scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1078748405 |
P356 | DOI | 10.3275/9021 |
P698 | PubMed publication ID | 23800691 |
P50 | author | Natalia S. Pellegata | Q55691848 |
P2093 | author name string | M Lee | |
P2860 | cites work | Multiple endocrine neoplasia type 2 | Q21203027 |
Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans | Q24679314 | ||
SKP2 is required for ubiquitin-mediated degradation of the CDK inhibitor p27 | Q28137860 | ||
Phosphorylation of p27Kip1 on serine 10 is required for its binding to CRM1 and nuclear export | Q28206256 | ||
Inhibitors of mammalian G1 cyclin-dependent kinases | Q29547907 | ||
Role of the ubiquitin-proteasome pathway in regulating abundance of the cyclin-dependent kinase inhibitor p27 | Q29617346 | ||
Polymorphisms cMyc-N11S and p27-V109G and breast cancer risk and prognosis | Q33287624 | ||
Forkhead transcription factor FKHR-L1 modulates cytokine-dependent transcriptional regulation of p27(KIP1). | Q33606105 | ||
Regulation of the cdk inhibitor p27 and its deregulation in cancer | Q33853211 | ||
Characterization of a naturally-occurring p27 mutation predisposing to multiple endocrine tumors. | Q33898315 | ||
Guidelines for diagnosis and therapy of MEN type 1 and type 2. | Q34104591 | ||
PKB/Akt mediates cell-cycle progression by phosphorylation of p27(Kip1) at threonine 157 and modulation of its cellular localization | Q34150579 | ||
A polymorphism in the CDKN1B gene is associated with increased risk of hereditary prostate cancer | Q34306506 | ||
Cytoplasmic ubiquitin ligase KPC regulates proteolysis of p27(Kip1) at G1 phase | Q34365993 | ||
Increased proteasome-dependent degradation of the cyclin-dependent kinase inhibitor p27 in aggressive colorectal carcinomas. | Q34415250 | ||
A novel germline CDKN1B mutation causing multiple endocrine tumors: clinical, genetic and functional characterization | Q34635679 | ||
A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype. | Q34649802 | ||
Somatic mutation and germline sequence abnormalities in CDKN1B, encoding p27Kip1, in sporadic parathyroid adenomas | Q34758456 | ||
The Cdk inhibitor p27 in human cancer: prognostic potential and relevance to anticancer therapy | Q34763495 | ||
Discovery of an oncogenic activity in p27Kip1 that causes stem cell expansion and a multiple tumor phenotype | Q35893635 | ||
Variable clinical expression in patients with a germline MEN1 disease gene mutation: clues to a genotype-phenotype correlation. | Q35895504 | ||
Molecular genetics of multiple endocrine neoplasia types 1 and 2. | Q36111935 | ||
Molecular pathogenesis of MEN2-associated tumors | Q36121928 | ||
Differential regulation of p27(Kip1) expression by mitogenic and hypertrophic factors: Involvement of transcriptional and posttranscriptional mechanisms | Q36327496 | ||
Impact of RET proto-oncogene analysis on the clinical management of multiple endocrine neoplasia type 2. | Q36419268 | ||
p27(Kip1) V109G polymorphism and cancer risk: a systematic review and meta-analysis | Q36451110 | ||
The multiple endocrine neoplasia syndromes | Q36622153 | ||
The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations | Q36735215 | ||
Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states | Q37198026 | ||
Cyclin-dependent kinase inhibitor 1B (CDKN1B) gene variants in AIP mutation-negative familial isolated pituitary adenoma kindreds | Q39403888 | ||
Enhanced ribosomal association of p27(Kip1) mRNA is a mechanism contributing to accumulation during growth arrest. | Q41120998 | ||
Alterations of the p27KIP1 gene in non-Hodgkin's lymphomas and adult T-cell leukemia/lymphoma | Q41302507 | ||
Cyclin E-CDK2 is a regulator of p27Kip1. | Q42800258 | ||
Association between the V109G polymorphism of the p27 gene and the risk and progression of oral squamous cell carcinoma | Q44951962 | ||
Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia | Q48079288 | ||
Allelic variant at -79 (C>T) in CDKN1B (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels. | Q53348388 | ||
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. | Q54546392 | ||
Recessive transmission of a multiple endocrine neoplasia syndrome in the rat | Q63951641 | ||
p27/Kip1 mutation found in breast cancer | Q71067651 | ||
The ETV6, CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberration in different hematological malignancies | Q71934956 | ||
Inverse relation between levels of p27(Kip1) and of its ubiquitin ligase subunit Skp2 in colorectal carcinomas | Q73833543 | ||
A novel p27 gene mutation in a case of unclassified myeloproliferative disorder | Q81164172 | ||
Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain | Q82192110 | ||
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | multiple endocrine neoplasia | Q1553018 |
P304 | page(s) | 781-787 | |
P577 | publication date | 2013-06-26 | |
P1433 | published in | Journal of Endocrinological Investigation | Q15766847 |
P1476 | title | Multiple endocrine neoplasia syndromes associated with mutation of p27 | |
P478 | volume | 36 |
Q37634917 | Decoding the Molecular and Mutational Ambiguities of Gastroenteropancreatic Neuroendocrine Neoplasm Pathobiology. |
Q54293020 | Early onset acromegaly associated with a novel deletion in CDKN1B 5'UTR region. |
Q47159773 | Functional characterization of a CDKN1B mutation in a Sardinian kindred with multiple endocrine neoplasia type 4 (MEN4). |
Q53683262 | Genetics of Cushing's Syndrome. |
Q53131281 | Loss of p27 expression is associated with MEN1 gene mutations in sporadic parathyroid adenomas. |
Q33904619 | Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's disease |
Q38313735 | MicroRNA deregulation in parathyroid tumours suggests an embryonic signature. |
Q39412594 | Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood |
Q91758387 | Multiple endocrine neoplasia-like syndrome in 24 baboons (Papio spp.). |
Q42695925 | Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features. |
Q38858270 | Towards a new classification of gastroenteropancreatic neuroendocrine neoplasms |
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