(Q51788318)

English

Expression and functional analysis of menin in a multiple endocrine neoplasia type 1 (MEN1) patient with somatic loss of heterozygosity in chromosome 11q13 and unidentified germline mutation of the MEN1 gene.

scientific article published in June 2006

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Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

Expression and functional analysis of menin in a multiple endocrine neoplasia type 1 (MEN1) patient with somatic loss of heterozygosity in chromosome 11q13 and unidentified germline mutation of the MEN1 gene. (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

multiple endocrine neoplasia

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multiple endocrine neoplasia type 1

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author name string

Junko Naito

1

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

Hiroshi Kaji

2

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

Hideaki Sowa

3

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

Riko Kitazawa

4

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

Sohei Kitazawa

5

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

Toshihiko Tsukada

6

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

Geoffrey N Hendy

7

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

Toshitsugu Sugimoto

8

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

Kazuo Chihara

9

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

publication date

1 June 2006

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

29

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Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

3

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

485-490

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

Role of transforming growth factor-beta signaling in cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential expression of menin in sporadic pituitary adenomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic features of patients with multiple endocrine tumors who have neither family history nor MEN1 germline mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple endocrine neoplasia type 1 with unusual concomitance of various neoplastic disorders

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https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

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inferred from PubMed ID database lookup

Somatic mutations in MEN type 1 tumors, consistent with the Knudson "two-hit" hypothesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Guidelines for diagnosis and therapy of MEN type 1 and type 2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

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Of mice and MEN1: Insulinomas in a conditional mouse knockout

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

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Alterations of the MEN1 gene in sporadic parathyroid tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

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Positional cloning of the gene for multiple endocrine neoplasia-type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic mutation of the MEN1 gene in parathyroid tumours

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous Men1 mutant mice develop a range of endocrine tumors mimicking multiple endocrine neoplasia type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inactivation of menin, a Smad3-interacting protein, blocks transforming growth factor type beta signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic deletions on chromosome 11q13 in multiple tumors from individual MEN1 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of different parathyroid hormone radioimmunoassays in uremic patients with secondary hyperparathyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline mutations of the MEN1 gene in Japanese kindred with multiple endocrine neoplasia type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the genetic defect in multiple endocrine neoplasia type 1 within a small region of chromosome 11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In situ analysis of human menin in normal and neoplastic pancreatic tissues: evidence for differential expression in exocrine and endocrine cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A large germline deletion of the MEN1 gene in a family with multiple endocrine neoplasia type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary hyperparathyroidism associatiated with aldosterone-producing adrenocortical adenoma and breast cancer: relation to MEN1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary cancer: two hits revisited

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype and phenocopy: the relationship between genotype and clinical phenotype in a single large family with multiple endocrine neoplasia type 1 (MEN 1)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Menin inactivation leads to loss of transforming growth factor beta inhibition of parathyroid cell proliferation and parathyroid hormone secretion

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of menin in parathyroid tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TGFbeta signaling and cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of mutations in patients with multiple endocrine neoplasia type 1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16943588

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1385/ENDO:29:3:485

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/16943588

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