A reappraisal of complete mtDNA variation in East Asian families with hearing impairment (Q42491866)

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English	A reappraisal of complete mtDNA variation in East Asian families with hearing impairment	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

16528519

retrieved

1 November 2017

title

A reappraisal of complete mtDNA variation in East Asian families with hearing impairment (English)

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Europe PubMed Central

PubMed publication ID

16528519

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1 November 2017

main subject

hearing loss

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author

Antonio Salas

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2

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Europe PubMed Central

PubMed publication ID

16528519

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1 November 2017

Yong-Gang Yao

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Yong-Gang Yao

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1

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Claudio M. Bravi

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3

object named as

Claudio M Bravi

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Europe PubMed Central

PubMed publication ID

16528519

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1 November 2017

Hans-Jürgen Bandelt

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4

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Hans-Jürgen Bandelt

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Europe PubMed Central

PubMed publication ID

16528519

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1 November 2017

publication date

10 March 2006

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Europe PubMed Central

PubMed publication ID

16528519

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1 November 2017

published in

Human Genetics

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Europe PubMed Central

PubMed publication ID

16528519

retrieved

1 November 2017

volume

119

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stated in

Europe PubMed Central

PubMed publication ID

16528519

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1 November 2017

issue

5

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Europe PubMed Central

PubMed publication ID

16528519

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1 November 2017

page(s)

505-515

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Europe PubMed Central

PubMed publication ID

16528519

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1 November 2017

cites work

Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00439-006-0154-9

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21 January 2018

Artificial recombination in forensic mtDNA population databases.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Commentary to mitDNA research for the pathogenesis of mitochondrial disorders

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Problems in FBI mtDNA database

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phantom mutation hotspots in human mitochondrial DNA.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence and organization of the human mitochondrial genome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phylogeographic analysis of mitochondrial DNA haplogroup F2 in China reveals T12338C in the initiation codon of the ND5 gene not to be pathogenic.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Emerging Limbs and Twigs of the East Asian mtDNA Tree

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA sequence polymorphisms of five ethnic populations from northern China

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence variation in mitochondrial complex I genes: mutation or polymorphism?

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

To err is human

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence polymorphisms of the mitochondrial DNA control region in 105 Chinese Han population.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigrees

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial genome variation in eastern Asia and the peopling of Japan

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quality assessment of DNA sequence data: autopsy of a mis-sequenced mtDNA population sample.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phylogeny of east Asian mitochondrial DNA lineages inferred from complete sequences

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple origins of a mitochondrial mutation conferring deafness.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The African diaspora: mitochondrial DNA and the Atlantic slave trade

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

mtDNA variation in the South African Kung and Khwe-and their genetic relationships to other African populations.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial genome variation and the origin of modern humans

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phylogeny of mitochondrial DNA macrohaplogroup N in India, based on complete sequencing: implications for the peopling of South Asia

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

To trust or not to trust an idiosyncratic mitochondrial data set.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA 5178A polymorphism and longevity

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A call for mtDNA data quality control in forensic science

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternally inherited deafness associated with a T1095C mutation in the mDNA.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype diversity in mitochondrial DNA hypervariable region I, II and III in a Korean ethnic group from northeast China

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A practical guide to mitochondrial DNA error prevention in clinical, forensic, and population genetics

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Etruscan artifacts

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disuniting uniformity: a pied cladistic canvas of mtDNA haplogroup H in Eurasia

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial genes and schizophrenia

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafness

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In search of geographical patterns in European mitochondrial DNA.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A critical reassessment of the role of mitochondria in tumorigenesis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phylogeographic differentiation of mitochondrial DNA in Han Chinese

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phylogenetic network for European mtDNA.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA control region sequences in Koreans: identification of useful variable sites and phylogenetic analysis for mtDNA data quality control.

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

About the "Pathological" role of the mtDNA T3308C mutationellipsis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

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Proving pathogenicity: when evolution is not enough

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

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Detecting errors in mtDNA data by phylogenetic analysis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

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Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

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Identification of Native American founder mtDNAs through the analysis of complete mtDNA sequences: some caveats.

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

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Diabetes mellitus: a "thrifty" genotype rendered detrimental by "progress"?

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

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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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

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Low "penetrance" of phylogenetic knowledge in mitochondrial disease studies

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

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Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

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Different matrilineal contributions to genetic structure of ethnic groups in the silk road region in china

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PubMed

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12 December 2020

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

More evidence for non-maternal inheritance of mitochondrial DNA?

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new database of mitochondrial DNA hypervariable regions I and II sequences from 162 Japanese individuals

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

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An annotated mtDNA database

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogenic DNA mutations.

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

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The fingerprint of phantom mutations in mitochondrial DNA data

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The making of the African mtDNA landscape

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaics of ancient mitochondrial DNA: positive indicators of nonauthenticity

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Forensic genetic analysis of mitochondrial DNA hypervariable region I/II sequences: an expanded Korean population database

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reconstructing the evolutionary history of China: a caveat about inferences drawn from ancient DNA

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16528519

retrieved

12 December 2020

based on heuristic

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The role of selection in the evolution of human mitochondrial genomes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16528519

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12 December 2020

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Identifiers

DOI

10.1007/S00439-006-0154-9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16528519

retrieved

1 November 2017

Dimensions Publication ID

1018484485

0 references

PubMed publication ID

16528519

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16528519

retrieved

1 November 2017

ResearchGate publication ID

7249004

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