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COG3
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Essential Genes and Their Role in Autism Spectrum Disorder
Chromosomal Rearrangements Are Commonly Post-Transcriptionally Attenuated in Cancer
Whole-Genome Cancer Analysis As an Approach to Deeper Understanding of Tumour Biology
Cog5–Cog7 Crystal Structure Reveals Interactions Essential for the Function of a Multisubunit Tethering Complex
Identification of a Clinically Relevant Androgen-Dependent Gene Signature in Prostate Cancer
Papadaki Et Al., 2009 Supplementary
1 Genome-Wide CRISPR-Cas9 Screen Reveals Common Factors in Dsrna and Sindbis Virus
Detection of H3k4me3 Identifies Neurohiv Signatures, Genomic
Increased RNA Editing in Maternal Immune Activation Model of Neurodevelopmental Disease
S41467-019-13965-X.Pdf
NIH Public Access Author Manuscript Mol Cell
THE USE of WHOLE EXOME SEQUENCING to DETECT NOVEL GENETIC DISORDERS: TWO CASES and an ASSESSMENT of the TECHNOLOGY by Lauren
Microrna-15A and -16-1 Act Via MYB to Elevate Fetal Hemoglobin Expression in Human Trisomy 13
Conserved Oligomeric Golgi Complex Subunit 1 Deficiency Reveals a Previously Uncharacterized Congenital Disorder of Glycosylation Type II
Pan-Cancer Molecular Subtypes Revealed by Mass-Spectrometry
Supplementary Information
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
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Assigned Reading
Germinal GLT8D1, GATAD2A and SLC25A39 Mutations in a Patient
University of California Santa Cruz the Identification And
Development of a Cellular Model for C9ORF72-Related Amyotrophic Lateral Sclerosis
An Improved Method to Align PPI Networks Based on Gene Ontology and Graphlets
Location Genename Changetype Aachange Typegenomicregion
Genome-Wide Characterization of RNA Editing in Chicken Embryos
The Extent of Mrna Editing Is Limited
COG Complexes Form Spatial Landmarks for Distinct SNARE Complexes
Germinal GLT8D1, GATAD2A and SLC25A39 Mutations in a Patient with a Glomangiopericytal Tumor and Fve Different Sarcomas Over a 10-Year Period
Systematic Evaluation of the Effect of Common Snps on Pre-Mrna Splicing
Verteporfin Inhibits PD-L1 Through Autophagy and the STAT1–IRF1
Phenotype Correlations in Patients with Retinoblastoma and Interstitial 13Q Deletions
Verteporfin Inhibits PD-L1 Through Autophagy and the STAT1–IRF1
RNA Sequencing Unravels the Genetics of Refractory/Relapsed T-Cell Acute Lymphoblastic Leukemia
Supplementary Table 1. a Full List of Cancer Genes
Deciphering the Genetic Heterogeneity in Acute Myeloid Leukemia: Association of Gene Mutations with Distinct Chromosomal Aberrations
Golgi Glycosylation and Human Inherited Diseases