Alterations of the SDHD gene locus in midgut carcinoids, Merkel cell carcinomas, pheochromocytomas, and abdominal paragangliomas (Q43990596)

28 November 2017

Alterations of the SDHD gene locus in midgut carcinoids, Merkel cell carcinomas, pheochromocytomas, and abdominal paragangliomas (English)

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28 November 2017

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Elisabeth Edström Elder

object named as

Elisabeth Edström Elder

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author name string

Soili Kytölä

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28 November 2017

Brita Nord

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28 November 2017

Elisabeth Edström Elder

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28 November 2017

Tobias Carling

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28 November 2017

Magnus Kjellman

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28 November 2017

Björn Cedermark

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28 November 2017

Claes Juhlin

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28 November 2017

Anders Höög

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28 November 2017

Jorma Isola

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28 November 2017

Catharina Larsson

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28 November 2017

language of work or name

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1 July 2002

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Genes, Chromosomes and Cancer

28 November 2017

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28 November 2017

34

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28 November 2017

3

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28 November 2017

325-332

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Germline SDHD mutation in familial phaeochromocytoma

28 November 2017

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology

21 January 2018

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Cytochrome b in human complex II (succinate-ubiquinone oxidoreductase): cDNA cloning of the components in liver mitochondria and chromosome assignment of the genes for the large (SDHC) and small (SDHD) subunits to 1q21 and 11q23

21 January 2018

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Characterization of the human SDHD gene encoding the small subunit of cytochrome b (cybS) in mitochondrial succinate-ubiquinone oxidoreductase.

21 January 2018

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Comparative genomic hybridization identifies loss of 18q22-qter as an early and specific event in tumorigenesis of midgut carcinoids

21 January 2018

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

21 January 2018

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Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

21 January 2018

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

21 January 2018

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A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease

21 January 2018

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Multiple endocrine neoplasia type 1

21 January 2018

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Loss of Heterozygosity on the Short Arm of Chromosome 1 in Pheochromocytoma and Abdominal Paraganglioma

21 January 2018

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Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation

21 January 2018

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MEN1 gene mutation analysis of sporadic adrenocortical lesions

21 January 2018

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Sporadic follicular thyroid tumors show loss of a 200-kb region in 11q13 without evidence for mutations in the MEN1 gene

21 January 2018

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Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/GCC.10081

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release_uw34drhakndw7epowmvy4n4o64

28 November 2017

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Fatcat

https://api.fatcat.wiki/v0/release/uw34drhakndw7epowmvy4n4o64

mapped directly with Wikidata item

24 November 2022

based on heuristic

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