WDR62 - Docslib

Sign Up
Log In
Upload

Sign Up
Log In
Upload

Home
» Tags
» WDR62

WDR62

A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Identification and Characterization of Genes Essential for Human Brain Development
Molecular Genetics of Microcephaly Primary Hereditary: an Overview
Ncomms4885.Pdf
(JNK)-Binding Protein WDR62 Is Recruited to Stress Granules And
Cenpj Regulates Cilia Disassembly and Neurogenesis in the Developing Mouse Cortex
A Novel Single Base Pair Duplication in WDR62 Causes Primary Microcephaly Verena Rupp1, Sobiah Rauf2, Ishrat Naveed2, Windpassinger Christian1 and Asif Mir2*
Modifier Genes in Microcephaly: a Report on WDR62, CEP63, RAD50
UC San Francisco Previously Published Works
Opposing Roles for JNK and Aurora a in Regulating the Association Of
Whole-Exome Sequencing Identifies Recessive WDR62 Mutations in Severe Brain Malformations
Title: Primary Autosomal Recessive Microcephalies and Seckel
Aurora a Protein Kinase: to the Centrosome and Beyond
A Novel Splice Site Mutation in CEP135 Is Associated with Primary Microcephaly in a Pakistani Family
Aurora-A Phosphorylates Splicing Factors and Regulates Alternative Splicing
Microcephaly-Associated Protein WDR62 Regulates Neurogenesis Through JNK1 in the Developing Neocortex
A Novel Non Sense Mutation in WDR62
Aurora a Protein Kinase to the Centrosome and Beyond Laura Magnaghi-Jaulin, Grégory Eot-Houllier, Emmanuel Gallaud, Régis Giet

Top View

WDR62 Is Involved in Spindle Assembly by Interacting with CEP170 in Spermatogenesis
WDR62 Mediates Tnfα-Dependent JNK Activation Via TRAF2-MLK3 Axis
Somatic Mutations and T-Cell Clonality in Patients with Immunodeficiency
Abnormal Centrosome and Spindle Morphology in a Patient With
MYC in Brain Development and Cancer
Further Delineation of Phenotype and Genotype of Primary Microcephaly Syndrome with Cortical Malformations Associated with Mutations in the WDR62 Gene
The Kinetochore Protein, CENPF, Is Mutated in Human Ciliopathy And
The Genetics of Primary Microcephaly.Pdf
Disruptions in Asymmetric Centrosome Inheritance and WDR62-Aurora
S41467-021-24919-7.Pdf
WDR62 Is Required for Centriole Duplication in Spermatogenesis and Manchette Removal in Spermiogenesis ✉ Uda Y
Technology Has Enabled Us to Learn About Primary Autosomal Recessive Microcephaly (MCPH)
Comprehensive Review on the Molecular Genetics of Autosomal Recessive Primary Cambridge.Org/Grh Microcephaly (MCPH)
WDR62 Regulates Early Neural and Glial Progenitor Specification of Human Pluripotent Stem Cells
Clinical Report Prenatal Identification of a Novel Mutation
WDR62 Regulates Early Neural and Glial Progenitor Specification of Human Pluripotent Stem Cells
Discovering Novel Feedback and Crosstalk Mechanisms in Cellular Signaling Pathways
Disorders of Neurogenesis and Cortical Development Fabrizia Claudia Guarnieri, Antoine De Chevigny, Antonio Falace, Carlos Cardoso

© 2024 Docslib.org Feedback