(Q61874674)

English

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

scientific article published in July 1997

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207786 AND SRC:MED&resulttype=core&format=json

4 November 2019

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207786 AND SRC:MED&resulttype=core&format=json

4 November 2019

1 reference

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inferred from title

mitochondrial myopathy

1 reference

based on heuristic

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1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207786 AND SRC:MED&resulttype=core&format=json

4 November 2019

4

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207786 AND SRC:MED&resulttype=core&format=json

4 November 2019

author name string

Waymire KG

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207786 AND SRC:MED&resulttype=core&format=json

4 November 2019

Cottrell B

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207786 AND SRC:MED&resulttype=core&format=json

4 November 2019

MacGregor GR

5

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4 November 2019

Wallace DC

6

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Europe PubMed Central

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4 November 2019

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1 July 1997

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Europe PubMed Central

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4 November 2019

Nature Genetics

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9207786 AND SRC:MED&resulttype=core&format=json

4 November 2019

16

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Europe PubMed Central

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4 November 2019

3

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Europe PubMed Central

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4 November 2019

226-234

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Europe PubMed Central

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4 November 2019

Molecular basis of mitochondrial DNA disease

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Structure-function of the ADP/ATP carrier

1 reference

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7 January 2021

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Bovine cardiac mitochondrial ADP/ATP-carrier: two distinct mRNAs and an unusually short 3'-noncoding sequence

1 reference

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7 January 2021

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Two bovine genes for mitochondrial ADP/ATP translocase expressed differences in various tissues

1 reference

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Isolation and characterization of cDNA clones and a genomic clone encoding rat mitochondrial adenine nucleotide translocator

1 reference

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7 January 2021

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DNA sequences of two expressed nuclear genes for human mitochondrial ADP/ATP translocase

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A human ADP/ATP translocase gene has seven pseudogenes and localizes to chromosome X.

1 reference

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Mitochondrial DNA mutations in human degenerative diseases and aging

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The Ant1 gene maps near Klk3 on proximal mouse chromosome 8

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Genetic mapping of human heart-skeletal muscle adenine nucleotide translocator and its relationship to the facioscapulohumeral muscular dystrophy locus

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7 January 2021

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The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus

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7 January 2021

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Rapid evolution of human pseudoautosomal genes and their mouse homologs

1 reference

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7 January 2021

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Promoter traps in embryonic stem cells: a genetic screen to identify and mutate developmental genes in mice

1 reference

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7 January 2021

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Mitochondrial myopathies

1 reference

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7 January 2021

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Ultrastructural quantitation of mitochondria and myofilaments in cardiac muscle from 10 different animal species including man

1 reference

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7 January 2021

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Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

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7 January 2021

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Adenine nucleotide translocator deficiency in muscle: Potential therapeutic value of vitamin E

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7 January 2021

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Neural control of phenotypic expression in mammalian muscle fibers

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The adaptive response of skeletal muscle to increased use.

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Muscle-specific overexpression of lipoprotein lipase causes a severe myopathy characterized by proliferation of mitochondria and peroxisomes in transgenic mice

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7 January 2021

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cDNA sequence of a human skeletal muscle ADP/ATP translocator: lack of a leader peptide, divergence from a fibroblast translocator cDNA, and coevolution with mitochondrial DNA genes

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7 January 2021

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Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice

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Gene targeting in embryonic stem cells

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7 January 2021

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Production of chimeras between embryonic stem cells and embryos.

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7 January 2021

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Ragged red fibers in normal aging and inflammatory myopathy

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Entry and release of measles virus are polarized in epithelial cells

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Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines

1 reference

https://api.crossref.org/works/10.1038/NG0797-226

7 January 2021

based on heuristic

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