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 *

144 related articles for article (PubMed ID: 12555937)

  • 1. Hartnup disorder: polymorphisms identified in the neutral amino acid transporter SLC1A5.
    Potter SJ; Lu A; Wilcken B; Green K; Rasko JE
    J Inherit Metab Dis; 2002 Oct; 25(6):437-48. PubMed ID: 12555937
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association study of polymorphisms in the neutral amino acid transporter genes SLC1A4, SLC1A5 and the glycine transporter genes SLC6A5, SLC6A9 with schizophrenia.
    Deng X; Sagata N; Takeuchi N; Tanaka M; Ninomiya H; Iwata N; Ozaki N; Shibata H; Fukumaki Y
    BMC Psychiatry; 2008 Jul; 8():58. PubMed ID: 18638388
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Search for mutations in SLC1A5 (19q13) in cystinuria patients.
    Brauers E; Vester U; Zerres K; Eggermann T
    J Inherit Metab Dis; 2005; 28(6):1169-71. PubMed ID: 16435221
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19.
    Seow HF; Bröer S; Bröer A; Bailey CG; Potter SJ; Cavanaugh JA; Rasko JE
    Nat Genet; 2004 Sep; 36(9):1003-7. PubMed ID: 15286788
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neutral amino acid transport in epithelial cells and its malfunction in Hartnup disorder.
    Bröer S; Cavanaugh JA; Rasko JE
    Biochem Soc Trans; 2005 Feb; 33(Pt 1):233-6. PubMed ID: 15667315
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular cloning of mouse amino acid transport system B0, a neutral amino acid transporter related to Hartnup disorder.
    Bröer A; Klingel K; Kowalczuk S; Rasko JE; Cavanaugh J; Bröer S
    J Biol Chem; 2004 Jun; 279(23):24467-76. PubMed ID: 15044460
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.
    Kleta R; Romeo E; Ristic Z; Ohura T; Stuart C; Arcos-Burgos M; Dave MH; Wagner CA; Camargo SR; Inoue S; Matsuura N; Helip-Wooley A; Bockenhauer D; Warth R; Bernardini I; Visser G; Eggermann T; Lee P; Chairoungdua A; Jutabha P; Babu E; Nilwarangkoon S; Anzai N; Kanai Y; Verrey F; Gahl WA; Koizumi A
    Nat Genet; 2004 Sep; 36(9):999-1002. PubMed ID: 15286787
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel mutation in SLC6A19 causing late-onset seizures in Hartnup disorder.
    Cheon CK; Lee BH; Ko JM; Kim HJ; Yoo HW
    Pediatr Neurol; 2010 May; 42(5):369-71. PubMed ID: 20399395
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Further evidence for allelic heterogeneity in Hartnup disorder.
    Azmanov DN; Kowalczuk S; Rodgers H; Auray-Blais C; Giguère R; Rasko JE; Bröer S; Cavanaugh JA
    Hum Mutat; 2008 Oct; 29(10):1217-21. PubMed ID: 18484095
    [TBL] [Abstract][Full Text] [Related]  

  • 10. ATB(0)/SLC1A5 gene. Fine localisation and exclusion of association with the intestinal phenotype of cystic fibrosis.
    Larriba S; Sumoy L; Ramos MD; Giménez J; Estivill X; Casals T; Nunes V
    Eur J Hum Genet; 2001 Nov; 9(11):860-6. PubMed ID: 11781704
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hartnup disorder: unraveling the mystery.
    Kraut JA; Sachs G
    Trends Pharmacol Sci; 2005 Feb; 26(2):53-5. PubMed ID: 15681018
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Occurrences of methylmalonic aciduria and Hartnup disorder in the same family.
    Shih VE; Coulombe JT; Wadman SK; Duran M; Waelkens JJ
    Clin Genet; 1984 Sep; 26(3):216-20. PubMed ID: 6478642
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical Role of ASCT2 (SLC1A5) in KRAS-Mutated Colorectal Cancer.
    Toda K; Nishikawa G; Iwamoto M; Itatani Y; Takahashi R; Sakai Y; Kawada K
    Int J Mol Sci; 2017 Jul; 18(8):. PubMed ID: 28749408
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exclusion of linkage between schizophrenia and the gene encoding a neutral amino acid glutamate/aspartate transporter, SLC1A5.
    Chen AC; Kalsi G; Brynjolfsson J; Sigmundsson T; Curtis D; Butler R; Read T; Murphy P; Barnard EA; Petursson H; Gurling HM
    Am J Med Genet; 1997 Feb; 74(1):50-2. PubMed ID: 9034006
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Hartnup phenotype: Mendelian transport disorder, multifactorial disease.
    Scriver CR; Mahon B; Levy HL; Clow CL; Reade TM; Kronick J; Lemieux B; Laberge C
    Am J Hum Genet; 1987 May; 40(5):401-12. PubMed ID: 3578280
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Homozygosity mapping to chromosome 5p15 of a gene responsible for Hartnup disorder.
    Nozaki J; Dakeishi M; Ohura T; Inoue K; Manabe M; Wada Y; Koizumi A
    Biochem Biophys Res Commun; 2001 Jun; 284(2):255-60. PubMed ID: 11394870
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel missense mutation in the SLC6A19 gene in a Chinese family with Hartnup disorder.
    Zheng Y; Zhou C; Huang Y; Bu D; Zhu X; Jiang W
    Int J Dermatol; 2009 Apr; 48(4):388-92. PubMed ID: 19335424
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tissue-specific amino acid transporter partners ACE2 and collectrin differentially interact with hartnup mutations.
    Camargo SM; Singer D; Makrides V; Huggel K; Pos KM; Wagner CA; Kuba K; Danilczyk U; Skovby F; Kleta R; Penninger JM; Verrey F
    Gastroenterology; 2009 Mar; 136(3):872-82. PubMed ID: 19185582
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Maternal Hartnup disorder.
    Mahon BE; Levy HL
    Am J Med Genet; 1986 Jul; 24(3):513-8. PubMed ID: 3728570
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A candidate mouse model for Hartnup disorder deficient in neutral amino acid transport.
    Symula DJ; Shedlovsky A; Guillery EN; Dove WF
    Mamm Genome; 1997 Feb; 8(2):102-7. PubMed ID: 9060408
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.