Histopathological analysis of renal cystic epithelia in the Pkd2WS25/- mouse model of ADPKD.
about
Pericentrin forms a complex with intraflagellar transport proteins and polycystin-2 and is required for primary cilia assemblyRole of PDZK1 in membrane expression of renal brush border ion exchangers.Novel role of ouabain as a cystogenic factor in autosomal dominant polycystic kidney diseaseDisruption of Myosin 1e promotes podocyte injuryRegulation of anion exchanger Slc26a6 by protein kinase CAcceleration of polycystic kidney disease progression in cpk mice carrying a deletion in the homeodomain protein Cux1Zebrafish mutations affecting cilia motility share similar cystic phenotypes and suggest a mechanism of cyst formation that differs from pkd2 morphants.Hepato-renal pathology in pkd2ws25/- mice, an animal model of autosomal dominant polycystic kidney diseaseCyst formation and activation of the extracellular regulated kinase pathway after kidney specific inactivation of Pkd1.The C-terminal tail of the polycystin-1 protein interacts with the Na,K-ATPase alpha-subunit.The fate of bone marrow-derived cells carrying a Polycystic Kidney Disease mutation in the genetically normal kidneyCyclic AMP-mediated cyst expansionAntisense-mediated angiotensinogen inhibition slows polycystic kidney disease in mice with a targeted mutation in Pkd2Tolvaptan inhibits ERK-dependent cell proliferation, Cl⁻ secretion, and in vitro cyst growth of human ADPKD cells stimulated by vasopressinAltered renal proximal tubular endocytosis and histology in mice lacking myosin-VI.Calmodulin-sensitive adenylyl cyclases mediate AVP-dependent cAMP production and Cl- secretion by human autosomal dominant polycystic kidney cells.Human ADPKD primary cyst epithelial cells with a novel, single codon deletion in the PKD1 gene exhibit defective ciliary polycystin localization and loss of flow-induced Ca2+ signaling.TRPpathies.Tight junction composition is altered in the epithelium of polycystic kidneys.Transcriptome analysis reveals manifold mechanisms of cyst development in ADPKD.Mouse models of polycystic kidney disease induced by defects of ciliary proteinsHaploinsufficiency of Pkd2 is associated with increased tubular cell proliferation and interstitial fibrosis in two murine Pkd2 models.The zebrafish Kupffer's vesicle as a model system for the molecular mechanisms by which the lack of Polycystin-2 leads to stimulation of CFTR.Pkd1 regulates immortalized proliferation of renal tubular epithelial cells through p53 induction and JNK activation.Immunolocalization of NHE8 in rat kidney.Cux1 promotes cell proliferation and polycystic kidney disease progression in an ADPKD mouse model.
P2860
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P2860
Histopathological analysis of renal cystic epithelia in the Pkd2WS25/- mouse model of ADPKD.
description
2003 nî lūn-bûn
@nan
2003 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Histopathological analysis of ...... d2WS25/- mouse model of ADPKD.
@ast
Histopathological analysis of ...... d2WS25/- mouse model of ADPKD.
@en
Histopathological analysis of ...... d2WS25/- mouse model of ADPKD.
@nl
type
label
Histopathological analysis of ...... d2WS25/- mouse model of ADPKD.
@ast
Histopathological analysis of ...... d2WS25/- mouse model of ADPKD.
@en
Histopathological analysis of ...... d2WS25/- mouse model of ADPKD.
@nl
prefLabel
Histopathological analysis of ...... d2WS25/- mouse model of ADPKD.
@ast
Histopathological analysis of ...... d2WS25/- mouse model of ADPKD.
@en
Histopathological analysis of ...... d2WS25/- mouse model of ADPKD.
@nl
P2093
P2860
P1476
Histopathological analysis of ...... d2WS25/- mouse model of ADPKD.
@en
P2093
Eric Delpire
Karen Earle
Peter S Aronson
R Brent Thomson
Robert Kim
Stefan Somlo
SueAnn Mentone
P2860
P304
P356
10.1152/AJPRENAL.00153.2003
P577
2003-07-08T00:00:00Z