DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» ASPM (Gene)
ASPM (Gene)
A Nonsense (C.3978G>A) Abnormal Spindle-Like, Microcephaly Associated (ASPM) Gene Mutation Is a Major Cause of Primary Microc
Molecular Genetics of Microcephaly Primary Hereditary: an Overview
The Molecular Landscape of ASPM Mutations in Primary Microcephaly
(ASPM) Gene in an Iranian Patient with Primary Microcephaly: a Case Report
Gene List of the Targeted NGS MCD and CCA Gene Panel AKT3,ALX1
Supplementary Information
Markers of Clinical Utility in the Differential Diagnosis and Prognosis of Prostate Cancer Glen Kristiansen
New Experimental Evidence and Its Consequences for Linguistics
Real and Spurious Correlations Involving Tonal Languages Jeremy Collins Radboud University, Nijmegen
Primary Microcephaly Caused by Novel Compound Heterozygous Mutations in ASPM
Human Microcephaly ASPM Protein Is a Spindle Pole-Focusing Factor That Functions Redundantly with CDK5RAP2 Elsa A
Regulation of Human Cerebral Cortical Development by EXOC7
ASPM Combined with KIF11 Promotes the Malignant Progression of Hepatocellular Carcinoma Via the Wnt/Β‑Catenin Signaling Pathway
Recapitulating Cortical Development with Organoid Culture in Vitro and Modeling Abnormal Spindle-Like (ASPM Related Primary) Microcephaly Disease
Open Full Page
Human Microcephaly ASPM Protein Is a Spindle Pole-Focusing Factor That Functions Redundantly with CDK5RAP2
Ciliary Signalling and Mechanotransduction in the Pathophysiology of Craniosynostosis
Mutations in Mouse Aspm (Abnormal Spindle-Like Microcephaly Associated) Cause Not Only Microcephaly but Also Major Defects in the Germline
Top View
Expression of Iq-Motif Genes in Human Cells and Aspm Domain Structure
The Genomic Grade Assay Compared with Ki67 to Determine Risk Of
Evolution of ASPM Coding Variation in Apes and Associations with Brain Structure in Chimpanzees
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
The Cell Biology of Neurogenesis
Supplementary Information
Role of Sonic Hedgehog Signalling in Regulating Neural Stem Cell Activity in the Adult and Aged Murine Hippocampus
(4) Building Brain
Hypothalamic Orexin Prevents Hepatic Insulin Resistance Via Daily Bidirectional Regulation of Autonomic Nervous System in Mice
Early Loss of Scribble Affects Cortical Development, Interhemispheric
Single-Cell Transcriptional Dynamics and Origins of Neuronal Diversity in the Developing Mouse Neocortex
Table S1. Complete List of Up- and Down-Regulated Genes in C1 Cells
How Culture Shaped the Human Genome: Bringing Genetics and the Human Sciences Together
ASPM Gene Abnormal Spindle Microtubule Assembly
Overexpression of the ASPM Gene Is Associated with Aggressiveness and Poor Outcome in Bladder Cancer
The Evolution of Neural-Progenitor-Cell Division
Evolution of the Human ASPM Gene, a Major Determinant of Brain Size
ASPM Regulates Wnt Signaling Pathway Activity in the Developing Brain
Analysing Human Neural Stem Cell Ontogeny by Consecutive Isolation of Notch Active Neural Progenitors
An Integrated Approach Identifies Nhlh1 and Insm1 As Sonic
Race and IQ in the Postgenomic Age: the Microcephaly Case
ASPM Regulates Symmetric Stem Cell Division by Tuning Cyclin E Ubiquitination
Supplementary Data
A Novel Splice-Site Mutation in the ASPM Gene Underlies Autosomal Recessive Primary Microcephaly Jamil A
Human Cerebral Organoids Recapitulate Gene Expression Programs of Fetal Neocortex Development
Supplementary Table 7
The Evolution of Neuronal Progenitor Cell Division in Mammals: the Role
MARCKS Modulates Radial Progenitor Placement, Proliferation and Organization in the Developing Cerebral Cortex Jill M
Disorders of Neurogenesis and Cortical Development Fabrizia Claudia Guarnieri, Antoine De Chevigny, Antonio Falace, Carlos Cardoso
Aspm Sustains Postnatal Cerebellar Neurogenesis and Medulloblastoma Growth in Mice Scott E
Novel Pathogenic Mutation Mapping of ASPM Gene in Consanguineous Pakistani Families with Primary Microcephaly
Aspm Sustains Postnatal Cerebellar Neurogenesis and Medulloblastoma Growth in Mice Scott E
Mutations in Mouse Aspm (Abnormal Spindle-Like Microcephaly Associated) Cause Not Only Microcephaly but Also Major Defects in the Germline
FAM72, Glioblastoma Multiforme (GBM) and Beyond
Mutation Update of the ASPM Gene Causing Autosomal Recessive Primary Microcephaly
Supplementary Table 1. a Full List of Cancer Genes
The University of Chicago Genetic Services Laboratories