(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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18 September 2017

14

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18 September 2017

L Pasquali

4

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Stefano Parodi

object named as

S Parodi

6

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Gianluca Caridi

object named as

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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18 September 2017

R Oleggini

2

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18 September 2017

A Di Donato

5

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18 September 2017

R Bertelli

7

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18 September 2017

G Frasca

9

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18 September 2017

G Cerullo

10

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18 September 2017

A Amoroso

11

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18 September 2017

F P Schena

12

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18 September 2017

F Scolari

13

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18 September 2017

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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18 September 2017

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18 September 2017

volume

70

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18 September 2017

issue

7

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18 September 2017

page(s)

1332-1341

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https://scigraph.springernature.com/pub.10.1038/sj.ki.5001767

18 September 2017

exact match

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cites work

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Changing patterns in the histopathology of idiopathic nephrotic syndrome in children

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Renal disease susceptibility and hypertension are under independent genetic control in the fawn-hooded rat

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Strain differences rather than hyperglycemia determine the severity of glomerulosclerosis in mice

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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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CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility

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

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Early glomerular filtration defect and severe renal disease in podocin-deficient mice

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

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Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin

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NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms

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Expression of podocyte-associated molecules in acquired human kidney diseases

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Expression of nephrin, podocin, alpha-actinin, and WT1 in children with 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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The IgA nephropathy Biobank. An important starting point for the genetic dissection of a complex trait.

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Haploview: analysis and visualization of LD and haplotype maps

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A New Statistical Method for Haplotype Reconstruction from Population Data

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Pedigree disequilibrium tests for multilocus haplotypes.

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Nephrin redistribution on podocytes is a potential mechanism for proteinuria in patients with primary acquired nephrotic syndrome

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Nephrin expression is reduced in human diabetic nephropathy: evidence for a distinct role for glycated albumin and angiotensin II.

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Natural history of idiopathic IgA nephropathy and factors predictive of disease outcome

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Urinary albumin excretion: a predictor of glomerular findings in adults with microscopic haematuria

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Angiotensin-converting enzyme inhibitors and angiotensin receptor blockers for IgA nephropathy

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7 January 2021

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

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7 January 2021

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7 January 2021

NPHS2 mutation associated with recurrence of proteinuria after transplantation

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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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7 January 2021

Identifiers

DOI

10.1038/SJ.KI.5001767

1 reference

Dimensions Publication ID

18 September 2017

1052271181

0 references

1 reference