Association analysis of podocyte slit diaphragm genes as candidates for diabetic nephropathy (Q57671529)

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9 January 2020

title

Association analysis of podocyte slit diaphragm genes as candidates for diabetic nephropathy (English)

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9 January 2020

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3

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9 January 2020

author name string

P Ihalmo

1

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9 January 2020

M Wessman

2

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9 January 2020

R Kilpikari

4

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9 January 2020

M Parkkonen

5

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9 January 2020

C Forsblom

6

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H Holthöfer

7

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P-H Groop

8

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FinnDiane Study Group

9

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publication date

30 October 2007

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9 January 2020

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9 January 2020

volume

51

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9 January 2020

issue

1

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9 January 2020

page(s)

86-90

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https://scigraph.springernature.com/pub.10.1007/s00125-007-0854-2

9 January 2020

exact match

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cites work

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

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12 December 2020

Proteinuria and perinatal lethality in mice lacking NEPH1, a novel protein with homology to NEPHRIN

1 reference

12 December 2020

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

1 reference

12 December 2020

TRPC6 - a new podocyte gene involved in focal segmental glomerulosclerosis

1 reference

12 December 2020

NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele

1 reference

12 December 2020

High glucose and advanced glycosylated end-products affect the expression of alpha-actinin-4 in glomerular epithelial cells

1 reference

12 December 2020

Population-based assessment of familial clustering of diabetic nephropathy in type 1 diabetes

1 reference

12 December 2020

Linkage analysis of candidate loci for end-stage renal disease due to diabetic nephropathy

1 reference

12 December 2020

Prediction of creatinine clearance from serum creatinine

1 reference

12 December 2020

A novel protein, densin, expressed by glomerular podocytes

1 reference

12 December 2020

Record-high incidence of Type I (insulin-dependent) diabetes mellitus in Finnish children. The Finnish Childhood Type I Diabetes Registry Group.

1 reference

12 December 2020

NPHS2 R229Q functional variant is associated with microalbuminuria in the general population

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12 December 2020

Altered transcapillary escape of albumin and microalbuminuria reflects two different pathogenetic mechanisms

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12 December 2020

10.1007/S00125-007-0854-2

Identifiers

DOI

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