Collagen IV alpha 3, alpha 4, and alpha 5 chains in rodent basal laminae: sequence, distribution, association with laminins, and developmental switches
about
Form and function: the laminin family of heterotrimersIdentification and characterization of AMACO, a new member of the von Willebrand factor A-like domain protein superfamily with a regulated expression in the kidneyAnuria, omphalocele, and perinatal lethality in mice lacking the CD34-related protein podocalyxinThe laminin alpha chains: expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11, and cloning of a novel alpha3 isoformLaminin isoforms in endothelial and perivascular basement membranesGenetic Background is a Key Determinant of Glomerular Extracellular Matrix Composition and OrganizationInsight into podocyte differentiation from the study of human genetic disease: nail-patella syndrome and transcriptional regulation in podocytesStructural organization of the human and mouse laminin beta2 chain genes, and alternative splicing at the 5' end of the human transcriptComparative distribution of the alpha 1(IV), alpha 5(IV), and alpha 6(IV) collagen chains in normal human adult and fetal tissues and in kidneys from X-linked Alport syndrome patientsThe renal glomerulus of mice lacking s-laminin/laminin beta 2: nephrosis despite molecular compensation by laminin beta 1Distribution and function of laminins in the neuromuscular system of developing, adult, and mutant miceCD4(+) T cells specific to a glomerular basement membrane antigen mediate glomerulonephritis.The inner ear of dogs with X-linked nephritis provides clues to the pathogenesis of hearing loss in X-linked Alport syndromeLMX1B is essential for the maintenance of differentiated podocytes in adult kidneys.Recombinant non-collagenous domain of alpha2(IV) collagen causes involution of choroidal neovascularization by inducing apoptosis.Laminin alpha4-null mutant mice develop chronic kidney disease with persistent overexpression of platelet-derived growth factor.Commitment and differentiation of lung cell lineages.A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers.Maintenance of glomerular filtration barrier integrity requires laminin alpha5.Every breath you take: the impact of environment on resident memory CD8 T cells in the lung.Basement membrane collagen type IV expression by human mesenchymal stem cells during adipogenic differentiationAlport syndrome: abnormalities of type IV collagen genes and proteins.Transgenic isolation of skeletal muscle and kidney defects in laminin beta2 mutant mice: implications for Pierson syndromeSearching for a treatment for Alport syndrome using mouse modelsLaminin-5 in the progression of carcinomas.Basement membranes: cell scaffoldings and signaling platforms.Rapid identification of a disease allele in mouse through whole genome sequencing and bulk segregation analysis.Dystroglycan does not contribute significantly to kidney development or function, in health or after injury.The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes.New functional roles for non-collagenous domains of basement membrane collagensThe basement membrane/basal lamina of skeletal muscle.MMP mediated degradation of type IV collagen alpha 1 and alpha 3 chains reflects basement membrane remodeling in experimental and clinical fibrosis--validation of two novel biomarker assays.Transcriptome analysis in prenatal IGF1-deficient mice identifies molecular pathways and target genes involved in distal lung differentiation.Sequential expression of type IV collagen networks: testis as a model and relevance to spermatogenesisMolecular Cloning and Functional Characterization of Mouse α3(IV)NC1.Low-dose irradiation affects expression of inflammatory markers in the heart of ApoE -/- miceReview series: The cell biology of renal filtration.Type IV procollagen missense mutations associated with defects of the eye, vascular stability, the brain, kidney function and embryonic or postnatal viability in the mouse, Mus musculus: an extension of the Col4a1 allelic series and the identificatiGelatinase B (MMP-9) is not essential in the normal kidney and does not influence progression of renal disease in a mouse model of Alport syndrome.Extrasynaptic location of laminin beta 2 chain in developing and adult human skeletal muscle.
P2860
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P2860
Collagen IV alpha 3, alpha 4, and alpha 5 chains in rodent basal laminae: sequence, distribution, association with laminins, and developmental switches
description
1994 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1994
@ast
im November 1994 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1994/11/01)
@sk
vědecký článek publikovaný v roce 1994
@cs
wetenschappelijk artikel (gepubliceerd op 1994/11/01)
@nl
наукова стаття, опублікована в листопаді 1994
@uk
مقالة علمية (نشرت في نوفمبر 1994)
@ar
name
Collagen IV alpha 3, alpha 4, ...... ns, and developmental switches
@ast
Collagen IV alpha 3, alpha 4, ...... ns, and developmental switches
@en
Collagen IV alpha 3, alpha 4, ...... ns, and developmental switches
@nl
type
label
Collagen IV alpha 3, alpha 4, ...... ns, and developmental switches
@ast
Collagen IV alpha 3, alpha 4, ...... ns, and developmental switches
@en
Collagen IV alpha 3, alpha 4, ...... ns, and developmental switches
@nl
prefLabel
Collagen IV alpha 3, alpha 4, ...... ns, and developmental switches
@ast
Collagen IV alpha 3, alpha 4, ...... ns, and developmental switches
@en
Collagen IV alpha 3, alpha 4, ...... ns, and developmental switches
@nl
P2860
P3181
P356
P1476
Collagen IV alpha 3, alpha 4, ...... ns, and developmental switches
@en
P2093
J. H. Miner
J. R. Sanes
P2860
P304
P3181
P356
10.1083/JCB.127.3.879
P407
P577
1994-11-01T00:00:00Z