(Q42944161)

11 November 2017

title

Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families (English)

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11 November 2017

5

Fuxin Zhao

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20691156

18 June 2024

15

Min-Xin Guan

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20691156

18 June 2024

author name string

Juanjuan Zhang

1

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11 November 2017

Xiangtian Zhou

2

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11 November 2017

Jian Zhou

3

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11 November 2017

Chengwu Li

4

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11 November 2017

Yan Wang

6

1 reference

11 November 2017

Yanzi Meng

7

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11 November 2017

Jiying Wang

8

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11 November 2017

Meixia Yuan

9

1 reference

11 November 2017

Wanshi Cai

10

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11 November 2017

Yi Tong

11

1 reference

11 November 2017

Yan-Hong Sun

12

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11 November 2017

Li Yang

13

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11 November 2017

Jia Qu

14

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11 November 2017

language of work or name

English

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publication date

4 August 2010

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full work available at URL

11 November 2017

https://api.elsevier.com/content/article/PII:S0006291X10014683?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

https://api.elsevier.com/content/article/PII:S0006291X10014683?httpAccept=text/plain

18 June 2024

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

Biochemical and Biophysical Research Communications

18 June 2024

published in

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11 November 2017

volume

399

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11 November 2017

issue

4

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11 November 2017

page(s)

647-653

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Inherited mitochondrial optic neuropathies

11 November 2017

cites work

3

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https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

18 June 2024

4

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https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

LHON and other optic nerve atrophies: the mitochondrial connection

18 June 2024

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https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

Mitochondrial encephalomyopathies: gene mutation

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https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

MITOMAP: a human mitochondrial genome database--2004 update

18 June 2024

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Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations

18 June 2024

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https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy

18 June 2024

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A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

18 June 2024

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Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation

18 June 2024

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https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

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

18 June 2024

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https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy

18 June 2024

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The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.

18 June 2024

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Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy

18 June 2024

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Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy

18 June 2024

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The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation

18 June 2024

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The mitochondrial tRNA(Thr) A15951G mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in a Chinese family.

18 June 2024

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https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family

18 June 2024

21

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https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation

18 June 2024

22

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https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation

18 June 2024

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Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation

18 June 2024

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Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

18 June 2024

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

18 June 2024

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Sequence and gene organization of mouse mitochondrial DNA

18 June 2024

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The complete nucleotide sequence of the Rattus norvegicus mitochondrial genome: cryptic signals revealed by comparative analysis between vertebrates

18 June 2024

28

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https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese family

18 June 2024

30

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Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson's disease and mitochondrial encephalomyopathy

18 June 2024

31

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Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation

18 June 2024

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Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations

18 June 2024

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The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

18 June 2024

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Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation

18 June 2024

37

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation

18 June 2024

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1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families

18 June 2024

39

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2010.07.135

18 June 2024

Identifiers

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11 November 2017

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