-
1
-
-
0024562578
-
Characterization of site-directed mutants in the lac permease of Escherichia coli. 2. Glutamate-325 replacements
-
Carrasco N, Puttner IB, Antes LM, Lee JA, Larigan JD, Lolkema JS, Roepe PD, Kaback HR 1989 Characterization of site-directed mutants in the lac permease of Escherichia coli. 2. Glutamate-325 replacements. Biochemistry 28:2533-2539
-
(1989)
Biochemistry
, vol.28
, pp. 2533-2539
-
-
Carrasco, N.1
Puttner, I.B.2
Antes, L.M.3
Lee, J.A.4
Larigan, J.D.5
Lolkema, J.S.6
Roepe, P.D.7
Kaback, H.R.8
-
3
-
-
0033922682
-
Molecular analysis of the sodium/iodide symporter: Impact on thyroid and extrathyroid pathophysiology
-
De la Vieja A, Dohan O, Levy O, Carrasco N 2000 Molecular analysis of the sodium/iodide symporter: impact on thyroid and extrathyroid pathophysiology. Physiol Rev 80:1083-1105
-
(2000)
Physiol Rev
, vol.80
, pp. 1083-1105
-
-
De La Vieja, A.1
Dohan, O.2
Levy, O.3
Carrasco, N.4
-
4
-
-
0037326161
-
The sodium/iodide Symporter (NIS): Characterization, regulation, and medical significance
-
Dohan O, De la Vieja A, Paroder V, Riedel C, Artani M, Reed M, Ginter CS, Carrasco N 2003 The sodium/iodide Symporter (NIS): characterization, regulation, and medical significance. Endocr Rev 24:48-77
-
(2003)
Endocr Rev
, vol.24
, pp. 48-77
-
-
Dohan, O.1
De La Vieja, A.2
Paroder, V.3
Riedel, C.4
Artani, M.5
Reed, M.6
Ginter, C.S.7
Carrasco, N.8
-
5
-
-
0036425965
-
The sodium iodide symporter: Its pathophysiological and therapeutic implications
-
Oxf
-
Spitzweg C, Morris JC 2002 The sodium iodide symporter: its pathophysiological and therapeutic implications. Clin Endocrinol (Oxf) 57:559-574
-
(2002)
Clin Endocrinol
, vol.57
, pp. 559-574
-
-
Spitzweg, C.1
Morris, J.C.2
-
6
-
-
0033835541
-
The mammary gland iodide transporter is expressed during lactation and in breast cancer
-
Tazebay UH, Wapnir IL, Levy O, Dohan O, Zuckier LS, Zhao QH, Deng HF, Amenta PS, Fineberg S, Pestell RG, Carrasco N 2000 The mammary gland iodide transporter is expressed during lactation and in breast cancer. Nat Med 6:871-878
-
(2000)
Nat Med
, vol.6
, pp. 871-878
-
-
Tazebay, U.H.1
Wapnir, I.L.2
Levy, O.3
Dohan, O.4
Zuckier, L.S.5
Zhao, Q.H.6
Deng, H.F.7
Amenta, P.S.8
Fineberg, S.9
Pestell, R.G.10
Carrasco, N.11
-
7
-
-
0002083634
-
Carcinoma of follicular epithelium: Radioiodide and other treatments and outcomes
-
Braverman LE, Utiger RD, eds. Philadelphia: Lippincott-Raven
-
Mazzaferri EL 1996 Carcinoma of follicular epithelium: radioiodide and other treatments and outcomes. In: Braverman LE, Utiger RD, eds. The thyroid: a fundamental and clinical text. 7th ed. Philadelphia: Lippincott-Raven; 922-945
-
(1996)
The Thyroid: A Fundamental and Clinical Text. 7th Ed.
, pp. 922-945
-
-
Mazzaferri, E.L.1
-
8
-
-
0027943619
-
Long-term impact of initial surgical and medical therapy on papillary and follicular thyroid cancer
-
Mazzaferri EL, Jhiang SM 1994 Long-term impact of initial surgical and medical therapy on papillary and follicular thyroid cancer. Am J Med 97:418-428
-
(1994)
Am J Med
, vol.97
, pp. 418-428
-
-
Mazzaferri, E.L.1
Jhiang, S.M.2
-
9
-
-
0030053759
-
Cloning and characterization of the thyroid iodide transporter
-
Dai G, Levy O, Carrasco N 1996 Cloning and characterization of the thyroid iodide transporter. Nature 379:458-460
-
(1996)
Nature
, vol.379
, pp. 458-460
-
-
Dai, G.1
Levy, O.2
Carrasco, N.3
-
10
-
-
0030800654
-
Thyroid Na+/I- symporter. Mechanism, stoichiometry, and specificity
-
Eskandari S, Loo DD, Dai G, Levy O, Wright EM, Carrasco N 1997 Thyroid Na+/I- symporter. Mechanism, stoichiometry, and specificity. J Biol Chem 272:27230-27238
-
(1997)
J Biol Chem
, vol.272
, pp. 27230-27238
-
-
Eskandari, S.1
Loo, D.D.2
Dai, G.3
Levy, O.4
Wright, E.M.5
Carrasco, N.6
-
11
-
-
0027288003
-
Iodide transport in the thyroid gland
-
Carrasco N 1993 Iodide transport in the thyroid gland. Biochim Biophys Acta 1154:65-82
-
(1993)
Biochim Biophys Acta
, vol.1154
, pp. 65-82
-
-
Carrasco, N.1
-
12
-
-
0030582379
-
Cloning of the human sodium iodide symporter
-
Smanik PA, Liu Q, Furminger TL, Ryu K, Xing S, Mazzaferri EL, Jhiang SM 1996 Cloning of the human sodium iodide symporter. Biochem Biophys Res Commun 226:339-345
-
(1996)
Biochem Biophys Res Commun
, vol.226
, pp. 339-345
-
-
Smanik, P.A.1
Liu, Q.2
Furminger, T.L.3
Ryu, K.4
Xing, S.5
Mazzaferri, E.L.6
Jhiang, S.M.7
-
13
-
-
0030739949
-
Expression, exon-intron organization, and chromosome mapping of the human sodium iodide symporter
-
Smanik PA, Ryu KY, Theil KS, Mazzaferri EL, Jhiang SM 1997 Expression, exon-intron organization, and chromosome mapping of the human sodium iodide symporter. Endocrinology 138:3555-3558
-
(1997)
Endocrinology
, vol.138
, pp. 3555-3558
-
-
Smanik, P.A.1
Ryu, K.Y.2
Theil, K.S.3
Mazzaferri, E.L.4
Jhiang, S.M.5
-
14
-
-
0030978104
-
Characterization of the thyroid Na+/I- symporter with an anti-COOH terminus antibody
-
USA
-
Levy O, Dai G, Riedel C, Ginter CS, Paul EM, Lebowitz AN, Carrasco N 1997 Characterization of the thyroid Na+/I- symporter with an anti-COOH terminus antibody. Proc Natl Acad Sci USA 94:5568-5573
-
(1997)
Proc Natl Acad Sci
, vol.94
, pp. 5568-5573
-
-
Levy, O.1
Dai, G.2
Riedel, C.3
Ginter, C.S.4
Paul, E.M.5
Lebowitz, A.N.6
Carrasco, N.7
-
15
-
-
0032575638
-
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 1998 N-linked glycosylation of the thyroid Na+/I- symporter (NIS). Implications for its secondary structure model. J Biol Chem 273:22657-22663
-
(1998)
J Biol Chem
, vol.273
, pp. 22657-22663
-
-
Levy, O.1
De La Vieja, A.2
Ginter, C.S.3
Riedel, C.4
Dai, G.5
Carrasco, N.6
-
16
-
-
0020776042
-
Congenital goiter with defective iodide transport
-
Wolff J 1983 Congenital goiter with defective iodide transport. Endocr Rev 4:240-254
-
(1983)
Endocr Rev
, vol.4
, pp. 240-254
-
-
Wolff, J.1
-
17
-
-
0031156646
-
Congenital hypothyroidism caused by a mutation in the Na+/I- symporter
-
Fujiwara H, Tatsumi K, Miki K, Harada T, Miyai K, Takai S, Amino N 1997 Congenital hypothyroidism caused by a mutation in the Na+/I- symporter. Nat Genet 16:124-125
-
(1997)
Nat Genet
, vol.16
, pp. 124-125
-
-
Fujiwara, H.1
Tatsumi, K.2
Miki, K.3
Harada, T.4
Miyai, K.5
Takai, S.6
Amino, N.7
-
18
-
-
0031727120
-
Recurrent T354P mutation of the Na+/I- symporter in patients with iodide transport defect
-
Fujiwara H, Tatsumi K, Miki K, Harada T, Okada S, Nose O, Kodama S, Amino N 1998 Recurrent T354P mutation of the Na+/I- symporter in patients with iodide transport defect. J Clin Endocrinol Metab 83:2940-2943
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 2940-2943
-
-
Fujiwara, H.1
Tatsumi, K.2
Miki, K.3
Harada, T.4
Okada, S.5
Nose, O.6
Kodama, S.7
Amino, N.8
-
19
-
-
0033917722
-
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 2000 A novel V59E missense mutation in the sodium iodide symporter gene in a family with iodide transport defect. Thyroid 10:471-474
-
(2000)
Thyroid
, vol.10
, pp. 471-474
-
-
Fujiwara, H.1
Tatsumi, K.2
Tanaka, S.3
Kimura, M.4
Nose, O.5
Amino, N.6
-
20
-
-
0031797296
-
Novel, missense and loss-of-function mutations in the sodium/iodide symporter gene causing iodide transport defect in three Japanese patients
-
Kosugi S, Inoue S, Matsuda A, Jhiang SM 1998 Novel, missense and loss-of-function mutations in the sodium/iodide symporter gene causing iodide transport defect in three Japanese patients. J Clin Endocrinol Metab 83:3373-3376
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 3373-3376
-
-
Kosugi, S.1
Inoue, S.2
Matsuda, A.3
Jhiang, S.M.4
-
21
-
-
0031763451
-
High prevalence of T354P sodium/iodide symporter gene mutation in Japanese patients with iodide transport defect who have heterogeneous clinical pictures
-
Kosugi S, Sato Y, Matsuda A, Ohyama Y, Fujieda K, Inomata H, Kameya T, Isozaki O, Jhiang SM 1998 High prevalence of T354P sodium/iodide symporter gene mutation in Japanese patients with iodide transport defect who have heterogeneous clinical pictures. J Clin Endocrinol Metab 83:4123-4129
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 4123-4129
-
-
Kosugi, S.1
Sato, Y.2
Matsuda, A.3
Ohyama, Y.4
Fujieda, K.5
Inomata, H.6
Kameya, T.7
Isozaki, O.8
Jhiang, S.M.9
-
22
-
-
0033304901
-
A novel mutation in the sodium/iodide symporter gene in the largest family with iodide transport defect
-
Kosugi S, Bhayana S, Dean HJ 1999 A novel mutation in the sodium/iodide symporter gene in the largest family with iodide transport defect. J Clin Endocrinol Metab 84:3248-3253
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 3248-3253
-
-
Kosugi, S.1
Bhayana, S.2
Dean, H.J.3
-
23
-
-
0036348487
-
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 2002 A novel peculiar mutation in the sodium/iodide symporter gene in Spanish siblings with iodide transport defect. J Clin Endocrinol Metab 87:3830-3836
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 3830-3836
-
-
Kosugi, S.1
Okamoto, H.2
Tamada, A.3
Sanchez-Franco, F.4
-
24
-
-
0031576397
-
Hypothyroidism in a Brazilian kindred due to iodide trapping defect caused by a homozygous mutation in the sodium/iodide symporter gene
-
Pohlenz J, Medeiros-Neto G, Gross JL, Silveiro SP, Knobel M, Refetoff S 1997 Hypothyroidism in a Brazilian kindred due to iodide trapping defect caused by a homozygous mutation in the sodium/iodide symporter gene. Biochem Biophys Res Commun 240:488-491
-
(1997)
Biochem Biophys Res Commun
, vol.240
, pp. 488-491
-
-
Pohlenz, J.1
Medeiros-Neto, G.2
Gross, J.L.3
Silveiro, S.P.4
Knobel, M.5
Refetoff, S.6
-
25
-
-
0032031728
-
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 1998 Congenital hypothyroidism due to mutations in the sodium/iodide symporter. Identification of a nonsense mutation producing a downstream cryptic 3′ splice site. J Clin Invest 101:1028-1035
-
(1998)
J Clin Invest
, vol.101
, pp. 1028-1035
-
-
Pohlenz, J.1
Rosenthal, I.M.2
Weiss, R.E.3
Jhiang, S.M.4
Burant, C.5
Refetoff, S.6
-
26
-
-
0141839677
-
Congenital hypothyroidism due to a new deletion in the sodium/iodide symporter protein
-
Oxf
-
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 2003 Congenital hypothyroidism due to a new deletion in the sodium/iodide symporter protein. Clin Endocrinol (Oxf) 59:500-506
-
(2003)
Clin Endocrinol
, vol.59
, pp. 500-506
-
-
Tonacchera, M.1
Agretti, P.2
De Marco, G.3
Elisei, R.4
Perri, A.5
Ambrogini, E.6
De Servi, M.7
Ceccarelli, C.8
Viacava, P.9
Refetoff, S.10
Panunzi, C.11
Bitti, M.L.12
Vitti, P.13
Chiovato, L.14
Pinchera, A.15
-
27
-
-
0032486458
-
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 1998 Identification of a structural requirement for thyroid Na+/I- symporter (NIS) function from analysis of a mutation that causes human congenital hypothyroidism. FEBS Lett 429:36-40
-
(1998)
FEBS Lett
, vol.429
, pp. 36-40
-
-
Levy, O.1
Ginter, C.S.2
De La Vieja, A.3
Levy, D.4
Carrasco, N.5
-
28
-
-
0036020509
-
Na(+)/I(-) symporter activity requires a small and uncharged amino acid residue at position 395
-
Dohan O, Gavrielides MV, Ginter C, Amzel LM, Carrasco N 2002 Na(+)/I(-) symporter activity requires a small and uncharged amino acid residue at position 395. Mol Endocrinol 16:1893-1902
-
(2002)
Mol Endocrinol
, vol.16
, pp. 1893-1902
-
-
Dohan, O.1
Gavrielides, M.V.2
Ginter, C.3
Amzel, L.M.4
Carrasco, N.5
-
29
-
-
1342305177
-
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 2004 The Q267E mutation in the sodium/iodide symporter (NIS) causes congenital iodide transport defect (ITD) by decreasing the NIS turnover number. J Cell Sci 117:677-687
-
(2004)
J Cell Sci
, vol.117
, pp. 677-687
-
-
De La Vieja, A.1
Ginter, C.S.2
Carrasco, N.3
-
30
-
-
0034455711
-
Failure of membrane targeting causes the functional defect of two mutant sodium iodide symporters
-
Pohlenz J, Duprez L, Weiss RE, Vassart G, Refetoff S, Costagliola S 2000 Failure of membrane targeting causes the functional defect of two mutant sodium iodide symporters. J Clin Endocrinol Metab 85:2366-2369
-
(2000)
J Clin Endocrinol Metab
, vol.85
, pp. 2366-2369
-
-
Pohlenz, J.1
Duprez, L.2
Weiss, R.E.3
Vassart, G.4
Refetoff, S.5
Costagliola, S.6
-
31
-
-
0017429069
-
Areas, volumes, packing and protein structure
-
Richards FM 1977 Areas, volumes, packing and protein structure. Annu Rev Biophys Bioeng 6:151-176
-
(1977)
Annu Rev Biophys Bioeng
, vol.6
, pp. 151-176
-
-
Richards, F.M.1
-
32
-
-
0028175767
-
Na(+)-I- symport activity is present in membrane vesicles from thyrotropin-deprived non-I(-)-transporting cultured thyroid cells
-
USA
-
Kaminsky SM, Levy O, Salvador C, Dai G, Carrasco N 1994 Na(+)-I- symport activity is present in membrane vesicles from thyrotropin-deprived non-I(-)-transporting cultured thyroid cells. Proc Natl Acad Sci USA 91:3789-3793
-
(1994)
Proc Natl Acad Sci
, vol.91
, pp. 3789-3793
-
-
Kaminsky, S.M.1
Levy, O.2
Salvador, C.3
Dai, G.4
Carrasco, N.5
-
33
-
-
0035877782
-
Post-transcriptional regulation of the sodium/iodide symporter by thyrotropin
-
Riedel C, Levy O, Carrasco N 2001 Post-transcriptional regulation of the sodium/iodide symporter by thyrotropin. J Biol Chem 276:21458-21463
-
(2001)
J Biol Chem
, vol.276
, pp. 21458-21463
-
-
Riedel, C.1
Levy, O.2
Carrasco, N.3
-
34
-
-
0030042386
-
Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation
-
Sato S, Ward CL, Krouse ME, Wine JJ, Kopito RR 1996 Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation. J Biol Chem 271:635-638
-
(1996)
J Biol Chem
, vol.271
, pp. 635-638
-
-
Sato, S.1
Ward, C.L.2
Krouse, M.E.3
Wine, J.J.4
Kopito, R.R.5
-
35
-
-
0033557197
-
Novel pharmacologic therapies for cystic fibrosis
-
Zeitlin PL 1999 Novel pharmacologic therapies for cystic fibrosis. J Clin Invest 103:447-452
-
(1999)
J Clin Invest
, vol.103
, pp. 447-452
-
-
Zeitlin, P.L.1
-
36
-
-
0032524048
-
Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones
-
Tamarappoo BK, Verkman AS 1998 Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones. J Clin Invest 101:2257-2267
-
(1998)
J Clin Invest
, vol.101
, pp. 2257-2267
-
-
Tamarappoo, B.K.1
Verkman, A.S.2
-
37
-
-
0030070055
-
Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption
-
Martin MG, Turk E, Lostao MP, Kerner C, Wright EM 1996 Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption. Nat Genet 12:216-220
-
(1996)
Nat Genet
, vol.12
, pp. 216-220
-
-
Martin, M.G.1
Turk, E.2
Lostao, M.P.3
Kerner, C.4
Wright, E.M.5
-
38
-
-
1242272759
-
The sodium/glucose cotransport family SLC5
-
Wright EM, Turk E 2004 The sodium/glucose cotransport family SLC5. Pflugers Arch 447:510-518
-
(2004)
Pflugers Arch
, vol.447
, pp. 510-518
-
-
Wright, E.M.1
Turk, E.2
-
39
-
-
0036937335
-
Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2)
-
van den Heuvel LP, Assink K, Willemsen M, Monnens L 2002 Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2). Hum Genet 111:544-547
-
(2002)
Hum Genet
, vol.111
, pp. 544-547
-
-
Van Den Heuvel, L.P.1
Assink, K.2
Willemsen, M.3
Monnens, L.4
-
40
-
-
0021273667
-
Iodide transport in a continuous line of cultured cells from rat thyroid
-
Weiss SJ, Philp NJ, Grollman EF 1984 Iodide transport in a continuous line of cultured cells from rat thyroid. Endocrinology 114:1090-1098
-
(1984)
Endocrinology
, vol.114
, pp. 1090-1098
-
-
Weiss, S.J.1
Philp, N.J.2
Grollman, E.F.3
-
41
-
-
0004161838
-
-
Cambridge, UK: Cambridge University Press
-
Press WH, Flannery BP, Teukolsky SA, Wetterling WT 1986 Numerical recipes: the art of scientific computing. Cambridge, UK: Cambridge University Press; 523-528
-
(1986)
Numerical Recipes: The Art of Scientific Computing
, pp. 523-528
-
-
Press, W.H.1
Flannery, B.P.2
Teukolsky, S.A.3
Wetterling, W.T.4
-
42
-
-
0013592069
-
Intracellular antigen staining: Quantitative immunofluorescence
-
Jacobberger JW 1991 Intracellular antigen staining: quantitative immunofluorescence. Methods 2:207-218
-
(1991)
Methods
, vol.2
, pp. 207-218
-
-
Jacobberger, J.W.1
-
43
-
-
0022486949
-
Analysis of intracellular antigens by flow cytometry
-
Jacobberger JW, Fogleman D, Lehman JM 1986 Analysis of intracellular antigens by flow cytometry. Cytometry 7:356-364
-
(1986)
Cytometry
, vol.7
, pp. 356-364
-
-
Jacobberger, J.W.1
Fogleman, D.2
Lehman, J.M.3
-
44
-
-
0032524637
-
Determination of external loop topology in the serotonin transporter by site-directed chemical labeling
-
Chen JG, Liu-Chen S, Rudnick G 1998 Determination of external loop topology in the serotonin transporter by site-directed chemical labeling. J Biol Chem 273:12675-12681
-
(1998)
J Biol Chem
, vol.273
, pp. 12675-12681
-
-
Chen, J.G.1
Liu-Chen, S.2
Rudnick, G.3
-
45
-
-
0031473847
-
SWISS-MODEL and the Swiss-PdbViewer: An environment for comparative protein modeling
-
Guex N, Peitsch MC 1997 SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling. Electrophoresis 18:2714-2723
-
(1997)
Electrophoresis
, vol.18
, pp. 2714-2723
-
-
Guex, N.1
Peitsch, M.C.2
-
46
-
-
0026244229
-
MOLSCRIPT: A program to produce both detailed and schematic plots of protein structures
-
Kraulis PJ 1991 MOLSCRIPT: a program to produce both detailed and schematic plots of protein structures. J Appl Cryst 24:946-950
-
(1991)
J Appl Cryst
, vol.24
, pp. 946-950
-
-
Kraulis, P.J.1
-
47
-
-
0030815133
-
Raster3D: Photorealistic molecular graphics
-
Merritt EA, Bacon DJ 1997 Raster3D: photorealistic molecular graphics. Methods Enzymol 277:505-524
-
(1997)
Methods Enzymol
, vol.277
, pp. 505-524
-
-
Merritt, E.A.1
Bacon, D.J.2
|