Results 151 to 160 of about 12,302 (171)

Molecular Pathology of the MEN1 Gene

Annals of the New York Academy of Sciences, 2004
Multiple endocrine neoplasia type 1 (MEN1), among all syndromes, causes tumors in the highest number of tissue types. Most of the tumors are hormone producing (e.g., parathyroid, enteropancreatic endocrine, anterior pituitary) but some are not (e.g ...
Sunita Agarwal, Allen M Spiegel
exaly   +2 more sources

Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database [PDF]

Endocrine, 2018
Purpose: Multiple endocrine neoplasia type 1 (MEN1) is caused by germline inactivating mutations of the MEN1 gene. Currently, no direct genotype–phenotype correlation is identified.
Laura Masi, Claudio Marcocci, Annamaria Colao   +2 more
exaly   +2 more sources

Sarcomas arising in MEN1 patients: demonstrating LOH of the MEN1 locus and loss of menin expression [PDF]

Familial Cancer
Multiple endocrine neoplasia type 1 (MEN1) is a hereditary tumor syndrome characterized by endocrine tumors, typically from parathyroid, pancreatic, or anterior pituitary origin.
Rachel van Leeuwaarde, Thorvardur Halfdanarson, Andrew Folpe   +2 more
exaly   +3 more sources

Some of the next articles are maybe not open access.

Related searches:

Mixed gangliocytoma–pituitary adenoma in MEN1 syndrome: A case report and literature review

Neuropathology, 2022
Benjamin F Bitner
exaly  

Plasma Polyamines as an Additional to Imaging Biomarker in MEN1 Patients With Duodenopancreatic Neuroendocrine Tumors

Journal of Clinical Endocrinology and Metabolism, 2022
Gregory Kaltsas
exaly  

Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene

Human Mutation, 2008
Manuel C Lemos, Rajesh Thakker
exaly  

MEN1 mutations and potentially MEN1-targeting miRNAs are responsible for menin deficiency in sporadic and MEN1 syndrome-associated primary hyperparathyroidism

Virchows Archiv Fur Pathologische Anatomie Und Physiologie Und Fur Klinische Medizin, 2017
Attila Patocs, Annamaria Kovesdi, Kinga Nemeth   +2 more
exaly  

Germline mutation profile ofMEN1in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein

Human Mutation, 2002
Alain Calender, Christophe Beroud
exaly  

Pancreatic neuroendocrine tumors in MEN1 disease: a mono-centric longitudinal and prognostic study

Endocrine, 2017
Antonella Giampietro, Sabrina Chiloiro, Antonio Bianchi   +2 more
exaly