Pages that link to "Q41921410"
The following pages link to Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate (Q41921410):
Displaying 27 items.
- Regulation of cytokinesis during corticogenesis: focus on the midbody (Q39298424) (← links)
- WDR62 Regulates Early Neural and Glial Progenitor Specification of Human Pluripotent Stem Cells. (Q41037948) (← links)
- PLK1-mediated phosphorylation of WDR62/MCPH2 ensures proper mitotic spindle orientation (Q41918159) (← links)
- The Role of WD40-Repeat Protein 62 (MCPH2) in Brain Growth: Diverse Molecular and Cellular Mechanisms Required for Cortical Development. (Q41918329) (← links)
- Human microcephaly ASPM protein is a spindle pole-focusing factor that functions redundantly with CDK5RAP2. (Q41918485) (← links)
- Human accelerated regions and other human-specific sequence variations in the context of evolution and their relevance for brain development (Q46259543) (← links)
- Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development. (Q47595186) (← links)
- The evolution of cortical development: the synapsid-diapsid divergence. (Q47595678) (← links)
- STIL balancing primary microcephaly and cancer (Q47851151) (← links)
- Same but different: pleiotropy in centrosome-related microcephaly (Q49571261) (← links)
- Once and only once: mechanisms of centriole duplication and their deregulation in disease (Q49831825) (← links)
- Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size. (Q52593078) (← links)
- Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disorders. (Q52674255) (← links)
- A genetic mosaic screen identifies genes modulating Notch signaling in Drosophila (Q58713670) (← links)
- Wdr62 is involved in meiotic initiation via activating JNK signaling and associated with POI in humans (Q58785275) (← links)
- Malformations of Human Neocortex in Development - Their Progenitor Cell Basis and Experimental Model Systems (Q66679187) (← links)
- Tight junction protein occludin regulates progenitor Self-Renewal and survival in developing cortex (Q83226328) (← links)
- Cortical Malformations: Lessons in Human Brain Development (Q84957742) (← links)
- The Yin and Yang of Autosomal Recessive Primary Microcephaly Genes: Insights from Neurogenesis and Carcinogenesis (Q89978236) (← links)
- Control of Intestinal Cell Fate by Dynamic Mitotic Spindle Repositioning Influences Epithelial Homeostasis and Longevity (Q90060993) (← links)
- MEKK3 coordinates with FBW7 to regulate WDR62 stability and neurogenesis (Q90634984) (← links)
- Digenic inheritance of human primary microcephaly delineates centrosomal and non-centrosomal pathways (Q91161146) (← links)
- SFI1 promotes centriole duplication by recruiting USP9X to stabilize the microcephaly protein STIL (Q92732818) (← links)
- Modeling microcephaly with cerebral organoids reveals a WDR62-CEP170-KIF2A pathway promoting cilium disassembly in neural progenitors (Q92733484) (← links)
- Centriole Positioning: Not Just a Little Dot in the Cell (Q92763174) (← links)
- A Novel Frameshift Mutation in Abnormal Spindle-Like Microcephaly (ASPM) Gene in an Iranian Patient with Primary Microcephaly: A Case Report (Q92862894) (← links)
- Unusual context of CENPJ variants and primary microcephaly: compound heterozygosity and nonconsanguinity in an Argentinian patient (Q96439694) (← links)