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KMT2E
Modes of Interaction of KMT2 Histone H3 Lysine 4 Methyltransferase/COMPASS Complexes with Chromatin
S41467-020-18249-3.Pdf
Get.Com Oncotarget, 2018, Vol
Open Data for Differential Network Analysis in Glioma
Deletions of Chromosome 7Q Affect Nuclear Organization And
Decreased DNA Methylation at Promoters and Gene-Specific Neuronal
Variation in Protein Coding Genes Identifies Information Flow
The Changing Chromatome As a Driver of Disease: a Panoramic View from Different Methodologies
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
Enabling Efficient and Streamlined Access to Large Scale Genomic Expression and Splicing Data
Supplementary Materials For
Genome-Wide Gene Expression Profiling of Randall's Plaques In
Abstracts Selected for Poster Presentations
Epigenome Alterations in Aortic Valve Stenosis and Its Related Left
Evidence Supporting Whole Exome Sequencing As a First-Tier Test
1 SUPPLEMENTARY METHODS Scoring the Schizophrenia Risk Gene
180K Probe Array-CGH Test Returned Normal Results
Whole Genome Sequencing of the Mutamouse Model Reveals Strain
Top View
Leveraging Large Genomic Datasets to Illuminate the Pathobiology of Autism Spectrum Disorders
Molecular Basis for Chromatin Binding and Regulation of MLL5
Supplementary Data)
Promoterless Transposon Mutagenesis Drives Solid Cancers Via Tumor Suppressor Inactivation
MLL5 Antibody (N-Term) Blocking Peptide Synthetic Peptide Catalog # Bp14173a
The Chromatin Architecture of the Chromosomal Region 7Q36.3, Frequently Rearranged in Leukemic Cells, Is Evolutionary Conserved
Loss and Gain of N-Linked Glycosylation Sequons Due to Single
Structure-Function Relationships of Rna and Protein in Synaptic Plasticity
Insights Into Early Development from Genetic and Epigenetic Data Across Tissue Types
Identification of Common Genetic Risk Variants for Autism Spectrum Disorder
Molecular Dysregulation in Autism Spectrum Disorder
Demographic Histories and Genome-Wide Patterns of Divergence in Incipient Species of Shorebirds
A Child with Multiple Congenital Anomalies Due to Partial Trisomy
A Transcriptome-Wide Association Study Based on 27 Tissues Identifies 106 Genes Potentially Relevant for Disease Pathology in Age-Related Macular Degeneration
An MXD1-Derived Repressor Peptide Identifies Noncoding Mediators of MYC-Driven Cell Proliferation
Somatic Variants in Epigenetic Modifiers Can Predict Failure of Response to Imatinib but Not to Second-Generation Tyrosine Kinase Inhibitors
MLL5 Antibody (N-Term) Affinity Purified Rabbit Polyclonal Antibody (Pab) Catalog # Ap14173a
Isoform Transcriptome of Developing Human Brain Provides New Insights