A common variant of CDKN2A (p16) predisposes to breast cancer. - Wikidata - wikimedia - TriplyDB

A common variant of CDKN2A (p16) predisposes to breast cancer.

A common variant of CDKN2A (p16) predisposes to breast cancer.

http://www.wikidata.org/entity/Q35447197

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Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression Association between melanocytic nevi and risk of breast diseases: The French E3N prospective cohort.Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment Potential dual immunomodulatory role of VEGF in ulcerative colitis and colorectal carcinoma Franklin H. Epstein Lecture. Both ends of the leash--the human links to good dogs with bad genes.The chromosome 9p21.3 coronary heart disease risk allele is associated with altered gene expression in normal heart and vascular tissues Common low-penetrance risk variants associated with breast cancer in Polish women.Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counseling.Identification of a comprehensive spectrum of genetic factors for hereditary breast cancer in a Chinese population by next-generation sequencing.CDKN2A mutations and melanoma risk in the Icelandic population.Risk of second primary cancer in men with breast cancer Precursors and preinvasive lesions of the breast: the role of molecular prognostic markers in the diagnostic and therapeutic dilemma.Risk of non-melanoma cancers in first-degree relatives of CDKN2A mutation carriers Hypermethylation of the 5' CpG island of the p14ARF flanking exon 1β in human colorectal cancer displaying a restricted pattern of p53 overexpression concomitant with increased MDM2 expression.DNA testing for variants conferring low or moderate increase in the risk of cancer.Genetic mechanisms mediating atherosclerosis susceptibility at the chromosome 9p21 locus.Coverage of the genetic background of breast cancer in the polish population.Low-risk Genes and Multi-organ Cancer Risk in the Polish Population.The CDKN2A p.A148T variant is associated with cutaneous melanoma in Southern Brazil.A genetic variant in CDKN2A/B gene is associated with the increased risk of breast cancer.Malignant melanoma and breast carcinoma: a bidirectional correlation.Oncogenic BRAF mutations and p16 expression in melanocytic nevi and melanoma in the Polish population.The genetics of melanoma

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P2860

A common variant of CDKN2A (p16) predisposes to breast cancer.

http://www.wikidata.org/entity/Q35447197

description

2005 nî lūn-bûn

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2005 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2005 թվականի մայիսին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

A common variant of CDKN2A (p16) predisposes to breast cancer.

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A common variant of CDKN2A (p16) predisposes to breast cancer.

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type

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A common variant of CDKN2A (p16) predisposes to breast cancer.

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A common variant of CDKN2A (p16) predisposes to breast cancer.

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A common variant of CDKN2A (p16) predisposes to breast cancer.

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A common variant of CDKN2A (p16) predisposes to breast cancer.

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JMG.2005.031476

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Journal of Medical Genetics

P1476

A common variant of CDKN2A (p16) predisposes to breast cancer.

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Debniak T

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Gozdecka-Grodecka S

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Gronwald J

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Grzybowska E

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Górski B

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Góźdź S

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Haus O

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Huzarski T

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Kowalska E

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Mackiewicz A

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P2860

A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4

CHEK2 is a multiorgan cancer susceptibility gene.

Identification of a splice acceptor site mutation in p16INK4A/p14ARF within a breast cancer, melanoma, neurofibroma prone kindred

Aberrant methylation of p16(INK4a) is an early event in lung cancer and a potential biomarker for early diagnosis

Alterations of p16-pRb pathway and chromosome locus 9p21-22 in sporadic invasive breast carcinomas.

Germ-line p53 mutations predispose to a wide spectrum of early-onset cancers.

Methylation silencing and mutations of the p14ARF and p16INK4a genes in colon cancer.

Cancer-associated mis-sense and deletion mutations impair p16INK4 CDK inhibitory activity.

Hereditary p16-Leiden mutation in a patient with multiple head and neck tumors.

CDKN2A common variants and their association with melanoma risk: a population-based study.

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10.1136/JMG.2005.031476

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Cezary Cybulski

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