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CDK5RAP2
Mutations in CDK5RAP2 Cause Seckel Syndrome Go¨ Khan Yigit1,2,3,A, Karen E
Supplemental Information Proximity Interactions Among Centrosome
Genetic and Genomic Analysis of Hyperlipidemia, Obesity and Diabetes Using (C57BL/6J × TALLYHO/Jngj) F2 Mice
Autosomal Recessive Primary Microcephaly
Molecular Genetics of Microcephaly Primary Hereditary: an Overview
E-Mutpath: Computational Modelling Reveals the Functional Landscape of Genetic Mutations Rewiring Interactome Networks
CDK5RAP2 Functions in Centrosome to Spindle Pole Attachment and DNA Damage Response
Genetic and Informatic Analyses Implicate Kif12 As a Candidate Gene Within the Mpkd2 Locus That Modulates Renal Cystic Disease Severity in the Cys1cpk Mouse
Modifier Genes in Microcephaly: a Report on WDR62, CEP63, RAD50
De Novo Transcriptome Assembly and Positive Selection Analysis of An
Cell-Cycle Dependent Phosphorylation of Yeast Pericentrin Regulates Γ-Tusc
Centriolar Satellites Assemble Centrosomal Microcephaly Proteins
Mechanisms of Centriole Duplication and Their Deregulation in Disease
Molecular Genetics of Human Primary Microcephaly: an Overview
Fyn Regulates Binding Partners of Cyclic-AMP Dependent Protein Kinase A
Cep68 and Cep215 (Cdk5rap2) Are Required for Centrosome Cohesion
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Fyn-Mediated Regulation of Protein Kinase A
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Identifying Human Interactors of SARS-Cov-2 Proteins and Drug Targets for COVID-19 Using Network-Based Label Propagation Arxiv:2
Analysis of Protein-Protein Interaction Network Based on Transcriptome
A Proteomic Approach Reveals Integrin Activation State-Dependent Control of Microtubule Cortical Targeting
The University of Chicago Genetic Services Laboratories Genetic
Deficient Adaptation to Centrosome Duplication Defects in Neural Progenitors Causes Microcephaly and Subcortical Heterotopias
Cdk5rap2 Interacts with Pericentrin to Maintain the Neural Progenitor Pool in the Developing Neocortex
EB1-Binding–Myomegalin Protein Complex Promotes Centrosomal Microtubules Functions
Analysis of the Genome and Viral Transcriptome of Epstein-Barr Virus
Comprehensive Review on the Molecular Genetics of Autosomal Recessive Primary Cambridge.Org/Grh Microcephaly (MCPH)
CDK5RAP2 Primary Microcephaly Is Associated With
HHS Public Access Author Manuscript
Remodeling of the Neuronal Microtubules in the Brain by Cdk5
The Genetics of Primary Microcephaly.Pdf
A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal Function
Genome-Wide Analysis Identifies Germ-Line Risk Factors Associated with Canine Mammary Tumours
Cyclin-Dependent Kinase 5 Is Essential for Neuronal Cell Cycle Arrest and Differentiation
Mechanisms of Centriole Duplication and Spindle Assembly in Human Cells
Oligopvp: Phenotype-Driven Analysis of Individual Genomic Information to Prioritize Oligogenic Disease Variants
An Extensive Program of Periodic Alternative Splicing Linked to Cell Cycle
Exome Sequencing Identifies Recessive CDK5RAP2 Variants In
Mouse Cdk5rap2 Conditional Knockout Project (CRISPR/Cas9)
Mixed-Species Rnaseq Analysis of Human Lymphoma Cells Adhering to Mouse Stromal Cells Identifies a Core Gene Set That Is Also Di
A Novel Deletion Mutation in CENPJ Gene in a Pakistani Family with Autosomal Recessive Primary Microcephaly
Myomegalin Is Necessary for the Formation of Centrosomal and Golgi-Derived Microtubules
Aspm Sustains Postnatal Cerebellar Neurogenesis and Medulloblastoma Growth in Mice Scott E
Overexpression of Dnmt3b Target Genes During Enteric Nervous
A Unique Set of Centrosome Proteins Requires Pericentrin for Spindle-Pole Localization and Spindle Orientation
Microtubule Nucleation at the Centrosome and Beyond
Centriole and PCM Cooperatively Recruit CEP192 to Spindle Poles To
CDK5RAP2 Primary Microcephaly Is
Sex-Dependent Association of Common Variants of Microcephaly Genes with Brain Structure