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 *

321 related articles for article (PubMed ID: 24107611)

  • 1. Molecular background of urate transporter genes in patients with exercise-induced acute kidney injury.
    Kaito H; Ishimori S; Nozu K; Shima Y; Nakanishi K; Yoshikawa N; Iijima K
    Am J Nephrol; 2013; 38(4):316-20. PubMed ID: 24107611
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Diagnostic tests for primary renal hypouricemia.
    Sebesta I; Stiburkova B; Bartl J; Ichida K; Hosoyamada M; Taylor J; Marinaki A
    Nucleosides Nucleotides Nucleic Acids; 2011 Dec; 30(12):1112-6. PubMed ID: 22132965
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Non-urate transporter 1, non-glucose transporter member 9-related renal hypouricemia and acute renal failure accompanied by hyperbilirubinemia after anaerobic exercise: a case report.
    Furuto Y; Kawamura M; Namikawa A; Takahashi H; Shibuya Y; Mori T; Sohara E
    BMC Nephrol; 2019 Nov; 20(1):433. PubMed ID: 31771519
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Recurrent exercise-induced acute renal failure in a young Pakistani man with severe renal hypouricemia and SLC2A9 compound heterozygosity.
    Jeannin G; Chiarelli N; Gaggiotti M; Ritelli M; Maiorca P; Quinzani S; Verzeletti F; Possenti S; Colombi M; Cancarini G
    BMC Med Genet; 2014 Jan; 15():3. PubMed ID: 24397858
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Recurrent EIARF and PRES with severe renal hypouricemia by compound heterozygous SLC2A9 mutation.
    Shima Y; Nozu K; Nozu Y; Togawa H; Kaito H; Matsuo M; Iijima K; Nakanishi K; Yoshikawa N
    Pediatrics; 2011 Jun; 127(6):e1621-5. PubMed ID: 21536615
    [TBL] [Abstract][Full Text] [Related]  

  • 6. URAT1 and GLUT9 mutations in Spanish patients with renal hypouricemia.
    Claverie-Martin F; Trujillo-Suarez J; Gonzalez-Acosta H; Aparicio C; Justa Roldan ML; Stiburkova B; Ichida K; Martín-Gomez MA; Herrero Goñi M; Carrasco Hidalgo-Barquero M; Iñigo V; Enriquez R; Cordoba-Lanus E; Garcia-Nieto VM;
    Clin Chim Acta; 2018 Jun; 481():83-89. PubMed ID: 29486147
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel homozygous insertion in SLC2A9 gene caused renal hypouricemia.
    Stiburkova B; Ichida K; Sebesta I
    Mol Genet Metab; 2011 Apr; 102(4):430-5. PubMed ID: 21256783
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deciphering genetic signatures by whole exome sequencing in a case of co-prevalence of severe renal hypouricemia and diabetes with impaired insulin secretion.
    Sekiya M; Matsuda T; Yamamoto Y; Furuta Y; Ohyama M; Murayama Y; Sugano Y; Ohsaki Y; Iwasaki H; Yahagi N; Yatoh S; Suzuki H; Shimano H
    BMC Med Genet; 2020 May; 21(1):91. PubMed ID: 32375679
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A heterozygous variant in the SLC22A12 gene in a Sri Lanka family associated with mild renal hypouricemia.
    Vidanapathirana DM; Jayasena S; Jasinge E; Stiburkova B
    BMC Pediatr; 2018 Jun; 18(1):210. PubMed ID: 29958533
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2.
    Mancikova A; Krylov V; Hurba O; Sebesta I; Nakamura M; Ichida K; Stiburkova B
    Clin Exp Nephrol; 2016 Aug; 20(4):578-584. PubMed ID: 26500098
    [TBL] [Abstract][Full Text] [Related]  

  • 11. URAT1 mutations cause renal hypouricemia type 1 in Iraqi Jews.
    Dinour D; Bahn A; Ganon L; Ron R; Geifman-Holtzman O; Knecht A; Gafter U; Rachamimov R; Sela BA; Burckhardt G; Holtzman EJ
    Nephrol Dial Transplant; 2011 Jul; 26(7):2175-81. PubMed ID: 21148271
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Renal hypouricemia caused by novel compound heterozygous mutations in the SLC22A12 gene: a case report with literature review.
    Zhou Z; Ma L; Zhou J; Song Z; Zhang J; Wang K; Chen B; Pan D; Li Z; Li C; Shi Y
    BMC Med Genet; 2018 Aug; 19(1):142. PubMed ID: 30097038
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of acute renal failure after exercise with renal hypouricemia demonstrated compound heterozygous mutations of uric acid transporter 1.
    Ochi A; Takei T; Ichikawa A; Kojima C; Moriyama T; Itabashi M; Mochizuki T; Taniguchi A; Nitta K
    Clin Exp Nephrol; 2012 Apr; 16(2):316-9. PubMed ID: 22045201
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A Novel Homozygous SLC2A9 Mutation Associated with Renal-Induced Hypouricemia.
    Windpessl M; Ritelli M; Wallner M; Colombi M
    Am J Nephrol; 2016; 43(4):245-50. PubMed ID: 27116386
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Depletion of Uric Acid Due to SLC22A12 (URAT1) Loss-of-Function Mutation Causes Endothelial Dysfunction in Hypouricemia.
    Sugihara S; Hisatome I; Kuwabara M; Niwa K; Maharani N; Kato M; Ogino K; Hamada T; Ninomiya H; Higashi Y; Ichida K; Yamamoto K
    Circ J; 2015; 79(5):1125-32. PubMed ID: 25739858
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary Renal Hypouricemia Type 1 and Autosomal Dominant Polycystic Kidney Disease.
    Stiburkova B; Stekrova J; Nakamura M; Ichida K
    Am J Med Sci; 2015 Oct; 350(4):268-71. PubMed ID: 26418379
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Amplicon targeted resequencing for SLC2A9 and SLC22A12 identified novel mutations in hypouricemia subjects.
    Zhou Z; Wang K; Zhou J; Wang C; Li X; Cui L; Han L; Liu Z; Ren W; Wang X; Zhang K; Li Z; Pan D; Li C; Shi Y
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00722. PubMed ID: 31131560
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel allelic variants and evidence for a prevalent mutation in URAT1 causing renal hypouricemia: biochemical, genetics and functional analysis.
    Stiburkova B; Sebesta I; Ichida K; Nakamura M; Hulkova H; Krylov V; Kryspinova L; Jahnova H
    Eur J Hum Genet; 2013 Oct; 21(10):1067-73. PubMed ID: 23386035
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel homozygous GLUT9 mutation cause recurrent exercise-induced acute renal failure and posterior reversible encephalopathy syndrome.
    Mou LJ; Jiang LP; Hu Y
    J Nephrol; 2015 Jun; 28(3):387-92. PubMed ID: 24643436
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High frequency of SLC22A12 variants causing renal hypouricemia 1 in the Czech and Slovak Roma population; simple and rapid detection method by allele-specific polymerase chain reaction.
    Gabrikova D; Bernasovska J; Sokolova J; Stiburkova B
    Urolithiasis; 2015 Oct; 43(5):441-5. PubMed ID: 26033041
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.