Rewiring of Glutamine Metabolism Is a Bioenergetic Adaptation of Human Cells with Mitochondrial DNA Mutations

about

Rewiring of Glutamine Metabolism Is a Bioenergetic Adaptation of Human Cells with Mitochondrial DNA Mutations

Item

http://www.wikidata.org/entity/Q56384006

description

scientific article published on 12 April 2018

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована в травні 2018

@uk

name

Rewiring of Glutamine Metaboli ...... th Mitochondrial DNA Mutations

@en

Rewiring of Glutamine Metaboli ...... th Mitochondrial DNA Mutations

@nl

type

Item

label

Rewiring of Glutamine Metaboli ...... th Mitochondrial DNA Mutations

@en

Rewiring of Glutamine Metaboli ...... th Mitochondrial DNA Mutations

@nl

prefLabel

Rewiring of Glutamine Metaboli ...... th Mitochondrial DNA Mutations

@en

Rewiring of Glutamine Metaboli ...... th Mitochondrial DNA Mutations

@nl

P1476

Rewiring of Glutamine Metaboli ...... th Mitochondrial DNA Mutations

@en

P2093

Dazhi Zhao

http://www.w3.org/2001/XMLSchema#string

Elizabeth L Calder

http://www.w3.org/2001/XMLSchema#string

Federica Valsecchi

http://www.w3.org/2001/XMLSchema#string

Giovanni Manfredi

http://www.w3.org/2001/XMLSchema#string

Guido Primiano

http://www.w3.org/2001/XMLSchema#string

Ifrah Shahi

http://www.w3.org/2001/XMLSchema#string

Kathryne Kirk

http://www.w3.org/2001/XMLSchema#string

M Flint Beal

http://www.w3.org/2001/XMLSchema#string

Marilena D'Aurelio

http://www.w3.org/2001/XMLSchema#string

Qiuying Chen

http://www.w3.org/2001/XMLSchema#string

P2860

Cloning and analysis of unique human glutaminase isoforms generated by tissue-specific alternative splicing

N-linked glycosylation and sequence changes in a critical negative control region of the ASCT1 and ASCT2 neutral amino acid transporters determine their retroviral receptor functions

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Hypoxia and metabolic adaptation of cancer cells

Skeletal muscle autophagy: a new metabolic regulator

The serine/threonine kinases SGK1, 3 and PKB stimulate the amino acid transporter ASCT2

The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia

Untargeted plasma metabolite profiling reveals the broad systemic consequences of xanthine oxidoreductase inactivation in mice

AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1

Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency.

P304

1007-1025.e5

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1016/J.CMET.2018.03.002

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Andrea J Arreguin

Travis T Denton

P577

2018-04-12T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29657030

http://www.w3.org/2001/XMLSchema#string

P921

P932

5932217

http://www.w3.org/2001/XMLSchema#string