Type IV collagen is detectable in most, but not all, basement membranes of Caenorhabditis elegans and assembles on tissues that do not express it
about
Gene CATCHR--gene cloning and tagging for Caenorhabditis elegans using yeast homologous recombination: a novel approach for the analysis of gene expressionThe Caenorhabditis elegans epidermis as a model skin. II: differentiation and physiological rolesMorphogenesis of the C. elegans Intestine Involves Axon Guidance GenesSPARC Promotes Cell Invasion In Vivo by Decreasing Type IV Collagen Levels in the Basement MembraneA widespread distribution of genomic CeMyoD binding sites revealed and cross validated by ChIP-Chip and ChIP-Seq techniquesThe C. elegans F-spondin family protein SPON-1 maintains cell adhesion in neural and non-neural tissues.Genetic interaction between Caenorhabditis elegans teneurin ten-1 and prolyl 4-hydroxylase phy-1 and their function in collagen IV-mediated basement membrane integrity during late elongation of the embryoLaminin is required to orient epithelial polarity in the C. elegans pharynx.Receptors and other signaling proteins required for serotonin control of locomotion in Caenorhabditis elegans.The union of somatic gonad precursors and primordial germ cells during Caenorhabditis elegans embryogenesisShaping cells and organs in Drosophila by opposing roles of fat body-secreted Collagen IV and perlecanRegulation of synaptic extracellular matrix composition is critical for proper synapse morphology.Gonad morphogenesis and distal tip cell migration in the Caenorhabditis elegans hermaphrodite.Analysis of the role of Caenorhabditis elegans GC-AG introns in regulated splicing.dpy-18 encodes an alpha-subunit of prolyl-4-hydroxylase in caenorhabditis elegans.Nidogen is nonessential and not required for normal type IV collagen localization in Caenorhabditis elegansComparative RNA-Seq analysis reveals pervasive tissue-specific alternative polyadenylation in Caenorhabditis elegans intestine and muscles.An active role for basement membrane assembly and modification in tissue sculptingTissue architecture in the Caenorhabditis elegans gonad depends on interactions among fibulin-1, type IV collagen and the ADAMTS extracellular protease.Membrane-associated collagens with interrupted triple-helices (MACITs): evolution from a bilaterian common ancestor and functional conservation in C. elegans.COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.Development of Caenorhabditis elegans pharynx, with emphasis on its nervous system.The C. elegans Discoidin Domain Receptor DDR-2 Modulates the Met-like RTK-JNK Signaling Pathway in Axon RegenerationCharacterization of alpha1(IV) collagen mutations in Caenorhabditis elegans and the effects of alpha1 and alpha2(IV) mutations on type IV collagen distribution.Laminin polymerization induces a receptor-cytoskeleton networkThe NC1/endostatin domain of Caenorhabditis elegans type XVIII collagen affects cell migration and axon guidance.STAR family RNA-binding protein ASD-2 regulates developmental switching of mutually exclusive alternative splicing in vivoBasement Membranes in the Worm: A Dynamic Scaffolding that Instructs Cellular Behaviors and Shapes Tissues.Laminins in basement membrane assemblyHemicentins: what have we learned from worms?Caenorhabditis elegans teneurin, ten-1, is required for gonadal and pharyngeal basement membrane integrity and acts redundantly with integrin ina-1 and dystroglycan dgn-1Complex patterns of alternative splicing mediate the spatial and temporal distribution of perlecan/UNC-52 in Caenorhabditis elegansMIG-17/ADAMTS controls cell migration by recruiting nidogen to the basement membrane in C. elegans.Extension of the Caenorhabditis elegans Pharyngeal M1 neuron axon is regulated by multiple mechanismsDevelopmental genetics of the Caenorhabditis elegans pharynxAn emerging model organism Caenorhabditis elegans for alternative pre-mRNA processing in vivo.A novel metalloproteinase virulence factor is involved in Bacillus thuringiensis pathogenesis in nematodes and insects.Lipocalin signaling controls unicellular tube development in the Caenorhabditis elegans excretory system.Roles for beta(pat-3) integrins in development and function of Caenorhabditis elegans muscles and gonads.Egg shell collagen formation in Caenorhabditis elegans involves a novel prolyl 4-hydroxylase expressed in spermatheca and embryos and possessing many unique properties.
P2860
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P2860
Type IV collagen is detectable in most, but not all, basement membranes of Caenorhabditis elegans and assembles on tissues that do not express it
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh
1997年學術文章
@zh-hant
name
Type IV collagen is detectable ...... tissues that do not express it
@ast
Type IV collagen is detectable ...... tissues that do not express it
@en
type
label
Type IV collagen is detectable ...... tissues that do not express it
@ast
Type IV collagen is detectable ...... tissues that do not express it
@en
prefLabel
Type IV collagen is detectable ...... tissues that do not express it
@ast
Type IV collagen is detectable ...... tissues that do not express it
@en
P2093
P2860
P356
P1476
Type IV collagen is detectable ...... tissues that do not express it
@en
P2093
P2860
P304
P356
10.1083/JCB.137.5.1171
P407
P577
1997-06-01T00:00:00Z