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Genetically modeled mice with mutations in mitochondrial metabolic enzymes for the study of cancer
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Europe PubMed Central
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4115665
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25126540%20AND%20SRC:MED&resulttype=core&format=json
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12 March 2020
title
Genetically modeled mice with mutations in mitochondrial metabolic enzymes for the study of cancer
(English)
1 reference
stated in
Europe PubMed Central
PMCID
4115665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25126540%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 March 2020
author
Africa Millán-Uclés
series ordinal
2
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Europe PubMed Central
PMCID
4115665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25126540%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 March 2020
author name string
José I Piruat
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1
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Europe PubMed Central
PMCID
4115665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25126540%20AND%20SRC:MED&resulttype=core&format=json
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12 March 2020
publication date
30 July 2014
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Europe PubMed Central
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4115665
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retrieved
12 March 2020
published in
Frontiers in Oncology
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Europe PubMed Central
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4115665
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12 March 2020
volume
4
1 reference
stated in
Europe PubMed Central
PMCID
4115665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25126540%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 March 2020
page(s)
200
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stated in
Europe PubMed Central
PMCID
4115665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25126540%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 March 2020
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HIF overexpression correlates with biallelic loss of fumarate hydratase in renal cancer: novel role of fumarate in regulation of HIF stability
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6 September 2017
The mitochondrial SDHD gene is required for early embryogenesis, and its partial deficiency results in persistent carotid body glomus cell activation with full responsiveness to hypoxia
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6 September 2017
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6 September 2017
Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma
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6 September 2017
Aberrant succination of proteins in fumarate hydratase-deficient mice and HLRCC patients is a robust biomarker of mutation status
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Inhibition of succinate dehydrogenase dysregulates histone modification in mammalian cells
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Loss of the SdhB, but Not the SdhA, subunit of complex II triggers reactive oxygen species-dependent hypoxia-inducible factor activation and tumorigenesis.
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14 September 2017
A mutation in the SDHC gene of complex II increases oxidative stress, resulting in apoptosis and tumorigenesis.
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Differential impairment of catecholaminergic cell maturation and survival by genetic mitochondrial complex II dysfunction
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23 June 2018
Expression profiling in progressive stages of fumarate-hydratase deficiency: the contribution of metabolic changes to tumorigenesis
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23 June 2018
An O2-sensitive glomus cell-stem cell synapse induces carotid body growth in chronic hypoxia.
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SDH mutations establish a hypermethylator phenotype in paraganglioma.
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31 August 2018
Structural basis of fumarate hydratase deficiency
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31 August 2018
Mitochondrial reactive oxygen species generation by the SDHC V69E mutation causes low birth weight and neonatal growth retardation
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31 August 2018
Hypoxia, HIF1 and glucose metabolism in the solid tumour
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=4115665
retrieved
31 August 2018
Succinate inhibition of alpha-ketoglutarate-dependent enzymes in a yeast model of paraganglioma
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=4115665
retrieved
31 August 2018
Mitochondrial succinate is instrumental for HIF1alpha nuclear translocation in SDHA-mutant fibroblasts under normoxic conditions
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=4115665
retrieved
31 August 2018
Accumulation of Krebs cycle intermediates and over-expression of HIF1alpha in tumours which result from germline FH and SDH mutations
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=4115665
retrieved
31 August 2018
Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families.
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=4115665
retrieved
31 August 2018
A complex II defect affects mitochondrial structure, leading to ced-3- and ced-4-dependent apoptosis and aging
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=4115665
retrieved
31 August 2018
Structural biology. Complex II is complex too.
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=4115665
retrieved
31 August 2018
Mutations in SDHC cause autosomal dominant paraganglioma, type 3.
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=4115665
retrieved
31 August 2018
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3
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=4115665
retrieved
3 December 2018
Adult Leydig Cell Tumors of the Testis Caused by Germline Fumarate Hydratase Mutations
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=4115665
retrieved
3 December 2018
Hereditary leiomyomatosis and renal cell cancer: update on clinical and molecular characteristics
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25126540
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
SDHA mutations in adult and pediatric wild-type gastrointestinal stromal tumors
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25126540
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
SDHA Immunohistochemistry Detects GermlineSDHAGene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25126540
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Increases in mitochondrial reactive oxygen species trigger hypoxia-induced calcium responses in pulmonary artery smooth muscle cells
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/25126540
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.3389/FONC.2014.00200
1 reference
stated in
Europe PubMed Central
PMCID
4115665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25126540%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 March 2020
PMCID
4115665
1 reference
stated in
Europe PubMed Central
PMCID
4115665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25126540%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 March 2020
PubMed ID
25126540
1 reference
stated in
Europe PubMed Central
PMCID
4115665
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25126540%20AND%20SRC:MED&resulttype=core&format=json
retrieved
12 March 2020
ResearchGate publication ID
264832730
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