(Q44770885)

6 December 2017

title

Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility (English)

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6 December 2017

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6 December 2017

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6 December 2017

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6 December 2017

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6 December 2017

Ashley B Grossman

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6 December 2017

Eamonn R Maher

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6 December 2017

Dewi Astuti

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6 December 2017

Niki Hart-Holden

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6 December 2017

Farida Latif

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6 December 2017

Fiona Lalloo

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6 December 2017

Caron Lim

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6 December 2017

Anthony Moran

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6 December 2017

Shirley V Hodgson

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6 December 2017

Richard Ramsden

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6 December 2017

publication date

1 December 2003

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6 December 2017

published in

Clinical Endocrinology

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6 December 2017

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6 December 2017

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6 December 2017

page(s)

728-733

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Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group

6 December 2017

cites work

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https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

Germline SDHD mutation in familial phaeochromocytoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

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/10.1046%2FJ.1365-2265.2003.01914.X

Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

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/10.1046%2FJ.1365-2265.2003.01914.X

Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

Mitochondrial reactive oxygen species trigger hypoxia-induced transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

Mitochondria and apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

Inhibition of HIF is necessary for tumor suppression by the von Hippel-Lindau protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

The pressure rises: update on the genetics of phaeochromocytoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

Genomic imprinting in hereditary glomus tumours: evidence for new genetic theory

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

Germ-line mutations in nonsyndromic pheochromocytoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

Familial malignant catecholamine-secreting paraganglioma with prolonged survival associated with mutation in the succinate dehydrogenase B gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2003.01914.X

10.1046/J.1365-2265.2003.01914.X

21 January 2018

Identifiers

DOI

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6 December 2017

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