(Q36470441)

English

The creation of cybrids harboring mitochondrial haplogroups in the Taiwanese population of ethnic Chinese background: an extensive in vitro tool for the study of mitochondrial genomic variations

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

The creation of cybrids harboring mitochondrial haplogroups in the Taiwanese population of ethnic Chinese background: an extensive in vitro tool for the study of mitochondrial genomic variations (English)

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

author name string

Tsu-Kung Lin

1

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Hung-Yu Lin

2

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Shang-Der Chen

3

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Yao-Chung Chuang

4

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Jiin-Haur Chuang

5

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Pei-Wen Wang

6

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Sheng-Teng Huang

7

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Mao-Meng Tiao

8

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Jin-Bor Chen

9

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Chia-Wei Liou

10

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

publication date

6 December 2012

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Oxidative medicine and cellular longevity

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

2012

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

824275

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

copyright license

Creative Commons Attribution 3.0 Unported

1 January 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

1 reference

April 2022 Public Data File from Crossref

Mitochondrial DNA coding and control region variants as genetic risk factors for type 2 diabetes.

1 reference

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30 September 2017

Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.

1 reference

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30 September 2017

Nutrient-sensitized screening for drugs that shift energy metabolism from mitochondrial respiration to glycolysis

1 reference

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30 September 2017

Mitochondrial DNA variants in the pathogenesis of type 2 diabetes - relevance of asian population studies

1 reference

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30 September 2017

Mitochondrial variants in schizophrenia, bipolar disorder, and major depressive disorder

1 reference

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30 September 2017

Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease.

1 reference

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30 September 2017

Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility

1 reference

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30 September 2017

Mitochondrial DNA haplogroup D4a is a marker for extreme longevity in Japan

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians

1 reference

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30 September 2017

Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations

1 reference

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30 September 2017

Inhibitory effects of Bcl-2 on mitochondrial respiration

1 reference

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30 September 2017

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

1 reference

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30 September 2017

Mitochondria make a come back

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Mitochondrial diseases in man and mouse

1 reference

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30 September 2017

Mitochondrial evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Oxidative stress and mitochondrial DNA mutations in human aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Platelet-mediated transformation of human mitochondrial DNA-less cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Creation and characterization of mitochondrial DNA-depleted cell lines with "neuronal-like" properties.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Crosstalk between nuclear and mitochondrial genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Sequence and organization of the human mitochondrial genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Sites of inhibition of mitochondrial electron transport in macrophage-injured neoplastic cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Mitochondrial DNA and human evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

Evidence that glutamine, not sugar, is the major energy source for cultured HeLa cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

30 September 2017

The structure of human mitochondrial DNA variation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

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Association between a common mitochondrial DNA D-loop polycytosine variant and alteration of mitochondrial copy number in human peripheral blood cells

1 reference

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1 reference

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21 September 2018

Mitochondrial SNPs associated with Japanese centenarians, Alzheimer's patients, and Parkinson's patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

21 September 2018

Mitochondrial haplogroup A is a genetic risk factor for atherothrombotic cerebral infarction in Japanese females.

1 reference

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Mitochondrial disease and stroke.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

21 September 2018

Mitochondrial DNA haplogroups and susceptibility to AD and dementia with Lewy bodies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

21 September 2018

Clinical features, investigation, and management of patients with defects of mitochondrial DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523582

21 September 2018

Mitochondrial DNA haplogroups and age at onset of schizophrenia

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F824275

21 January 2018

Large deletions in mitochondrial DNA in radiation-associated human thyroid tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/23304256

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/23304256

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Toll-like receptor-3-induced mitochondrial dysfunction in cultured human hepatocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23304256

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/23304256

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1155/2012/824275

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

ResearchGate publication ID

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