(Q73806653)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Male infertility associated with multiple mitochondrial DNA rearrangements (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

1

1 reference

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6 November 2019

author name string

M F Chrétien

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

I Penisson-Besnier

3

1 reference

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6 November 2019

Y Malthièry

4

1 reference

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6 November 2019

V Rohmer

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

P Lestienne

6

1 reference

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6 November 2019

publication date

1 August 1997

1 reference

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Comptes rendus de l'Académie des sciences. Série 3, Sciences de la vie

6 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

320

1 reference

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6 November 2019

issue

8

1 reference

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6 November 2019

page(s)

629-636

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json

Abnormal spermatogenesis in RXR beta mutant mice.

6 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

The development of intracytoplasmic sperm injection.

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Mitochondrial DNA mutations in human diseases: a review

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Accumulation of deletions in MtDNA during tissue aging: analysis by long PCR

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Mitochondrial disease and reduced sperm motility

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

An autosomal locus predisposing to deletions of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Mitochondrial mutations and male infertility

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Mitochondrial deoxyribonucleic acid 4977-bp deletion is associated with diminished fertility and motility of human sperm

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

MELAS syndrome with mitochondrial tRNA(Leu(UUR)) gene mutation in a Chinese family

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Mitochondrial and nuclear DNA complementation in the respiratory chain function and defects

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

Viable offspring derived from fetal and adult mammalian cells

1 reference

https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X

7 January 2021

10.1016/S0764-4469(97)85696-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference