Similar articles for PMID: 8651296

Year	Number of Results
1990	1
1991	1
1992	8
1993	10
1994	12
1995	9
1996	9
1997	2
1998	7
1999	5
2000	5
2001	4
2002	4
2003	1
2004	2
2005	2
2006	1
2007	1
2008	4
2009	2
2010	1
2011	2
2012	4
2013	3
2014	3
2015	3
2016	4
2017	3
2020	4
2021	3
2022	5
2023	1
2024	0

1

X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene.

Renieri A, Bruttini M, Galli L, Zanelli P, Neri T, Rossetti S, Turco A, Heiskari N, Zhou J, Gusmano R, Massella L, Banfi G, Scolari F, Sessa A, Rizzoni G, Tryggvason K, Pignatti PF, Savi M, Ballabio A, De Marchi M. Renieri A, et al. Am J Hum Genet. 1996 Jun;58(6):1192-204. Am J Hum Genet. 1996. PMID: 8651296 Free PMC article.

2

Alport syndrome. Molecular genetic aspects.

Hertz JM. Hertz JM. Dan Med Bull. 2009 Aug;56(3):105-52. Dan Med Bull. 2009. PMID: 19728970

3

Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndrome.

Knebelmann B, Breillat C, Forestier L, Arrondel C, Jacassier D, Giatras I, Drouot L, Deschênes G, Grünfeld JP, Broyer M, Gubler MC, Antignac C. Knebelmann B, et al. Am J Hum Genet. 1996 Dec;59(6):1221-32. Am J Hum Genet. 1996. PMID: 8940267 Free PMC article.

4

Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome.

Hertz JM, Juncker I, Persson U, Matthijs G, Schmidtke J, Petersen MB, Kjeldsen M, Gregersen N. Hertz JM, et al. Hum Mutat. 2001 Aug;18(2):141-8. doi: 10.1002/humu.1163. Hum Mutat. 2001. PMID: 11462238 Free article.

5

Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome.

Renieri A, Galli L, Grillo A, Bruttini M, Neri T, Zanelli P, Rizzoni G, Massella L, Sessa A, Meroni M, Peratoner L, Riegler P, Scolari F, Mileti M, Giani M, Cossu M, Savi M, Ballabio A, De Marchi M. Renieri A, et al. Am J Med Genet. 1995 Nov 20;59(3):380-5. doi: 10.1002/ajmg.1320590320. Am J Med Genet. 1995. PMID: 8599366

6

Detection of mutations in COL4A5 in patients with Alport syndrome.

Plant KE, Green PM, Vetrie D, Flinter FA. Plant KE, et al. Hum Mutat. 1999;13(2):124-32. doi: 10.1002/(SICI)1098-1004(1999)13:2<124::AID-HUMU4>3.0.CO;2-Z. Hum Mutat. 1999. PMID: 10094548

7

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. doi: 10.1681/ASN.V75702. J Am Soc Nephrol. 1996. PMID: 8738805

8

The COL4A5 gene in Japanese Alport syndrome patients: spectrum of mutations of all exons. The Japanese Alport Network.

Kawai S, Nomura S, Harano T, Harano K, Fukushima T, Osawa G. Kawai S, et al. Kidney Int. 1996 Mar;49(3):814-22. doi: 10.1038/ki.1996.113. Kidney Int. 1996. PMID: 8648925 Free article.

9

Identification of four novel mutations in the COL4A5 gene of patients with Alport syndrome.

Lemmink HH, Schröder CH, Brunner HG, Nelen MR, Zhou J, Tryggvason K, Haagsma-Schouten WA, Roodvoets AP, Rascher W, van Oost BA, et al. Lemmink HH, et al. Genomics. 1993 Aug;17(2):485-9. doi: 10.1006/geno.1993.1351. Genomics. 1993. PMID: 8406498

10

Detection of 12 novel mutations in the collagenous domain of the COL4A5 gene in Alport syndrome patients.

Boye E, Flinter F, Zhou J, Tryggvason K, Bobrow M, Harris A. Boye E, et al. Hum Mutat. 1995;5(3):197-204. doi: 10.1002/humu.1380050303. Hum Mutat. 1995. PMID: 7599631

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