(Q38889446)

7 September 2017

title

Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men. (English)

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7 September 2017

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8

Faiza Fakhfakh

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7 September 2017

author name string

Siwar Baklouti-Gargouri

1

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7 September 2017

Myriam Ghorbel

2

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7 September 2017

Afif Ben Mahmoud

3

1 reference

7 September 2017

Emna Mkaouar-Rebai

4

1 reference

7 September 2017

Meriam Cherif

5

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7 September 2017

Nozha Chakroun

6

1 reference

7 September 2017

Afifa Sellami

7

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7 September 2017

Leila Ammar-Keskes

9

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7 September 2017

publication date

6 May 2013

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Molecular Biology Reports

7 September 2017

published in

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7 September 2017

volume

40

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7 September 2017

issue

8

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7 September 2017

page(s)

4705-4712

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The thankless task of playing genetics with mammalian mitochondrial DNA: a 30-year review.

7 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Fate during cell growth of yeast mitochondrial and nuclear DNA after photolytic attachment of the monoazide analog of ethidium

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Mitochondrial DNA damage is more extensive and persists longer than nuclear DNA damage in human cells following oxidative stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Repair of mtDNA in vertebrates

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Mammalian mitochondrial genetics: heredity, heteroplasmy and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Recent developments in the molecular genetics of mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Mitochondrial diseases in man and mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Accumulation of somatic mutation in mitochondrial DNA extracted from peripheral blood cells in diabetic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

MtDNA mutations in maternally inherited diabetes: presence of the 3397 ND1 mutation previously associated with Alzheimer's and Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Molecular biology of human male infertility: links with aging, mitochondrial genetics, and oxidative stress?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Misconceptions about mitochondria and mammalian fertilization: implications for theories on human evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Prediction of deleterious human alleles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Sperm Mitochondrial Mutations as a Cause of Low Sperm Motility

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11033-013-2566-7

Mitochondrial disease and reduced sperm motility

21 January 2018

1 reference

12 December 2020

Oxidative stress and sperm mitochondrial DNA mutation in idiopathic oligoasthenozoospermic men.

1 reference

12 December 2020

Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa

1 reference

12 December 2020

[Mutation of MTCYB and MTATP6 is associated with asthenospermia]

1 reference

12 December 2020

NADH-dependent oxidoreductase (diaphorase) activity and isozyme pattern of sperm in infertile men

1 reference

12 December 2020

A role for mitochondrial DNA and sperm survival

1 reference

12 December 2020

High incidence of single nucleotide substitutions in the mitochondrial genome is associated with poor semen parameters in men

1 reference

12 December 2020

Can mitochondrial DNA mutations cause sperm dysfunction?

1 reference

12 December 2020

Oxidative phosphorylation diseases and mitochondrial DNA mutations: diagnosis and treatment

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

Necessity of nuclear and mitochondrial genome analysis prior to assisted reproductive techniques/intracytoplasmic sperm injection

1 reference

12 December 2020

Oligoasthenospermia associated with multiple mitochondrial DNA rearrangements

1 reference

12 December 2020

Association of a novel human mtDNA ATPase6 mutation with immature sperm cells

1 reference

12 December 2020

10.1007/S11033-013-2566-7

Identifiers

DOI

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Dimensions Publication ID

7 September 2017

1033140351

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Fatcat ID

release_ugdipimn7jgfjepauarsxtbrli

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ugdipimn7jgfjepauarsxtbrli

24 November 2022

mapped directly with Wikidata item

1 reference