Sdhd and SDHD/H19 knockout mice do not develop paraganglioma or pheochromocytoma (Q30945414)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19956719%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

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

1 reference

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13 February 2020

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1 reference

Pancras C.W. Hogendoorn

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13 February 2020

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13 February 2020

Luc Teppema

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13 February 2020

Albert Dahan

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13 February 2020

Jean-Pierre Bayley

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13 February 2020

Ivonne van Minderhout

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13 February 2020

Cees J Cornelisse

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13 February 2020

Annemieke van der Wal

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13 February 2020

Frans A Prins

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13 February 2020

Peter Devilee

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13 February 2020

language of work or name

English

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publication date

24 November 2009

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13 February 2020

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13 February 2020

volume

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13 February 2020

issue

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13 February 2020

page(s)

e7987

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Creative Commons Attribution 4.0 International

13 February 2020

start time

24 November 2009

1 reference

April 2022 Public Data File from Crossref

copyrighted

0 references

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

The H19 locus acts in vivo as a tumor suppressor

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

A highly efficient Escherichia coli-based chromosome engineering system adapted for recombinogenic targeting and subcloning of BAC DNA

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

Disruption of imprinting caused by deletion of the H19 gene region in mice

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

HPRT-deficient (Lesch-Nyhan) mouse embryos derived from germline colonization by cultured cells

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

Exchangeable gene trap using the Cre/mutated lox system.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2776493

Epigenetic analysis of HIC1, CASP8, FLIP, TSP1, DCR1, DCR2, DR4, DR5, KvDMR1, H19 and preferential 11p15.5 maternal-allele loss in von Hippel-Lindau and sporadic phaeochromocytomas

25 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19956719

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0007987

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19956719%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

0 references

1 reference

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13 February 2020

PubMed publication ID

19956719

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19956719%20AND%20SRC:MED&resulttype=core&format=json