-
1
-
-
48249155076
-
Molecular mechanisms of epithelial cell-specific expression and regulation of the human anion exchanger (pendrin) gene
-
Adler L., Efrati E., Zelikovic I. Molecular mechanisms of epithelial cell-specific expression and regulation of the human anion exchanger (pendrin) gene. Am. J. Physiol. Cell. Physiol. 2008, 294:1261-1276.
-
(2008)
Am. J. Physiol. Cell. Physiol.
, vol.294
, pp. 1261-1276
-
-
Adler, L.1
Efrati, E.2
Zelikovic, I.3
-
3
-
-
0034904523
-
Expression pattern of the pendrin and sodium/iodide symporter genes in human thyroid carcinoma cell lines and human thyroid tumors
-
Arturi F., Russo D., Bidart J.M., Scarpelli D., Schlumberger M., Filetti S. Expression pattern of the pendrin and sodium/iodide symporter genes in human thyroid carcinoma cell lines and human thyroid tumors. Eur. J. Endocrinol. 2001, 145:129-135.
-
(2001)
Eur. J. Endocrinol.
, vol.145
, pp. 129-135
-
-
Arturi, F.1
Russo, D.2
Bidart, J.M.3
Scarpelli, D.4
Schlumberger, M.5
Filetti, S.6
-
4
-
-
77957332163
-
Absence of anti-Pendrin auto-antibodies in the sera of Tunisian patients with autoimmune thyroid disease
-
Belguith-Maalej S., Hadj-Kacem H., Rebuffat S.A., Mnif-Feki M., Nguyen B., Abid M., Gross R., Ayadi H., Peraldi-Roux S. Absence of anti-Pendrin auto-antibodies in the sera of Tunisian patients with autoimmune thyroid disease. Clin Lab. 2010, 56:335-343.
-
(2010)
Clin Lab.
, vol.56
, pp. 335-343
-
-
Belguith-Maalej, S.1
Hadj-Kacem, H.2
Rebuffat, S.A.3
Mnif-Feki, M.4
Nguyen, B.5
Abid, M.6
Gross, R.7
Ayadi, H.8
Peraldi-Roux, S.9
-
5
-
-
0034455756
-
Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
-
Bidart J.M., Mian C., Lazar V., Russo D., Filetti S., Caillou B., Schlumberger M. Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues. J. Clin. Endocrinol. Metab. 2000, 85:2028-2033.
-
(2000)
J. Clin. Endocrinol. Metab.
, vol.85
, pp. 2028-2033
-
-
Bidart, J.M.1
Mian, C.2
Lazar, V.3
Russo, D.4
Filetti, S.5
Caillou, B.6
Schlumberger, M.7
-
6
-
-
67649836744
-
Minireview: the sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroid
-
Bizhanova A., Kopp P. Minireview: the sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroid. Endocrinology 2009, 150:1084-1090.
-
(2009)
Endocrinology
, vol.150
, pp. 1084-1090
-
-
Bizhanova, A.1
Kopp, P.2
-
7
-
-
26244454529
-
Modulation of thyroid-specific gene expression in normal and nodular human thyroid tissues from adults: an in vivo effect of thyrotropin
-
Bruno R., Ferretti E., Tosi E., Arturi F., Giannasio P., Mattei T., Scipioni A., Presta I., Morisi R., Gulino A., Filetti S., Russo D. Modulation of thyroid-specific gene expression in normal and nodular human thyroid tissues from adults: an in vivo effect of thyrotropin. J. Clin. Endocrinol. Metab. 2005, 90:5692-5697.
-
(2005)
J. Clin. Endocrinol. Metab.
, vol.90
, pp. 5692-5697
-
-
Bruno, R.1
Ferretti, E.2
Tosi, E.3
Arturi, F.4
Giannasio, P.5
Mattei, T.6
Scipioni, A.7
Presta, I.8
Morisi, R.9
Gulino, A.10
Filetti, S.11
Russo, D.12
-
8
-
-
63749096761
-
Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?
-
Choi B.Y., Stewart A.K., Madeo A.C., Pryor S.P., Lenhard S., Kittles R., Eisenman D., Kim H.J., Niparko J., Thomsen J., Arnos K.S., Nance W.E., King K.A., Zalewski C.K., Brewer C.C., Shawker T., Reynolds J.C., Butman J.A., Karniski L.P., Alper S.L., Griffith A.J. Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?. Hum. Mutat. 2009, 30:599-608.
-
(2009)
Hum. Mutat.
, vol.30
, pp. 599-608
-
-
Choi, B.Y.1
Stewart, A.K.2
Madeo, A.C.3
Pryor, S.P.4
Lenhard, S.5
Kittles, R.6
Eisenman, D.7
Kim, H.J.8
Niparko, J.9
Thomsen, J.10
Arnos, K.S.11
Nance, W.E.12
King, K.A.13
Zalewski, C.K.14
Brewer, C.C.15
Shawker, T.16
Reynolds, J.C.17
Butman, J.A.18
Karniski, L.P.19
Alper, S.L.20
Griffith, A.J.21
more..
-
9
-
-
79953278430
-
Response to: the c.-103T>C variant in the 5'-UTR of SLC26A4 gene: a pathogenic mutation or coincidental polymorphism?
-
Choi B.Y., Alper S.L., Griffith A.J. Response to: the c.-103T>C variant in the 5'-UTR of SLC26A4 gene: a pathogenic mutation or coincidental polymorphism?. Hum. Mutat. 2009, 30:1471.
-
(2009)
Hum. Mutat.
, vol.30
, pp. 1471
-
-
Choi, B.Y.1
Alper, S.L.2
Griffith, A.J.3
-
10
-
-
0032476116
-
Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome
-
Cremers C.W., Admiraal R.J., Huygen P.L., Bolder C., Everett L.A., Joosten F.B., Green E.D., Van Camp G., Otten B.J. Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome. Int. J. Pediatr. Otorhinolaryngol. 1998, 45:113-123.
-
(1998)
Int. J. Pediatr. Otorhinolaryngol.
, vol.45
, pp. 113-123
-
-
Cremers, C.W.1
Admiraal, R.J.2
Huygen, P.L.3
Bolder, C.4
Everett, L.A.5
Joosten, F.B.6
Green, E.D.7
Van Camp, G.8
Otten, B.J.9
-
11
-
-
0033999085
-
In situ hybridization and immunohistochemistry study of thyroid peroxidase expression in thyroid tumors
-
De Micco C., Kopp F., Vassko V., Grino M. In situ hybridization and immunohistochemistry study of thyroid peroxidase expression in thyroid tumors. Thyroid 2000, 10:109-115.
-
(2000)
Thyroid
, vol.10
, pp. 109-115
-
-
De Micco, C.1
Kopp, F.2
Vassko, V.3
Grino, M.4
-
12
-
-
0025732156
-
Immunohistochemical study of thyroid peroxidase in normal, hyperplastic, and neoplastic human thyroid tissues
-
De Micco C., Ruf J., Chrestian M.A., Gros N., Henry J.F., Carayon P. Immunohistochemical study of thyroid peroxidase in normal, hyperplastic, and neoplastic human thyroid tissues. Cancer 1991, 67:3036-3041.
-
(1991)
Cancer
, vol.67
, pp. 3036-3041
-
-
De Micco, C.1
Ruf, J.2
Chrestian, M.A.3
Gros, N.4
Henry, J.F.5
Carayon, P.6
-
13
-
-
27644592904
-
Pendrin is a novel in vivo downstream target gene of the TTF-1/Nkx-2.1 homeodomain transcription factor in differentiated thyroid cells
-
Dentice M., Luongo C., Elefante A., Ambrosio R., Salzano S., Zannini M., Nitsch R., Di Lauro R., Rossi G., Fenzi G., Salvatore D. Pendrin is a novel in vivo downstream target gene of the TTF-1/Nkx-2.1 homeodomain transcription factor in differentiated thyroid cells. Mol. Cell. Biol. 2005, 25:10171-10182.
-
(2005)
Mol. Cell. Biol.
, vol.25
, pp. 10171-10182
-
-
Dentice, M.1
Luongo, C.2
Elefante, A.3
Ambrosio, R.4
Salzano, S.5
Zannini, M.6
Nitsch, R.7
Di Lauro, R.8
Rossi, G.9
Fenzi, G.10
Salvatore, D.11
-
14
-
-
0036317991
-
Androgen-dependent expression of FcgammaRIIB2 by thyrocytes from patients with autoimmune Graves' disease: a possible molecular clue for sex dependence of autoimmune disease
-
Estienne V., Duthoit C., Reichert M., Praetor A., Carayon P., Hunziker W., Ruf J. Androgen-dependent expression of FcgammaRIIB2 by thyrocytes from patients with autoimmune Graves' disease: a possible molecular clue for sex dependence of autoimmune disease. FASEB J. 2002, 16:1087-1092.
-
(2002)
FASEB J.
, vol.16
, pp. 1087-1092
-
-
Estienne, V.1
Duthoit, C.2
Reichert, M.3
Praetor, A.4
Carayon, P.5
Hunziker, W.6
Ruf, J.7
-
15
-
-
16944366606
-
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)
-
Everett L.A., Glaser B., Beck J.C., Idol J.R., Buchs A., Heyman M., Adawi F., Hazani E., Nassir E., Baxevanis A.D., Sheffield V.C., Green E.D. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). Nat. Genet. 1997, 17:411-422.
-
(1997)
Nat. Genet.
, vol.17
, pp. 411-422
-
-
Everett, L.A.1
Glaser, B.2
Beck, J.C.3
Idol, J.R.4
Buchs, A.5
Heyman, M.6
Adawi, F.7
Hazani, E.8
Nassir, E.9
Baxevanis, A.D.10
Sheffield, V.C.11
Green, E.D.12
-
16
-
-
0033578352
-
Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
-
Everett L.A., Morsli H., Wu D.K., Green E.D. Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear. Proc. Natl. Acad. Sci. U. S. A. 1999, 96:9727-9732.
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 9727-9732
-
-
Everett, L.A.1
Morsli, H.2
Wu, D.K.3
Green, E.D.4
-
17
-
-
0346154518
-
Association of congenital deafness with goitre (Pendred's syndrome): a study of 207 families
-
Fraser G.R. Association of congenital deafness with goitre (Pendred's syndrome): a study of 207 families. Ann. Hum. Genet. 1965, 28:201-249.
-
(1965)
Ann. Hum. Genet.
, vol.28
, pp. 201-249
-
-
Fraser, G.R.1
-
18
-
-
0023930772
-
Thyroid function in patients with Pendred's syndrome
-
Friis J., Johnsen T., Feldt-Rasmussen U., Bech K., Friis T. Thyroid function in patients with Pendred's syndrome. J. Endocrinol. Invest. 1988, 11:97-101.
-
(1988)
J. Endocrinol. Invest.
, vol.11
, pp. 97-101
-
-
Friis, J.1
Johnsen, T.2
Feldt-Rasmussen, U.3
Bech, K.4
Friis, T.5
-
19
-
-
10744222193
-
Correlation between the loss of thyroglobulin iodination and the expression of thyroid-specific proteins involved in iodine metabolism in thyroid carcinomas
-
Gerard A.C., Daumerie C., Mestdagh C., Gohy S., De Burbure C., Costagliola S., Miot F., Nollevaux M.C., Denef J.F., Rahier J., Franc B., De Vijlder J.J., Colin I.M., Many M.C. Correlation between the loss of thyroglobulin iodination and the expression of thyroid-specific proteins involved in iodine metabolism in thyroid carcinomas. J. Clin. Endocrinol. Metab. 2003, 88:4977-4983.
-
(2003)
J. Clin. Endocrinol. Metab.
, vol.88
, pp. 4977-4983
-
-
Gerard, A.C.1
Daumerie, C.2
Mestdagh, C.3
Gohy, S.4
De Burbure, C.5
Costagliola, S.6
Miot, F.7
Nollevaux, M.C.8
Denef, J.F.9
Rahier, J.10
Franc, B.11
De Vijlder, J.J.12
Colin, I.M.13
Many, M.C.14
-
20
-
-
1842581804
-
Functional characterization of pendrin in a polarized cell system: evidence for pendrin-mediated apical iodide efflux
-
Gillam M.P., Sidhaye A.R., Lee E.J., Rutishauser J., Stephan C.W., Kopp P. Functional characterization of pendrin in a polarized cell system: evidence for pendrin-mediated apical iodide efflux. J. Biol. Chem. 2004, 279:13004-13010.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 13004-13010
-
-
Gillam, M.P.1
Sidhaye, A.R.2
Lee, E.J.3
Rutishauser, J.4
Stephan, C.W.5
Kopp, P.6
-
21
-
-
0038368918
-
PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage study
-
Hadj Kacem H., Rebai A., Kaffel N., Masmoudi S., Abid M., Ayadi H. PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage study. J. Clin. Endocrinol. Metab. 2003, 88:2274-2280.
-
(2003)
J. Clin. Endocrinol. Metab.
, vol.88
, pp. 2274-2280
-
-
Hadj Kacem, H.1
Rebai, A.2
Kaffel, N.3
Masmoudi, S.4
Abid, M.5
Ayadi, H.6
-
22
-
-
0024514347
-
The WHO histological classification of thyroid tumors: a commentary on the second edition
-
Hedinger C., Williams E.D., Sobin L.H. The WHO histological classification of thyroid tumors: a commentary on the second edition. Cancer 1989, 63:908-911.
-
(1989)
Cancer
, vol.63
, pp. 908-911
-
-
Hedinger, C.1
Williams, E.D.2
Sobin, L.H.3
-
24
-
-
79953290984
-
Graves' hyperthyroidism in a patient with pendred's dyshormonogenesis
-
Ibrahim I.M., McDonald D.O., Owen C.J., Kendall-Taylor P., Pearce S.H.S. Graves' hyperthyroidism in a patient with pendred's dyshormonogenesis. Hot. Thyroidol. 2009, 13:09.
-
(2009)
Hot. Thyroidol.
, vol.13
, pp. 09
-
-
Ibrahim, I.M.1
McDonald, D.O.2
Owen, C.J.3
Kendall-Taylor, P.4
Pearce, S.H.S.5
-
25
-
-
0035235633
-
Effects of thyroglobulin and pendrin on iodide flux through the thyrocyte
-
Kohn L.D., Suzuki K., Nakazato M., Royaux I.E., Green E.D. Effects of thyroglobulin and pendrin on iodide flux through the thyrocyte. Trends Endocrinol. Metab. 2001, 12:10-16.
-
(2001)
Trends Endocrinol. Metab.
, vol.12
, pp. 10-16
-
-
Kohn, L.D.1
Suzuki, K.2
Nakazato, M.3
Royaux, I.E.4
Green, E.D.5
-
26
-
-
0037311506
-
Expression of human pendrin in diseased thyroids
-
Kondo T., Nakamura N., Suzuki K., Murata S.I., Muramatsu A., Kawaoi A., Katoh R. Expression of human pendrin in diseased thyroids. J. Histochem. Cytochem. 2003, 51:167-173.
-
(2003)
J. Histochem. Cytochem.
, vol.51
, pp. 167-173
-
-
Kondo, T.1
Nakamura, N.2
Suzuki, K.3
Murata, S.I.4
Muramatsu, A.5
Kawaoi, A.6
Katoh, R.7
-
27
-
-
0035065054
-
Na(+)/I(-) symporter and Pendred syndrome gene and protein expressions in human extra-thyroidal tissues
-
Lacroix L., Mian C., Caillou B., Talbot M., Filetti S., Schlumberger M., Bidart J.M. Na(+)/I(-) symporter and Pendred syndrome gene and protein expressions in human extra-thyroidal tissues. Eur. J. Endocrinol. 2001, 144:297-302.
-
(2001)
Eur. J. Endocrinol.
, vol.144
, pp. 297-302
-
-
Lacroix, L.1
Mian, C.2
Caillou, B.3
Talbot, M.4
Filetti, S.5
Schlumberger, M.6
Bidart, J.M.7
-
28
-
-
0034857446
-
Sodium iodide symporter and pendrin expression in human thyroid tissues
-
Mian C., Lacroix L., Alzieu L., Nocera M., Talbot M., Bidart J.M., Schlumberger M., Caillou B. Sodium iodide symporter and pendrin expression in human thyroid tissues. Thyroid 2001, 11:825-830.
-
(2001)
Thyroid
, vol.11
, pp. 825-830
-
-
Mian, C.1
Lacroix, L.2
Alzieu, L.3
Nocera, M.4
Talbot, M.5
Bidart, J.M.6
Schlumberger, M.7
Caillou, B.8
-
29
-
-
49649086716
-
PKC-epsilon-dependent cytosol-to-membrane translocation of pendrin in rat thyroid PCCl3 cells
-
Muscella A., Marsigliante S., Verri T., Urso L., Dimitri C., Bottà G., Paulmichl M., Beck-Peccoz P., Fugazzola L., Storelli C. PKC-epsilon-dependent cytosol-to-membrane translocation of pendrin in rat thyroid PCCl3 cells. J. Cell. Physiol. 2008, 217:103-112.
-
(2008)
J. Cell. Physiol.
, vol.217
, pp. 103-112
-
-
Muscella, A.1
Marsigliante, S.2
Verri, T.3
Urso, L.4
Dimitri, C.5
Bottà, G.6
Paulmichl, M.7
Beck-Peccoz, P.8
Fugazzola, L.9
Storelli, C.10
-
30
-
-
73149096698
-
Thyroglobulin (Tg) induces thyroid cell growth in a concentration-specific manner by a mechanism other than thyrotropin/cAMP stimulation
-
Noguchi Y., Harii N., Giuliani C., Tatsuno I., Suzuki K., Kohn L.D. Thyroglobulin (Tg) induces thyroid cell growth in a concentration-specific manner by a mechanism other than thyrotropin/cAMP stimulation. Biochem. Biophys. Res. Commun. 2009, 391:890-894.
-
(2009)
Biochem. Biophys. Res. Commun.
, vol.391
, pp. 890-894
-
-
Noguchi, Y.1
Harii, N.2
Giuliani, C.3
Tatsuno, I.4
Suzuki, K.5
Kohn, L.D.6
-
31
-
-
50549149000
-
Deaf mutism and goitre
-
Pendred V. Deaf mutism and goitre. Lancet 1896, 11:532.
-
(1896)
Lancet
, vol.11
, pp. 532
-
-
Pendred, V.1
-
32
-
-
17344392308
-
A new mathematical model for relative quantification in real-time RT-PCR
-
Pfaffl M.W. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001, 29(9):e45.
-
(2001)
Nucleic Acids Res.
, vol.29
, Issue.9
-
-
Pfaffl, M.W.1
-
33
-
-
0036581160
-
©) for group-wise comparison and statistical analysis of relative expression results in real-time PCR
-
©) for group-wise comparison and statistical analysis of relative expression results in real-time PCR. Nucleic Acids Res. 2002, 30(9):e36.
-
(2002)
Nucleic Acids Res.
, vol.30
, Issue.9
-
-
Pfaffl, M.W.1
Horgan, G.W.2
Dempfle, L.3
-
34
-
-
0036277794
-
Characterization and semiquantitative analyses of pendrin expressed in normal and tumoral human thyroid tissues
-
Porra V., Bernier-Valentin F., Trouttet-Masson S., Berger-Dutrieux N., Peix J.L., Perrin A., Selmi-Ruby S., Rousset B. Characterization and semiquantitative analyses of pendrin expressed in normal and tumoral human thyroid tissues. J. Clin. Endocrinol. Metab. 2002, 87:1700-1707.
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 1700-1707
-
-
Porra, V.1
Bernier-Valentin, F.2
Trouttet-Masson, S.3
Berger-Dutrieux, N.4
Peix, J.L.5
Perrin, A.6
Selmi-Ruby, S.7
Rousset, B.8
-
35
-
-
21044448948
-
Silencing of the tumor suppressor gene SLC5A8 is associated with BRAF mutations in classical papillary thyroid carcinomas
-
Porra V., Ferraro-Peyret C., Durand C., Selmi-Ruby S., Giroud H., Berger-Dutrieux N., Decaussin M., Peix J.L., Bournaud C., Orgiazzi J., Borson-Chazot F., Dante R., Rousset B. Silencing of the tumor suppressor gene SLC5A8 is associated with BRAF mutations in classical papillary thyroid carcinomas. J. Clin. Endocrinol. Metab. 2005, 90:3028-3035.
-
(2005)
J. Clin. Endocrinol. Metab.
, vol.90
, pp. 3028-3035
-
-
Porra, V.1
Ferraro-Peyret, C.2
Durand, C.3
Selmi-Ruby, S.4
Giroud, H.5
Berger-Dutrieux, N.6
Decaussin, M.7
Peix, J.L.8
Bournaud, C.9
Orgiazzi, J.10
Borson-Chazot, F.11
Dante, R.12
Rousset, B.13
-
37
-
-
0032773714
-
Prevalence, age of onset, and natural history of thyroid disease in Pendred syndrome
-
Reardon W., Coffey R., Chowdhury T., Grossman A., Jan H., Britton K., Kendall-Taylor P., Trembath R. Prevalence, age of onset, and natural history of thyroid disease in Pendred syndrome. J. Med. Genet. 1999, 36:595-598.
-
(1999)
J. Med. Genet.
, vol.36
, pp. 595-598
-
-
Reardon, W.1
Coffey, R.2
Chowdhury, T.3
Grossman, A.4
Jan, H.5
Britton, K.6
Kendall-Taylor, P.7
Trembath, R.8
-
38
-
-
0030815949
-
Pendred syndrome-100 years of under ascertainment
-
Reardon W., Coffey R., Phelps P.D., Luxon L.M., Stephens D., Kendall-Taylor P., Britton K.E., Grossman A., Trembath R. Pendred syndrome-100 years of under ascertainment. Quart. J. Med. 1997, 90:443-447.
-
(1997)
Quart. J. Med.
, vol.90
, pp. 443-447
-
-
Reardon, W.1
Coffey, R.2
Phelps, P.D.3
Luxon, L.M.4
Stephens, D.5
Kendall-Taylor, P.6
Britton, K.E.7
Grossman, A.8
Trembath, R.9
-
39
-
-
0037225536
-
Prolactin regulation of the pendrin-iodide transporter in the mammary gland
-
Rillema J.A., Hill M.A. Prolactin regulation of the pendrin-iodide transporter in the mammary gland. Am. J. Physiol. Endocrinol. Metab. 2003, 284:E25-E28.
-
(2003)
Am. J. Physiol. Endocrinol. Metab.
, vol.284
-
-
Rillema, J.A.1
Hill, M.A.2
-
40
-
-
0036322911
-
Identification and characterization of a putative human iodide transporter located at the apical membrane of thyrocytes
-
Rodriguez A.M., Perron B., Lacroix L., Caillou B., Leblanc G., Schlumberger M., Bidart J.M., Pourcher T. Identification and characterization of a putative human iodide transporter located at the apical membrane of thyrocytes. J. Clin. Endocrinol. Metab. 2002, 87:3500-3503.
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 3500-3503
-
-
Rodriguez, A.M.1
Perron, B.2
Lacroix, L.3
Caillou, B.4
Leblanc, G.5
Schlumberger, M.6
Bidart, J.M.7
Pourcher, T.8
-
41
-
-
0036797830
-
Retention of pendrin in the endoplasmic reticulum is a major mechanism for Pendred syndrome
-
Rotman-Pikielny P., Hirschberg K., Maruvada P., Suzuki K., Royaux I.E., Green E.D., Kohn L.D., Lippincott-Schwartz J., Yen P.M. Retention of pendrin in the endoplasmic reticulum is a major mechanism for Pendred syndrome. Hum. Mol. Genet. 2002, 11:2625-2633.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2625-2633
-
-
Rotman-Pikielny, P.1
Hirschberg, K.2
Maruvada, P.3
Suzuki, K.4
Royaux, I.E.5
Green, E.D.6
Kohn, L.D.7
Lippincott-Schwartz, J.8
Yen, P.M.9
-
42
-
-
0141729459
-
Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in Pendred syndrome
-
Royaux I.E., Belyantseva I.A., Wu T., Kachar B., Everett L.A., Marcus D.C., Green E.D. Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in Pendred syndrome. J. Assoc. Res. Otolaryngol. 2003, 4:394-404.
-
(2003)
J. Assoc. Res. Otolaryngol.
, vol.4
, pp. 394-404
-
-
Royaux, I.E.1
Belyantseva, I.A.2
Wu, T.3
Kachar, B.4
Everett, L.A.5
Marcus, D.C.6
Green, E.D.7
-
43
-
-
0034463973
-
Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells
-
Royaux I.E., Suzuki K., Mori A., Katoh R., Everett L.A., Kohn L.D., Green E.D. Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells. Endocrinology 2000, 141:839-845.
-
(2000)
Endocrinology
, vol.141
, pp. 839-845
-
-
Royaux, I.E.1
Suzuki, K.2
Mori, A.3
Katoh, R.4
Everett, L.A.5
Kohn, L.D.6
Green, E.D.7
-
44
-
-
0035957363
-
Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion
-
Royaux I.E., Wall S.M., Karniski L.P., Everett L.A., Suzuki K., Knepper M.A., Green E.D. Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion. Proc. Natl. Acad. Sci. U. S. A. 2001, 98:4221-4226.
-
(2001)
Proc. Natl. Acad. Sci. U. S. A.
, vol.98
, pp. 4221-4226
-
-
Royaux, I.E.1
Wall, S.M.2
Karniski, L.P.3
Everett, L.A.4
Suzuki, K.5
Knepper, M.A.6
Green, E.D.7
-
45
-
-
0033990048
-
Primer 3 on the WWW for general users and for biologist programmers
-
Humana Press, Totowa, NJ, S. Krawetz, S. Misener (Eds.)
-
Rozen S., Skaletsky H.J. Primer 3 on the WWW for general users and for biologist programmers. Bioinformatics Methods and Protocols: Methods in Molecular Biology 2000, 365-386. Humana Press, Totowa, NJ. S. Krawetz, S. Misener (Eds.).
-
(2000)
Bioinformatics Methods and Protocols: Methods in Molecular Biology
, pp. 365-386
-
-
Rozen, S.1
Skaletsky, H.J.2
-
46
-
-
0024430122
-
Relationship between immunological structure and biochemical properties of human thyroid peroxidase
-
Ruf J., Toubert M.E., Czarnocka B., Durand-Gorde J.M., Ferrand M., Carayon P. Relationship between immunological structure and biochemical properties of human thyroid peroxidase. Endocrinology 1989, 125:1211-1218.
-
(1989)
Endocrinology
, vol.125
, pp. 1211-1218
-
-
Ruf, J.1
Toubert, M.E.2
Czarnocka, B.3
Durand-Gorde, J.M.4
Ferrand, M.5
Carayon, P.6
-
47
-
-
0035171063
-
Sodium/iodide symporter (NIS) and pendrin are expressed differently in hot and cold nodules of thyroid toxic multinodular goiter
-
Russo D., Bulotta S., Bruno R., Arturi F., Giannasio P., Derwahl M., Bidart J.M., Schlumberger M., Filetti S. Sodium/iodide symporter (NIS) and pendrin are expressed differently in hot and cold nodules of thyroid toxic multinodular goiter. Eur. J. Endocrinol. 2001, 145:591-597.
-
(2001)
Eur. J. Endocrinol.
, vol.145
, pp. 591-597
-
-
Russo, D.1
Bulotta, S.2
Bruno, R.3
Arturi, F.4
Giannasio, P.5
Derwahl, M.6
Bidart, J.M.7
Schlumberger, M.8
Filetti, S.9
-
48
-
-
0034235222
-
Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4)
-
Scott D.A., Wang R., Kreman T.M., Andrews M., McDonald J.M., Bishop J.R., Smith R.J., Karniski L.P., Sheffield V.C. Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4). Hum. Mol. Genet. 2000, 9:1709-1715.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1709-1715
-
-
Scott, D.A.1
Wang, R.2
Kreman, T.M.3
Andrews, M.4
McDonald, J.M.5
Bishop, J.R.6
Smith, R.J.7
Karniski, L.P.8
Sheffield, V.C.9
-
49
-
-
0032901865
-
The Pendred syndrome gene encodes a chloride-iodide transport protein
-
Scott D.A., Wang R., Kreman T.M., Sheffield V.C., Karniski L.P. The Pendred syndrome gene encodes a chloride-iodide transport protein. Nat. Genet. 1999, 21:440-443.
-
(1999)
Nat. Genet.
, vol.21
, pp. 440-443
-
-
Scott, D.A.1
Wang, R.2
Kreman, T.M.3
Sheffield, V.C.4
Karniski, L.P.5
-
50
-
-
23044460719
-
Expression of pendrin in benign and malignant human thyroid tissues
-
Skubis-Zegadło J., Nikodemska A., Przytuła E., Mikula M., Bardadin K., Ostrowski J., Wenzel B.E., Czarnocka B. Expression of pendrin in benign and malignant human thyroid tissues. Br. J. Cancer 2005, 93:144-151.
-
(2005)
Br. J. Cancer
, vol.93
, pp. 144-151
-
-
Skubis-Zegadło, J.1
Nikodemska, A.2
Przytuła, E.3
Mikula, M.4
Bardadin, K.5
Ostrowski, J.6
Wenzel, B.E.7
Czarnocka, B.8
-
51
-
-
33646811842
-
Differential regulation of apical and basal iodide transporters in the thyroid by thyroglobulin
-
Suzuki K., Kohn L.D. Differential regulation of apical and basal iodide transporters in the thyroid by thyroglobulin. J. Endocrinol. 2006, 189:247-255.
-
(2006)
J. Endocrinol.
, vol.189
, pp. 247-255
-
-
Suzuki, K.1
Kohn, L.D.2
-
52
-
-
18244386042
-
Expression of PDS/Pds, the Pendred syndrome gene, in endometrium
-
Suzuki K., Royaux I.E., Everett L.A., Mori-Aoki A., Suzuki S., Nakamura K., Sakai T., Katoh R., Toda S., Green E.D., Kohn L.D. Expression of PDS/Pds, the Pendred syndrome gene, in endometrium. J. Clin. Endocrinol. Metab. 2002, 87:938.
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 938
-
-
Suzuki, K.1
Royaux, I.E.2
Everett, L.A.3
Mori-Aoki, A.4
Suzuki, S.5
Nakamura, K.6
Sakai, T.7
Katoh, R.8
Toda, S.9
Green, E.D.10
Kohn, L.D.11
-
53
-
-
0036283790
-
Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome
-
Taylor J.P., Metcalfe R.A., Watson P.F., Weetman A.P., Trembath R.C. Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome. J. Clin. Endocrinol. Metab. 2002, 87:1778-1784.
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 1778-1784
-
-
Taylor, J.P.1
Metcalfe, R.A.2
Watson, P.F.3
Weetman, A.P.4
Trembath, R.C.5
-
54
-
-
0033344689
-
Concurrence of Pendred syndrome, autoimmune thyroiditis, and simple goiter in one family
-
Vaidya B., Coffey R., Coyle B., Trembath R., San Lazaro C., Reardon W., Kendall-Taylor P. Concurrence of Pendred syndrome, autoimmune thyroiditis, and simple goiter in one family. J. Clin. Endocrinol. Metab. 1999, 84:2736-2738.
-
(1999)
J. Clin. Endocrinol. Metab.
, vol.84
, pp. 2736-2738
-
-
Vaidya, B.1
Coffey, R.2
Coyle, B.3
Trembath, R.4
San Lazaro, C.5
Reardon, W.6
Kendall-Taylor, P.7
-
55
-
-
13844299001
-
Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model
-
Wangemann P., Itza E.M., Albrecht B., Wu T., Jabba S.V., Maganti R.J., Lee J.H., Everett L.A., Wall S.M., Royaux I.E., Green E.D., Marcus D.C. Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model. BMC Med. 2004, 2:30.
-
(2004)
BMC Med.
, vol.2
, pp. 30
-
-
Wangemann, P.1
Itza, E.M.2
Albrecht, B.3
Wu, T.4
Jabba, S.V.5
Maganti, R.J.6
Lee, J.H.7
Everett, L.A.8
Wall, S.M.9
Royaux, I.E.10
Green, E.D.11
Marcus, D.C.12
-
56
-
-
73349102851
-
The c.-103T>C variant in the 5'-UTR of SLC26A4 gene: a pathogenic mutation or coincidental polymorphism?
-
Yang T., Smith R.J. The c.-103T>C variant in the 5'-UTR of SLC26A4 gene: a pathogenic mutation or coincidental polymorphism?. Hum. Mutat. 2009, 30:1469-1470.
-
(2009)
Hum. Mutat.
, vol.30
, pp. 1469-1470
-
-
Yang, T.1
Smith, R.J.2
-
57
-
-
34250803246
-
Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4)
-
Yang T., Vidarsson H., Rodrigo-Blomqvist S., Rosengren S.S., Enerback S., Smith R.J. Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4). Am. J. Hum. Genet. 2007, 80:1055-1063.
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 1055-1063
-
-
Yang, T.1
Vidarsson, H.2
Rodrigo-Blomqvist, S.3
Rosengren, S.S.4
Enerback, S.5
Smith, R.J.6
-
58
-
-
47149095245
-
Heterogeneity in the processing defect of SLC26A4 mutants
-
Yoon J.S., Park H.J., Yoo S.Y., Namkung W., Jo M.J., Koo S.K., Park H.Y., Lee W.S., Kim K.H., Lee M.G. Heterogeneity in the processing defect of SLC26A4 mutants. J. Med. Genet. 2008, 45:411-419.
-
(2008)
J. Med. Genet.
, vol.45
, pp. 411-419
-
-
Yoon, J.S.1
Park, H.J.2
Yoo, S.Y.3
Namkung, W.4
Jo, M.J.5
Koo, S.K.6
Park, H.Y.7
Lee, W.S.8
Kim, K.H.9
Lee, M.G.10
-
59
-
-
59749093970
-
Pendrin is a novel autoantigen recognized by patients with autoimmune thyroid diseases
-
Yoshida A., Hisatome I., Taniguchi S., Shirayoshi Y., Yamamoto Y., Miake J., Ohkura T., Akama T., Igawa O., Shigemasa C., Kamijo K., Ikuyama S., Caturegli P., Suzuki K. Pendrin is a novel autoantigen recognized by patients with autoimmune thyroid diseases. J. Clin. Endocrinol. Metab. 2009, 94(2):442-448.
-
(2009)
J. Clin. Endocrinol. Metab.
, vol.94
, Issue.2
, pp. 442-448
-
-
Yoshida, A.1
Hisatome, I.2
Taniguchi, S.3
Shirayoshi, Y.4
Yamamoto, Y.5
Miake, J.6
Ohkura, T.7
Akama, T.8
Igawa, O.9
Shigemasa, C.10
Kamijo, K.11
Ikuyama, S.12
Caturegli, P.13
Suzuki, K.14
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