BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

412 related articles for article (PubMed ID: 29277510)

  • 1. HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.
    Adeyemo A; Esezobor C; Solarin A; Abeyagunawardena A; Kari JA; El Desoky S; Greenbaum LA; Kamel M; Kallash M; Silva C; Young A; Hunley TE; de Jesus-Gonzalez N; Srivastava T; Gbadegesin R
    Am J Kidney Dis; 2018 Mar; 71(3):399-406. PubMed ID: 29277510
    [TBL] [Abstract][Full Text] [Related]  

  • 2. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome.
    Gbadegesin RA; Adeyemo A; Webb NJ; Greenbaum LA; Abeyagunawardena A; Thalgahagoda S; Kale A; Gipson D; Srivastava T; Lin JJ; Chand D; Hunley TE; Brophy PD; Bagga A; Sinha A; Rheault MN; Ghali J; Nicholls K; Abraham E; Janjua HS; Omoloja A; Barletta GM; Cai Y; Milford DD; O'Brien C; Awan A; Belostotsky V; Smoyer WE; Homstad A; Hall G; Wu G; Nagaraj S; Wigfall D; Foreman J; Winn MP;
    J Am Soc Nephrol; 2015 Jul; 26(7):1701-10. PubMed ID: 25349203
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of HLA-DR/DQ alleles and haplotypes with nephrotic syndrome.
    Ramanathan AS; Senguttuvan P; Chinniah R; Vijayan M; Thirunavukkarasu M; Raju K; Mani D; Ravi PM; Rajendran P; Krishnan JI; Karuppiah B
    Nephrology (Carlton); 2016 Sep; 21(9):745-52. PubMed ID: 26566811
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic Basis of Health Disparity in Childhood Nephrotic Syndrome.
    Varner JD; Matory A; Gbadegesin RA
    Am J Kidney Dis; 2018 Nov; 72(5 Suppl 1):S22-S25. PubMed ID: 30343718
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
    Debiec H; Dossier C; Letouzé E; Gillies CE; Vivarelli M; Putler RK; Ars E; Jacqz-Aigrain E; Elie V; Colucci M; Debette S; Amouyel P; Elalaoui SC; Sefiani A; Dubois V; Simon T; Kretzler M; Ballarin J; Emma F; Sampson MG; Deschênes G; Ronco P
    J Am Soc Nephrol; 2018 Jul; 29(7):2000-2013. PubMed ID: 29903748
    [No Abstract]   [Full Text] [Related]  

  • 6. Genetics of childhood steroid-sensitive nephrotic syndrome.
    Karp AM; Gbadegesin RA
    Pediatr Nephrol; 2017 Sep; 32(9):1481-1488. PubMed ID: 27470160
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The podocin V260E mutation predicts steroid resistant nephrotic syndrome in black South African children with focal segmental glomerulosclerosis.
    Govender MA; Fabian J; Gottlich E; Levy C; Moonsamy G; Maher H; Winkler CA; Ramsay M
    Commun Biol; 2019; 2():416. PubMed ID: 31754646
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Strong Association of the
    Jia X; Horinouchi T; Hitomi Y; Shono A; Khor SS; Omae Y; Kojima K; Kawai Y; Nagasaki M; Kaku Y; Okamoto T; Ohwada Y; Ohta K; Okuda Y; Fujimaru R; Hatae K; Kumagai N; Sawanobori E; Nakazato H; Ohtsuka Y; Nakanishi K; Shima Y; Tanaka R; Ashida A; Kamei K; Ishikura K; Nozu K; Tokunaga K; Iijima K;
    J Am Soc Nephrol; 2018 Aug; 29(8):2189-2199. PubMed ID: 30012571
    [No Abstract]   [Full Text] [Related]  

  • 9. Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome.
    Dorval G; Gribouval O; Martinez-Barquero V; Machuca E; Tête MJ; Baudouin V; Benoit S; Chabchoub I; Champion G; Chauveau D; Chehade H; Chouchane C; Cloarec S; Cochat P; Dahan K; Dantal J; Delmas Y; Deschênes G; Dolhem P; Durand D; Ekinci Z; El Karoui K; Fischbach M; Grunfeld JP; Guigonis V; Hachicha M; Hogan J; Hourmant M; Hummel A; Kamar N; Krummel T; Lacombe D; Llanas B; Mesnard L; Mohsin N; Niaudet P; Nivet H; Parvex P; Pietrement C; de Pontual L; Noble CP; Ribes D; Ronco P; Rondeau E; Sallee M; Tsimaratos M; Ulinski T; Salomon R; Antignac C; Boyer O
    Pediatr Nephrol; 2018 Mar; 33(3):473-483. PubMed ID: 29058154
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome.
    Dufek S; Cheshire C; Levine AP; Trompeter RS; Issler N; Stubbs M; Mozere M; Gupta S; Klootwijk E; Patel V; Hothi D; Waters A; Webb H; Tullus K; Jenkins L; Godinho L; Levtchenko E; Wetzels J; Knoers N; Teeninga N; Nauta J; Shalaby M; Eldesoky S; Kari JA; Thalgahagoda S; Ranawaka R; Abeyagunawardena A; Adeyemo A; Kristiansen M; Gbadegesin R; Webb NJ; Gale DP; Stanescu HC; Kleta R; Bockenhauer D
    J Am Soc Nephrol; 2019 Aug; 30(8):1375-1384. PubMed ID: 31263063
    [TBL] [Abstract][Full Text] [Related]  

  • 11. APOL1 risk genotype in European steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis patients of different African ancestries.
    Gribouval O; Boyer O; Knebelmann B; Karras A; Dantal J; Fourrage C; Alibeu O; Hogan J; Dossier C; Tête MJ; Antignac C; Servais A
    Nephrol Dial Transplant; 2019 Nov; 34(11):1885-1893. PubMed ID: 29992269
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association of DQB1*0302 alloantigens in Japanese pediatric patients with steroid-sensitive nephrotic syndrome.
    Abe KK; Michinaga I; Hiratsuka T; Ogahara S; Naito S; Arakawa K; Tsuru N; Tokieda K
    Nephron; 1995; 70(1):28-34. PubMed ID: 7617114
    [TBL] [Abstract][Full Text] [Related]  

  • 13. APOL1-associated glomerular disease among African-American children: a collaboration of the Chronic Kidney Disease in Children (CKiD) and Nephrotic Syndrome Study Network (NEPTUNE) cohorts.
    Ng DK; Robertson CC; Woroniecki RP; Limou S; Gillies CE; Reidy KJ; Winkler CA; Hingorani S; Gibson KL; Hjorten R; Sethna CB; Kopp JB; Moxey-Mims M; Furth SL; Warady BA; Kretzler M; Sedor JR; Kaskel FJ; Sampson MG
    Nephrol Dial Transplant; 2017 Jun; 32(6):983-990. PubMed ID: 27190333
    [TBL] [Abstract][Full Text] [Related]  

  • 14. HLA-DQA1 and -DQB1 alleles in Latino and African American children with diabetes mellitus.
    McCarthy BJ; Lipton R; Nichol L
    J Pediatr Endocrinol Metab; 2004 Mar; 17(3):297-306. PubMed ID: 15112906
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Shared genetic risk across different presentations of gene test-negative idiopathic nephrotic syndrome.
    Downie ML; Gupta S; Chan MMY; Sadeghi-Alavijeh O; Cao J; Parekh RS; Diz CB; Bierzynska A; Levine AP; Pepper RJ; Stanescu H; Saleem MA; Kleta R; Bockenhauer D; Koziell AB; Gale DP
    Pediatr Nephrol; 2023 Jun; 38(6):1793-1800. PubMed ID: 36357634
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetics of Childhood Steroid Sensitive Nephrotic Syndrome: An Update.
    Lane BM; Cason R; Esezobor CI; Gbadegesin RA
    Front Pediatr; 2019; 7():8. PubMed ID: 30761277
    [TBL] [Abstract][Full Text] [Related]  

  • 17. ACE I/D gene polymorphism can't predict the steroid responsiveness in Asian children with idiopathic nephrotic syndrome: a meta-analysis.
    Zhou TB; Qin YH; Su LN; Lei FY; Huang WF; Zhao YJ
    PLoS One; 2011; 6(5):e19599. PubMed ID: 21611163
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association of HLA-DQA1 gene polymorphisms with the risk of children primary nephrotic syndrome in Chinese population.
    Zhu B; Zhang R; Yang H; Yuan T; Lv J; Peng Q; Tian L
    J Clin Lab Anal; 2019 Jan; 33(1):e22623. PubMed ID: 30006974
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Polymorphic variants of MIF gene and prognosis in steroid therapy in children with idiopathic nephrotic syndrome.
    Świerczewska M; Ostalska-Nowicka D; Kempisty B; Szczepankiewicz A; Nowicki M
    Acta Biochim Pol; 2014; 61(1):67-75. PubMed ID: 24644543
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An investigation of APOL1 risk genotypes and preterm birth in African American population cohorts.
    Robertson CC; Gillies CE; Putler RKB; Ng D; Reidy KJ; Crawford B; Sampson MG
    Nephrol Dial Transplant; 2017 Dec; 32(12):2051-2058. PubMed ID: 27638911
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.