CCDC88A - Docslib

Biological Models of Colorectal Cancer Metastasis and Tumor Suppression
A High-Throughput Approach to Uncover Novel Roles of APOBEC2, a Functional Orphan of the AID/APOBEC Family
Combinatorial Strategies Using CRISPR/Cas9 for Gene Mutagenesis in Adult Mice
1 Fibrillar Αβ Triggers Microglial Proteome Alterations and Dysfunction in Alzheimer Mouse 1 Models 2 3 4 Laura Sebastian
ID AKI Vs Control Fold Change P Value Symbol Entrez Gene Name *In
14200 Girdin Antibody
Infant High-Grade Gliomas Comprise Multiple Subgroups Characterized by Novel Targetable Gene Fusions and Favorable Outcomes
Pan-Cancer Network Analysis Identifies Combinations of Rare Somatic Mutations Across Pathways and Protein Complexes
Assessing Mitochondrial Theory of Aging on the Transcriptome Level
Systematic Detection of Brain Protein-Coding Genes Under Positive Selection During Primate Evolution and Their Roles in Cognition
Genome-Wide Association Study of Alcohol Dependence: Signiﬁcant ﬁndings in African- and European-Americans Including Novel Risk Loci
A CRISPR Screen to Identify Combination Therapies of Cytotoxic
Exome Sequencing for Bipolar Disorder Points to Roles of De Novo Loss-Of-Function and Protein-Altering Mutations
Revised Manuscript ID CJP-2016-11-0031R1
SUPPLEMENTARY MATERIAL Differential Expression Profile Of
CCDC88A Mutations Cause PEHO-Like Syndrome in Humans and Mouse
Gene Expression in the Mouse Eye: an Online Resource for Genetics Using 103 Strains of Mice
Supplementary Materials: Small-Molecule Inhibition of Rho

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