BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

79 related articles for article (PubMed ID: 9288112)

  • 21. [Neonatal hypothyroidism].
    Arisaka O; Kanazawa S; Hoshi M; Kuribayashi T
    Ryoikibetsu Shokogun Shirizu; 2000; (31):514-7. PubMed ID: 11269150
    [No Abstract]   [Full Text] [Related]  

  • 22. Promoter characterization of the rat Na+/I- symporter gene.
    Tong Q; Ryu KY; Jhiang SM
    Biochem Biophys Res Commun; 1997 Oct; 239(1):34-41. PubMed ID: 9345265
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Apical Na+-Cl- symport in rabbit gallbladder epithelium: a thiazide-sensitive cotransporter (TSC).
    Cremaschi D; Porta C; Bottà G; Bazzini C; Baroni MD; Garavaglia M
    J Membr Biol; 2000 Jul; 176(1):53-65. PubMed ID: 10882428
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Evolutionary relationship between K(+) channels and symporters.
    Durell SR; Hao Y; Nakamura T; Bakker EP; Guy HR
    Biophys J; 1999 Aug; 77(2):775-88. PubMed ID: 10423425
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Expression cloning of NaDC-2, an intestinal Na(+)- or Li(+)-dependent dicarboxylate transporter.
    Bai L; Pajor AM
    Am J Physiol; 1997 Aug; 273(2 Pt 1):G267-74. PubMed ID: 9277403
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Establishment and characterization of a Chinese hamster ovary cell line, CHO-4J, stably expressing a number of Na+/I- symporters.
    Kosugi S; Sasaki N; Hai N; Sugawa H; Aoki N; Shigemasa C; Mori T; Yoshida A
    Biochem Biophys Res Commun; 1996 Oct; 227(1):94-101. PubMed ID: 8858109
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Absence of sodium/iodide symporter gene mutations in differentiated human thyroid carcinomas.
    Russo D; Manole D; Arturi F; Suarez HG; Schlumberger M; Filetti S; Derwahl M
    Thyroid; 2001 Jan; 11(1):37-9. PubMed ID: 11272095
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35.
    Kos CH; Tihy F; Econs MJ; Murer H; Lemieux N; Tenenhouse HS
    Genomics; 1994 Jan; 19(1):176-7. PubMed ID: 8188224
    [No Abstract]   [Full Text] [Related]  

  • 29. A novel peculiar mutation in the sodium/iodide symporter gene in spanish siblings with iodide transport defect.
    Kosugi S; Okamoto H; Tamada A; Sanchez-Franco F
    J Clin Endocrinol Metab; 2002 Aug; 87(8):3830-6. PubMed ID: 12161518
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Primary bile acid malabsorption caused by mutations in the ileal sodium-dependent bile acid transporter gene (SLC10A2).
    Oelkers P; Kirby LC; Heubi JE; Dawson PA
    J Clin Invest; 1997 Apr; 99(8):1880-7. PubMed ID: 9109432
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Implications of the molecular characterization of the sodium-iodide symporter (NIS).
    Schmutzler C; Köhrle J
    Exp Clin Endocrinol Diabetes; 1998; 106 Suppl 3():S1-10. PubMed ID: 9865544
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Congenital central isolated hypothyroidism caused by a homozygous mutation in the TSH-beta subunit gene.
    Heinrichs C; Parma J; Scherberg NH; Delange F; Van Vliet G; Duprez L; Bourdoux P; Bergmann P; Vassart G; Refetoff S
    Thyroid; 2000 May; 10(5):387-91. PubMed ID: 10884185
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Iodide transport defect: functional characterization of a novel mutation in the Na+/I- symporter 5'-untranslated region in a patient with congenital hypothyroidism.
    Nicola JP; Nazar M; Serrano-Nascimento C; Goulart-Silva F; Sobrero G; Testa G; Nunes MT; Muñoz L; Miras M; Masini-Repiso AM
    J Clin Endocrinol Metab; 2011 Jul; 96(7):E1100-7. PubMed ID: 21565787
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular cloning and functional expression of a sodium-dicarboxylate cotransporter from human kidney.
    Pajor AM
    Am J Physiol; 1996 Apr; 270(4 Pt 2):F642-8. PubMed ID: 8967342
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Extending the clinical heterogeneity of iodide transport defect (ITD): a novel mutation R124H of the sodium/iodide symporter gene and review of genotype-phenotype correlations in ITD.
    Szinnai G; Kosugi S; Derrien C; Lucidarme N; David V; Czernichow P; Polak M
    J Clin Endocrinol Metab; 2006 Apr; 91(4):1199-204. PubMed ID: 16418213
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Detection of binding and blocking autoantibodies to the human sodium-iodide symporter in patients with autoimmune thyroid disease.
    Ajjan RA; Kemp EH; Waterman EA; Watson PF; Endo T; Onaya T; Weetman AP
    J Clin Endocrinol Metab; 2000 May; 85(5):2020-7. PubMed ID: 10843191
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Assignment of SLC17A6 (alias DNPI), the gene encoding brain/pancreatic islet-type Na+-dependent inorganic phosphate cotransporter to human chromosome 11p14.3.
    Aihara Y; Onda H; Teraoka M; Yokoyama Y; Seino Y; Kasuya H; Hori T; Tomura H; Inoue I; Kojima I; Takeda J
    Cytogenet Cell Genet; 2001; 92(1-2):167-9. PubMed ID: 11306821
    [No Abstract]   [Full Text] [Related]  

  • 38. Congenital isolated central hypothyroidism caused by a "hot spot" mutation in the thyrotropin-beta gene.
    McDermott MT; Haugen BR; Black JN; Wood WM; Gordon DF; Ridgway EC
    Thyroid; 2002 Dec; 12(12):1141-6. PubMed ID: 12593729
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Evolutionary and experimental analyses of inorganic phosphate transporter PiT family reveals two related signature sequences harboring highly conserved aspartic acids critical for sodium-dependent phosphate transport function of human PiT2.
    Bøttger P; Pedersen L
    FEBS J; 2005 Jun; 272(12):3060-74. PubMed ID: 15955065
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Early cellular abnormalities induced by RET/PTC1 oncogene in thyroid-targeted transgenic mice.
    Cho JY; Sagartz JE; Capen CC; Mazzaferri EL; Jhiang SM
    Oncogene; 1999 Jun; 18(24):3659-65. PubMed ID: 10380889
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.