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English
Male infertility associated with multiple mitochondrial DNA rearrangements
scientific article published on 01 August 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
title
Male infertility associated with multiple mitochondrial DNA rearrangements
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
main subject
male infertility
1 reference
based on heuristic
inferred from title
author
Pascal Reynier
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
author name string
M F Chrétien
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
I Penisson-Besnier
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
Y Malthièry
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
V Rohmer
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
P Lestienne
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
publication date
1 August 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
published in
Comptes rendus de l'Académie des sciences. Série 3, Sciences de la vie
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
volume
320
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
issue
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
page(s)
629-636
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
cites work
Abnormal spermatogenesis in RXR beta mutant mice.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The development of intracytoplasmic sperm injection.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sequence and organization of the human mitochondrial genome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutations in human diseases: a review
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of heteroplasmic mitochondrial DNA deletions in Kearns-Sayre syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Accumulation of deletions in MtDNA during tissue aging: analysis by long PCR
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial disease and reduced sperm motility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An autosomal locus predisposing to deletions of mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial mutations and male infertility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial deoxyribonucleic acid 4977-bp deletion is associated with diminished fertility and motility of human sperm
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MELAS syndrome with mitochondrial tRNA(Leu(UUR)) gene mutation in a Chinese family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial and nuclear DNA complementation in the respiratory chain function and defects
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Viable offspring derived from fetal and adult mammalian cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0764-4469%2897%2985696-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0764-4469(97)85696-X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
PubMed publication ID
9337998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9337998
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9337998%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 November 2019
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