A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo - Wikidata - awgldk - TriplyDB

A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo

A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo

http://www.wikidata.org/entity/Q30856481

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Caenorhabditis elegans cyclin B3 is required for multiple mitotic processes including alleviation of a spindle checkpoint-dependent block in anaphase chromosome segregation Unstable microtubule capture at kinetochores depleted of the centromere-associated protein CENP-F.The retromer coat complex coordinates endosomal sorting and dynein-mediated transport, with carrier recognition by the trans-Golgi network Characterization of sub-nuclear changes in Caenorhabditis elegans embryos exposed to brief, intermediate and long-term anoxia to analyze anoxia-induced cell cycle arrest Suspended animation, diapause and quiescence: arresting the cell cycle in C. elegans The KLP-7 Residue S546 Is a Putative Aurora Kinase Site Required for Microtubule Regulation at the Centrosome in C. elegans TRIP13PCH-2 promotes Mad2 localization to unattached kinetochores in the spindle checkpoint response A cell cycle timer for asymmetric spindle positioning Conditional dominant mutations in the Caenorhabditis elegans gene act-2 identify cytoplasmic and muscle roles for a redundant actin isoform.Model of chromosome motility in Drosophila embryos: adaptation of a general mechanism for rapid mitosis.Barrier to autointegration factor blocks premature cell fusion and maintains adult muscle integrity in C. elegans.Genetic analysis of the spindle checkpoint genes san-1, mdf-2, bub-3 and the CENP-F homologues hcp-1 and hcp-2 in Caenorhabditis elegans.RAB-11 permissively regulates spindle alignment by modulating metaphase microtubule dynamics in Caenorhabditis elegans early embryos.Cell cycle progression requires the CDC-48UFD-1/NPL-4 complex for efficient DNA replication SPDL-1 functions as a kinetochore receptor for MDF-1 in Caenorhabditis elegans.Systematic analysis in Caenorhabditis elegans reveals that the spindle checkpoint is composed of two largely independent branches.NPP-16/Nup50 function and CDK-1 inactivation are associated with anoxia-induced prophase arrest in Caenorhabditis elegans Spindle assembly checkpoint genes reveal distinct as well as overlapping expression that implicates MDF-2/Mad2 in postembryonic seam cell proliferation in Caenorhabditis elegans Dynamic SUMO modification regulates mitotic chromosome assembly and cell cycle progression in Caenorhabditis elegans.Cell Size Determines the Strength of the Spindle Assembly Checkpoint during Embryonic Development.Functional analysis of cytoplasmic dynein heavy chain in Caenorhabditis elegans with fast-acting temperature-sensitive mutations A survey of new temperature-sensitive, embryonic-lethal mutations in C. elegans: 24 alleles of thirteen genes.The function of a spindle checkpoint gene bub-1 in C. elegans development.Mutual antagonism between the anaphase promoting complex and the spindle assembly checkpoint contributes to mitotic timing in Caenorhabditis elegans Components of the spindle assembly checkpoint regulate the anaphase-promoting complex during meiosis in Caenorhabditis elegans.Kinetochore-localized BUB-1/BUB-3 complex promotes anaphase onset in C. elegans Suppressors of spindle checkpoint defect (such) mutants identify new mdf-1/MAD1 interactors in Caenorhabditis elegans.Progression from mitotic catastrophe to germ cell death in Caenorhabditis elegans lis-1 mutants requires the spindle checkpoint Cytokinesis is not controlled by calmodulin or myosin light chain kinase in the Caenorhabditis elegans early embryo.Spindle assembly checkpoint gene mdf-1 regulates germ cell proliferation in response to nutrition signals in C. elegans The spindle assembly checkpoint in Caenorhabditis elegans: one who lacks Mad1 becomes mad one Key players in chromosome segregation in Caenorhabditis elegans.Condensin and the spindle midzone prevent cytokinesis failure induced by chromatin bridges in C. elegans embryos Proper cyclin B3 dosage is important for precision of metaphase-to-anaphase onset timing in Caenorhabditis elegans.Synthetic lethal interactions identify phenotypic "interologs" of the spindle assembly checkpoint components.Caenorhabditis elegans oocytes detect meiotic errors in the absence of canonical end-on kinetochore attachments.UBASH3B-mediated silencing of the mitotic checkpoint: Therapeutic perspectives in cancer.

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P2860

A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo

http://www.wikidata.org/entity/Q30856481

description

2004 nî lūn-bûn

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2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

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2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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name

A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo

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A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo

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type

label

A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo

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A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo

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prefLabel

A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo

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A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo

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P356

MBC.E04-08-0712

P1433

Molecular Biology of the Cell

P1476

A spindle checkpoint functions during mitosis in the early Caenorhabditis elegans embryo

@en

P2093

Bruce Bowerman

http://www.w3.org/2001/XMLSchema#string

John Willis

http://www.w3.org/2001/XMLSchema#string

Rebecca Lyczak

http://www.w3.org/2001/XMLSchema#string

Sandra E Encalada

http://www.w3.org/2001/XMLSchema#string

P2860

Characterization of the kinetochore binding domain of CENP-E reveals interactions with the kinetochore proteins CENP-F and hBUBR1

CENP-F is a protein of the nuclear matrix that assembles onto kinetochores at late G2 and is rapidly degraded after mitosis

Centromere-associated protein-E is essential for the mammalian mitotic checkpoint to prevent aneuploidy due to single chromosome loss

The C terminus of mitosin is essential for its nuclear localization, centromere/kinetochore targeting, and dimerization

The genetics of Caenorhabditis elegans

Checkpoint genes required to delay cell division in response to nocodazole respond to impaired kinetochore function in the yeast Saccharomyces cerevisiae.

Aurora-A kinase is required for centrosome maturation in Caenorhabditis elegans

Mad1p, a phosphoprotein component of the spindle assembly checkpoint in budding yeast

Functional analysis of kinetochore assembly in Caenorhabditis elegans.

Activation of the budding yeast spindle assembly checkpoint without mitotic spindle disruption.

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1056-1070

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scholarly article

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10.1091/MBC.E04-08-0712

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3

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P478

16

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2004-12-22T00:00:00Z

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15616189

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Caenorhabditis elegans

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551473

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