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EP400
ARID2 Deficiency Promotes Tumor Progression and Is Associated with Higher
Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK/ERK and PI3K/AKT Signaling Pathways
Natural Genetic Variation Caused by Small Insertions and Deletions in the Human Genome
1 Novel Expression Signatures Identified by Transcriptional Analysis
The Clinical Significance of Small Copy Number Variants In
RUVBL1 Antibody Cat
Anti-RUVBL1 / Pontin Antibody [1D6] (ARG57073)
Supplementary Material and Methods
Modeling Cancer Driver Events in Vitro Using Barrier Bypass-Clonal Expansion Assays and Massively Parallel Sequencing
Function and Regulation of the Tip60-P400 Complex in Embryonic Stem Cells: a Dissertation
Pan-Cancer Multi-Omics Analysis and Orthogonal Experimental Assessment of Epigenetic Driver Genes
Anti-TIP49 / RUVBL1 Antibody (Aa1-268) Rabbit Anti Human Polyclonal Antibody Catalog # ALS17399
Landscape of Protein–Protein Interactions in Drosophila Immune Deficiency Signaling During Bacterial Challenge
2021.05.30.446361.Full.Pdf
Sex Differences in Cancer Driver Genes and Biomarkers Constance H
Integrative Framework for Identification of Key Cell Identity Genes Uncovers
Functional Characterization of the TRRAP Pseudokinase and Its Chaperone TTT During Transcriptional Regulation in Colorectal Cancer Dylane Detilleux
Locally Disordered Methylation Forms the Basis of Intratumor Methylome Variation in Chronic Lymphocytic Leukemia
Top View
Somatic Genetic Variation in Solid Pseudopapillary Tumor of the Pancreas by Whole Exome Sequencing
Ruvb-Like 1 Antibody / RUVBL1 / TIP49A (F54729)
A Unique Missense Variant in the E1A-Binding Protein P400 Gene Is
Merkel Cell Polyomavirus Recruits MYCL to the EP400 Complex to Promote Oncogenesis
Potential Roles for ATP-Dependent Chromatin Remodelers in the Regulation of CTCF-Mediated 3D Architecture
Epilepsy Kinase CDKL5 Is a DNA Damage Sensor Which Controls Transcriptional Activity at DNA Breaks
Promoterless Transposon Mutagenesis Drives Solid Cancers Via Tumor Suppressor Inactivation
Genome-Wide Sirna Screen Identifies SMCX, EP400, and Brd4 As E2
Molecular Complexes at Euchromatin, Heterochromatin and Centromeric Chromatin
Significant Linkage to Chromosome 12Q24.32– Q24.33 And
Description: Uniprot:Q9Y265 Alternative Names: Specificity
Identification of Monotonically Differentially Expressed Genes for Non-Small Cell Lung Cancer Suyan Tian
RUVBL1 Antibody Mouse Monoclonal Antibody (Mab) Catalog # Am2039b
ZMYM3 Regulates BRCA1 Localization at Damaged Chromatin to Promote DNA Repair
Enhanced MYC Association with the Nua4 Histone Acetyltransferase
Microrna Binding Microrna Binding Probe Set Entrez Gene Gene
Recognition of Histone Acetylation by the GAS41 YEATS Domain Promotes H2A.Z Deposition in Non-Small Cell Lung Cancer
Haploinsufficiency of RREB1 Causes a Noonan-Like Rasopathy Via
2021.08.11.456009.Full.Pdf
GEM Development Breast Cancer Previous Breast Patient Population Cancer Patient Set (N=251, Miller 2005) NCI-60 Panel (N=133, Hess Et Al `05)
Natural Genetic Variation Caused by Small Insertions and Deletions in the Human Genome
Inbreeding and Inbreeding Depression in Linebred Beef Cattle (PDF)
Proteomic Analysis of Mouse Oocytes Reveals 28 Candidate Factors of the “Reprogrammome” Martin J
Cohesin Disrupts Polycomb-Dependent Chromosome Interactions
Genetic Variation and Autism: a Field Synopsis and Systematic Meta-Analysis