Katanin p80 regulates human cortical development by limiting centriole and cilia number.
about
Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary MicrocephalySevere NDE1-mediated microcephaly results from neural progenitor cell cycle arrests at multiple specific stagesCellular Mechanisms of Ciliary Length ControlKIAA0556 is a novel ciliary basal body component mutated in Joubert syndromeKatanin p80, NuMA and cytoplasmic dynein cooperate to control microtubule dynamicsCPAP promotes timely cilium disassembly to maintain neural progenitor poolMicrotubule minus-end regulation at spindle poles by an ASPM-katanin complexFidgetin-like 1 is a ciliogenesis-inhibitory centrosome proteinMutations in KATNB1 cause complex cerebral malformations by disrupting asymmetrically dividing neural progenitorsNovel POC1A mutation in primordial dwarfism reveals new insights for centriole biogenesis.SPEF2 functions in microtubule-mediated transport in elongating spermatids to ensure proper male germ cell differentiation.A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies.Regulation of cytokinesis during corticogenesis: focus on the midbody.RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in Humans.WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells.Microcephaly Proteins Wdr62 and Aspm Define a Mother Centriole Complex Regulating Centriole Biogenesis, Apical Complex, and Cell Fate.A novel family of katanin-like 2 protein isoforms (KATNAL2), interacting with nucleotide-binding proteins Nubp1 and Nubp2, are key regulators of different MT-based processes in mammalian cells.Katanin-like 2 (KATNAL2) functions in multiple aspects of haploid male germ cell development in the mouse.Structural basis of katanin p60:p80 complex formation.Primary cilia proteins: ciliary and extraciliary sites and functions.Of rings and spines: The multiple facets of Citron proteins in neural development.The evolution of cortical development: the synapsid-diapsid divergence.Mutations in the Katnb1 gene cause left-right asymmetry and heart defects.Katanin spiral and ring structures shed light on power stroke for microtubule severing.A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutation.Two novel POC1A mutations in the primordial dwarfism, SOFT syndrome: Clinical homogeneity but also unreported malformations.A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.Katanin-like protein Katnal2 is required for ciliogenesis and brain development in Xenopus embryosSonic Hedgehog Signaling Rises to the Surface: Emerging Roles in Neocortical Development
P2860
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P2860
Katanin p80 regulates human cortical development by limiting centriole and cilia number.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Katanin p80 regulates human cortical development by limiting centriole and cilia number.
@ast
Katanin p80 regulates human cortical development by limiting centriole and cilia number.
@en
type
label
Katanin p80 regulates human cortical development by limiting centriole and cilia number.
@ast
Katanin p80 regulates human cortical development by limiting centriole and cilia number.
@en
prefLabel
Katanin p80 regulates human cortical development by limiting centriole and cilia number.
@ast
Katanin p80 regulates human cortical development by limiting centriole and cilia number.
@en
P2093
P2860
P50
P1433
P1476
Katanin p80 regulates human cortical development by limiting centriole and cilia number.
@en
P2093
Amira Masri
Anas Alazami
Andrew Kodani
Bruno Reversade
Carine Bonnard
Christopher A Walsh
Grace Selva Raj
Hanan Hamamy
Jennifer N Partlow
Jeremy F Reiter
P2860
P304
P356
10.1016/J.NEURON.2014.12.017
P407
P577
2014-12-01T00:00:00Z