki Moriyama

11

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1 September 2017

Kazuhiro Eto

12

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1 September 2017

Takashi Kadowaki

13

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1 September 2017

David S Sinasac

14

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1 September 2017

Lap-Chee Tsui

15

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1 September 2017

Mihoko Tsuji

16

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1 September 2017

Akira Okano

17

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1 September 2017

Tsuyoshi Kobayashi

18

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1 September 2017

language of work or name

English

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publication date

25 June 2007

1 reference

Journal of Biological Chemistry

1 September 2017

number of pages

12

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based on heuristic

inferred from page(s)

published in

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1 September 2017

volume

282

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1 September 2017

issue

34

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1 September 2017

page(s)

25041-25052

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

1 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Molecular cloning of Aralar, a new member of the mitochondrial carrier superfamily that binds calcium and is present in human muscle and brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Expression of three mitochondrial solute carriers, citrin, aralar1 and ornithine transporter, in relation to urea cycle in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype-phenotype correlation in 38 classical citrullinemia patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Type II (adult onset) citrullinaemia: clinical pictures and the therapeutic effect of liver transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Metabolic derangements in deficiency of citrin, a liver-type mitochondrial aspartate-glutamate carrier

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Application of mutation analysis for the previously uncertain cases of adult-onset type II citrullinemia (CTLN2) and their clinical profiles

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Adult onset type II citrullinemia as a cause of non-alcoholic steatohepatitis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Risk of worsened encephalopathy after intravenous glycerol therapy in patients with adult-onset type II citrullinemia (CTLN2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Diurnal fluctuation of blood ammonia levels in adult-type citrullinemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Screening of SLC25A13 mutations in early and late onset patients with citrin deficiency and in the Japanese population: Identification of two novel mutations and establishment of multiple DNA diagnosis methods for nine mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Neonatal intrahepatic cholestasis caused by citrin deficiency: severe hepatic dysfunction in an infant requiring liver transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Stimulation of mouse liver glutathione S-transferase activity in propylthiouracil-treated mice in vivo by tri-iodothyronine

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Molecular analysis of argininosuccinate synthetase deficiency in human fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

The redox state of free nicotinamide-adenine dinucleotide in the cytoplasm and mitochondria of rat liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Normal thyroid thermogenesis but reduced viability and adiposity in mice lacking the mitochondrial glycerol phosphate dehydrogenase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

The distribution of L-asparagine synthetase in the principal organs of several mammalian and avian species

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Effects of citrin deficiency in the perinatal period: feasibility of newborn mass screening for citrin deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

Citrin deficiency presenting with ketotic hypoglycaemia and hepatomegaly in childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M702031200

21 January 2018

Identifiers

DOI

10.1074/JBC.M702031200

1 reference

release_vhssngdmoffuhij5x2mxqgcc2y

1 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/vhssngdmoffuhij5x2mxqgcc2y

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference