نتایج جستجو برای: pkd1 gene

تعداد نتایج: 1141754  

Journal: :Cancer research 2005
Meena Jaggi Prema S Rao David J Smith Margaret J Wheelock Keith R Johnson George P Hemstreet K C Balaji

The cadherin family of transmembrane glycoproteins plays a critical role in cell-to-cell adhesion and cadherin dysregulation is strongly associated with cancer metastasis and progression. In this study, we report a novel interaction between protein kinase D1 [PKD1; formerly known as protein kinase C mu (PKCmu)] and E-cadherin. PKD1 is a serine/threonine-specific kinase known to play a role in m...

2012
Vitalyi O. Rybin Jianfen Guo Erin Harleton Fan Zhang Susan F. Steinberg

The canonical pathway for Protein kinase D1 (PKD1) activation by growth factor receptors involves diacylglycerol binding to the C1 domain and protein kinase C-dependent phosphorylation at the activation loop. PKD1 then autophosphorylates at Ser 916 , a modification frequently used as a surrogate marker of PKD1 activity. PKD1 also is cleaved by caspase-3 at a site in the C1-PH interdomain during...

Journal: :F1000Research 2023

Background: Polycystic kidney disease (PKD) has a complex phenotype partly explained by genetic variants related to this disease. Ultrasonography is promising approach for defining clinical signs. This study aimed assess characteristics in cats with Polycystin-1 (PKD1) gene mutations and wild-type cats. Kidney were identified ultrasonography. <ns4:bold...

Journal: :American journal of physiology. Cell physiology 2014
Weihua Qiu Fan Zhang Susan F Steinberg

Protein kinase D1 (PKD1) is a Ser/Thr kinase implicated in a wide variety of cellular responses. PKD1 activation is generally attributed to a PKC-dependent pathway that leads to phosphorylation of the activation loop at Ser(744)/Ser(748). This modification increases catalytic activity, including that toward an autophosphorylation site (Ser(916)) in a postsynaptic density-95/disks large/zonula o...

Journal: :European Journal of Human Genetics 2000

Journal: :Journal of the American Society of Nephrology : JASN 2010
Michelle Liu Sally Shi Sean Senthilnathan Julie Yu Elliot Wu Carsten Bergmann Klaus Zerres Nadja Bogdanova Eliecer Coto Constantinos Deltas Alkis Pierides Kyproula Demetriou Olivier Devuyst Berenice Gitomer Marku Laakso Anne Lumiaho Klea Lamnissou Riccardo Magistroni Patrick Parfrey Martijn Breuning Dorien J M Peters Roser Torra Christopher G Winearls Vicente E Torres Peter C Harris Andrew D Paterson York Pei

Significant variation in the course of autosomal dominant polycystic kidney disease ( ADPKD) within families suggests the presence of effect modifiers. Recent studies of the variation within families harboring PKD1 mutations indicate that genetic background may account for 32 to 42% of the variance in estimated GFR (eGFR) before ESRD and 43 to 78% of the variance in age at ESRD onset, but the g...

2010
Sharon A. Matthews Maria N. Navarro Linda V. Sinclair Elizabeth Emslie Carmen Feijoo-Carnero Doreen A. Cantrell

Mammalian PKD (protein kinase D) isoforms have been implicated in the regulation of diverse biological processes in response to diacylglycerol and PKC (protein kinase C) signalling. To compare the functions of PKD1 and PKD2 in vivo, we generated mice deficient in either PKD1 or PKD2 enzymatic activity, via homozygous expression of PKD1(S744A/S748A) or PKD2(S707A/S711A) 'knockin' alleles. We als...

Journal: :American journal of physiology. Renal physiology 2011
Wouter N Leonhard Annemieke van der Wal Zlata Novalic Steven J Kunnen Ron T Gansevoort Martijn H Breuning Emile de Heer Dorien J M Peters

Autosomal dominant polycystic kidney disease (ADPKD) caused by mutations in either the PKD1 or PKD2 gene is a major cause of end-stage renal failure. A number of compounds targeting specific signaling pathways were able to inhibit cystogenesis in rodent models and are currently being tested in clinical trials. However, given the complex signaling in ADPKD, an ideal therapy would likely have to ...

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