(Q43197988)

15 November 2017

Mitochondrial haplogroup B increases the risk for hearing loss among the Eastern Asian pedigrees carrying 12S rRNA 1555A>G mutation (English)

1 reference

15 November 2017

1 reference

Ye Chen

13

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author name string

Zhengbiao Ying

1

1 reference

15 November 2017

Jing Zheng

2

1 reference

15 November 2017

Zhaoyang Cai

3

1 reference

15 November 2017

Li Liu

4

1 reference

15 November 2017

Yu Dai

5

1 reference

15 November 2017

Juan Yao

6

1 reference

15 November 2017

Hui Wang

7

1 reference

15 November 2017

Yinglong Gao

8

1 reference

15 November 2017

Binjiao Zheng

9

1 reference

15 November 2017

Xiaowen Tang

10

1 reference

15 November 2017

Yi Zhu

11

1 reference

15 November 2017

Min-Xin Guan

12

1 reference

15 November 2017

11 September 2015

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15 November 2017

1 reference

15 November 2017

6

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15 November 2017

11

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15 November 2017

844-848

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Creative Commons Attribution 4.0 International

15 November 2017

start time

11 September 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1007/s13238-015-0203-z

0 references

cites work

A peep into mitochondrial disorder: multifaceted from mitochondrial DNA mutations to nuclear gene modulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

MtDNA haplogroups M7 and B in southwestern Han Chinese at risk for acute mountain sickness

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

Cancer type-specific modulation of mitochondrial haplogroups in breast, colorectal and thyroid cancer.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

Interaction of aminoglycosides with human mitochondrial 12S rRNA carrying the deafness-associated mutation

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

Mitochondrial deafness mutations reviewed

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

Alzheimer disease: Variations in mitochondrial DNA predict AD-related brain atrophy

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

Mitochondrial DNA haplogroup associated with hereditary hearing loss in a Japanese population.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4624676

10.1007/S13238-015-0203-Z

15 August 2018

Identifiers

DOI

1 reference

15 November 2017

1 reference

15 November 2017

1 reference