| scholarly article | Q13442814 |
| P356 | DOI | 10.1093/HMG/DDX330 |
| P698 | PubMed publication ID | 28973348 |
| P50 | author | Takashi Yamamoto | Q46522287 |
| Tatsuo Miyamoto | Q50621962 | ||
| Shinya Matsuura | Q59304325 | ||
| Hideshi Kawakami | Q71016675 | ||
| Hiroyuki Morino | Q75186077 | ||
| P2093 | author name string | Hirofumi Ohashi | |
| Kenji Shimizu | |||
| Akihiro Fukumitsu | |||
| Kosuke Hosoba | |||
| Silvia Natsuko Akutsu | |||
| Yoshinori Masatsuna | |||
| P2860 | cites work | Efficient introduction of specific homozygous and heterozygous mutations using CRISPR/Cas9. | Q48789186 |
| Evidence for a pioneer round of mRNA translation: mRNAs subject to nonsense-mediated decay in mammalian cells are bound by CBP80 and CBP20 | Q24291673 | ||
| Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations | Q24296941 | ||
| Dishevelled, a Wnt signalling component, is involved in mitotic progression in cooperation with Plk1 | Q24299033 | ||
| Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture | Q24301645 | ||
| WDR62 is associated with the spindle pole and is mutated in human microcephaly | Q24301673 | ||
| Microcephaly-associated protein WDR62 regulates neurogenesis through JNK1 in the developing neocortex | Q24317320 | ||
| A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia | Q28116910 | ||
| Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors | Q28594217 | ||
| Centrioles, centrosomes, and cilia in health and disease | Q29615173 | ||
| MISP is a novel Plk1 substrate required for proper spindle orientation and mitotic progression | Q30537786 | ||
| Identification of a consensus motif for Plk (Polo-like kinase) phosphorylation reveals Myt1 as a Plk1 substrate. | Q34195806 | ||
| Opposing roles for JNK and Aurora A in regulating the association of WDR62 with spindle microtubules. | Q35029169 | ||
| Regulation of NDR1 activity by PLK1 ensures proper spindle orientation in mitosis | Q35701372 | ||
| Mitotic spindle (DIS)orientation and DISease: cause or consequence? | Q36486600 | ||
| WD40-repeat protein 62 is a JNK-phosphorylated spindle pole protein required for spindle maintenance and timely mitotic progression | Q36497538 | ||
| Aurora A phosphorylation of WD40-repeat protein 62 in mitotic spindle regulation. | Q37091944 | ||
| Genetic causes of microcephaly and lessons for neuronal development | Q37158051 | ||
| The Microtubule-Depolymerizing Activity of a Mitotic Kinesin Protein KIF2A Drives Primary Cilia Disassembly Coupled with Cell Proliferation. | Q37398735 | ||
| TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome. | Q37543719 | ||
| Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly | Q37685924 | ||
| What next-generation sequencing (NGS) technology has enabled us to learn about primary autosomal recessive microcephaly (MCPH). | Q38518978 | ||
| Nonsense-mediated mRNA decay: an intricate machinery that shapes transcriptomes | Q38591386 | ||
| ASPM and CITK regulate spindle orientation by affecting the dynamics of astral microtubules. | Q38750052 | ||
| Regulation of mitotic spindle orientation: an integrated view. | Q38901748 | ||
| Insufficiency of BUBR1, a mitotic spindle checkpoint regulator, causes impaired ciliogenesis in vertebrates. | Q39578797 | ||
| PLK1-dependent activation of LRRK1 regulates spindle orientation by phosphorylating CDK5RAP2. | Q41569146 | ||
| Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate | Q41921410 | ||
| The Microcephaly-Associated Protein Wdr62/CG7337 Is Required to Maintain Centrosome Asymmetry in Drosophila Neuroblasts | Q41926666 | ||
| Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis. | Q42522587 | ||
| P433 | issue | 22 | |
| P304 | page(s) | 4429-4440 | |
| P577 | publication date | 2017-08-26 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | PLK1-mediated phosphorylation of WDR62/MCPH2 ensures proper mitotic spindle orientation | |
| P478 | volume | 26 |
| Q90060993 | Control of Intestinal Cell Fate by Dynamic Mitotic Spindle Repositioning Influences Epithelial Homeostasis and Longevity |
| Q91941027 | Endoplasmic reticulum and Golgi stress in microcephaly |
| Q55273319 | Exploration of genetic basis underlying individual differences in radiosensitivity within human populations using genome editing technology. |
| Q61810522 | Expression of polo-like kinase 1 in pre-implantation stage murine somatic cell nuclear transfer embryos |
| Q92733484 | Modeling microcephaly with cerebral organoids reveals a WDR62-CEP170-KIF2A pathway promoting cilium disassembly in neural progenitors |
| Q64981854 | Novel compound heterozygous mutations in WDR62 gene leading to developmental delay and Primary Microcephaly in Saudi Family. |
| Q59136612 | Plk1 regulates spindle orientation by phosphorylating NuMA in human cells |
| Q58555874 | Regulating a key mitotic regulator, Polo-like Kinase 1 (PLK1) |
| Q89978236 | The Yin and Yang of Autosomal Recessive Primary Microcephaly Genes: Insights from Neurogenesis and Carcinogenesis |
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