(Q57040614)

Emmanuel Milot

1

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Alan A Cohen

Alan A Cohen

4

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Bernard Brais

5

Bernard Brais

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Claudia Moreau

2

Claudia Moreau

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author name string

Damian Labuda

Nature Ecology and Evolution

6

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language of work or name

English

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publication date

September 2017

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published in

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volume

1

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issue

9

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page(s)

1400-1406

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cites work

Revealing the hidden complexities of mtDNA inheritance

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Mitochondria and male disease.

21 January 2018

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Cytoplasmic inheritance and intragenomic conflict

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Mitochondria, maternal inheritance, and asymmetric fitness: why males die younger

21 January 2018

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Human mtDNA haplogroups associated with high or reduced spermatozoa motility

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Mother's curse: the effect of mtDNA on individual fitness and population viability

21 January 2018

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Reversing mother's curse: selection on male mitochondrial fitness effects

21 January 2018

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Can paternal leakage maintain sexually antagonistic polymorphism in the cytoplasm?

21 January 2018

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The costs of being male: are there sex-specific effects of uniparental mitochondrial inheritance?

21 January 2018

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Sex-specific mitonuclear epistasis and the evolution of mitochondrial bioenergetics, ageing, and life history in seed beetles.

21 January 2018

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Nuclear-mitochondrial epistasis: a gene's eye view of genomic conflict

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Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing.

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Mitochondria, maternal inheritance, and male aging

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Introducing mother's curse: low male fertility associated with an imported mtDNA haplotype in a captive colony of brown hares.

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Experimental evidence supports a sex-specific selective sieve in mitochondrial genome evolution.

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Evolution of sex differences in lifespan and aging: causes and constraints

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A mitochondrial bioenergetic etiology of disease

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Medicine. Mitochondrial replacement, evolution, and the clinic.

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Genotype-phenotype correlations in Leber hereditary optic neuropathy

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Leber hereditary optic neuropathy - historical report in comparison with the current knowledge.

21 January 2018

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Pedigree analysis of French Canadian families with T14484C Leber's hereditary optic neuropathy

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Leber hereditary optic neuropathy

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Three subgroups of patients from the United Kingdom with Leber hereditary optic neuropathy

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Leber's hereditary optic neuropathy with childhood onset

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The challenges of mitochondrial replacement.

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A "Fille du Roy" introduced the T14484C Leber hereditary optic neuropathy mutation in French Canadians

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Individual fitness and phenotypic selection in age-structured populations with constant growth rates

21 January 2018

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Does exposure to infectious diseases in infancy affect old-age mortality? Evidence from a pre-industrial population

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The decline of adult smallpox in eighteenth-century London

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Cardiac arrhythmia and Leber's hereditary optic neuropathy

21 January 2018

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Leber's hereditary optic neuropathy associated with a multiple-sclerosis-like picture in a man.

21 January 2018

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Variable clinical manifestation of homoplasmic G14459A mitochondrial DNA mutation.

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Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy

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A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance

21 January 2018

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Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?

21 January 2018

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Leber's hereditary optic neuropathy: a multifactorial disease.

21 January 2018

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A demographic transition altered the strength of selection for fitness and age-specific survival and fertility in a 19th century American population

21 January 2018

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Phylogenetic and familial estimates of mitochondrial substitution rates: study of control region mutations in deep-rooting pedigrees

21 January 2018

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

21 January 2018

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7 January 2021

Reversing mother's curse revisited

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7 January 2021

Population genetics of sexually antagonistic mitochondrial mutants under inbreeding

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7 January 2021

Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation

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7 January 2021