173 related articles for article (PubMed ID: 27934798)
1. Identification of a novel collagen type IV alpha-4 (
Deng S; Xu H; Yuan J; Xiao J; Yuan L; Deng X; Guan L; Zhu A; Rong P; Zhang J; Deng H
Indian J Med Res; 2016 Aug; 144(2):200-205. PubMed ID: 27934798
[TBL] [Abstract][Full Text] [Related]
2. Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing.
Guo Y; Yuan J; Liang H; Xiao J; Xu H; Yuan L; Gao K; Wu B; Tang Y; Li X; Deng H
Mol Biol Rep; 2014 Jun; 41(6):3631-5. PubMed ID: 24522658
[TBL] [Abstract][Full Text] [Related]
3. A novel frameshift mutation of COL4A5 in a Chinese family with presumed IgA nephropathy and chronic glomerulonephritis.
Zhu Q; Zhou C; Wang J
J Clin Lab Anal; 2020 Dec; 34(12):e23558. PubMed ID: 32893410
[TBL] [Abstract][Full Text] [Related]
4. A novel COL4A5 mutation identified in a Chinese Han family using exome sequencing.
Xiu X; Yuan J; Deng X; Xiao J; Xu H; Zeng Z; Guan L; Xu F; Deng S
Biomed Res Int; 2014; 2014():186048. PubMed ID: 25110662
[TBL] [Abstract][Full Text] [Related]
5. Identification of a novel COL4A5 mutation in the proband initially diagnosed as IgAN from a Chinese family with X-linked Alport syndrome.
Li Z; Zhu P; Huang H; Pan Y; Han P; Cui H; Kang Z; Xun M; Zhang Y; Liu S; Wang J; Wu J
Sci China Life Sci; 2019 Dec; 62(12):1572-1579. PubMed ID: 31209800
[TBL] [Abstract][Full Text] [Related]
6. Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome.
Kamiyoshi N; Nozu K; Fu XJ; Morisada N; Nozu Y; Ye MJ; Imafuku A; Miura K; Yamamura T; Minamikawa S; Shono A; Ninchoji T; Morioka I; Nakanishi K; Yoshikawa N; Kaito H; Iijima K
Clin J Am Soc Nephrol; 2016 Aug; 11(8):1441-1449. PubMed ID: 27281700
[TBL] [Abstract][Full Text] [Related]
7. Autosomal dominant Alport syndrome due to a COL4A4 mutation with an additional ESPN variant detected by whole-exome analysis.
Izumi Y; Hamaguchi A; Miura R; Nakagawa T; Nakagawa M; Saida K; Miyake N; Nagayoshi Y; Kakizoe Y; Miyoshi T; Kohda Y; Misumi Y; Matsumoto N; Ando Y; Mukoyama M
CEN Case Rep; 2020 Feb; 9(1):59-64. PubMed ID: 31677115
[TBL] [Abstract][Full Text] [Related]
8. Whole exome sequencing reveals novel COL4A3 and COL4A4 mutations and resolves diagnosis in Chinese families with kidney disease.
Lin F; Bian F; Zou J; Wu X; Shan J; Lu W; Yao Y; Jiang G; Gale DP
BMC Nephrol; 2014 Nov; 15():175. PubMed ID: 25381091
[TBL] [Abstract][Full Text] [Related]
9. A COL4A5 Missense Variant in a Han-Chinese Family with X-linked Alport Syndrome.
Wu Y; Guo Y; Yuan J; Xu H; Chen Y; Zhang H; Yuan M; Deng H; Yuan L
Curr Mol Med; 2019; 19(10):758-765. PubMed ID: 31490752
[TBL] [Abstract][Full Text] [Related]
10. COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi family.
Ramzan K; Imtiaz F; Taibah K; Alnufiee S; Akhtar M; Al-Hazzaa SA; Al-Owain M
Int J Pediatr Otorhinolaryngol; 2014 Mar; 78(3):427-32. PubMed ID: 24398087
[TBL] [Abstract][Full Text] [Related]
11. Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and clinical outcome.
Marcocci E; Uliana V; Bruttini M; Artuso R; Silengo MC; Zerial M; Bergesio F; Amoroso A; Savoldi S; Pennesi M; Giachino D; Rombolà G; Fogazzi GB; Rosatelli C; Martinhago CD; Carmellini M; Mancini R; Di Costanzo G; Longo I; Renieri A; Mari F
Nephrol Dial Transplant; 2009 May; 24(5):1464-71. PubMed ID: 19129241
[TBL] [Abstract][Full Text] [Related]
12. Mutation analysis of COL4A3 and COL4A4 genes in a Chinese autosomal-dominant Alport syndrome family.
Guo L; Li D; Dong S; Wan D; Yang B; Huang Y
J Genet; 2017 Jun; 96(2):389-392. PubMed ID: 28674241
[TBL] [Abstract][Full Text] [Related]
13. Mutation c.359_363delGTATTinsATAC in the COL4A5 causes Alport syndrome in a Chinese family.
Wang Q; Liu F; Xing Y; Wei X; Li H; Zhang S; Liu J; Wang Q; Tang Z; Liu M
Gene; 2013 Jan; 512(2):482-5. PubMed ID: 23085274
[TBL] [Abstract][Full Text] [Related]
14. Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene.
Pescucci C; Mari F; Longo I; Vogiatzi P; Caselli R; Scala E; Abaterusso C; Gusmano R; Seri M; Miglietti N; Bresin E; Renieri A
Kidney Int; 2004 May; 65(5):1598-603. PubMed ID: 15086897
[TBL] [Abstract][Full Text] [Related]
15. Identification of a new mutation in the alpha4(IV) collagen gene in a family with autosomal dominant Alport syndrome and hypercholesterolaemia.
Ciccarese M; Casu D; Ki Wong F; Faedda R; Arvidsson S; Tonolo G; Luthman H; Satta A
Nephrol Dial Transplant; 2001 Oct; 16(10):2008-12. PubMed ID: 11572889
[TBL] [Abstract][Full Text] [Related]
16. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically.
Imafuku A; Nozu K; Sawa N; Hasegawa E; Hiramatsu R; Kawada M; Hoshino J; Tanaka K; Ishii Y; Takaichi K; Fujii T; Ohashi K; Iijima K; Ubara Y
Nephrology (Carlton); 2018 Oct; 23(10):940-947. PubMed ID: 28704582
[TBL] [Abstract][Full Text] [Related]
18. A Novel
Graziani L; Minotti C; Carriero ML; Bengala M; Lai S; Terracciano A; Novelli A; Novelli G
Genes (Basel); 2024 May; 15(5):. PubMed ID: 38790225
[TBL] [Abstract][Full Text] [Related]
19. Novel Mutations of
Gong WY; Liu FN; Yin LH; Zhang J
Biomed Res Int; 2021; 2021():6664973. PubMed ID: 33748275
[TBL] [Abstract][Full Text] [Related]
20. Autosomal dominant Alport syndrome linked to the type IV collage alpha 3 and alpha 4 genes (COL4A3 and COL4A4).
Jefferson JA; Lemmink HH; Hughes AE; Hill CM; Smeets HJ; Doherty CC; Maxwell AP
Nephrol Dial Transplant; 1997 Aug; 12(8):1595-9. PubMed ID: 9269635
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
