(Q80385508)

English

LOH on chromosome 11q, but not SDHD and Men1 mutations was frequently detectable in Chinese patients with pheochromocytoma and paraganglioma

scientific article published on 01 December 2006

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

LOH on chromosome 11q, but not SDHD and Men1 mutations was frequently detectable in Chinese patients with pheochromocytoma and paraganglioma (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

phaeochromocytoma

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Hai-Yan Sun

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Bin Cui

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Din-Wei Su

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Xiao-Long Jin

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Fu-Kang Sun

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Yu Zu

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Lei Jiang

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Wei-Qing Wang

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Guang Ning

9

1 reference

Europe PubMed Central

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31 December 2019

publication date

1 December 2006

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

30

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

3

1 reference

Europe PubMed Central

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31 December 2019

307-312

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

https://scigraph.springernature.com/pub.10.1007/s12020-006-0009-0

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing in pheochromocytoma or functional paraganglioma

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alterations of the SDHD gene locus in midgut carcinoids, Merkel cell carcinomas, pheochromocytomas, and abdominal paragangliomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the SDHD gene, the susceptibility gene for familial paraganglioma syndrome (PGL1), in pheochromocytomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Active succinate dehydrogenase (SDH) and lack of SDHD mutations in sporadic paragangliomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular and genetic mechanisms of tumorigenesis in multiple endocrine neoplasia type-1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of somatic SDHD mutations in sporadic neuroendocrine tumors and detection of two germline variants in paraganglioma patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germ-line mutations in nonsyndromic pheochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel candidate region linked to development of both pheochromocytoma and head/neck paraganglioma

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetics of neuroendocrine and carcinoid tumours

1 reference

https://pubmed.ncbi.nlm.nih.gov/17526943

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12020-006-0009-0

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17526943%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

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