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 *

78 related articles for article (PubMed ID: 1491459)

  • 1. [Recent progress in molecular biology of inherited tubular transport abnormalities].
    Indo Y; Matsuda I
    Nihon Rinsho; 1992 Dec; 50(12):3086-92. PubMed ID: 1491459
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase.
    Attree O; Olivos IM; Okabe I; Bailey LC; Nelson DL; Lewis RA; McInnes RR; Nussbaum RL
    Nature; 1992 Jul; 358(6383):239-42. PubMed ID: 1321346
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the V2 vasopressin receptor gene are associated with X-linked nephrogenic diabetes insipidus.
    Pan Y; Metzenberg A; Das S; Jing B; Gitschier J
    Nat Genet; 1992 Oct; 2(2):103-6. PubMed ID: 1303257
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cloning and characterization of a vasopressin V2 receptor and possible link to nephrogenic diabetes insipidus.
    Lolait SJ; O'Carroll AM; McBride OW; Konig M; Morel A; Brownstein MJ
    Nature; 1992 May; 357(6376):336-9. PubMed ID: 1534150
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two novel mutations in the vasopressin V2 receptor gene in unrelated Japanese kindreds with nephrogenic diabetes insipidus.
    Tsukaguchi H; Matsubara H; Aritaki S; Kimura T; Abe S; Inada M
    Biochem Biophys Res Commun; 1993 Dec; 197(2):1000-10. PubMed ID: 8267567
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cloning and chromosomal localization of a human kidney cDNA involved in cystine, dibasic, and neutral amino acid transport.
    Lee WS; Wells RG; Sabbag RV; Mohandas TK; Hediger MA
    J Clin Invest; 1993 May; 91(5):1959-63. PubMed ID: 8486766
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndrome.
    Hodgson SV; Heckmatt JZ; Hughes E; Crolla JA; Dubowitz V; Bobrow M
    Am J Med Genet; 1986 Mar; 23(3):837-47. PubMed ID: 3953680
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus.
    van den Ouweland AM; Dreesen JC; Verdijk M; Knoers NV; Monnens LA; Rocchi M; van Oost BA
    Nat Genet; 1992 Oct; 2(2):99-102. PubMed ID: 1303271
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Recent advances in the biochemical and molecular biological basis of cystinuria.
    Gitomer WL; Pak CY
    J Urol; 1996 Dec; 156(6):1907-12. PubMed ID: 8911353
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Recent advances in vasopressin receptors and signal transduction system].
    Terada Y; Marumo F
    Nihon Rinsho; 1993 Oct; 51(10):2655-60. PubMed ID: 8254935
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Brief report: a mutation in the vasopressin V2-receptor gene in a kindred with X-linked nephrogenic diabetes insipidus.
    Merendino JJ; Speigel AM; Crawford JD; O'Carroll AM; Brownstein MJ; Lolait SJ
    N Engl J Med; 1993 May; 328(21):1538-41. PubMed ID: 8479491
    [No Abstract]   [Full Text] [Related]  

  • 12. Biology and genetics of inherited renal tubular disorders.
    van't Hoff WG
    Exp Nephrol; 1996; 4(5):253-62. PubMed ID: 8931979
    [No Abstract]   [Full Text] [Related]  

  • 13. The amino acid transport system b(o,+) and cystinuria.
    Palacin M; Fernández E; Chillarón J; Zorzano A
    Mol Membr Biol; 2001; 18(1):21-6. PubMed ID: 11396607
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human neutral amino acid transporter ASCT1: structure of the gene (SLC1A4) and localization to chromosome 2p13-p15.
    Hofmann K; Düker M; Fink T; Lichter P; Stoffel W
    Genomics; 1994 Nov; 24(1):20-6. PubMed ID: 7896285
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Renal transport of amino acids in children with oculocerebrorenal syndrome.
    Manz F; Bremer HJ; Brodehl J
    Helv Paediatr Acta; 1978 Apr; 33(1):37-44. PubMed ID: 669970
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Slc7a9-deficient mice develop cystinuria non-I and cystine urolithiasis.
    Feliubadaló L; Arbonés ML; Mañas S; Chillarón J; Visa J; Rodés M; Rousaud F; Zorzano A; Palacín M; Nunes V
    Hum Mol Genet; 2003 Sep; 12(17):2097-108. PubMed ID: 12915471
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A mouse model for cystinuria type I.
    Peters T; Thaete C; Wolf S; Popp A; Sedlmeier R; Grosse J; Nehls MC; Russ A; Schlueter V
    Hum Mol Genet; 2003 Sep; 12(17):2109-20. PubMed ID: 12923163
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel human amino acid transporter, hNAT3: cDNA cloning, chromosomal mapping, genomic structure, expression, and functional characterization.
    Gu S; Adan-Rice D; Leach RJ; Jiang JX
    Genomics; 2001 Jun; 74(3):262-72. PubMed ID: 11414754
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Human cystinuria-related transporter: localization and functional characterization.
    Mizoguchi K; Cha SH; Chairoungdua A; Kim DK; Shigeta Y; Matsuo H; Fukushima J; Awa Y; Akakura K; Goya T; Ito H; Endou H; Kanai Y
    Kidney Int; 2001 May; 59(5):1821-33. PubMed ID: 11318953
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment.
    Reilly DS; Lewis RA; Ledbetter DH; Nussbaum RL
    Am J Hum Genet; 1988 May; 42(5):748-55. PubMed ID: 2895982
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.