Deficiency of the tensin2 gene in the ICGN mouse: an animal model for congenital nephrotic syndrome (Q83318688)

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21 January 2020

title

Deficiency of the tensin2 gene in the ICGN mouse: an animal model for congenital nephrotic syndrome (English)

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21 January 2020

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A-Ri Cho

1

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21 January 2020

Kozue Uchio-Yamada

2

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21 January 2020

Takeshi Torigai

3

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21 January 2020

Tomomi Miyamoto

4

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21 January 2020

Ichiro Miyoshi

5

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21 January 2020

Junichiro Matsuda

6

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21 January 2020

Tsutomu Kurosawa

7

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21 January 2020

Yasuhiro Kon

8

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21 January 2020

Atsushi Asano

9

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21 January 2020

Nobuya Sasaki

10

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21 January 2020

Takashi Agui

11

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21 January 2020

publication date

1 May 2006

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21 January 2020

number of pages

10

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inferred from page(s)

published in

Mammalian Genome

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21 January 2020

volume

17

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21 January 2020

issue

5

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21 January 2020

page(s)

407-416

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https://scigraph.springernature.com/pub.10.1007/s00335-005-0167-z

21 January 2020

exact match

0 references

cites work

Tensin1 and a previously undocumented family member, tensin2, positively regulate cell migration

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-005-0167-Z

Evolution of Glomerular Lesions in Nephrotic ICGN Mice: Serial Biopsy Study with Electron Microscopy

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-005-0167-Z

Tensin is expressed in glomerular mesangial cells and is related to their attachment to surrounding extracellular matrix

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-005-0167-Z

Linkage mapping of the mouse nephrosis (nep) gene to chromosome 15

21 January 2018

1 reference

12 December 2020

1 reference

12 December 2020

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

1 reference

12 December 2020

An ultrastructural study of the mechanisms of proteinuria in aminonucleoside nephrosis

1 reference

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

Development of nephrotic ICGN mice--the origin, reproductive ability, and incidence of glomerulonephritis

1 reference

12 December 2020

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

1 reference

12 December 2020

Evaluation of a Thick and Thin Section Method for Estimation of Podocyte Number, Glomerular Volume, and Glomerular Volume Per Podocyte in Rat Kidney with Wilms’ Tumor-1 Protein Used as a Podocyte Nuclear Marker

1 reference

12 December 2020

Progressive kidney degeneration in mice lacking tensin

1 reference

12 December 2020

Novel concepts in understanding and management of glomerular proteinuria.

1 reference

12 December 2020

Nonradioactive in situ hybridization to xenopus tissue sections

1 reference

12 December 2020

Getting a foothold in nephrotic syndrome

1 reference

12 December 2020

Regulation of tensin-promoted cell migration by its focal adhesion binding and Src homology domain 2.

1 reference

12 December 2020

When the message goes awry: disease-producing mutations that influence mRNA content and performance.

1 reference

12 December 2020

Hepatocyte growth factor prevents renal fibrosis and dysfunction in a mouse model of chronic renal disease

1 reference

12 December 2020

Podocyte biology and response to injury

1 reference

12 December 2020

Hereditary nephrotic syndrome with progression to renal failure in a mouse model (ICGN strain): clinical study

1 reference

12 December 2020

Decreased matrix metalloproteinase activity in the kidneys of hereditary nephrotic mice (ICGN strain)

1 reference

12 December 2020

Localization of extracellular matrix receptors in ICGN mice, a strain of mice with hereditary nephrotic syndrome

1 reference

12 December 2020

Caught flat-footed: podocyte damage and the molecular bases of focal glomerulosclerosis

1 reference

12 December 2020

Early Ultrastructural Glomerular Alterations in Neonatal Nephrotic Mice (ICGN Strain)

1 reference

12 December 2020

Abnormalities of extracellular matrices and transforming growth factor beta1 localization in the kidney of the hereditary nephrotic mice (ICGN strain).

1 reference

12 December 2020

Alterations of the glomerular epithelium in acute aminonucleoside nephrosis. Evidence for formation of occluding junctions and epithelial cell detachment

1 reference

12 December 2020

Focal and segmental glomerulosclerosis in mice with podocyte-specific expression of mutant alpha-actinin-4

1 reference

12 December 2020

Ultrastructural organization of contractile and cytoskeletal proteins in glomerular podocytes of chicken, rat, and man.

1 reference

12 December 2020

Characteristics of mutant mice (ICGN) with spontaneous renal lesions: a new model for human nephrotic syndrome

1 reference

12 December 2020

Podocyte depletion and glomerulosclerosis have a direct relationship in the PAN-treated rat

1 reference

12 December 2020

Congenital nephrotic syndrome in mice lacking CD2-associated protein

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12 December 2020

Regulation of podocyte structure during the development of nephrotic syndrome

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12 December 2020

Occurrence of an actin-inserting domain in tensin

1 reference

12 December 2020

10.1007/S00335-005-0167-Z

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16688531%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

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