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 *

136 related articles for article (PubMed ID: 37356184)

  • 41. Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies.
    Gianesello L; Ceol M; Bertoldi L; Terrin L; Priante G; Murer L; Peruzzi L; Giordano M; Paglialonga F; Cantaluppi V; Musetti C; Valle G; Del Prete D; Anglani F; Network DDI
    Int J Mol Sci; 2020 Jan; 21(2):. PubMed ID: 31947599
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Generation of the integration-free induced pluripotent stem cell line (FHUSTCi001-A) from a patient with glomerulopathy with fibronectin deposits harboring FN1 mutation.
    Yu X; Wang H; Xiao F; Jiang S; Li K; Chen Q; Wang G; Kong F; Zhao S
    Stem Cell Res; 2022 May; 61():102751. PubMed ID: 35395622
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Generation of induced pluripotent stem cell PLAFMCi002-A derived from peripheral blood mononuclear cells of polycystic kidney disease patient with PKD1 mutation.
    Wang T; Li J; Xiao Y; Fu B; Wang P; Bai X; Cai G; Chen X; Li Q
    Stem Cell Res; 2020 Dec; 49():102039. PubMed ID: 33068887
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Generation of the induced pluripotent stem cell line UHOMi002-A from peripheral blood mononuclear cells of a healthy male donor.
    Fieldes M; Ahmed E; Bourguignon C; Mianné J; Martin M; Arnould C; Vachier I; Assou S; De Vos J; Bourdin A
    Stem Cell Res; 2020 Dec; 49():102037. PubMed ID: 33099111
    [TBL] [Abstract][Full Text] [Related]  

  • 45. A novel mutation of Dent's disease in an 11-year-old male with nephrolithiasis and nephrocalcinosis.
    Sancakli O; Kulu B; Sakallioglu O
    Arch Argent Pediatr; 2018 Jun; 116(3):e442-e444. PubMed ID: 29756720
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Phenotypic spectrum and antialbuminuric response to angiotensin converting enzyme inhibitor and angiotensin receptor blocker therapy in pediatric Dent disease.
    Deng H; Zhang Y; Xiao H; Yao Y; Zhang H; Liu X; Su B; Guan N; Zhong X; Wang S; Ding J; Wang F
    Mol Genet Genomic Med; 2020 Aug; 8(8):e1306. PubMed ID: 32495484
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Generation of a human induced pluripotent stem cell line (BIHi002-A) from a patient with CLCN7-related infantile malignant autosomal recessive osteopetrosis.
    Hennig AF; Rössler U; Boiti F; von der Hagen M; Gossen M; Kornak U; Stachelscheid H
    Stem Cell Res; 2019 Mar; 35():101367. PubMed ID: 30763735
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Generation of induced pluripotent stem cells from peripheral blood mononuclear cells obtained from an adult with autosomal recessive polycystic kidney disease.
    Sun M; Li J; Shang S; Bai X; Cai G; Li Q
    Stem Cell Res; 2022 May; 61():102772. PubMed ID: 35405383
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [A rare tubulopathy: Dent's disease in the background of focal segmental glomerular sclerosis].
    Jakab D; Maróti Z; Iványi B; Bereczki C; Kalmár T
    Orv Hetil; 2023 May; 164(20):788-791. PubMed ID: 37210717
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Generation and characterization of a human induced pluripotent stem cell line (SDQLCHi052-A) from peripheral blood mononuclear cells derived from a healthy Chinese donor.
    Wan Z; Guan J; Li Y; Zhang H; Wang B; Yang X; Jin X; Ma X; Liu Y
    Stem Cell Res; 2023 Sep; 71():103139. PubMed ID: 37320988
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Generation of human induced pluripotent stem cell line from a patient with restrictive cardiomyopathy.
    Li J; Jiang J; Ye L; Lian Z; Gong H; Lei W; Dai Y; Hu S
    Stem Cell Res; 2024 Apr; 76():103370. PubMed ID: 38428347
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Renal manifestations of Dent disease and Lowe syndrome.
    Cho HY; Lee BH; Choi HJ; Ha IS; Choi Y; Cheong HI
    Pediatr Nephrol; 2008 Feb; 23(2):243-9. PubMed ID: 18038239
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq).
    Ye Y; Wang J; Quan X; Xu K; Fu H; Gu W; Mao J
    BMC Nephrol; 2020 May; 21(1):171. PubMed ID: 32393202
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Generation of human induced pluripotent stem cell line FDCHDPi001-A from a Chinese Han Tourette's syndrome patient.
    Yuan A; Tao R; Yu S; Jing N; Sun J
    Stem Cell Res; 2021 Apr; 52():102227. PubMed ID: 33607468
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Generation of two human induced pluripotent stem cell lines derived from myoblasts (MDCi014-A) and from peripheral blood mononuclear cells (MDCi014-B) from the same donor.
    Metzler E; Telugu N; Diecke S; Spuler S; Escobar H
    Stem Cell Res; 2020 Oct; 48():101998. PubMed ID: 32979629
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Human induced pluripotent stem cells line (PNUSCRi002-A) from a patient with Parkinson's disease carrying a R159W mutation in the GBA gene.
    Moon HJ; Lee N; Moon JY; Park KK; Lee JH; Kim JH
    Stem Cell Res; 2022 Dec; 65():102948. PubMed ID: 36274270
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Generation of a hiPSC line ZZUNEUi017-A from a patient with dilated cardiomyopathy caused by mutation in TTN.
    Huang S; Fu W; Guo G; Tiana X; Zhao X; Dong J; Li X; Yang H
    Stem Cell Res; 2021 Apr; 52():102248. PubMed ID: 33610015
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Generation and characterization of human induced pluripotent stem cell (hiPSC) lines from an Alzheimer's disease (ASUi003-A) and non-demented control (ASUi004-A) patient homozygous for the Apolipoprotein e4 (APOE4) risk variant.
    Brookhouser N; Zhang P; Caselli R; Kim JJ; Brafman DA
    Stem Cell Res; 2017 Dec; 25():266-269. PubMed ID: 29246571
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Characterization of human induced pluripotent stem cells line (PNUSCRi004-A) from a Parkinson's disease patient carrying L483P, A495P and V499V mutations.
    Moon HJ; Lee N; Moon JY; Lee JH; Kim JH
    Stem Cell Res; 2023 Apr; 68():103051. PubMed ID: 36805467
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Identification of a novel mutation in the CLCN5 gene in a Chinese family with Dent-1 disease.
    Zhang H; Wang C; Yue H; Hu WW; Gu JM; He JW; Fu WZ; Liu YJ; Zhang Z; Zhang ZL
    Nephrology (Carlton); 2014 Feb; 19(2):80-3. PubMed ID: 24428215
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.