(Q24538797)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10936107%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Human mtDNA haplogroups associated with high or reduced spermatozoa motility (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10936107%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

0 references

José Antonio Enríquez

11

1 reference

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9 November 2019

author name string

Ruiz-Pesini E

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10936107%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Lapeña AC

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10936107%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Díez-Sánchez C

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10936107%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Pérez-Martos A

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10936107%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Montoya J

5

1 reference

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9 November 2019

Alvarez E

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10936107%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Díaz M

7

1 reference

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9 November 2019

Urriés A

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10936107%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Montoro L

9

1 reference

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9 November 2019

López-Pérez MJ

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10936107%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

language of work or name

English

0 references

publication date

9 August 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10936107%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

9 November 2019

published in

1 reference

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9 November 2019

volume

67

1 reference

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9 November 2019

issue

3

1 reference

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9 November 2019

page(s)

682-696

1 reference

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The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs

9 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Classification of European mtDNAs from an analysis of three European populations

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Paleolithic and neolithic lineages in the European mitochondrial gene pool

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Normal variants of human mitochondrial DNA and translation products: the building of a reference data base

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Tight control of respiration by NADH dehydrogenase ND5 subunit gene expression in mouse mitochondria

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Molecular phenotype of a human lymphoblastoid cell-line homoplasmic for the np 7445 deafness-associated mitochondrial mutation.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Molecular genetic aspects of human mitochondrial disorders

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Mitochondrial mutation associated with nonsyndromic deafness

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Mitochondrial DNA mutations and pathogenesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Interdependence of mitochondrial ATP production and extramitochondrial ATP utilization in intact spermatozoa

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Mitochondria and male disease.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287528

Mitochondrial mutations and male infertility

29 November 2018

1 reference

12 December 2020

Mitochondrial disorders

1 reference

12 December 2020

Analysis of the mitochondrial DNA from patients with Wolfram (DIDMOAD) syndrome

1 reference

12 December 2020

Mitochondrial DNA mutations in multiple sclerosis

1 reference

12 December 2020

Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease

1 reference

12 December 2020

Semen levels of mitochondrial DNA deletions in men attending an infertility clinic do not correlate with phenotype

1 reference

12 December 2020

Correlation of sperm motility with mitochondrial enzymatic activities

1 reference

12 December 2020

Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine

1 reference

12 December 2020

Characterization of the mitochondrial genome in childhood multiple sclerosis. I. Optic neuritis and LHON mutations

1 reference

12 December 2020

Human mitochondrial diseases: answering questions and questioning answers

1 reference

12 December 2020

Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes

1 reference

12 December 2020

The role of oxidative phosphorylation in the generation of ATP in human spermatozoa

1 reference

12 December 2020

Determination of L-carnitine in serum, and implementation on the ABA-100 and CentrifiChem 600

1 reference

12 December 2020

Mitochondrial disease and reduced sperm motility

1 reference

12 December 2020

Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy

1 reference

12 December 2020

Clinical male infertility. II. Critical evaluation of the prospects for therapy

1 reference

12 December 2020

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

1 reference

12 December 2020

Short-term inhibition of the energy metabolism affects motility but not surface properties of sperm cells

1 reference

12 December 2020

Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement

1 reference

12 December 2020

Identifiers

DOI

10.1086/303040

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10936107%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10936107%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

2 references