Early onset acromegaly associated with a novel deletion in CDKN1B 5'UTR region. (Q54293020)

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29 February 2020

title

Early onset acromegaly associated with a novel deletion in CDKN1B 5'UTR region (English)

1 reference

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29 February 2020

8

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29 February 2020

Natalia S. Pellegata

4

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29 February 2020

author name string

Silvia Sambugaro

1

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29 February 2020

Mauro Di Ruvo

2

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29 February 2020

Maria Rosaria Ambrosio

3

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29 February 2020

Mariaenrica Bellio

5

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29 February 2020

Alessandra Guerra

6

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29 February 2020

Mattia Buratto

7

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29 February 2020

Federico Tagliati

9

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29 February 2020

Ettore degli Uberti

10

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29 February 2020

Maria Chiara Zatelli

11

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29 February 2020

publication date

4 February 2015

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29 February 2020

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29 February 2020

volume

49

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29 February 2020

issue

1

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29 February 2020

page(s)

58-64

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https://scigraph.springernature.com/pub.10.1007/s12020-015-0540-y

29 February 2020

exact match

0 references

cites work

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Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans

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Cyclin-dependent kinase inhibitor 1B (CDKN1B) gene variants in AIP mutation-negative familial isolated pituitary adenoma kindreds

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Prevalence of AIP mutations in a large series of sporadic Italian acromegalic patients and evaluation of CDKN1B status in acromegalic patients with multiple endocrine neoplasia

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Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states

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A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype.

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Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia.

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A novel germline CDKN1B mutation causing multiple endocrine tumors: clinical, genetic and functional characterization

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Mutation and expression analysis of the cyclin-dependent kinase inhibitor gene p27/Kip1 in pituitary tumors.

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Functional characterization of a rare germline mutation in the gene encoding the cyclin-dependent kinase inhibitor p27Kip1 (CDKN1B) in a Spanish patient with multiple endocrine neoplasia-like phenotype.

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BRAF V600E mutation analysis increases diagnostic accuracy for papillary thyroid carcinoma in fine-needle aspiration biopsies.

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Magmas, a gene newly identified as overexpressed in human and mouse ACTH-secreting pituitary adenomas, protects pituitary cells from apoptotic stimuli

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Role of the ubiquitin-proteasome pathway in regulating abundance of the cyclin-dependent kinase inhibitor p27

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Overexpression of the S-phase kinase-associated protein 2 in thyroid cancer

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CDK2 is involved in the S-phase lengthening induced by glucocorticoids in normal human lymphocytes

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The p27-Skp2 axis mediates glucocorticoid-induced cell cycle arrest in T-lymphoma cells.

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PubMed

https://pubmed.ncbi.nlm.nih.gov/25645465

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Multiple endocrine neoplasia syndromes associated with mutation of p27.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25645465