Results 1 to 10 of about 61,476 (246)
The CDKN2A (cyclin dependent kinase inhibitor 2A/multiple tumor suppressor 1) gene, also known as the P16 gene, encodes multiple tumor suppressor 1 (MTS1), which belongs to the INK4 family.
Quan Zou, Yingjie Guo, Da Zhao
exaly +3 more sources
Homozygous deletion (HD) of CDKN2A and CDKN2B (CDKN2A/BHD) is the most frequent copy‐number variation (CNV) in lung adenocarcinoma (LUAD). CDKN2A/BHD has been associated with poor outcomes in LUAD; however, the mechanisms of its prognostic effect remain ...
Liyan Ji, Pansong Li, Zhenzhou Yang
exaly +2 more sources
Transcriptomic Analysis Identifies CDKN2A-Associated Transcriptional Alterations in Primary Melanocytes of Lueyang Black-Boned Chicken [PDF]
Pronounced melanin enrichment characterizes the Lueyang black-boned chicken, yet the transcriptional basis underlying this pigmentation phenotype remains incompletely understood.
Fan Li +7 more
doaj +2 more sources
Association of CDKN2A overexpression with poor prognosis, radioresistance, and immunosuppression in colorectal cancer [PDF]
BackgroundIn colorectal cancer (CRC), dysregulated cyclin-dependent kinase inhibitor 2A (CDKN2A) contributes to disease progression. This investigation sought to explore the link between CDKN2A expression and the effectiveness of radiotherapy in CRC, and
Yaobin Lin +7 more
doaj +2 more sources
CDKN2A Deletion Leading to Hematogenous Metastasis of Human Gastric Carcinoma
IntroductionSomatic copy number deletion (SCND) of CDKN2A gene is the most frequent event in cancer genomes. Whether CDKN2A SCND drives human cancer metastasis is far from clear.
Dajun Deng, Jiafu Ji, Jing Zhou
exaly +3 more sources
The prognostic significance of p16 expression pattern in diffuse gliomas [PDF]
Background CDKN2A is a tumor suppressor gene that encodes the cell cycle inhibitor protein p16. Homozygous deletion of the CDK-N2A gene has been associated with shortened survival in isocitrate dehydrogenase (IDH)–mutant gliomas.
Jin Woo Park +7 more
doaj +1 more source
Methylation of F2RL3, CDKN2A genes and sudden cardiac death
The aim of the study was to evaluate the association of methylation of the F2RL3, CDKN2A gene with sudden cardiac death (SCD). Material and methods. Case-control study design.
Anastasiya A. Ivanova +5 more
doaj +1 more source
Introduction: We have observed that most cutaneous melanoma patients under our supervision lack characteristic phenotypical features for melanoma. In contrast; history of cancers other than melanoma and age at onset before 50 were common.
Aysel Çakır +5 more
doaj +1 more source
BackgroundA feasible method to detect somatic copy number deletion (SCND) of genes is still absent to date.MethodsInterstitial base-resolution deletion/fusion coordinates for CDKN2A were extracted from published articles and our whole genome sequencing ...
Yuan Tian +8 more
doaj +1 more source
Aim. Study the effect of single nucleotide polymorphism genes TP53 (rsl042522, rsl 800371), CDKN2A (rs3731217, rs3088440) and MDM2 (rs2279744) on the risk of development of colorectal cancer (CRC) in population of Perm Region. Materials and methods. Case
M. Kh. Alyeva +5 more
doaj +1 more source

