BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 35264234)

  • 1. Primary URECs: a source to better understand the pathology of renal tubular epithelia in pediatric hereditary cystic kidney diseases.
    Ziegler WH; Lüdiger S; Hassan F; Georgiadis ME; Swolana K; Khera A; Mertens A; Franke D; Wohlgemuth K; Dahmer-Heath M; König J; Dafinger C; Liebau MC; Cetiner M; Bergmann C; Soetje B; Haffner D
    Orphanet J Rare Dis; 2022 Mar; 17(1):122. PubMed ID: 35264234
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Use of patient derived urine renal epithelial cells to confirm pathogenicity of PKHD1 alleles.
    Molinari E; Srivastava S; Dewhurst RM; Sayer JA
    BMC Nephrol; 2020 Oct; 21(1):435. PubMed ID: 33059616
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Urine-Derived Renal Epithelial Cells (URECs) from Transplanted Kidneys as a Promising Immunomodulatory Cell Population.
    Pizzuti V; Donadei C; Balducelli E; Conte D; Gessaroli E; Paris F; Bini C; Demetri M; Di Nunzio M; Corradetti V; Alviano F; La Manna G; Comai G
    Cells; 2023 Jun; 12(12):. PubMed ID: 37371100
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Results of targeted next-generation sequencing in children with cystic kidney diseases often change the clinical diagnosis.
    Obeidova L; Seeman T; Fencl F; Blahova K; Hojny J; Elisakova V; Reiterova J; Stekrova J
    PLoS One; 2020; 15(6):e0235071. PubMed ID: 32574212
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Systematic evaluation of olfaction in patients with hereditary cystic kidney diseases/renal ciliopathies.
    Dahmer-Heath M; Schriever V; Kollmann S; Schleithoff C; Titieni A; Cetiner M; Patzer L; Tönshoff B; Hansen M; Pennekamp P; Gerß J; Konrad M; König J
    J Med Genet; 2021 Sep; 58(9):629-636. PubMed ID: 32917769
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New Insights into Cystic Kidney Diseases.
    Mochizuki T; Makabe S; Aoyama Y; Kataoka H; Nitta K
    Contrib Nephrol; 2018; 195():31-41. PubMed ID: 29734148
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nephronophthisis-associated ciliopathies.
    Hildebrandt F; Zhou W
    J Am Soc Nephrol; 2007 Jun; 18(6):1855-71. PubMed ID: 17513324
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.
    Otto EA; Schermer B; Obara T; O'Toole JF; Hiller KS; Mueller AM; Ruf RG; Hoefele J; Beekmann F; Landau D; Foreman JW; Goodship JA; Strachan T; Kispert A; Wolf MT; Gagnadoux MF; Nivet H; Antignac C; Walz G; Drummond IA; Benzing T; Hildebrandt F
    Nat Genet; 2003 Aug; 34(4):413-20. PubMed ID: 12872123
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Recent advances in the molecular diagnosis of polycystic kidney disease.
    Bergmann C
    Expert Rev Mol Diagn; 2017 Dec; 17(12):1037-1054. PubMed ID: 28952822
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ciliopathies and the Kidney: A Review.
    McConnachie DJ; Stow JL; Mallett AJ
    Am J Kidney Dis; 2021 Mar; 77(3):410-419. PubMed ID: 33039432
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical Scenarios in Chronic Kidney Disease: Cystic Renal Diseases.
    Meola M; Samoni S; Petrucci I
    Contrib Nephrol; 2016; 188():120-30. PubMed ID: 27169740
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Pathology and genetic hereditary kidney cysts].
    Hermanns B; Alfer J; Fischedick K; Stojanovic-Dedic A; Rudnik-Schöneborn S; Büttner R; Zerres K
    Pathologe; 2003 Oct; 24(6):410-20. PubMed ID: 14605845
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rapidly Progressive Nephronophthisis in a 2-Year-Old Boy with a Homozygous SDCCAG8 Mutation.
    Watanabe Y; Fujinaga S; Sakuraya K; Morisada N; Nozu K; Iijima K
    Tohoku J Exp Med; 2019 Sep; 249(1):29-32. PubMed ID: 31534065
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Urine-Derived Epithelial Cells as a New Model to Study Renal Metabolic Phenotypes of Patients with Glycogen Storage Disease 1a.
    Lenzini L; Iori E; Scannapieco F; Carraro G; Avogaro A; Vitturi N
    Int J Mol Sci; 2022 Dec; 24(1):. PubMed ID: 36613675
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fibrocystin/polyductin modulates renal tubular formation by regulating polycystin-2 expression and function.
    Kim I; Fu Y; Hui K; Moeckel G; Mai W; Li C; Liang D; Zhao P; Ma J; Chen XZ; George AL; Coffey RJ; Feng ZP; Wu G
    J Am Soc Nephrol; 2008 Mar; 19(3):455-68. PubMed ID: 18235088
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expression of nuclear transcription factor PAX2 in renal biopsies of juvenile nephronophthisis.
    Murer L; Caridi G; Della Vella M; Montini G; Carasi C; Ghiggeri G; Zacchello G
    Nephron; 2002 Aug; 91(4):588-93. PubMed ID: 12138259
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PKHD1 gene silencing may cause cell abnormal proliferation through modulation of intracellular calcium in autosomal recessive polycystic kidney disease.
    Yang J; Zhang S; Zhou Q; Guo H; Zhang K; Zheng R; Xiao C
    J Biochem Mol Biol; 2007 Jul; 40(4):467-74. PubMed ID: 17669261
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Adult renal cystic disease: a genetic, biological, and developmental primer.
    Katabathina VS; Kota G; Dasyam AK; Shanbhogue AK; Prasad SR
    Radiographics; 2010 Oct; 30(6):1509-23. PubMed ID: 21071372
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and genetic characteristics of autosomal recessive polycystic kidney disease in Oman.
    Al Alawi I; Molinari E; Al Salmi I; Al Rahbi F; Al Mawali A; Sayer JA
    BMC Nephrol; 2020 Aug; 21(1):347. PubMed ID: 32799815
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hippo signaling-a central player in cystic kidney disease?
    Müller RU; Schermer B
    Pediatr Nephrol; 2020 Jul; 35(7):1143-1152. PubMed ID: 31297585
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.