Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation
Author:
Publisher
Elsevier BV
Subject
Biochemistry,Biophysics
Reference29 articles.
1. Hereditary familial congenital haemorrhagic nephritis;Alport;Br. Med. J.,1927
2. Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus;Spear;Am. J. Pathol.,1972
3. Identification of mutations in the COL4A5 collagen gene in Alport syndrome;Barker;Science,1990
4. Role of distinct type IV collagen networks in glomerular development and function;Harvey;Kidney Int.,1998
5. Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome;Hostikka;Proc. Natl. Acad. Sci. USA,1990
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3. A mouse model for X-linked Alport syndrome induced by Del-ATGG in the Col4a5 gene;Frontiers in Medicine;2023-03-08
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5. A Comparative Presentation of Mouse Models That Recapitulate Most Features of Alport Syndrome;Genes;2022-10-18
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