(Q43990596)

28 November 2017

title

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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Merkel cell carcinoma

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based on heuristic

inferred from title

author

Elisabeth Edström Elder

object named as

Elisabeth Edström Elder

3

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author name string

Soili Kytölä

1

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28 November 2017

Brita Nord

2

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28 November 2017

Elisabeth Edström Elder

3

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28 November 2017

Tobias Carling

4

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28 November 2017

Magnus Kjellman

5

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28 November 2017

Björn Cedermark

6

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28 November 2017

Claes Juhlin

7

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28 November 2017

Anders Höög

8

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28 November 2017

Jorma Isola

9

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28 November 2017

Catharina Larsson

10

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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

published in

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28 November 2017

volume

34

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28 November 2017

issue

3

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28 November 2017

page(s)

325-332

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Germline SDHD mutation in familial phaeochromocytoma

28 November 2017

cites work

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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

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

1 reference

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

21 January 2018

1 reference

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

1 reference

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

1 reference

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

1 reference

MEN1 gene mutation analysis of sporadic adrenocortical lesions

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/GCC.10081

1 reference

release_uw34drhakndw7epowmvy4n4o64

28 November 2017

Fatcat ID

1 reference

Fatcat

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

mapped directly with Wikidata item

24 November 2022

based on heuristic

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