نتایج جستجو برای: nphs2 protein

تعداد نتایج: 1234819  

Journal: :American journal of nephrology 2009
Hiroshi Kajiyama Steve Titus Christopher P Austin Kathleen Chiotos Takayuki Matsumoto Toru Sakairi Jeffrey B Kopp

BACKGROUND Conditionally immortalized podocytes are valuable research tools but are difficult to efficiently transfect and do not provide graded transgene expression. METHODS Conditionally immortalized mouse podocyte cell lines were established employing a tetracycline-inducible system. Glomerular cells, isolated from transgenic mice bear- ing two transgenes, NPHS2-reverse tetracycline-contro...

Journal: :The Journal of clinical investigation 2002
Jeffrey H Miner Roy Morello Kaya L Andrews Cong Li Corinne Antignac Andrey S Shaw Brendan Lee

LMX1B encodes a LIM-homeodomain transcription factor. Mutations in LMX1B cause nail-patella syndrome (NPS), an autosomal dominant disease with skeletal abnormalities, nail hypoplasia, and nephropathy. Expression of glomerular basement membrane (GBM) collagens is reduced in Lmx1b(-/-) mice, suggesting one basis for NPS nephropathy. Here, we show that Lmx1b(-/-) podocytes have reduced numbers of ...

Journal: :Human molecular genetics 2013
Teresa Esposito Rod A Lea Bridget H Maher Dianne Moses Hannah C Cox Sara Magliocca Andrea Angius Dale R Nyholt Thomas Titus Troy Kay Nicholas A Gray Maria P Rastaldi Alan Parnham Fernando Gianfrancesco Lyn R Griffiths

Focal segmental glomerulosclerosis (FSGS) is the consequence of a disease process that attacks the kidney's filtering system, causing serious scarring. More than half of FSGS patients develop chronic kidney failure within 10 years, ultimately requiring dialysis or renal transplantation. There are currently several genes known to cause the hereditary forms of FSGS (ACTN4, TRPC6, CD2AP, INF2, MYO...

2015
Mariya T. Sweetwyne Antje Gruenwald Thiruvur Niranjan Ryuichi Nishinakamura Lothar J. Strobl Katalin Susztak

Notch pathway activation in podocytes has been shown to play an important role in diabetic kidney disease (DKD) development; however, the receptors and ligands involved in the process have not been identified. Here, we report that conditional deletion of Notch1 in podocytes using NPHS2(cre)Notch1(flox/flox) animals resulted in marked amelioration of DKD. On the contrary, podocyte-specific genet...

Journal: :Journal of the American Society of Nephrology : JASN 2002
Susan E Quaggin

One of the many challenges facing researchers in the postgenomic era is the assignment of biologic functions to all the gene sequences now publicly available. In many centers, the mouse is the experimental model of choice for studying the genetics of human development and disease. The mouse is a powerful tool to study human biology because of the remarkable similarities of the genetic, cellular...

Journal: :Journal of the American Society of Nephrology : JASN 2007
Kin-Wai Lai Chang-Li Wei Li-Kiang Tan Puay-Hoon Tan Gilbert S C Chiang Caroline G L Lee Stanley C Jordan Hui-Kim Yap

IL-13 has been implicated in the pathogenesis of minimal-change nephrotic syndrome. This study aimed to investigate the role of IL-13 on the development of proteinuria and expression of podocyte-related genes that are associated with nephrotic syndrome. IL-13 was overexpressed in Wistar rats through transfection of a mammalian expression vector cloned with the rat IL-13 gene, into the quadricep...

Journal: :Seminars in nephrology 2003
Martin R Pollak

Studies of Mendelian forms of focal segmental glomerulosclerosis (FSGS) and nephrotic syndrome have provided new insights into the mechanism of these diseases. Congenital nephrotic syndrome and familial forms of FSGS form a spectrum of podocyte diseases of varying severity and age of onset. Mutations in both nephrin gene (NPHS1) alleles lead to congenital nephrosis, podocyte foot process efacem...

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