Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations. - Wikidata - awgldk - TriplyDB

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

http://www.wikidata.org/entity/Q34651788

about

Syndromic gastrointestinal stromal tumors Energy metabolism in neuroblastoma and Wilms tumor Paragangliomas: À Propos of Two Cases. Diagnostics and Treatment.The role of miRNAs in the pheochromocytomas.Parent-of-origin tumourigenesis is mediated by an essential imprinted modifier in SDHD-linked paragangliomas: SLC22A18 and CDKN1C are candidate tumour modifiers.A comprehensive characterization of rare mitochondrial DNA variants in neuroblastoma.Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas.Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.Metabologenomics of Phaeochromocytoma and Paraganglioma: An Integrated Approach for Personalised Biochemical and Genetic Testing.Measurement of head and neck paragangliomas: is volumetric analysis worth the effort? A method comparison study.Tumour risks and genotype–phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.

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P2860

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

http://www.wikidata.org/entity/Q34651788

description

2014 nî lūn-bûn

@nan

2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

@ast

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

@en

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

@nl

type

label

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

@ast

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

@en

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

@nl

prefLabel

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

@ast

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

@en

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

@nl

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P356

S12881-014-0111-8

P1433

BMC Medical Genetics

P1476

Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations.

@en

P2093

Attje S Hoekstra

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

Barbara McGillivray

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Conny A van der Meer

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Eleonora P M Corssmit

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Esther Korpershoek

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Frederik J Hes

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Jean-Pierre Bayley

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

Jennifer Nuk

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

Jeroen C Jansen

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

Rogier A Oldenburg

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P2860

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

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

The mitochondrial SDHD gene is required for early embryogenesis, and its partial deficiency results in persistent carotid body glomus cell activation with full responsiveness to hypoxia

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

Sdhd and SDHD/H19 knockout mice do not develop paraganglioma or pheochromocytoma

SDHA is a tumor suppressor gene causing paraganglioma.

Genomic imprinting at a boundary element flanking the SDHD locus

Differential loss of chromosome 11q in familial and sporadic parasympathetic paragangliomas detected by comparative genomic hybridization

P2888

s12881-014-0111-8

P304

111

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scholarly article

P356

10.1186/S12881-014-0111-8

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P478

15

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P50

P577

2014-10-10T00:00:00Z

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266745118

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1034757656

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P698

25300370

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P921

phaeochromocytoma

P932

4259087

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