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Exploring Autophagy with Gene Ontology
The Genetics of Bipolar Disorder
1 Supplementary Materials: Fig
Agricultural University of Athens
Detection of H3k4me3 Identifies Neurohiv Signatures, Genomic
Interactions of the Human LIP5 Regulatory Protein with Endosomal Sorting Complexes Required for Transport Jack J
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
S41467-019-13965-X.Pdf
Mass Spectrometry-Based Proteomic Discovery of Prognostic Biomarkers in Adrenal Cortical Carcinoma
Molecular Genetics of Frontotemporal Dementia Elucidated by Drosophila Models—Defects in Endosomal–Lysosomal Pathway
Supplementary Information
The Glomerular Transcriptome and a Predicted Protein–Protein Interaction Network
Combining Genome Wide Association Studies and Differential Gene
Whole-Exome Sequencing and Genome-Wide Evolutionary
Detection of Rare Germline Variants in the Genomes of Patients with B-Cell Neoplasms
Microsatellite Scanning of the Immunogenome for Associations with Graft-Versus-Host Disease Following Haematopoietic Stem Cell Transplantation
Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants
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Large-Scale Neuroanatomical Study Uncovers 198 Gene Associations in Mouse Brain Morphogenesis
Identifying Proteins Controlling Key Disease Signaling Pathways
Modeling Microcephaly Caused by Inactivation of the Minor
RUNX1-EVI1 Disrupts Lineage Determination and the Cell Cycle by Interfering with RUNX1 and EVI1 Driven Gene Regulatory Networks
The Aryl Hydrocarbon Receptor Pathway: a Key Component of the Microrna-Mediated AML Signalisome
Generating and Characterising Knockout and Transgenic Mouse Models of Frontotemporal Dementia Caused by CHMP2B Mutation
Attractor Metafeatures and Their Application in Biomolecular Data Analysis
Insights Into Herpesvirus Assembly from the Structure of the Pul7