Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseases (Q40245141)

18 September 2017

title

Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseases (English)

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14

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L Pasquali

4

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Stefano Parodi

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S Parodi

6

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Gianluca Caridi

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G Caridi

8

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Simone Sanna-Cherchi

3

object named as

S Sanna-Cherchi

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18 September 2017

M Di Duca

1

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R Oleggini

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A Di Donato

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R Bertelli

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G Frasca

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G Cerullo

10

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A Amoroso

11

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F P Schena

12

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F Scolari

13

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European IgA Nephropathy Consortium

15

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18 September 2017

language of work or name

English

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publication date

9 August 2006

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volume

70

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issue

7

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18 September 2017

page(s)

1332-1341

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Changing incidence of glomerular diseases in adults

18 September 2017

cites work

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Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations

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Molecular basis of the functional podocin-nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains

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Identification of podocin (NPHS2) gene mutations in African Americans with nondiabetic end-stage renal disease

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NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

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Gene Expression Profiles of Podocyte-Associated Molecules as Diagnostic Markers in Acquired Proteinuric Diseases

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Disease-causing missense mutations in NPHS2 gene alter normal nephrin trafficking to the plasma membrane

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Two gene fragments that direct podocyte-specific expression in transgenic mice

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Podocyte-specific expression of cre recombinase in transgenic mice

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Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome.

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Angiotensin-converting-enzyme inhibitors slow renal decline in IgA nephropathy, independent of tubulointerstitial fibrosis at presentation

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Lysyl Oxidase Activates the Transcription Activity of Human Collagene III Promoter

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Segregation at three loci explains familial and population risk in Hirschsprung disease

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Identifiers

DOI

10.1038/SJ.KI.5001767

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Dimensions Publication ID

18 September 2017

1052271181

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