Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans
about
Acromegaly pathogenesis and treatmentDifferential gene expression of p27Kip1 and Rb knockout pituitary tumors associated with altered growth and angiogenesisThe PI3K/Akt Pathway in Tumors of Endocrine TissuesMurine models and cell lines for the investigation of pheochromocytoma: applications for future therapies?The molecular pathogenesis of pituitary adenomas: an updateAdvances in small bowel neuroendocrine neoplasiaGenetic and epigenetic changes in sporadic endocrine tumors: parathyroid tumorsMEN1, MEN4, and Carney Complex: Pathology and Molecular GeneticsMultiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4)High-throughput screening reveals alsterpaullone, 2-cyanoethyl as a potent p27Kip1 transcriptional inhibitorGastrinoma and neurofibromatosis type 2: the first case report and review of the literature.A functional genome-wide RNAi screen identifies TAF1 as a regulator for apoptosis in response to genotoxic stress.Temozolomide and pasireotide treatment for aggressive pituitary adenoma: expertise at a tertiary care center.Secretin receptor promotes the proliferation of endocrine tumor cells via the PI3K/AKT pathway.Familial isolated pituitary adenomas: from genetics to therapy.AHR over-expression in papillary thyroid carcinoma: clinical and molecular assessments in a series of Italian acromegalic patients with a long-term follow-up.Characterization of a naturally-occurring p27 mutation predisposing to multiple endocrine tumors.Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's diseaseLoss of function of the tumor suppressor DKC1 perturbs p27 translation control and contributes to pituitary tumorigenesis.Clinical and molecular genetics of parathyroid neoplasmsMouse models of endocrine tumours.Genetic screening for multiple endocrine neoplasia syndrome type 1 (MEN-1): when and howSolid tumors associated with multiple endocrine neoplasias.Genetic characterization of large parathyroid adenomasPheochromocytoma in rats with multiple endocrine neoplasia (MENX) shares gene expression patterns with human pheochromocytoma.Mutation analysis of inhibitory guanine nucleotide binding protein alpha (GNAI) loci in young and familial pituitary adenomas.p27 Loss Is Associated with Poor Prognosis in Gastroenteropancreatic Neuroendocrine Tumors.Anterior pituitary adenomas: inherited syndromes, novel genes and molecular pathways.Hyperparathyroid genes: sequences reveal answers and questions.The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes.A novel germline CDKN1B mutation causing multiple endocrine tumors: clinical, genetic and functional characterization.A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype.Components of the canonical and non-canonical Wnt pathways are not mis-expressed in pituitary tumorsSomatic mutation and germline sequence abnormalities in CDKN1B, encoding p27Kip1, in sporadic parathyroid adenomasPrimary hyperparathyroidism: an overview.Multiple endocrine neoplasias: advances and challenges for the futureDeconstructing pancreas development to reconstruct human islets from pluripotent stem cells.Glucagon receptor gene mutations with hyperglucagonemia but without the glucagonoma syndrome.p27(Kip1) is required to maintain proliferative quiescence in the adult cochlea and pituitary.Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations
P2860
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P2860
Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans
description
2006 nî lūn-bûn
@nan
2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Germ-line mutations in p27Kip1 ...... ia syndrome in rats and humans
@ast
Germ-line mutations in p27Kip1 ...... ia syndrome in rats and humans
@en
Germ-line mutations in p27Kip1 ...... ia syndrome in rats and humans
@nl
type
label
Germ-line mutations in p27Kip1 ...... ia syndrome in rats and humans
@ast
Germ-line mutations in p27Kip1 ...... ia syndrome in rats and humans
@en
Germ-line mutations in p27Kip1 ...... ia syndrome in rats and humans
@nl
prefLabel
Germ-line mutations in p27Kip1 ...... ia syndrome in rats and humans
@ast
Germ-line mutations in p27Kip1 ...... ia syndrome in rats and humans
@en
Germ-line mutations in p27Kip1 ...... ia syndrome in rats and humans
@nl
P2093
P2860
P50
P3181
P356
P1476
Germ-line mutations in p27Kip1 ...... ia syndrome in rats and humans
@en
P2093
Elenore Samson
Heide Siggelkow
Heinz Höfler
Karin Bink
P2860
P304
P3181
P356
10.1073/PNAS.0603877103
P407
P50
P577
2006-10-17T00:00:00Z