A new mutation in the menin gene causes the multiple endocrine neoplasia type 1 syndrome with adrenocortical carcinoma

scientific article published on November 11, 2010

A new mutation in the menin gene causes the multiple endocrine neoplasia type 1 syndrome with adrenocortical carcinoma is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/S12020-010-9424-3
P953full work available at URLhttp://link.springer.com/content/pdf/10.1007/s12020-010-9424-3.pdf
http://link.springer.com/article/10.1007/s12020-010-9424-3/fulltext.html
http://link.springer.com/content/pdf/10.1007/s12020-010-9424-3
P698PubMed publication ID21069576

P2093author name stringM. Schott
E. Kaminsky
W. A. Scherbaum
M. Haase
Holger S. Willenberg
M. Anlauf
S. Schinner
P2860cites workPositional cloning of the gene for multiple endocrine neoplasia-type 1Q28307577
Mechanisms of disease: adrenocortical tumors--molecular advances and clinical perspectives.Q36643559
In search of tumor suppressing functions of meninQ36707655
Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related statesQ37198026
MEN1 gene and its mutations: basic and clinical implicationsQ37345051
Pathophysiological aspects of Wnt-signaling in endocrine diseaseQ37402178
Recognizing genes differentially regulated in vitro by the multiple endocrine neoplasia type 1 (MEN1) gene, using RNA interference and oligonucleotide microarrays.Q40190607
Adrenal lesions in a large kindred with multiple endocrine neoplasia type 1.Q41014429
Adrenal involvement in multiple endocrine neoplasia type 1: results of 7 years prospective screeningQ44521493
Menin promotes the Wnt signaling pathway in pancreatic endocrine cellsQ46613774
Differential expression of menin in various adrenal tumors. The role of menin in adrenal tumorsQ46731496
Adrenal lesion in multiple endocrine neoplasia type 1.Q50593991
Multiple endocrine neoplasias in the era of translational medicine.Q53270846
MEN1 gene analysis in sporadic adrenocortical neoplasms.Q53938524
Genotyping of Adrenocortical Tumors: Very Frequent Deletions of the MEN1 Locus in 11q13 and of a 1-Centimorgan Region in 2p16Q57274823
Clinical and genetic features of adrenocortical lesions in multiple endocrine neoplasia type 1Q67518300
MEN I gene mutations in sporadic adrenal adenomasQ73385722
Multiple endocrine neoplasia type 1 gene expression is normal in sporadic adrenocortical tumorsQ73816222
Adrenal involvement in multiple endocrine neoplasia type 1Q74119309
Genotyping of adrenocortical tumors: very frequent deletions of the MEN1 locus in 11q13 and of a 1-centimorgan region in 2p16Q74449566
MEN1 gene mutation analysis of sporadic adrenocortical lesionsQ77959348
P433issue2
P407language of work or nameEnglishQ1860
P921main subjectadrenocortical carcinomaQ918285
multiple endocrine neoplasiaQ1553018
multiple endocrine neoplasia type 1Q3347154
P304page(s)153-159
P577publication date2010-11-11
P1433published inEndocrineQ15757048
P1476titleA new mutation in the menin gene causes the multiple endocrine neoplasia type 1 syndrome with adrenocortical carcinoma
P478volume39

Reverse relations

cites work (P2860)
Q64230407Adrenocortical carcinoma in patients with MEN1: a kindred report and review of the literature
Q37972482Association of adrenocortical carcinoma with familial cancer susceptibility syndromes
Q37056120Causes of death and prognostic factors in multiple endocrine neoplasia type 1: a prospective study: comparison of 106 MEN1/Zollinger-Ellison syndrome patients with 1613 literature MEN1 patients with or without pancreatic endocrine tumors
Q39229792The tumor suppressor protein menin inhibits NF-κB-mediated transactivation through recruitment of Sirt1 in hepatocellular carcinoma

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