(Q46764503)

English

Modifier locus for mitochondrial DNA disease: linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness

scientific article published in May 2001

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

Modifier locus for mitochondrial DNA disease: linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

mitochondrial DNA

0 references

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

linkage disequilibrium

1 reference

based on heuristic

inferred from title

Xavier Estivill i Pallejà

6

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

author name string

Bykhovskaya Y

1

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

Yang H

2

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

Taylor K

3

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

Hang T

4

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

Tun RY

5

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

Casano RA

7

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

Majamaa K

8

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

Shohat M

9

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

Fischel-Ghodsian N

10

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

language of work or name

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publication date

1 May 2001

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

Genetics in Medicine

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

3

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

3

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

177-180

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

https://scigraph.springernature.com/pub.10.1097/00125817-200105000-00005

0 references

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

Mitochondrial mutations and hearing loss: paradigm for mitochondrial genetics

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

Candidate locus for a nuclear modifier gene for maternally inherited deafness

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

Allele-sharing models: LOD scores and accurate linkage tests

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

Faster multipoint linkage analysis using Fourier transforms.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice.

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

Genetic factors in aminoglycoside toxicity

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

Angiopoietin-2, a natural antagonist for Tie2 that disrupts in vivo angiogenesis

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

Defensins: key players or bystanders in infection, injury, and repair in the lung?

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00005

21 January 2018

Identifiers

10.1097/00125817-200105000-00005

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 December 2017

http://europepmc.org/abstract/MED/11388757

ResearchGate publication ID

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