BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

29 related articles for article (PubMed ID: 23085274)

  • 1. A novel COL4A5 splicing mutation causes alport syndrome in a Chinese family.
    Chen S; Xu G; Zhao Z; Du J; Shen B; Li C
    BMC Med Genomics; 2024 Apr; 17(1):108. PubMed ID: 38671472
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Aberrant Splicing of
    Li Y; Yan X; Luo Z; Fu X; Li Z; Xu Q; Chen J; Yang J; Lu D
    Int J Nephrol Renovasc Dis; 2024; 17():167-174. PubMed ID: 38855711
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Trimerization profile of type IV collagen COL4A5 exon deletion in X-linked Alport syndrome.
    Koyama Y; Suico MA; Owaki A; Sato R; Kuwazuru J; Kaseda S; Sannomiya Y; Horizono J; Omachi K; Horinouchi T; Yamamura T; Tsuhako H; Nozu K; Shuto T; Kai H
    Clin Exp Nephrol; 2024 Apr; ():. PubMed ID: 38658441
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Long-term follow-up of an Alport syndrome patient with a novel mutation of
    Xiang R; Li JJ; Liu JS; Fan LL; Li L; Xia K; Zhang H
    Int J Clin Exp Pathol; 2017; 10(8):8709-8714. PubMed ID: 31966729
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X-Linked Glomerulopathy Due to COL4A5 Founder Variant.
    Barua M; John R; Stella L; Li W; Roslin NM; Sharif B; Hack S; Lajoie-Starkell G; Schwaderer AL; Becknell B; Wuttke M; Köttgen A; Cattran D; Paterson AD; Pei Y
    Am J Kidney Dis; 2018 Mar; 71(3):441-445. PubMed ID: 29198386
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel splice site mutation in the COL4A5 gene in a Chinese female patient with rare ocular abnormalities.
    Zhao C; Wang F; Zhang Y; Wen Y; Su Y; Zhang C; Sui R; Xu F; Ding J; Dong F
    Mol Vis; 2012; 18():2205-12. PubMed ID: 22919268
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. [A novel COL4A5 splicing mutation causing Alport syndrome in a Chinese family].
    Tang Z; Dai Y; Wan Z; Zhan T; Tan J; Ren X; Liu J; Wang Q; Liu M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):649-52. PubMed ID: 19065523
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 14.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 15.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 16.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 17.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 2.