Characterization of alpha1(IV) collagen mutations in Caenorhabditis elegans and the effects of alpha1 and alpha2(IV) mutations on type IV collagen distribution.
about
Tyrosine cross-linking of extracellular matrix is catalyzed by Duox, a multidomain oxidase/peroxidase with homology to the phagocyte oxidase subunit gp91phoxNovel mutations in three families confirm a major role of COL4A1 in hereditary porencephalyBromine is an essential trace element for assembly of collagen IV scaffolds in tissue development and architectureCOL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humansLoss of assembly of the main basement membrane collagen, type IV, but not fibril-forming collagens and embryonic death in collagen prolyl 4-hydroxylase I null miceGenetic 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.Distinct functions of the laminin β LN domain and collagen IV during cardiac extracellular matrix formation and stabilization of alary muscle attachments revealed by EMS mutagenesis in Drosophila.Collagen IV and basement membrane at the evolutionary dawn of metazoan tissues.Prolyl 4-hydroxylase is an essential procollagen-modifying enzyme required for exoskeleton formation and the maintenance of body shape in the nematode Caenorhabditis elegansPeroxidasin forms sulfilimine chemical bonds using hypohalous acids in tissue genesis.Collagens: building blocks at the end of the development line.Regulation of synaptic extracellular matrix composition is critical for proper synapse morphology.The C. elegans peroxidasin PXN-2 is essential for embryonic morphogenesis and inhibits adult axon regeneration.The C terminus of collagen SQT-3 has complex and essential functions in nematode collagen assembly.Nidogen is nonessential and not required for normal type IV collagen localization in Caenorhabditis elegansA role for peroxidasin PXN-1 in aspects of C. elegans development.COL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic stroke.Prolyl 4-hydroxylase is required for viability and morphogenesis in Caenorhabditis elegansGlomerular expression of type IV collagen chains in normal and X-linked Alport syndrome kidneysTissue 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.The Effect of In Vitro Cultivation on the Transcriptome of Adult Brugia malayi.COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.COL4A2 mutation associated with familial porencephaly and small-vessel disease.Type IV collagen is detectable in most, but not all, basement membranes of Caenorhabditis elegans and assembles on tissues that do not express itA genome-wide RNAi screen for enhancers of par mutants reveals new contributors to early embryonic polarity in Caenorhabditis elegans.Organ Length Control by an ADAMTS Extracellular Protease in Caenorhabditis elegans.Extracellular chloride signals collagen IV network assembly during basement membrane formationMIG-17/ADAMTS controls cell migration by recruiting nidogen to the basement membrane in C. elegans.C. elegans mig-6 encodes papilin isoforms that affect distinct aspects of DTC migration, and interacts genetically with mig-17 and collagen IVThe PAPS transporter PST-1 is required for heparan sulfation and is essential for viability and neural development in C. elegans.A unique covalent bond in basement membrane is a primordial innovation for tissue evolution.Border patrol: insights into the unique role of perlecan/heparan sulfate proteoglycan 2 at cell and tissue bordersAllelic heterogeneity contributes to variability in ocular dysgenesis, myopathy and brain malformations caused by Col4a1 and Col4a2 mutations.COL4A1 and COL4A2 mutations and disease: insights into pathogenic mechanisms and potential therapeutic targets.Lens capsule as a model to study type IV collagen.Lean forward: Genetic analysis of temperature-sensitive mutants unfolds the secrets of oligomeric protein complex assembly.Egg shell collagen formation in Caenorhabditis elegans involves a novel prolyl 4-hydroxylase expressed in spermatheca and embryos and possessing many unique properties.Characterization of a novel Caenorhabditis elegans prolyl 4-hydroxylase with a unique substrate specificity and restricted expression in the pharynx and excretory duct.
P2860
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P2860
Characterization of alpha1(IV) collagen mutations in Caenorhabditis elegans and the effects of alpha1 and alpha2(IV) mutations on type IV collagen distribution.
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
Characterization of alpha1(IV) ...... type IV collagen distribution.
@ast
Characterization of alpha1(IV) ...... type IV collagen distribution.
@en
type
label
Characterization of alpha1(IV) ...... type IV collagen distribution.
@ast
Characterization of alpha1(IV) ...... type IV collagen distribution.
@en
prefLabel
Characterization of alpha1(IV) ...... type IV collagen distribution.
@ast
Characterization of alpha1(IV) ...... type IV collagen distribution.
@en
P2093
P2860
P356
P1476
Characterization of alpha1(IV) ...... type IV collagen distribution.
@en
P2093
P2860
P304
P356
10.1083/JCB.137.5.1185
P407
P577
1997-06-01T00:00:00Z