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Microcephalin
The University of Chicago Genetic Services Laboratories Genetic
Congenital Microcephaly
Identification and Characterization of Genes Essential for Human Brain Development
Microcephaly Genes and Risk of Late-Onset Alzheimer Disease
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
Review Article Molecular and Cellular Basis of Autosomal Recessive Primary Microcephaly
New Experimental Evidence and Its Consequences for Linguistics
Print ACNR MA05
Expression of DNA Damage Response Proteins and Associations with Clinicopathologic Characteristics in Chinese Familial Breast Cancer Patients with BRCA1/2 Mutations
Novel SASS6 Compound Heterozygous Mutations in A
Autosomal Recessive Primary Microcephaly (MCPH): an Update
Phosphorylation of MCPH1 Isoforms During Mitosis Followed by Isoform-Specific Degradation by APC/C-CDH1 † Stephanie K
Human Evolution
The Mitotic Apparatus and Kinetochores in Microcephaly and Neurodevelopmental Diseases
Evidence That the Adaptive Allele of the Brain Size Gene Microcephalin Introgressed Into Homo Sapiens from an Archaic Homo Lineage
Molecular Genetics of Human Primary Microcephaly: an Overview
Investigating the Role of CK2 in the DNA Damage Response
Top View
Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4
A Novel Single Base Pair Duplication in WDR62 Causes Primary Microcephaly Verena Rupp1, Sobiah Rauf2, Ishrat Naveed2, Windpassinger Christian1 and Asif Mir2*
Microcephalin Is a New Novel Prognostic Indicator in Breast Cancer Associated with BRCA1 Inactivation Julie Richardson, Abeer M
ASPM Gene Abnormal Spindle Microtubule Assembly
Microcephalin, a Gene Regulating Brain Size, Continues to Evolve Adaptively in Humans
Cdk5rap2 Interacts with Pericentrin to Maintain the Neural Progenitor Pool in the Developing Neocortex
Phosphorylation-Mediated Interactions with TOPBP1 Couple
Comprehensive Review on the Molecular Genetics of Autosomal Recessive Primary Cambridge.Org/Grh Microcephaly (MCPH)
Genetic Determinants at the Interface of Cancer and Neurodegenerative Disease
Is Brain Evolution Still Continuing In
Molecular and Cellular Basis of Autosomal Recessive Primary Microcephaly
Race and IQ in the Postgenomic Age: the Microcephaly Case
The Genetics of Primary Microcephaly.Pdf
Reconstructing the Evolutionary History of Microcephalin, a Gene Controlling Human Brain Size
A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal Function
Comprehensive Review on the Molecular Genetics of Autosomal Recessive Primary Cambridge.Org/Grh Microcephaly (MCPH)
Clinical Report Prenatal Identification of a Novel Mutation
Exome Sequencing Identifies Recessive CDK5RAP2 Variants In
Cell Cycle-Dependent Localization of CHK2 at Centrosomes During Mitosis
A Novel Deletion Mutation in CENPJ Gene in a Pakistani Family with Autosomal Recessive Primary Microcephaly
Characterization of the Microcephaly Gene Wd40-Repeat Protein 62 (Wdr62) in Brain Growth and Development Belal Shohayeb, Mres Ma
Computational Identification of Mutually Homologous Zika Virus Mirnas That Target Microcephaly Genes
Molecular and Cellular Basis of Autosomal Recessive Primary Microcephaly
Distinct BRCT Domains in Mcph1/Brit1 Mediate Ionizing Radiation-Induced Focus Formation and Centrosomal Localization
Function of MCPH1 in Neurogenesis
Genetic Basis of Human Brain Evolution
Molecular Evolution of WDR62, a Gene That Regulates Neocorticogenesis
Sex-Dependent Association of Common Variants of Microcephaly Genes with Brain Structure