Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background - Wikidata - wikimedia - TriplyDB

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

http://www.wikidata.org/entity/Q24678122

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Mitochondrial DNA backgrounds might modulate diabetes complications rather than T2DM as a whole Mitochondrial genetics Leber hereditary optic neuropathy: current perspectives DLK-1, SEK-3 and PMK-3 Are Required for the Life Extension Induced by Mitochondrial Bioenergetic Disruption in C. elegans The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity Impact of the mitochondrial genetic background in complex III deficiency Historical perspective on mitochondrial medicine Mutation rate switch inside Eurasian mitochondrial haplogroups: impact of selection and consequences for dating settlement in Europe Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation: a case report A cytoplasmic suppressor of a nuclear mutation affecting mitochondrial functions in Drosophila.The utility of mitochondrial and y chromosome phylogenetic data to improve correction for population stratification Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifier Mitochondrial DNA copy number, but not haplogroup, confers a genetic susceptibility to leprosy in Han Chinese from Southwest China.Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy Minisequencing mitochondrial DNA pathogenic mutations.Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.Mitochondrial DNA and primary mitochondrial dysfunction in Parkinson's disease.OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background.Treatment strategies for inherited optic neuropathies: past, present and future Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases.ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait.Mitochondrial DNA haplogroup distribution in Chaoshanese with and without myopia.Mitochondrial disorders and the eye.Inherited mitochondrial DNA variants can affect complement, inflammation and apoptosis pathways: insights into mitochondrial-nuclear interactions.Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy.Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.Is mitochondrial tRNA(phe) variant m.593T>C a synergistically pathogenic mutation in Chinese LHON families with m.11778G>A?Mitochondrial DNA haplogroup background affects LHON, but not suspected LHON, in Chinese patients Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.The neuro-ophthalmology of mitochondrial disease The case for the continuing use of the revised Cambridge Reference Sequence (rCRS) and the standardization of notation in human mitochondrial DNA studies.Hypervariable region polymorphism of mtDNA of recurrent oral ulceration in Chinese.Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.Mitochondrial DNA haplogroups confer differences in risk for age-related macular degeneration: a case control study.Principal-component analysis for assessment of population stratification in mitochondrial medical genetics.The role of the mitochondrial genome in ageing and carcinogenesis.

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Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

http://www.wikidata.org/entity/Q24678122

description

2007 nî lūn-bûn

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2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի օգոստոսին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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Clinical expression of Leber h ...... rial DNA-haplogroup background

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Clinical expression of Leber h ...... rial DNA-haplogroup background

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Clinical expression of Leber h ...... rial DNA-haplogroup background

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Clinical expression of Leber h ...... rial DNA-haplogroup background

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Clinical expression of Leber h ...... rial DNA-haplogroup background

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Clinical expression of Leber h ...... rial DNA-haplogroup background

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Clinical expression of Leber h ...... rial DNA-haplogroup background

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Clinical expression of Leber h ...... rial DNA-haplogroup background

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Clinical expression of Leber h ...... rial DNA-haplogroup background

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American Journal of Human Genetics

P1476

Clinical expression of Leber h ...... rial DNA-haplogroup background

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P2093

Alfredo A Sadun

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Catherine Mowbray

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Eeva Nikoskelainen

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Gavin Hudson

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Hubert J T Smeets

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Joanna Elson

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Kirsi Huoponen

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Liesbeth Spruijt

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Marja-Liisa Savontaus

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Mike Gerards

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Respiratory complex III is required to maintain complex I in mammalian mitochondria

Saami and Berbers--an unexpected mitochondrial DNA link.

Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder

Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups.

Supercomplexes in the respiratory chains of yeast and mammalian mitochondria

The epidemiology of Leber hereditary optic neuropathy in the North East of England

Mitochondrial DNA variation of modern Tuscans supports the near eastern origin of Etruscans

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228-33

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4540431

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10.1086/519394

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2

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81

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Antonio Torroni

Massimo Zeviani

Patrick Yu-Wai-Man

Alessandro Achilli

Maria Lucia Valentino

Valerio Carelli

Chiara La Morgia

Patrick F. Chinnery

P577

2007-08-01T00:00:00Z

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6171683

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17668373

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mitochondrial DNA

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1950812

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