Clinical Heterogeneity, Tissue Distribution, and Intergenerational Segregation of mtDNA Mutation A3243G.

about

Clinical Heterogeneity, Tissue Distribution, and Intergenerational Segregation of mtDNA Mutation A3243G.

Item

http://www.wikidata.org/entity/Q51636769

description

2004 nî lūn-bûn

@nan

2004年の論文

@ja

2004年学术文章

@wuu

2004年学术文章

@zh

2004年学术文章

@zh-cn

2004年学术文章

@zh-hans

2004年学术文章

@zh-my

2004年学术文章

@zh-sg

2004年學術文章

@yue

2004年學術文章

@zh-hant

name

Clinical Heterogeneity, Tissue ...... tion of mtDNA Mutation A3243G.

@en

Clinical Heterogeneity, Tissue ...... tion of mtDNA Mutation A3243G.

@nl

type

Item

label

Clinical Heterogeneity, Tissue ...... tion of mtDNA Mutation A3243G.

@en

Clinical Heterogeneity, Tissue ...... tion of mtDNA Mutation A3243G.

@nl

prefLabel

Clinical Heterogeneity, Tissue ...... tion of mtDNA Mutation A3243G.

@en

Clinical Heterogeneity, Tissue ...... tion of mtDNA Mutation A3243G.

@nl

P1476

Clinical Heterogeneity, Tissue ...... tion of mtDNA Mutation A3243G.

@en

P2093

H Hansikova

http://www.w3.org/2001/XMLSchema#string

J Houstek

http://www.w3.org/2001/XMLSchema#string

J Kytnarova

http://www.w3.org/2001/XMLSchema#string

L Cerna

http://www.w3.org/2001/XMLSchema#string

M Bohm

http://www.w3.org/2001/XMLSchema#string

M Tesarova

http://www.w3.org/2001/XMLSchema#string

P2860

Decrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study.

Random genetic drift determines the level of mutant mtDNA in human primary oocytes

Mitochondrial DNA segregation in the developing embryo.

Lessons from mitochondrial DNA mutations.

Reactive oxygen species and mitochondrial diseases.

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

The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.

Studying the platelet cytoskeleton in Triton X-100 lysates.

P304

79-84

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1080/15376520490257527

http://www.w3.org/2001/XMLSchema#string

P433

1-2

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Jiri Zeman

Hana Houšťková

P577

2004-01-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

20021128

http://www.w3.org/2001/XMLSchema#string