(Q81191060)

English

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss

scientific article published on 01 October 2005

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scholarly article

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6 January 2020

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss (English)

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6 January 2020

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Huijun Yuan

1

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6 January 2020

Yaping Qian

2

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6 January 2020

Yanjun Xu

3

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6 January 2020

Juyang Cao

4

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6 January 2020

Linna Bai

5

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6 January 2020

Weidong Shen

6

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6 January 2020

Fei Ji

7

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6 January 2020

Xin Zhang

8

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6 January 2020

Dongyang Kang

9

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6 January 2020

Jun Qin Mo

10

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6 January 2020

John H Greinwald

11

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6 January 2020

Dongyi Han

12

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6 January 2020

Suoqiang Zhai

13

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6 January 2020

Wie-Yen Young

14

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6 January 2020

Min-Xin Guan

15

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6 January 2020

publication date

1 October 2005

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6 January 2020

American Journal of Medical Genetics

1 reference

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6 January 2020

138A

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6 January 2020

2

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6 January 2020

133-140

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16152638%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigree

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular pathogenetic mechanism of maternally inherited deafness

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial tRNA 3' end metabolism and human disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence and organization of the human mitochondrial genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment of aminoglycosides

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial deafness mutations reviewed

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MITOMAP: a human mitochondrial genome database--2004 update

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASerUCN gene in a Japanese family.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical characterization of the deafness-associated mitochondrial tRNASer(UCN) A7445G mutation in osteosarcoma cell cybrids.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phylogeographic differentiation of mitochondrial DNA in Han Chinese

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNA(Ser(UCN)) gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence and gene organization of mouse mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The complete nucleotide sequence of the Xenopus laevis mitochondrial genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A molecular basis for human hypersensitivity to aminoglycoside antibiotics

1 reference

https://pubmed.ncbi.nlm.nih.gov/16152638

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/AJMG.A.30952

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16152638%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16152638%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16152638%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

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