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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1959 1
1962 1
1965 1
1966 2
1974 2
1977 1
1981 1
1982 1
1983 1
1984 2
1985 1
1987 1
1988 1
1989 2
1990 9
1991 9
1992 15
1993 13
1994 24
1995 21
1996 19
1997 12
1998 12
1999 8
2000 12
2001 11
2002 6
2003 6
2004 8
2005 5
2006 1
2007 4
2008 5
2009 3
2010 8
2011 4
2012 5
2013 4
2014 4
2015 5
2016 7
2017 3
2018 2
2019 6
2020 5
2021 0
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Similar articles for PMID: 7579094

264 results
Results by year
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Page 1
Mutation in alpha 5(IV) collagen chain gene in nonfamilial hematuria.
Kitagawa K, Nakanishi K, Iijima K, Nishio H, Sado Y, Sano K, Nakamura H, Yoshikawa N. Kitagawa K, et al. J Am Soc Nephrol. 1995 Aug;6(2):264-8. J Am Soc Nephrol. 1995. PMID: 7579094 Free article.
Alport syndrome. Molecular genetic aspects.
Hertz JM. Hertz JM. Dan Med Bull. 2009 Aug;56(3):105-52. Dan Med Bull. 2009. PMID: 19728970
A deletion mutation in the 3' end of the alpha 5(IV) collagen gene in juvenile-onset Alport syndrome.
Saito A, Sakatsume M, Yamazaki H, Ogata F, Hirasawa Y, Arakawa M. Saito A, et al. J Am Soc Nephrol. 1994 Mar;4(9):1649-53. J Am Soc Nephrol. 1994. PMID: 8011973 Free article.
Autosomal recessive Alport syndrome: mutation in the COL4A3 gene in a woman with Alport syndrome and posttransplant antiglomerular basement membrane nephritis.
Ding J, Stitzel J, Berry P, Hawkins E, Kashtan CE. Ding J, et al. J Am Soc Nephrol. 1995 Mar;5(9):1714-7. J Am Soc Nephrol. 1995. PMID: 7780062 Free article.
COL4A5 deletions in three patients with Alport syndrome and posttransplant antiglomerular basement membrane nephritis.
Ding J, Zhou J, Tryggvason K, Kashtan CE. Ding J, et al. J Am Soc Nephrol. 1994 Aug;5(2):161-8. J Am Soc Nephrol. 1994. PMID: 7993995 Free article.
Identification of 17 mutations in ten exons in the COL4A5 collagen gene, but no mutations found in four exons in COL4A6: a study of 250 patients with hematuria and suspected of having Alport syndrome.
Heiskari N, Zhang X, Zhou J, Leinonen A, Barker D, Gregory M, Atkin CL, Netzer KO, Weber M, Reeders S, Grönhagen-Riska C, Neumann HP, Trembath R, Tryggvason K. Heiskari N, et al. J Am Soc Nephrol. 1996 May;7(5):702-9. J Am Soc Nephrol. 1996. PMID: 8738805 Free article.
Type IV collagen alpha 5 chain. Normal distribution and abnormalities in X-linked Alport syndrome revealed by monoclonal antibody.
Yoshioka K, Hino S, Takemura T, Maki S, Wieslander J, Takekoshi Y, Makino H, Kagawa M, Sado Y, Kashtan CE. Yoshioka K, et al. Am J Pathol. 1994 May;144(5):986-96. Am J Pathol. 1994. PMID: 8178947 Free PMC article.
Complete amino acid sequence of the human alpha 5 (IV) collagen chain and identification of a single-base mutation in exon 23 converting glycine 521 in the collagenous domain to cysteine in an Alport syndrome patient.
Zhou J, Hertz JM, Leinonen A, Tryggvason K. Zhou J, et al. J Biol Chem. 1992 Jun 25;267(18):12475-81. J Biol Chem. 1992. PMID: 1352287 Free article.
[Molecular genetics of Alport syndrome].
Yamazaki H, Saito A, Nakagawa Y, Arakawa M. Yamazaki H, et al. Nihon Rinsho. 1992 Dec;50(12):3021-6. Nihon Rinsho. 1992. PMID: 1491454 Review. Japanese.
Comparison of alpha5(IV) collagen chain expression in skin with disease severity in women with X-linked Alport syndrome.
Nakanishi K, Iijima K, Kuroda N, Inoue Y, Sado Y, Nakamura H, Yoshikawa N. Nakanishi K, et al. J Am Soc Nephrol. 1998 Aug;9(8):1433-40. J Am Soc Nephrol. 1998. PMID: 9697665 Free article.
264 results
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