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CCDC22
Transcriptome-Wide Profiling of Multiple RNA Modifications Simultaneously at Single-Base Resolution,” by Vahid Khoddami, Archana Yerra, Timothy L
Endosomal PI(3)P Regulation by the COMMD/CCDC22/CCDC93
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Evidence for Induction of the Ornithine Transcarbamylase Expression in Alzheimer's Disease
Investigating Common Pathogenic Mechanisms Between Homo Sapiens and Different Strains of Candida Albicans for Drug Design
COMMD1 Is Linked to the WASH Complex and Regulates Endosomal Trafficking of the Copper Transporter ATP7A
Dynamic Erasure of Random X-Chromosome Inactivation During Ipsc Reprogramming
Targeted Next-Generation Sequencing in Patients with Suggestive X-Linked Intellectual Disability
CCDC22 Shrna (H) Lentiviral Particles: Sc-91292-V
Understanding Regulatory Mechanisms Underlying Stem Cells Helps to Identify Cancer Biomarkers
Milger Et Al. Pulmonary CCR2+CD4+ T Cells Are Immune Regulatory And
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Genetic Disruption of WASHC4 Drives Endo-Lysosomal Dysfunction
Functional Relationships Between Recessive Inherited Genes and Genes with De Novo Variants in Autism Spectrum Disorder
Mosaic Origin of the Eukaryotic Kinetochore
Membranes of Human Neutrophils Secretory Vesicle Membranes And
1 Imipramine Treatment and Resiliency Exhibit Similar
X-Exome Sequencing of 405 Unresolved Families Identifies Seven
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University of Groningen Identification of a Novel Multiprotein Complex in Cargo Sorting That Preserves Metabolic Pathways In
Genes Potentially Associated with Familial Hypercholesterolemia
VPS29 Exerts Opposing Effects on Endocytic Viral Entry 2 3 4 Daniel Poston1,2*, Yiska Weisblum1*, Alvaro Hobbs1, Paul D
Extensive Cellular Heterogeneity of X Inactivation Revealed by Single-Cell Allele-Specific 2 Expression in Human Fibroblasts
Figure 1. APEX2:RAB Expression Lead to Endosomal Biotinylation
Autosomal Recessive Variants in Intellectual Disability and Autism Spectrum Disorder
Pervasive Chromatin Remodeling at X-Inactivation Escape Genes in Schizophrenic Males
THAP11F80L Cobalamin Disorder-Associated Mutation Reveals Normal and Pathogenic THAP11 Functions in Gene Expression and Cell Proliferation
Prognosis and Modulation Mechanisms of COMMD6 in Human Tumours Based on Expression Profiling and Comprehensive Bioinformatics An
Missense Variant in CCDC22 Causes X-Linked Recessive Intellectual Disability with Features of Ritscher-Schinzel/3C Syndrome
The Pennsylvania State University the Graduate School Department