BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 34486308)

  • 1. Molecular Screening of
    I El-Hallous E; Alharthi AA; Gaber A; M Hassan M
    Pak J Biol Sci; 2021 Jan; 24(4):492-499. PubMed ID: 34486308
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PAX2 polymorphisms and congenital abnormalities of the kidney and urinary tract in a Brazilian pediatric population: evidence for a role in vesicoureteral reflux.
    de Miranda DM; Dos Santos Júnior AC; Dos Reis GS; Freitas IS; Carvalho TG; de Marco LA; Oliveira EA; Simões E Silva AC
    Mol Diagn Ther; 2014 Aug; 18(4):451-7. PubMed ID: 24633556
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Vesicoureteral reflux and other urinary tract malformations in mice compound heterozygous for Pax2 and Emx2.
    Boualia SK; Gaitan Y; Murawski I; Nadon R; Gupta IR; Bouchard M
    PLoS One; 2011; 6(6):e21529. PubMed ID: 21731775
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease Database.
    Liu JL; Shen Q; Wu MY; Zhu GH; Li YF; Wang XW; Tang XS; Bi YL; Gong YN; Chen J; Fang XY; Zhai YH; Wu BB; Li GM; Sun YB; Gao XJ; Liu CH; Jiang XY; Hao S; Kang YL; Gong YL; Rong LP; Li D; Wang S; Ma D; Rao J; Xu H;
    World J Pediatr; 2021 Aug; 17(4):409-418. PubMed ID: 34059960
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The significance of Pax2 expression in the ureter epithelium of children with vesicoureteric reflux.
    Zheng Y; Xu J; Guo W; Xu H; Chen J; Shen Q; Zhang X; Zhai Y
    Hum Pathol; 2015 Jul; 46(7):963-70. PubMed ID: 25912758
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Absence of PAX2 gene mutations in patients with primary familial vesicoureteric reflux.
    Choi KL; McNoe LA; French MC; Guilford PJ; Eccles MR
    J Med Genet; 1998 Apr; 35(4):338-9. PubMed ID: 9598733
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in PAX2 associate with adult-onset FSGS.
    Barua M; Stellacci E; Stella L; Weins A; Genovese G; Muto V; Caputo V; Toka HR; Charoonratana VT; Tartaglia M; Pollak MR
    J Am Soc Nephrol; 2014 Sep; 25(9):1942-53. PubMed ID: 24676634
    [TBL] [Abstract][Full Text] [Related]  

  • 8. PAX2 and CAKUT Phenotypes: Report on Two New Variants and a Review of Mutations from the Leiden Open Variation Database.
    Negrisolo S; Benetti E
    Int J Mol Sci; 2023 Feb; 24(4):. PubMed ID: 36835576
    [No Abstract]   [Full Text] [Related]  

  • 9. ROBO2 gene variants in children with primary nonsyndromic vesicoureteral reflux with or without renal hypoplasia/dysplasia.
    Mitsioni AG; Siomou E; Bouba I; Petridi S; Siamopoulou A; Georgiou I
    Pediatr Res; 2016 Jul; 80(1):72-6. PubMed ID: 27002985
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Vesico-ureteric reflux and urinary tract development in the Pax2 1Neu+/- mouse.
    Murawski IJ; Myburgh DB; Favor J; Gupta IR
    Am J Physiol Renal Physiol; 2007 Nov; 293(5):F1736-45. PubMed ID: 17881463
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association of PAX2 and Other Gene Mutations with the Clinical Manifestations of Renal Coloboma Syndrome.
    Okumura T; Furuichi K; Higashide T; Sakurai M; Hashimoto S; Shinozaki Y; Hara A; Iwata Y; Sakai N; Sugiyama K; Kaneko S; Wada T
    PLoS One; 2015; 10(11):e0142843. PubMed ID: 26571382
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel truncating PAX2 mutation in a boy with renal coloboma syndrome with focal segmental glomerulosclerosis causing rapid progression to end-stage kidney disease.
    Saida K; Kamei K; Morisada N; Ogura M; Ogata K; Matsuoka K; Nozu K; Iijima K; Ito S
    CEN Case Rep; 2020 Feb; 9(1):19-23. PubMed ID: 31538321
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomalies.
    Cunliffe HE; McNoe LA; Ward TA; Devriendt K; Brunner HG; Eccles MR
    J Med Genet; 1998 Oct; 35(10):806-12. PubMed ID: 9783702
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Molecular basis of vesicoureteral reflux].
    Lama G; Esposito Salsano M
    Minerva Pediatr; 2002 Oct; 54(5):415-22. PubMed ID: 12244279
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.
    Madariaga L; Morinière V; Jeanpierre C; Bouvier R; Loget P; Martinovic J; Dechelotte P; Leporrier N; Thauvin-Robinet C; Jensen UB; Gaillard D; Mathieu M; Turlin B; Attie-Bitach T; Salomon R; Gübler MC; Antignac C; Heidet L
    Clin J Am Soc Nephrol; 2013 Jul; 8(7):1179-87. PubMed ID: 23539225
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux.
    Elahi S; Homstad A; Vaidya H; Stout J; Hall G; Wu G; Conlon P; Routh JC; Wiener JS; Ross SS; Nagaraj S; Wigfall D; Foreman J; Adeyemo A; Gupta IR; Brophy PD; Rabinovich CE; Gbadegesin RA
    Pediatr Nephrol; 2016 Feb; 31(2):247-53. PubMed ID: 26408188
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Significance of the tissue kallikrein promoter and transforming growth factor-beta1 polymorphisms with renal progression in children with vesicoureteral reflux.
    Lee-Chen GJ; Liu KP; Lai YC; Juang HS; Huang SY; Lin CY
    Kidney Int; 2004 Apr; 65(4):1467-72. PubMed ID: 15086490
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A Novel Missense Mutation (L44V) of
    Oh SH; Keum C; Her M; Chung WY; Kim YH; Kim T
    Ann Clin Lab Sci; 2020 Sep; 50(5):687-690. PubMed ID: 33067217
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lack of major involvement of human uroplakin genes in vesicoureteral reflux: implications for disease heterogeneity.
    Jiang S; Gitlin J; Deng FM; Liang FX; Lee A; Atala A; Bauer SB; Ehrlich GD; Feather SA; Goldberg JD; Goodship JA; Goodship TH; Hermanns M; Hu FZ; Jones KE; Malcolm S; Mendelsohn C; Preston RA; Retik AB; Schneck FX; Wright V; Ye XY; Woolf AS; Wu XR; Ostrer H; Shapiro E; Yu J; Sun TT
    Kidney Int; 2004 Jul; 66(1):10-9. PubMed ID: 15200408
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diverse phenotypes in children with PAX2-related disorder.
    Deng H; Zhang Y; Xiao H; Yao Y; Liu X; Su B; Zhang H; Xu K; Wang S; Wang F; Ding J
    Mol Genet Genomic Med; 2019 Jun; 7(6):e701. PubMed ID: 31060108
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.