MEN1 gene and its mutations: basic and clinical implications.

MEN1 gene and its mutations: basic and clinical implications.

Item
http://www.wikidata.org/entity/Q37345051
Loss of menin mediated by endothelial cells treated with CoPP is associated with increased maturation of adipocytesMenin represses tumorigenesis via repressing cell proliferation.Molecular alterations in sporadic primary hyperparathyroidismA new double substitution mutation in the MEN1 gene: a limited penetrance and a specific phenotype.Multiple Endocrine Neoplasia: A Genetically Diverse Group of Familial Tumor Syndromes.Menin and GIP are inversely regulated by food intake and diet via PI3/AKT signaling in the proximal duodenum.Expression and subcellular localization of menin in human cancer cells.Intracranial ependymoma associated with multiple endocrine neoplasia type 1.Correlation of mutant menin stability with clinical expression of multiple endocrine neoplasia type 1 and its incomplete forms.
P2860

MEN1 gene and its mutations: basic and clinical implications.

Item
http://www.wikidata.org/entity/Q37345051
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on February 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
MEN1 gene and its mutations: basic and clinical implications.
@en
MEN1 gene and its mutations: basic and clinical implications.
@nl
type
label
MEN1 gene and its mutations: basic and clinical implications.
@en
MEN1 gene and its mutations: basic and clinical implications.
@nl
prefLabel
MEN1 gene and its mutations: basic and clinical implications.
@en
MEN1 gene and its mutations: basic and clinical implications.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P577
P5875
P698
P356
P1433
P1476
MEN1 gene and its mutations: basic and clinical implications.
@en
P2093
P2860
P304
P31
P356
10.1111/J.1349-7006.2008.01034.X
P433
P478
P577
P5875
P698