Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma (Q25255910)

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English	Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

phaeochromocytoma

1 reference

based on heuristic

inferred from title

head and neck paraganglioma

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

13

object named as

Peter Devilee

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author name string

Jean-Pierre Bayley

1

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Europe PubMed Central

PubMed publication ID

6 July 2017

Ivonne van Minderhout

2

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Europe PubMed Central

PubMed publication ID

6 July 2017

Marjan M Weiss

3

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Europe PubMed Central

PubMed publication ID

6 July 2017

Jeroen C Jansen

4

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Europe PubMed Central

PubMed publication ID

6 July 2017

Peter H N Oomen

5

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Fred H Menko

6

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Barbara Pasini

7

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Barbara Ferrando

8

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Europe PubMed Central

PubMed publication ID

6 July 2017

Nora Wong

9

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Lesley C Alpert

10

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Europe PubMed Central

PubMed publication ID

6 July 2017

Rosie Williams

11

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Europe PubMed Central

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6 July 2017

Edward Blair

12

1 reference

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6 July 2017

Peter E M Taschner

14

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6 July 2017

language of work or name

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publication date

11 January 2006

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Europe PubMed Central

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6 July 2017

BMC Medical Genetics

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Europe PubMed Central

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6 July 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

1

0 references

1

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Architecture of succinate dehydrogenase and reactive oxygen species generation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

7 April 2017

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

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

7 April 2017

Structural organization of the gene encoding the human iron-sulfur subunit of succinate dehydrogenase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

7 April 2017

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

7 April 2017

K40E: a novel succinate dehydrogenase (SDH)B mutation causing familial phaeochromocytoma and paraganglioma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

The prevalence of SDHB, SDHC, and SDHD mutations in patients with head and neck paraganglioma and association of mutations with clinical features.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

Genetic and epigenetic profile of sporadic pheochromocytomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

The genetic basis of pheochromocytoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

SDHB mutation analysis in familial and sporadic phaeochromocytoma identifies a novel mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

Hereditary paraganglioma targets diverse paraganglia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

Germ-line mutations in nonsyndromic pheochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

Phaeochromocytomas discovered during coronial autopsies in Sydney, Melbourne and Auckland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

The quinone-binding site in succinate-ubiquinone reductase from Escherichia coli. Quinone-binding domain and amino acid residues involved in quinone binding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

A review of clinicopathologic features of pheochromocytomas in Hong Kong Chinese.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

A Chinese Hamster Mutant Cell Line with a Defect in the Integral Membrane Protein CII-3 of Complex II of the Mitochondrial Electron Transport Chain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 September 2017

Pheochromocytoma--death of an axiom

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

31 May 2018

Mammalian cells with defective mitochondrial functions: a Chinese hamster mutant cell line lacking succinate dehydrogenase activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

31 May 2018

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

PIRA PCR designer for restriction analysis of single nucleotide polymorphisms

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

SDHD mutations in head and neck paragangliomas result in destabilization of complex II in the mitochondrial respiratory chain with loss of enzymatic activity and abnormal mitochondrial morphology.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

A mutation in succinate dehydrogenase cytochrome b causes oxidative stress and ageing in nematodes

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

Germline SDHD mutation in familial phaeochromocytoma

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

Hereditary phaeochromocytomas and paragangliomas: a study of five susceptibility genes

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

Identification of the heme axial ligands in the cytochrome b562 of the Saccharomyces cerevisiae succinate dehydrogenase

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-7-1

21 January 2018

Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 November 2018

Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 November 2018

Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1343542

28 November 2018

Pheochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/16405730

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated families

1 reference

https://pubmed.ncbi.nlm.nih.gov/16405730

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2350-7-1

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

ResearchGate publication ID

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