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Cited by 533

The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.

The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death

Putaala, H.·2001·Human Molecular Genetics

Abstract

A mouse model for congenital nephrotic syndrome (NPHS1) was generated by inactivating the nephrin gene (Nphs1) in embryonic stem cells by homologous recombination. The targeting construct contained the Escherichia coli lacZ gene as a reporter for the Nphs1 promoter. Mice homozygous for inactivated Nphs1 were born at an expected frequency of 25%. Although seemingly normal at birth, they immediately developed massive proteinuria and edema and died within 24 h. The kidneys of null mice exhibited enlarged Bowman's spaces, dilated tubuli, effacement of podocyte foot processes and absence of the slit diaphragm, essentially as found in human NPHS1 patients. In addition to expression in glomerular podocytes, the reporter gene was expressed in the brain and pancreas of (+/-) and (-/-) mice. In the brain, expression was localized to the ventricular zone of the fourth ventricle, the developing spinal cord, cerebellum, hippocampus and olfactory bulb. In the cerebellum, the expression was seen in radial glial cells. Neither anatomical nor morphological abnormalities were observed in the brains of null mice.

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Metadata

Authors
Putaala, H.
Venue
Human Molecular Genetics
Published
2001-01-01
Volume
10
Issue
1
Pages
1-8
ISSN
  • 0964-6906 (ISSN-L)
  • 1460-2083
OpenAlex
W2153534186
Cited by
533
References
22
FWCI
26.60
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death. https://app.cochat.ai/papers/10.1093/hmg/10.1.1
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Putaala, H. (2001). The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death. Human Molecular Genetics. https://doi.org/10.1093/hmg/10.1.1

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