(Q28293107)

English

Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3

scientific article

In more languages

Statements

scholarly article

0 references

Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3 (English)

0 references

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Xavier Estivill i Pallejà

5

0 references

Mordechai Shohat

6

object named as

Mordechai Shohat

0 references

Yelena Bykhovskaya

1

object named as

Yelena Bykhovskaya

0 references

author name string

Emebet Mengesha

2

0 references

Dai Wang

3

0 references

Huiying Yang

4

0 references

Nathan Fischel-Ghodsian

7

0 references

language of work or name

0 references

publication date

November 2004

0 references

Molecular Genetics and Metabolism

0 references

83

0 references

3

0 references

199-206

0 references

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Candidate locus for a nuclear modifier gene for maternally inherited deafness

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Duplication of chromosome region 8p23.1 ? p23.3: A benign variant?

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Mitochondrial RNA processing and translation: link between mitochondrial mutations and hearing loss?

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Human mitochondrial transcription factor B1 methylates ribosomal RNA at a conserved stem-loop

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNA

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

A human mitochondrial GTP binding protein related to tRNA modification may modulate phenotypic expression of the deafness-associated mitochondrial 12S rRNA mutation

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

MTO1 codes for a mitochondrial protein required for respiration in paromomycin-resistant mutants of Saccharomyces cerevisiae.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

MSS1, a nuclear-encoded mitochondrial GTPase involved in the expression of COX1 subunit of cytochrome c oxidase

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Tandem repeats finder: a program to analyze DNA sequences

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Base composition-independent hybridization in tetramethylammonium chloride: a method for oligonucleotide screening of highly complex gene libraries

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Faster multipoint linkage analysis using Fourier transforms.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Chromosome-based method for rapid computer simulation in human genetic linkage analysis

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.009

7 January 2021

Identifiers

10.1016/J.YMGME.2004.07.009

0 references

PubMed publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28293107&oldid=2112439710"