Familial nonsyndromic pheochromocytoma.

about

Diseases of the adrenal medulla Cowden syndrome-associated germline succinate dehydrogenase complex subunit D (SDHD) variants cause PTEN-mediated down-regulation of autophagy in thyroid cancer cells.Metastatic paraganglioma.Surgical approaches in hereditary endocrine tumors.

P2860

Q24646015-958D5FA0-91AD-4EFB-9F38-919066B5B2AE Q33561627-437A4AB2-DFA9-4E75-96D4-4339B1A23550 Q34480015-C7A61264-2394-4630-A27E-C2EDE1608FE6 Q39271803-55394279-C268-4154-84D9-56B63D281C6E

P2860

Familial nonsyndromic pheochromocytoma.

Item

http://www.wikidata.org/entity/Q51776854

description

2006 nî lūn-bûn

@nan

2006年の論文

@ja

2006年学术文章

@wuu

2006年学术文章

@zh

2006年学术文章

@zh-cn

2006年学术文章

@zh-hans

2006年学术文章

@zh-my

2006年学术文章

@zh-sg

2006年學術文章

@yue

2006年學術文章

@zh-hant

name

Familial nonsyndromic pheochromocytoma.

@en

Familial nonsyndromic pheochromocytoma.

@nl

type

Item

label

Familial nonsyndromic pheochromocytoma.

@en

Familial nonsyndromic pheochromocytoma.

@nl

prefLabel

Familial nonsyndromic pheochromocytoma.

@en

Familial nonsyndromic pheochromocytoma.

@nl

P1476

Familial nonsyndromic pheochromocytoma.

@en

P2093

Alessandra Murgia

http://www.w3.org/2001/XMLSchema#string

Antonio Toniato

http://www.w3.org/2001/XMLSchema#string

Franco Mantero

http://www.w3.org/2001/XMLSchema#string

Gennaro Favia

http://www.w3.org/2001/XMLSchema#string

Isabella Merante Boschin

http://www.w3.org/2001/XMLSchema#string

Laura Zambonin

http://www.w3.org/2001/XMLSchema#string

Maddalena Martella

http://www.w3.org/2001/XMLSchema#string

Maria Rosa Pelizzo

http://www.w3.org/2001/XMLSchema#string

Maurizio Iacobone

http://www.w3.org/2001/XMLSchema#string

Paola De Lazzari

http://www.w3.org/2001/XMLSchema#string

P2860

Neuronal apoptosis linked to EglN3 prolyl hydroxylase and familial pheochromocytoma genes: developmental culling and cancer

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations

Germ-line mutations in nonsyndromic pheochromocytoma.

The molecular pathogenesis of hereditary and sporadic adrenocortical and adrenomedullary tumors.

New insights in the genetics of adrenocortical tumors, pheochromocytomas and paragangliomas.

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

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

Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma.

Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: a possible hot spot?

Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma.

P304

149-155

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P31

scholarly article

P356

10.1196/ANNALS.1353.015

http://www.w3.org/2001/XMLSchema#string

P478

1073

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P50

P577

2006-08-01T00:00:00Z

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P698

17102081

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P921

phaeochromocytoma

Familial nonsyndromic pheochromocytoma.

about

P2860

P2860

Familial nonsyndromic pheochromocytoma.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P50

P577

P698

P921