(Q36653563)

15 August 2017

Mitochondrial DNA variation and HIV-associated sensory neuropathy in CHARTER. (English)

1 reference

15 August 2017

0 references

David C Samuels

4

0 references

Ronald Ellis

object named as

Ronald J Ellis

3

0 references

Marylyn D. Ritchie

5

object named as

Marylyn D Ritchie

1 reference

15 August 2017

21

Igor Grant

1 reference

15 August 2017

20

Scott Letendre

1 reference

15 August 2017

15

Susan Morgello

1 reference

15 August 2017

22

CHARTER Group

1 reference

15 August 2017

17

Donald R Franklin

1 reference

15 August 2017

14

J Allen McCutchan

1 reference

15 August 2017

12

Christina M Marra

1 reference

15 August 2017

11

Benjamin B Gelman

1 reference

15 August 2017

13

Justin C McArthur

1 reference

15 August 2017

7

Asha R Kallianpur

1 reference

15 August 2017

18

Debralee Rosario

1 reference

15 August 2017

8

Cinnamon S Bloss

1 reference

15 August 2017

1

Emily R Holzinger

1 reference

15 August 2017

10

Ann C Collier

1 reference

15 August 2017

2

Todd Hulgan

1 reference

15 August 2017

6

David W Haas

1 reference

15 August 2017

David B Clifford

9

1 reference

15 August 2017

David M Simpson

16

1 reference

15 August 2017

Doug Selph

19

1 reference

15 August 2017

language of work or name

1 reference

17 October 2012

1 reference

15 August 2017

Journal of NeuroVirology

1 reference

15 August 2017

18

1 reference

15 August 2017

6

1 reference

15 August 2017

511-520

1 reference

Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Mitochondrial dysfunction in distal axons contributes to human immunodeficiency virus sensory neuropathy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

European mitochondrial DNA haplogroups and metabolic changes during antiretroviral therapy in AIDS Clinical Trials Group Study A5142

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Association of self-reported painful symptoms with clinical and neurophysiologic signs in HIV-associated sensory neuropathy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Continued high prevalence and adverse clinical impact of human immunodeficiency virus-associated sensory neuropathy in the era of combination antiretroviral therapy: the CHARTER Study

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

African mitochondrial DNA subhaplogroups and peripheral neuropathy during antiretroviral therapy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Mitochondrial haplogroups are associated with risk of neuroretinal disorder in HIV-positive patients

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Finding unique filter sets in PLATO: a precursor to efficient interaction analysis in GWAS data

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

HIV and antiretroviral therapy: impact on the central nervous system.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

The mitochondrial A10398G polymorphism, interaction with alcohol consumption, and breast cancer risk

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Mitochondrial DNA haplogroups influence lipoatrophy after highly active antiretroviral therapy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Multisystem manifestations of mitochondrial disorders

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Mitochondrial DNA haplogroups influence AIDS progression

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Ashkenazi Jewish centenarians do not demonstrate enrichment in mitochondrial haplogroup J

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

PLINK: a tool set for whole-genome association and population-based linkage analyses

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

An enhanced MITOMAP with a global mtDNA mutational phylogeny

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Identification of mitochondrial DNA polymorphisms that alter mitochondrial matrix pH and intracellular calcium dynamics

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Mitochondrial haplogroups and peripheral neuropathy during antiretroviral therapy: an adult AIDS clinical trials group study

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

The epidemiology of human immunodeficiency virus-associated neurological disease in the era of highly active antiretroviral therapy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Mitochondrial DNA polymorphisms associated with longevity in a Finnish population

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Mitochondrial DNA variation in human evolution and disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Mitochondrial toxicity induced by nucleoside-analogue reverse-transcriptase inhibitors is a key factor in the pathogenesis of antiretroviral-therapy-related lipodystrophy

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

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.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

Sequence and organization of the human mitochondrial genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587171

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

28 June 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13365-012-0133-Y

Expression of genes from the human active and inactive X chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13365-012-0133-Y

Cytokine genotype suggests a role for inflammation in nucleoside analog-associated sensory neuropathy (NRTI-SN) and predicts an individual's NRTI-SN risk.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13365-012-0133-Y

Mitochondrial alterations with mitochondrial DNA depletion in the nerves of AIDS patients with peripheral neuropathy induced by 2'3'-dideoxycytidine (ddC).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13365-012-0133-Y

Hemochromatosis gene polymorphisms, mitochondrial haplogroups, and peripheral lipoatrophy during antiretroviral therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13365-012-0133-Y

A common mitochondrial polymorphism 10398A>G is associated metabolic syndrome in a Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13365-012-0133-Y

Mitochondrial D-loop variation in leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13365-012-0133-Y

Controlling neuropathic pain in HIV.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13365-012-0133-Y

mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish

21 January 2018

1 reference

12 December 2020

Large scale screening of the mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians

1 reference

12 December 2020

mtDNA haplogroup J: a contributing factor of optic neuritis

1 reference

12 December 2020

A combination of three common inherited mitochondrial DNA polymorphisms promotes longevity in Finnish and Japanese subjects

1 reference

12 December 2020

Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women

1 reference

12 December 2020

Hemochromatosis (HFE) gene mutations and peripheral neuropathy during antiretroviral therapy

1 reference

12 December 2020

Mitochondrial DNA haplogroups and age-related maculopathy

1 reference

12 December 2020

Increased risk of oral cancer in relation to common Indian mitochondrial polymorphisms and Autosomal GSTP1 locus

1 reference

12 December 2020

Interaction between the UCP2-866G/A, mtDNA 10398G/A and PGC1alpha p.Thr394Thr and p.Gly482Ser polymorphisms in type 2 diabetes susceptibility in North Indian population

1 reference

12 December 2020

1 reference

12 December 2020

10.1007/S13365-012-0133-Y

Identifiers

DOI

1 reference

15 August 2017

1 reference

15 August 2017

PubMed publication ID

23073667

1 reference