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BNC1
Primepcr™Assay Validation Report
The DNA Methylation Landscape of Glioblastoma Disease Progression Shows Extensive Heterogeneity in Time and Space
Identification of Novel DNA-Methylated Genes
Rna-Sequencing Applications: Gene Expression Quantification and Methylator Phenotype Identification
The GALNT9, BNC1 and CCDC8 Genes Are Frequently Epigenetically Dysregulated in Breast Tumours That Metastasise to the Brain Rajendra P
Identification of Candidate Tumour Suppressor Genes Frequently
Genomic Anatomy of the Tyrp1 (Brown) Deletion Complex
393LN V 393P 344SQ V 393P Probe Set Entrez Gene
Genome-Wide Analysis of Promoter Methylation Associated with Gene Expression Profile in Pancreatic Adenocarcinoma
Basonuclin 2 Has a Function in the Multiplication of Embryonic Craniofacial Mesenchymal Cells and Is Orthologous to Disco Proteins
The Cancer Genome Atlas Dataset-Based Analysis of Aberrantly Expressed Genes by Geneanalytics in Thymoma Associated Myasthenia Gravis: Focusing on T Cells
BNC1 Regulates Human Epicardial Heterogeneity and Function
Title Analysis of the Genome Architecture of The
Positive Selection in Transcription Factor Genes
A 15Q25.2 Microdeletion Phenotype For
RNA-Seq Analysis of Broiler Liver Transcriptome Reveals Novel Responses to High Ambient Temperature Derrick Jamaal Coble Iowa State University
The Synthetic Histone-Binding Regulator Protein Pctf Activates Interferon Genes in Breast Cancer Cells Kimberly C
Introductory Remarks on the Milieux of the Egg and the Early Embryo
Top View
Syntabulin Regulates the Trafficking of PICK1-Containing Vesicles in Neurons
Supplemental Table 1. Exome Variant Filtering Strategy a Based on UCSC
Decreased Expression of BNC1 and BNC2 Is Associated with Genetic Or Epigenetic Regulation in Hepatocellular Carcinoma
Supplementary Table 6: Transcripts with a Significant Difference in Expression Between Insulin- and X10- Treated Animal
A Comprehensive Genomic Pan-Cancer Classification Using the Cancer Genome Atlas Gene Expression Data Yuanyuan Li1, Kai Kang1, Juno M
A Novel Microdeletion Syndrome Involving 5Q14.3-Q15: Clinical and Molecular Cytogenetic Characterization of Three Patients
CAMOS, a Nonprogressive, Autosomal Recessive, Congenital Cerebellar Ataxia, Is Caused by a Mutant Zinc-finger Protein, ZNF592
Basonuclin-1 Modulates Epithelial Plasticity and TGF-&Beta
Integration of a Single-Step Genome-Wide Association Study
Overexpression and Activation of Αvβ3 Integrin Differentially Affects Tgfβ2 Signaling in Human Trabecular Meshwork Cells
Mouse Bnc1 Conditional Knockout Project (CRISPR/Cas9)