About: Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease

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About: Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease Goto Sponge NotDistinct Permalink

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description	article scientifique publié en 2008 (fr) artículu científicu espublizáu en 2008 (ast) vědecký článek publikovaný v roce 2008 (cs) наукова стаття, опублікована в листопаді 2008 (uk) 2008 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած (hyw) 2008 թվականի նոյեմբերին հրատարակված գիտական հոդված (hy) wetenschappelijk artikel (gepubliceerd op 2008/11/03) (nl) vedecký článok (publikovaný 2008/11/03) (sk) scientific journal article (en) im November 2008 veröffentlichter wissenschaftlicher Artikel (de) مقالة علمية (نشرت في 3-11-2008) (ar)
publication date	wds:Q28592609-67CC9964-475C-43A0-B884-2AA515B0ED1E
publication date	2008-11-03 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28592609-FDBD3AC0-97D6-4C78-9BFB-9F6AB7AF0AE3
language of work or name	English
cites work	wds:Q28592609-002B1725-D00A-40C4-9686-AAE82C2081AF wds:Q28592609-0B9E5A5D-3D36-4A73-8126-4F48994E6A5B wds:Q28592609-13C1BB60-1866-46F9-ACD7-7A7C41BD761F wds:Q28592609-171B1CA1-7F18-491D-96FA-F0B35D4AB769 wds:Q28592609-2E5F90C5-444F-463A-ADBE-CD56FEEFF5E8 wds:Q28592609-38471DF5-8379-47E6-BC7D-4CD4D95128C1 wds:Q28592609-38C01AD3-EB4F-4E98-88F1-56A0E4043319 wds:Q28592609-40A24746-0E64-4D9D-92BC-658B2C734FE8 wds:Q28592609-6052C3F0-7F3F-4DD1-ADF0-578CA53655AD wds:Q28592609-61B30A7D-80F3-4A11-915F-F2E247E2392F wds:Q28592609-64CE5726-59EE-4504-B518-4DD5F73116C0 wds:Q28592609-73BF3887-B1B6-4409-B246-378C0270C012 wds:Q28592609-88CCD7D2-4844-4F61-9946-8F0C9FAD707D wds:Q28592609-895E8906-466D-4071-82D3-08B25DE95470 wds:Q28592609-8B9B2669-064D-4E20-89C4-F2A3A5DF65C4 wds:Q28592609-8E1CC400-A597-44B9-991D-CC1C9EB2448E wds:Q28592609-937871E6-B213-42FC-A644-889A1BBF1A1E wds:Q28592609-938492C2-95E1-4794-B9C2-093F2339845D wds:Q28592609-9A5AE66F-0EE1-4A5C-886D-0E31E988559D wds:Q28592609-AC7A6B64-E1C5-483D-8A9B-DBE702A65FBD wds:Q28592609-AF8760E3-FEF4-4528-9D38-A14811E9D109 wds:Q28592609-C824BEC2-2AEF-475F-BEED-9B5E6817B677 wds:Q28592609-D400B331-D9E9-4729-B849-53C07B6668E1 wds:Q28592609-D4403460-ADF4-4AF2-B085-B262B47BB800 wds:Q28592609-D47AFD87-2540-4453-B023-FCFE8DFC6CD1 wds:Q28592609-D5C5CF44-2117-430C-A2D6-135EF5BC8ABA wds:Q28592609-DA58963D-8063-4855-8A65-1C86697356FF wds:Q28592609-E139A1BA-ACF4-40B3-9645-606942B4A716 wds:Q28592609-F377DD59-55F2-4299-ABE4-A98C38DE55C6 wds:Q28592609-F412E456-86ED-40B8-9635-65FA47E67A32 wds:Q28592609-F62DE0B8-EA22-4FFF-9C80-D840DAF713E7 wds:Q28592609-F7E1E1A7-1D1D-4704-BC26-4453EDCBFF98
cites work	Sonic hedgehog regulates proliferation and differentiation of mesenchymal cells in the mouse metanephric kidney Early development of polycystic kidney disease in transgenic mice expressing an activated mutant of the beta-catenin gene Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells Polycystic kidney disease: cell division without a c(l)ue? beta-catenin signaling and cancer A role for a novel centrosome cycle in asymmetric cell division Functionally unequal centrosomes drive spindle orientation in asymmetrically dividing Drosophila neural stem cells. Wrch-1, a novel member of the Rho gene family that is regulated by Wnt-1 Acute kidney injury and aberrant planar cell polarity induce cyst formation in mice lacking renal cilia. Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease. Genetics and pathogenesis of polycystic kidney disease. Disruption of intraflagellar transport in adult mice leads to obesity and slow-onset cystic kidney disease Role for the PP2A/B56delta phosphatase in regulating 14-3-3 release from Cdc25 to control mitosis Loss of the retrograde motor for IFT disrupts localization of Smo to cilia and prevents the expression of both activator and repressor functions of Gli Widespread recombinase expression using FLPeR (flipper) mice Intraflagellar transport and cilia-dependent renal disease: the ciliary hypothesis of polycystic kidney disease. Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella A critical developmental switch defines the kinetics of kidney cyst formation after loss of Pkd1 Defective planar cell polarity in polycystic kidney disease Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways Protamine-Cre recombinase transgenes efficiently recombine target sequences in the male germ line of mice, but not in embryonic stem cells Kif3a constrains beta-catenin-dependent Wnt signalling through dual ciliary and non-ciliary mechanisms Overview of structure and function of mammalian cilia Intraflagellar Transport Intraflagellar transport Dorsalizing signal Wnt-7a required for normal polarity of D-V and A-P axes of mouse limb Molecular regulation of kidney development: is the answer blowing in the Wnt? Bending the MDCK cell primary cilium increases intracellular calcium TRPP2 and TRPV4 form a polymodal sensory channel complex Beta-catenin is necessary to keep cells of ureteric bud/Wolffian duct epithelium in a precursor state Renal malformations may be linked to mutations in the hepatocyte nuclear factor-1alpha (MODY3) gene The atypical Rho family GTPase Wrch-1 regulates focal adhesion formation and cell migration
author name string	wds:Q28592609-3B5A6A8A-5760-42C7-B989-B5FA7BA99313 wds:Q28592609-4EA76F2E-F585-4D56-8EAB-D9FB9BE22200 wds:Q28592609-558BC42A-5008-4DF2-9844-EE9BA4B69878 wds:Q28592609-D45EE3A7-846B-4CEF-9257-F383A42C5F8F
OpenCitations bibliographic resource ID	wds:Q28592609-4CBBE850-EAFE-4F93-80CB-7632697ED696
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/3304334
author name string	Gregory J. Pazour Julie A. Jonassen John A. Follit Jovenal San Agustin
OpenCitations bibliographic resource ID	3304334
rdfs:label	Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease (en) Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease (nl) Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease (ast)
skos:prefLabel	Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease (en) Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease (nl) Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease (ast)
name	Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease (en) Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease (nl) Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease (ast)

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