Functional characterization of a CDKN1B mutation in a Sardinian kindred with multiple endocrine neoplasia type 4 (MEN4).
about
Multiple Endocrine Neoplasia: Genetics and Clinical Management.Animal models of pituitary neoplasiaAn unusual phenotype of MEN1 syndrome with a SI-NEN associated with a deletion of the MEN1 geneMutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features.Heritable forms of primary hyperparathyroidism: a current perspective.MEN1 mutations and potentially MEN1-targeting miRNAs are responsible for menin deficiency in sporadic and MEN1 syndrome-associated primary hyperparathyroidism.MEN4 and CDKN1B mutations: the latest of the MEN syndromes.Loss of p27 expression is associated with MEN1 gene mutations in sporadic parathyroid adenomas.Genetics of Cushing's Syndrome.Landscape of CDKN1B Mutations in Luminal Breast Cancer and Other Hormone-Driven Human Tumors
P2860
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P2860
Functional characterization of a CDKN1B mutation in a Sardinian kindred with multiple endocrine neoplasia type 4 (MEN4).
description
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name
Functional characterization of ...... crine neoplasia type 4 (MEN4).
@en
Functional characterization of ...... ple endocrine neoplasia type 4
@nl
type
label
Functional characterization of ...... crine neoplasia type 4 (MEN4).
@en
Functional characterization of ...... ple endocrine neoplasia type 4
@nl
prefLabel
Functional characterization of ...... crine neoplasia type 4 (MEN4).
@en
Functional characterization of ...... ple endocrine neoplasia type 4
@nl
P2093
P2860
P356
P1476
Functional characterization of ...... crine neoplasia type 4 (MEN4).
@en
P2093
Antonello Cappai
Chiara Satta
Claudio Marcocci
Elena Pardi
Federica Saponaro
Filomena Cetani
Katiuscia Benfini
Liborio Torregrossa
Marco Mastinu
Natalia S Pellegata
P2860
P356
10.1530/EC-14-0116
P577
2014-11-21T00:00:00Z