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CDKN2BAS
Long Noncoding RNA and Cancer: a New Paradigm Arunoday Bhan, Milad Soleimani, and Subhrangsu S
Genetic Characterization of Endometriosis Patients: Review of the Literature and a Prospective Cohort Study on a Mediterranean Population
CDKN2A and CDKN2B Methylation in Coronary Heart Disease Cases and Controls
With Coronary Heart Disease: a Case-Control Study and a Meta-Analysis
Common Variants at 9P21 and 8Q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma
CDKN2BAS Gene Polymorphisms and the Risk of Intracranial Aneurysm In
LINC01106 Post-Transcriptionally Regulates ELK3 and HOXD8 to Promote Bladder Cancer Progression Liwei Meng1,Zhaoquanxing1, Zhaoxin Guo1 and Zhaoxu Liu1
Glycosyltransferase B4GALNT2 As a Predictor of Good Prognosis in Colon Cancer: Lessons from Databases
Centre for Arab Genomic Studies a Division of Sheikh Hamdan Award for Medical Sciences
CDKN2BAS Is Associated with Periodontitis
CDKN2BAS Polymorphisms Are Associated with Coronary Heart Disease Risk a Han Chinese Population
Original Article CDKN2BAS Polymorphisms Are Associated with Coronary Artery Disease in Chinese Han Population
Lncrna CDKN2BAS Aggravates the Progression of Ovarian Cancer by Positively Interacting with GAS6
CDKN2A/B Alterations Impair Prognosis in Adult BCR-ABL1– Positive Acute Lymphoblastic Leukemia Patients
The Severity of Internal Carotid Artery Stenosis Is Associated with the Cyclin-Dependent Kinase Inhibitor 2A Gene Expression
Non-Coding Rnas As Biomarkers of Tumor Progression and Metastatic Spread in Epithelial Ovarian Cancer
NIH Public Access Author Manuscript Nature
What Are Genome-Wide Association Studies Telling Us About B-Cell Tumor Development?
Top View
TCF21 and AP-1 Interact Through Epigenetic Modifications to Regulate
Meta-Analysis of Genome-Wide Association Studies Identifies Novel Loci That Influence Cupping and the Glaucomatous Process
TCF21 and AP-1 Interact Through Epigenetic Modifications to Regulate Coronary Artery Disease Gene Expression
Association of Polymorphisms in MALAT1 with Risk of Coronary
Association Analyses Based on False Discovery Rate Implicate New Loci for Coronary Artery Disease
Is Associated with Poor Prognosis in Ovarian Clear Cell Adenocarcinoma Via TRAIL-Induced Apoptotic Pathway Regulation
ANRIL: Molecular Mechanisms and Implications in Human Health
4487950.Pdf (473.3Kb)
ANRIL Is Implicated in the Regulation of Nucleus and Potential Transcriptional Target of E2F1
Roles As Sensors Regulating Gene Transcriptional Programs
Thirty-Five Common Variants for Coronary Artery Disease
Genome-Wide Association Analysis Identifies TXNRD2, ATXN2 and FOXC1 As Susceptibility Loci for Primary Open Angle Glaucoma
Genome-Wide Association Studies on Endometriosis and Endometriosis-Related Infertility
Variants As Novel Markers for Coronary Artery Disease
Genome-Wide Genetic Analyses Highlight Mitogen-Activated Protein Kinase (MAPK) Signaling in the Pathogenesis of Endometriosis
Type 1 Diabetic Mellitus Patients with Increased Atherosclerosis Risk
A Large De Novo 9P21.3 Deletion in a Girl Affected by Astrocytoma And
Long Noncoding RNA and Cancer: a New Paradigm Arunoday Bhan, Milad Soleimani, and Subhrangsu S