175 related articles for article (PubMed ID: 18339708)
1. Molecular characterization of V59E NIS, a Na+/I- symporter mutant that causes congenital I- transport defect.
Reed-Tsur MD; De la Vieja A; Ginter CS; Carrasco N
Endocrinology; 2008 Jun; 149(6):3077-84. PubMed ID: 18339708
[TBL] [Abstract][Full Text] [Related]
2. The Q267E mutation in the sodium/iodide symporter (NIS) causes congenital iodide transport defect (ITD) by decreasing the NIS turnover number.
De La Vieja A; Ginter CS; Carrasco N
J Cell Sci; 2004 Feb; 117(Pt 5):677-87. PubMed ID: 14734652
[TBL] [Abstract][Full Text] [Related]
3. The iodide-transport-defect-causing mutation R124H: a δ-amino group at position 124 is critical for maturation and trafficking of the Na+/I- symporter.
Paroder V; Nicola JP; Ginter CS; Carrasco N
J Cell Sci; 2013 Aug; 126(Pt 15):3305-13. PubMed ID: 23690546
[TBL] [Abstract][Full Text] [Related]
4. Na(+)/I(-) symporter activity requires a small and uncharged amino acid residue at position 395.
Dohán O; Gavrielides MV; Ginter C; Amzel LM; Carrasco N
Mol Endocrinol; 2002 Aug; 16(8):1893-902. PubMed ID: 12145342
[TBL] [Abstract][Full Text] [Related]
5. Molecular analysis of a congenital iodide transport defect: G543E impairs maturation and trafficking of the Na+/I- symporter.
De la Vieja A; Ginter CS; Carrasco N
Mol Endocrinol; 2005 Nov; 19(11):2847-58. PubMed ID: 15976004
[TBL] [Abstract][Full Text] [Related]
6. Asn441 plays a key role in folding and function of the Na+/I- symporter (NIS).
Li W; Nicola JP; Amzel LM; Carrasco N
FASEB J; 2013 Aug; 27(8):3229-38. PubMed ID: 23650190
[TBL] [Abstract][Full Text] [Related]
7. The Iodide Transport Defect-Causing Y348D Mutation in the Na
Reyna-Neyra A; Jung L; Chakrabarti M; Suárez MX; Amzel LM; Carrasco N
Thyroid; 2021 Aug; 31(8):1272-1281. PubMed ID: 33779310
[No Abstract] [Full Text] [Related]
8. Mechanism of anion selectivity and stoichiometry of the Na+/I- symporter (NIS).
Paroder-Belenitsky M; Maestas MJ; Dohán O; Nicola JP; Reyna-Neyra A; Follenzi A; Dadachova E; Eskandari S; Amzel LM; Carrasco N
Proc Natl Acad Sci U S A; 2011 Nov; 108(44):17933-8. PubMed ID: 22011571
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Conserved charged amino acid residues in the extracellular region of sodium/iodide symporter are critical for iodide transport activity.
Li CC; Ho TY; Kao CH; Wu SL; Liang JA; Hsiang CY
J Biomed Sci; 2010 Nov; 17(1):89. PubMed ID: 21092238
[TBL] [Abstract][Full Text] [Related]
11. The PDZ protein SCRIB regulates sodium/iodide symporter (NIS) expression at the basolateral plasma membrane.
Martín M; Salleron L; Peyret V; Geysels RC; Darrouzet E; Lindenthal S; Bernal Barquero CE; Masini-Repiso AM; Pourcher T; Nicola JP
FASEB J; 2021 Aug; 35(8):e21681. PubMed ID: 34196428
[TBL] [Abstract][Full Text] [Related]
12. A Carboxy-Terminal Monoleucine-Based Motif Participates in the Basolateral Targeting of the Na+/I- Symporter.
Martín M; Modenutti CP; Peyret V; Geysels RC; Darrouzet E; Pourcher T; Masini-Repiso AM; Martí MA; Carrasco N; Nicola JP
Endocrinology; 2019 Jan; 160(1):156-168. PubMed ID: 30496374
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. The porcine sodium/iodide symporter gene exhibits an uncommon expression pattern related to the use of alternative splice sites not present in the human or murine species.
Selmi-Ruby S; Watrin C; Trouttet-Masson S; Bernier-Valentin F; Flachon V; Munari-Silem Y; Rousset B
Endocrinology; 2003 Mar; 144(3):1074-85. PubMed ID: 12586784
[TBL] [Abstract][Full Text] [Related]
15. A Novel SLC5A5 Variant Reveals the Crucial Role of Kinesin Light Chain 2 in Thyroid Hormonogenesis.
Martín M; Modenutti CP; Gil Rosas ML; Peyret V; Geysels RC; Bernal Barquero CE; Sobrero G; Muñoz L; Signorino M; Testa G; Miras MB; Masini-Repiso AM; Calcaterra NB; Coux G; Carrasco N; Martí MA; Nicola JP
J Clin Endocrinol Metab; 2021 Jun; 106(7):1867-1881. PubMed ID: 33912899
[TBL] [Abstract][Full Text] [Related]
16. Congenital hypothyroidism due to a new deletion in the sodium/iodide symporter protein.
Tonacchera M; Agretti P; de Marco G; Elisei R; Perri A; Ambrogini E; De Servi M; Ceccarelli C; Viacava P; Refetoff S; Panunzi C; Bitti ML; Vitti P; Chiovato L; Pinchera A
Clin Endocrinol (Oxf); 2003 Oct; 59(4):500-6. PubMed ID: 14510914
[TBL] [Abstract][Full Text] [Related]
17. Identification of a structural requirement for thyroid Na+/I- symporter (NIS) function from analysis of a mutation that causes human congenital hypothyroidism.
Levy O; Ginter CS; De la Vieja A; Levy D; Carrasco N
FEBS Lett; 1998 Jun; 429(1):36-40. PubMed ID: 9657379
[TBL] [Abstract][Full Text] [Related]
18. N-linked glycosylation of the thyroid Na+/I- symporter (NIS). Implications for its secondary structure model.
Levy O; De la Vieja A; Ginter CS; Riedel C; Dai G; Carrasco N
J Biol Chem; 1998 Aug; 273(35):22657-63. PubMed ID: 9712895
[TBL] [Abstract][Full Text] [Related]
19. A novel V59E missense mutation in the sodium iodide symporter gene in a family with iodide transport defect.
Fujiwara H; Tatsumi K; Tanaka S; Kimura M; Nose O; Amino N
Thyroid; 2000 Jun; 10(6):471-4. PubMed ID: 10907989
[TBL] [Abstract][Full Text] [Related]
20. Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3' splice site.
Pohlenz J; Rosenthal IM; Weiss RE; Jhiang SM; Burant C; Refetoff S
J Clin Invest; 1998 Mar; 101(5):1028-35. PubMed ID: 9486973
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]