BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

41 related articles for article (PubMed ID: 36726441)

  • 1. Characterization of pre-mRNA Splicing Defects Caused by
    Mura-Escorche G; Perdomo-Ramírez A; Ramos-Trujillo E; Trujillo-Frías CJ; Claverie-Martín F;
    Biomedicines; 2023 Nov; 11(11):. PubMed ID: 38002082
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dent disease 1-linked novel CLCN5 mutations result in aberrant location and reduced ion currents.
    Wang Y; Xu L; Zhang Y; Fu H; Gao L; Guan Y; Gu W; Sun J; Chen X; Yang F; Lai E; Wang J; Jin Y; Kou Z; Qiu X; Mao J; Hu L
    Int J Biol Macromol; 2024 Feb; 257(Pt 2):128564. PubMed ID: 38061527
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel likely pathogenic CLCN5 variant in Dent's disease.
    Hayward S; Norton J; Bownass L; Platt C; ; Campbell H; Watson E; Forrester N; Smithson S; Menon A
    BMC Nephrol; 2023 Aug; 24(1):256. PubMed ID: 37641036
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Site and Type of
    Arnous MG; Arroyo J; Cogal AG; Anglani F; Kang HG; Sas D; Harris PC; Lieske JC
    Kidney Int Rep; 2023 Jun; 8(6):1220-1230. PubMed ID: 37284679
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A young man with recurrent kidney stones and renal failure.
    Gill J; Wiederkehr MR
    Clin Nephrol Case Stud; 2020; 8():85-90. PubMed ID: 33163328
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dent's disease.
    Devuyst O; Thakker RV
    Orphanet J Rare Dis; 2010 Oct; 5():28. PubMed ID: 20946626
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hemizygous loss of function mutations in
    Leggatt G; Gast C; Gilbert RD; Veighey K; Rahman T; Ennis S
    Clin Kidney J; 2023 Jan; 16(1):192-194. PubMed ID: 36726441
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Nephrolithiasis, kidney failure and bone disorders in Dent disease patients with and without CLCN5 mutations.
    Anglani F; D'Angelo A; Bertizzolo LM; Tosetto E; Ceol M; Cremasco D; Bonfante L; Addis MA; Del Prete D;
    Springerplus; 2015; 4():492. PubMed ID: 26389017
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene.
    Drosataki E; Maragkou S; Dermitzaki K; Stavrakaki I; Lygerou D; Latsoudis H; Pleros C; Petrakis I; Zaganas I; Stylianou K
    BMC Nephrol; 2022 May; 23(1):182. PubMed ID: 35549682
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypercalciuria in patients with CLCN5 mutations.
    Ludwig M; Utsch B; Balluch B; Fründ S; Kuwertz-Bröking E; Bökenkamp A
    Pediatr Nephrol; 2006 Sep; 21(9):1241-50. PubMed ID: 16807762
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Next-Generation Sequencing in Early Diagnosis of Dent Disease 1: Two Case Reports.
    Wen M; Shen T; Wang Y; Li Y; Shi X; Dang X
    Front Med (Lausanne); 2018; 5():347. PubMed ID: 30581818
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Observations of a large Dent disease cohort.
    Blanchard A; Curis E; Guyon-Roger T; Kahila D; Treard C; Baudouin V; Bérard E; Champion G; Cochat P; Dubourg J; de la Faille R; Devuyst O; Deschenes G; Fischbach M; Harambat J; Houillier P; Karras A; Knebelmann B; Lavocat MP; Loirat C; Merieau E; Niaudet P; Nobili F; Novo R; Salomon R; Ulinski T; Jeunemaître X; Vargas-Poussou R
    Kidney Int; 2016 Aug; 90(2):430-439. PubMed ID: 27342959
    [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 3.