Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q36481832)
Watch
English
Mechanisms of retinal ganglion specific-cell death in Leber hereditary optic neuropathy.
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
2258117
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18427623%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
title
Mechanisms of retinal ganglion specific-cell death in Leber hereditary optic neuropathy
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
2258117
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18427623%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
main subject
cell death
1 reference
based on heuristic
inferred from title
author name string
Leonard A Levin
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
2258117
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18427623%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
publication date
1 January 2007
1 reference
stated in
Europe PubMed Central
PMC publication ID
2258117
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18427623%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
published in
Transactions of the American Ophthalmological Society annual meeting
1 reference
stated in
Europe PubMed Central
PMC publication ID
2258117
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18427623%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
volume
105
1 reference
stated in
Europe PubMed Central
PMC publication ID
2258117
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18427623%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
page(s)
379-391
1 reference
stated in
Europe PubMed Central
PMC publication ID
2258117
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18427623%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
describes a project that uses
ImageJ
1 reference
stated in
Europe PubMed Central
retrieved
11 June 2022
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2258117/fullTextXML
based on heuristic
inferred from PubMed Central ID database lookup
cites work
Kinase-dependent differentiation of a retinal ganglion cell precursor
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Rotenone model of Parkinson disease: multiple brain mitochondria dysfunctions after short term systemic rotenone intoxication
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Severe impairment of complex I-driven adenosine triphosphate synthesis in leber hereditary optic neuropathy cybrids
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Isolation of transcriptomal changes attributable to LHON mutations and the cybridization process.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Inhibitors of the quinone-binding site allow rapid superoxide production from mitochondrial NADH:ubiquinone oxidoreductase (complex I).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
MitoProteome: mitochondrial protein sequence database and annotation system
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
LEBER'S DISEASE WITH SYMPTOMS RESEMBLING DISSEMINATED SCLEROSIS
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Topology of superoxide production from different sites in the mitochondrial electron transport chain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-Induced apoptosis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Characterization of a transformed rat retinal ganglion cell line
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Functional constraints of nuclear-mitochondrial DNA interactions in xenomitochondrial rodent cell lines
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Maternal inheritance of human mitochondrial DNA
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
Role of ubiquinone in the mitochondrial generation of hydrogen peroxide
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
30 September 2017
SOD2 gene transfer protects against optic neuropathy induced by deficiency of complex I.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
28 June 2018
Apoptotic cell death of cybrid cells bearing Leber's hereditary optic neuropathy mutations is caspase independent
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
28 June 2018
Optic neuropathy induced by reductions in mitochondrial superoxide dismutase
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
28 June 2018
Suppression of complex I gene expression induces optic neuropathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
28 June 2018
Generation of superoxide anion by the NADH dehydrogenase of bovine heart mitochondria
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
28 June 2018
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
28 June 2018
Difficulty differentiating Leber's from dominant optic neuropathy in a patient with remote visual loss
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
28 June 2018
Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
28 June 2018
Retinal ganglion cell axotomy induces an increase in intracellular superoxide anion
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
21 September 2018
Neuroprotective effect of sulfhydryl reduction in a rat optic nerve crush model.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
21 September 2018
Characterization of superoxide-producing sites in isolated brain mitochondria
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
21 September 2018
Amplification of a Reactive Oxygen Species Signal in Axotomized Retinal Ganglion Cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
21 September 2018
Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
21 September 2018
Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
21 September 2018
Reduced redox state allows prolonged survival of axotomized neonatal retinal ganglion cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
21 September 2018
Atypical Leber's hereditary optic neuropathy with molecular confirmation.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
21 September 2018
Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathy.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
21 September 2018
Clinical and genetical manifestations in 34 families with Leber's hereditary optic neuropathy (LHON).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
21 September 2018
Optic disk cupping and electrocardiographic abnormalities in an American pedigree with Leber's hereditary optic neuropathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2258117
retrieved
21 September 2018
Tissue culture of adult human retinal ganglion cells
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18427623
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Mitochondria and Leber's hereditary optic neuropathy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18427623
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Leber's hereditary optic neuropathy. Clinical manifestations of the 15257 mutation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18427623
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Late-onset Leber's hereditary optic neuropathy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18427623
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18427623
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
2258117
1 reference
stated in
Europe PubMed Central
PMC publication ID
2258117
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18427623%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
PubMed publication ID
18427623
1 reference
stated in
Europe PubMed Central
PMC publication ID
2258117
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18427623%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 January 2020
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
