(Q35622053)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14708972 AND SRC:MED&resulttype=core&format=json

17 November 2019

review article

1 reference

title

The TCA cycle and tumorigenesis: the examples of fumarate hydratase and succinate dehydrogenase (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14708972 AND SRC:MED&resulttype=core&format=json

17 November 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14708972 AND SRC:MED&resulttype=core&format=json

17 November 2019

3

Ian P M Tomlinson

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14708972 AND SRC:MED&resulttype=core&format=json

17 November 2019

author name string

Noel C Wortham

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14708972 AND SRC:MED&resulttype=core&format=json

17 November 2019

language of work or name

English

0 references

publication date

1 January 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14708972 AND SRC:MED&resulttype=core&format=json

17 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14708972 AND SRC:MED&resulttype=core&format=json

17 November 2019

volume

35

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14708972 AND SRC:MED&resulttype=core&format=json

17 November 2019

issue

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14708972 AND SRC:MED&resulttype=core&format=json

17 November 2019

page(s)

632-639

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14708972 AND SRC:MED&resulttype=core&format=json

Inborn errors of the Krebs cycle: a group of unusual mitochondrial diseases in human

17 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Subacute necrotizing encephalomyelopathy in an infant

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

A novel mutation in the SDHD gene in a family with inherited paragangliomas--implications of genetic diagnosis for follow up and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Crystallographic studies of the catalytic and a second site in fumarase C from Escherichia coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Hypoxia inducible factor-alpha binding and ubiquitylation by the von Hippel-Lindau tumor suppressor protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Contrasting effects on HIF-1alpha regulation by disease-causing pVHL mutations correlate with patterns of tumourigenesis in von Hippel-Lindau disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Quantification of vascular endothelial growth factor-A in leiomyomas and adjacent myometrium

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Bcl-2 family members and functional electron transport chain regulate oxygen deprivation-induced cell death

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

A role for mitochondrial enzymes in inherited neoplasia and beyond

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Glucose deprivation-induced cytotoxicity and alterations in mitogen-activated protein kinase activation are mediated by oxidative stress in multidrug-resistant human breast carcinoma cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Caspase-3 activation and DNA fragmentation in primary hippocampal neurons following glutamate excitotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Biochemical, physiological and medical aspects of ubiquinone function

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

A defect in the cytochrome b large subunit in complex II causes both superoxide anion overproduction and abnormal energy metabolism in Caenorhabditis elegans

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Alteration of mitochondrial DNA in human oncocytomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Pig heart fumarase contains two distinct substrate-binding sites differing in affinity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

von Hippel-Lindau Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080/07853890310018458

10.1080/07853890310018458

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14708972 AND SRC:MED&resulttype=core&format=json

17 November 2019

1 reference