Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus (Q34839861)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

4 August 2017

Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus (English)

1 reference

Europe PubMed Central

4 August 2017

0 references

mitochondrial DNA

0 references

1 reference

based on heuristic

inferred from title

Jukka S Moilanen

object named as

Jukka S Moilanen

2

0 references

author name string

Heidi K Soini

1

1 reference

Europe PubMed Central

4 August 2017

Tiina Vilmi-Kerälä

3

1 reference

Europe PubMed Central

4 August 2017

Saara Finnilä

4

1 reference

Europe PubMed Central

4 August 2017

Kari Majamaa

5

1 reference

Europe PubMed Central

4 August 2017

publication date

19 July 2013

1 reference

Europe PubMed Central

4 August 2017

BMC Medical Genetics

1 reference

Europe PubMed Central

4 August 2017

14

1 reference

Europe PubMed Central

4 August 2017

73

1 reference

Europe PubMed Central

4 August 2017

https://scigraph.springernature.com/pub.10.1186/1471-2350-14-73

0 references

Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Mitochondria, oxidative stress and neurodegeneration.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Epilepsy in mitochondrial disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Epigenetics, epidemiology and mitochondrial DNA diseases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Mitochondrial disease and epilepsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

HmtDB, a genomic resource for mitochondrion-based human variability studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

A mitochondrial etiology of Alzheimer and Parkinson disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

The mitochondrial genome is a "genetic sanctuary" during the oncogenic process.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Mitochondrial pathogenic mutations are population-specific

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Mitochondrial dysfunction in neurological disorders with epileptic phenotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

A method and server for predicting damaging missense mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Mitochondria, oxidative stress, and temporal lobe epilepsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Arlequin (version 3.0): an integrated software package for population genetics data analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Mitochondrial DNA haplogroups influence AIDS progression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Updated comprehensive phylogenetic tree of global 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=3726289

8 July 2018

Mamit-tRNA, a database of mammalian mitochondrial tRNA primary and secondary structures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

An enhanced MITOMAP with a global mtDNA mutational phylogeny

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

mtDB: Human Mitochondrial Genome Database, a resource for population genetics and medical sciences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Mitochondrial DNA analysis in clinical laboratory diagnostics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

mtDNA mutations increase tumorigenicity in prostate cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Mitochondrial dysfunction and oxidative stress: cause and consequence of epileptic seizures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Mitochondrial genome variation in eastern Asia and the peopling of Japan

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Metabolic consequences of a novel missense mutation of the mtDNA CO I gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Evidence for mtDNA admixture between the Finns and the Saami

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Phylogenetic network for European mtDNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Predicting deleterious amino acid substitutions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequence analysis of the complete coding region by conformation-sensitive gel electrophoresis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Conformation sensitive gel electrophoresis for simple and accurate detection of mutations: comparison with denaturing gradient gel electrophoresis and nucleotide sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Classification of European mtDNAs from an analysis of three European populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Mitochondrial portraits of human populations using median networks

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Family history and recurrence of febrile seizures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Convenient single-step, one tube purification of PCR products for direct sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726289

8 July 2018

Sacred disease secrets revealed: the genetics of human epilepsy

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

Increased variation in mtDNA in patients with familial sensorineural hearing impairment

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

Type 2 diabetes is associated with a common mitochondrial variant: evidence from a population-based case-control study.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

Phylogenetic network and physicochemical properties of nonsynonymous mutations in the protein-coding genes of human mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

Homoplasmy of the G7444A mtDNA and heterozygosity of the GJB2 c.35delG mutations in a family with hearing loss.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

Novel A14841G mutation is associated with high penetrance of LHON/C4171A family.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

Mitochondrial encephalomyopathy lactic acidosis and strokelike episodes mimicking occipital idiopathic epilepsy.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

Genes and languages in Europe: an analysis of mitochondrial lineages.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

An integrated approach for classifying mitochondrial DNA variants: one clinical diagnostic laboratory's experience.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

Functional characterization of novel mutations in the human cytochrome b gene.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

mtDNA tree Build 17 (18 Feb 2016)

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

Clinical spectrum of mitochondrial DNA mutation at base pair 8344

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-14-73

21 January 2018

Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/23870133

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/23870133

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence-based prediction of pathological mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/23870133

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA Haplogroups and Incidence of Lipodystrophy in HIV-Infected Patients on Long-Term Antiretroviral Therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/23870133

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

https://pubmed.ncbi.nlm.nih.gov/23870133

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2350-14-73

1 reference

Europe PubMed Central

4 August 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

4 August 2017

1 reference

Europe PubMed Central

4 August 2017

ResearchGate 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=Q34839861&oldid=1841144132"