These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 8264140)

  • 61. Detection of mutations in COL4A5 in patients with Alport syndrome.
    Plant KE; Green PM; Vetrie D; Flinter FA
    Hum Mutat; 1999; 13(2):124-32. PubMed ID: 10094548
    [TBL] [Abstract][Full Text] [Related]  

  • 62. X-linked Alport syndrome associated with a synonymous p.Gly292Gly mutation alters the splicing donor site of the type IV collagen alpha chain 5 gene.
    Fu XJ; Nozu K; Eguchi A; Nozu Y; Morisada N; Shono A; Taniguchi-Ikeda M; Shima Y; Nakanishi K; Vorechovsky I; Iijima K
    Clin Exp Nephrol; 2016 Oct; 20(5):699-702. PubMed ID: 26581810
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Distribution of familial nephritis antigen in normal tissue and renal basement membranes of patients with homozygous and heterozygous Alport familial nephritis. Relationship of familial nephritis and Goodpasture antigens to novel collagen chains and type IV collagen.
    Kleppel MM; Kashtan C; Santi PA; Wieslander J; Michael AF
    Lab Invest; 1989 Sep; 61(3):278-89. PubMed ID: 2671490
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Splicing mutations in the COL4A5 gene in Alport's syndrome: different mRNA expression between leukocytes and fibroblasts.
    Nakazato H; Hattori S; Ushijima T; Matsuura T; Karashima S; Uemura T; Endo F; Matsuda I
    Am J Kidney Dis; 1995 Nov; 26(5):732-9. PubMed ID: 7485125
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Glomerular expression of type IV collagen chains in normal and X-linked Alport syndrome kidneys.
    Heidet L; Cai Y; Guicharnaud L; Antignac C; Gubler MC
    Am J Pathol; 2000 Jun; 156(6):1901-10. PubMed ID: 10854213
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Relationship between COL4A5 gene mutation and distribution of type IV collagen in male X-linked Alport syndrome. Japanese Alport Network.
    Naito I; Kawai S; Nomura S; Sado Y; Osawa G
    Kidney Int; 1996 Jul; 50(1):304-11. PubMed ID: 8807602
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Sequence and localization of a partial cDNA encoding the human alpha 3 chain of type IV collagen.
    Morrison KE; Mariyama M; Yang-Feng TL; Reeders ST
    Am J Hum Genet; 1991 Sep; 49(3):545-54. PubMed ID: 1882840
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Targets of alloantibodies in Alport anti-glomerular basement membrane disease after renal transplantation.
    Brainwood D; Kashtan C; Gubler MC; Turner AN
    Kidney Int; 1998 Mar; 53(3):762-6. PubMed ID: 9507224
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Dot-and-fleck retinopathy in Alport syndrome caused by a novel mutation in the COL4A5 gene.
    Blasi MA; Rinaldi R; Renieri A; Petrucci R; De Bernardo C; Bruttini M; Grammatico P
    Am J Ophthalmol; 2000 Jul; 130(1):130-1. PubMed ID: 11004279
    [TBL] [Abstract][Full Text] [Related]  

  • 70. COL4A5 gene deletion and production of post-transplant anti-alpha 3(IV) collagen alloantibodies in Alport syndrome.
    Kalluri R; Weber M; Netzer KO; Sun MJ; Neilson EG; Hudson BG
    Kidney Int; 1994 Mar; 45(3):721-6. PubMed ID: 8196274
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Unusual deep intronic mutations in the COL4A5 gene cause X linked Alport syndrome.
    King K; Flinter FA; Nihalani V; Green PM
    Hum Genet; 2002 Dec; 111(6):548-54. PubMed ID: 12436246
    [TBL] [Abstract][Full Text] [Related]  

  • 72. [Application of multiplex ligation-dependent probe amplification in gene diagnosis of X-linked Alport syndrome].
    Zhang YQ; Zhao D; Yu LX; Ding J; Wang F
    Zhonghua Yi Xue Za Zhi; 2012 Oct; 92(40):2825-9. PubMed ID: 23290210
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Clinical and genetic mapping of X chromosome in the X-linked dominant inherited Alport's syndrome.
    Dai Y; Huang Y; He X; Wang S; Huang R; Tang M; Hu C
    Saudi J Kidney Dis Transpl; 2008 Sep; 19(5):767-74. PubMed ID: 18711293
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Meta-analysis of genotype-phenotype correlation in X-linked Alport syndrome: impact on clinical counselling.
    Gross O; Netzer KO; Lambrecht R; Seibold S; Weber M
    Nephrol Dial Transplant; 2002 Jul; 17(7):1218-27. PubMed ID: 12105244
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Major rearrangements in the alpha 5(IV) collagen gene in three patients with Alport syndrome.
    Boye E; Vetrie D; Flinter F; Buckle B; Pihlajaniemi T; Hamalainen ER; Myers JC; Bobrow M; Harris A
    Genomics; 1991 Dec; 11(4):1125-32. PubMed ID: 1783380
    [TBL] [Abstract][Full Text] [Related]  

  • 76. [Molecular genetics of Alport syndrome].
    Yamazaki H; Saito A; Nakagawa Y; Arakawa M
    Nihon Rinsho; 1992 Dec; 50(12):3021-6. PubMed ID: 1491454
    [TBL] [Abstract][Full Text] [Related]  

  • 77. [Detection of a novel mutation in COL4A5 gene from a Chinese family with X-linked alport syndrome].
    Peng CL; Liang H; Z ou QL; Wang J; Liu CS; Zhang XF; Chen J; Hu SN
    Yi Chuan Xue Bao; 2004 Nov; 31(11):1190-5. PubMed ID: 15651669
    [TBL] [Abstract][Full Text] [Related]  

  • 78. COL4A3/COL4A4 mutations: from familial hematuria to autosomal-dominant or recessive Alport syndrome.
    Longo I; Porcedda P; Mari F; Giachino D; Meloni I; Deplano C; Brusco A; Bosio M; Massella L; Lavoratti G; Roccatello D; Frascá G; Mazzucco G; Muda AO; Conti M; Fasciolo F; Arrondel C; Heidet L; Renieri A; De Marchi M
    Kidney Int; 2002 Jun; 61(6):1947-56. PubMed ID: 12028435
    [TBL] [Abstract][Full Text] [Related]  

  • 79. 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
    Hum Mutat; 2001 Aug; 18(2):141-8. PubMed ID: 11462238
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndrome.
    Lu W; Phillips CL; Killen PD; Hlaing T; Harrison WR; Elder FF; Miner JH; Overbeek PA; Meisler MH
    Genomics; 1999 Oct; 61(2):113-24. PubMed ID: 10534397
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.