-
1
-
-
0141629106
-
Chronic adaptations in proximal tubular H/HCO3 transporters
-
Alpern R.J., Horie S., Moe O., Tejedor A., Miller R.T., and Preisig P.A. Chronic adaptations in proximal tubular H/HCO3 transporters. Kidney Inter., Suppl. 33 (1991) S29-S32
-
(1991)
Kidney Inter., Suppl.
, vol.33
-
-
Alpern, R.J.1
Horie, S.2
Moe, O.3
Tejedor, A.4
Miller, R.T.5
Preisig, P.A.6
-
2
-
-
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., and 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. 145 (2001) 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
-
3
-
-
0034529826
-
Expression of Na+/I- symporter and Pendred syndrome genes in trophoblast cells
-
Bidart J.M., Lacroix L., Evain-Brion D., Caillou B., Lazar V., Frydman R., Bellet D., Filetti S., and Schlumberger M. Expression of Na+/I- symporter and Pendred syndrome genes in trophoblast cells. J. Clin. Endocrinol. Metab. 85 (2000) 4367-4372
-
(2000)
J. Clin. Endocrinol. Metab.
, vol.85
, pp. 4367-4372
-
-
Bidart, J.M.1
Lacroix, L.2
Evain-Brion, D.3
Caillou, B.4
Lazar, V.5
Frydman, R.6
Bellet, D.7
Filetti, S.8
Schlumberger, M.9
-
4
-
-
0033999397
-
Pendrin does not increase sulfate uptake in mammalian COS-7 cells
-
Bogazzi F., Bartalena L., Raggi F., Ultimieri F., and Martino E. Pendrin does not increase sulfate uptake in mammalian COS-7 cells. J. Endocrinol. Investig. 23 (2000) 170-172
-
(2000)
J. Endocrinol. Investig.
, vol.23
, pp. 170-172
-
-
Bogazzi, F.1
Bartalena, L.2
Raggi, F.3
Ultimieri, F.4
Martino, E.5
-
5
-
-
0042831021
-
Sugar transport by mammalian members of the SLC26 superfamily of anion-bicarbonate exchangers
-
Chambard J.M., and Ashmore J.F. Sugar transport by mammalian members of the SLC26 superfamily of anion-bicarbonate exchangers. J. Physiol. 550 (2003) 667-677
-
(2003)
J. Physiol.
, vol.550
, pp. 667-677
-
-
Chambard, J.M.1
Ashmore, J.F.2
-
6
-
-
8244263673
-
Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4
-
Coyle B., Coffey R., Armour J.A., Gausden E., Hochberg Z., Grossman A., Britton K., Pembrey M., Reardon W., and Trembath R. Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4. Nat. Genet. 12 (1996) 421-423
-
(1996)
Nat. Genet.
, vol.12
, pp. 421-423
-
-
Coyle, B.1
Coffey, R.2
Armour, J.A.3
Gausden, E.4
Hochberg, Z.5
Grossman, A.6
Britton, K.7
Pembrey, M.8
Reardon, W.9
Trembath, R.10
-
7
-
-
0034980216
-
Update on intrathyroidal iodine metabolism
-
Dunn J.T., and Dunn A.D. Update on intrathyroidal iodine metabolism. Thyroid 11 (2001) 407-414
-
(2001)
Thyroid
, vol.11
, pp. 407-414
-
-
Dunn, J.T.1
Dunn, A.D.2
-
8
-
-
0032837375
-
A family of mammalian anion transporters and their involvement in human genetic diseases
-
Everett L.A., and Green E.D. A family of mammalian anion transporters and their involvement in human genetic diseases. Hum. Mol. Genet. 8 (1999) 1883-1891
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1883-1891
-
-
Everett, L.A.1
Green, E.D.2
-
9
-
-
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., and Green E.D. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). Nat. Genet. 17 (1997) 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
-
10
-
-
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., and 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. 96 (1999) 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
-
11
-
-
0035862723
-
Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome
-
Everett L.A., Belyantseva I.A., Noben-Trauth K., Cantos R., Chen A., Thakkar S.I., Hoogstraten-Miller S.L., Kachar B., Wu D.K., and Green E.D. Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome. Hum. Mol. Genet. 10 (2001) 153-161
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 153-161
-
-
Everett, L.A.1
Belyantseva, I.A.2
Noben-Trauth, K.3
Cantos, R.4
Chen, A.5
Thakkar, S.I.6
Hoogstraten-Miller, S.L.7
Kachar, B.8
Wu, D.K.9
Green, E.D.10
-
12
-
-
1542714234
-
Age-dependent variation of follicular size and expression of iodine transporters in human thyroid tissue
-
Faggiano A., Coulot J., Bellon N., Talbot M., Caillou B., Ricard M., Bidart J.M., and Schlumberger M. Age-dependent variation of follicular size and expression of iodine transporters in human thyroid tissue. J. Nucl. Med. 45 (2004) 232-237
-
(2004)
J. Nucl. Med.
, vol.45
, pp. 232-237
-
-
Faggiano, A.1
Coulot, J.2
Bellon, N.3
Talbot, M.4
Caillou, B.5
Ricard, M.6
Bidart, J.M.7
Schlumberger, M.8
-
14
-
-
0035122341
-
The role of pendrin in iodide regulation
-
Fugazzola L., Cerutti N., Mannavola D., Vannucchi G., and Beck-Peccoz P. The role of pendrin in iodide regulation. Exp. Clin. Endocrinol. Diabetes 109 (2001) 18-22
-
(2001)
Exp. Clin. Endocrinol. Diabetes
, vol.109
, pp. 18-22
-
-
Fugazzola, L.1
Cerutti, N.2
Mannavola, D.3
Vannucchi, G.4
Beck-Peccoz, P.5
-
15
-
-
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., and Kopp P. Functional characterization of pendrin in a polarized cell system. Evidence for pendrin-mediated apical iodide efflux. J. Biol. Chem. 279 (2004) 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
-
16
-
-
0027978110
-
The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping
-
Hastbacka J., de la Chapelle A., Mahtani M.M., Clines G., Reeve-Daly M.P., Daly M., Hamilton B.A., Kusumi K., Trivedi B., and Weaver A. The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping. Cell 78 (1994) 1073-1087
-
(1994)
Cell
, vol.78
, pp. 1073-1087
-
-
Hastbacka, J.1
de la Chapelle, A.2
Mahtani, M.M.3
Clines, G.4
Reeve-Daly, M.P.5
Daly, M.6
Hamilton, B.A.7
Kusumi, K.8
Trivedi, B.9
Weaver, A.10
-
17
-
-
16144368521
-
Mutations of the down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea
-
Hoglund P., Haila S., Socha J., Tomaszewski L., Saarialho-Kere U., Karjalainen-Lindsberg M.L., Airola K., Holmberg C., de la Chapelle A., and Kere J. Mutations of the down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea. Nat. Genet. 14 (1996) 316-319
-
(1996)
Nat. Genet.
, vol.14
, pp. 316-319
-
-
Hoglund, P.1
Haila, S.2
Socha, J.3
Tomaszewski, L.4
Saarialho-Kere, U.5
Karjalainen-Lindsberg, M.L.6
Airola, K.7
Holmberg, C.8
de la Chapelle, A.9
Kere, J.10
-
18
-
-
0036783931
-
Immunocytochemical localization of pendrin in intercalated cell subtypes in rat and mouse kidney
-
Kim Y.H., Kwon T.H., Frische S., Kim J., Tisher C.C., Madsen K.M., and Nielsen S. Immunocytochemical localization of pendrin in intercalated cell subtypes in rat and mouse kidney. Am. J. Physiol. Renal. Physiol. 283 (2002) F744-F754
-
(2002)
Am. J. Physiol. Renal. Physiol.
, vol.283
-
-
Kim, Y.H.1
Kwon, T.H.2
Frische, S.3
Kim, J.4
Tisher, C.C.5
Madsen, K.M.6
Nielsen, S.7
-
19
-
-
0035235633
-
Effects of thyroglobulin and pendrin on iodide flux through the thyrocyte
-
Kohn L.D., Suzuki K., Nakazato M., Royaux I., and Green E.D. Effects of thyroglobulin and pendrin on iodide flux through the thyrocyte. Trends Endocrinol. Metab. 12 (2001) 10-16
-
(2001)
Trends Endocrinol. Metab.
, vol.12
, pp. 10-16
-
-
Kohn, L.D.1
Suzuki, K.2
Nakazato, M.3
Royaux, I.4
Green, E.D.5
-
20
-
-
0033062827
-
Pendred's syndrome: identification of the genetic defect a century after its recognition
-
Kopp P. Pendred's syndrome: identification of the genetic defect a century after its recognition. Thyroid 9 (1999) 65-69
-
(1999)
Thyroid
, vol.9
, pp. 65-69
-
-
Kopp, P.1
-
21
-
-
0033306085
-
Sulfate transport is not impaired in pendred syndrome thyrocytes
-
Kraiem Z., Heinrich R., Sadeh O., Shiloni E., Nassir E., Hazani E., and Glaser B. Sulfate transport is not impaired in pendred syndrome thyrocytes. J. Clin. Endocrinol. Metab. 84 (1999) 2574-2576
-
(1999)
J. Clin. Endocrinol. Metab.
, vol.84
, pp. 2574-2576
-
-
Kraiem, Z.1
Heinrich, R.2
Sadeh, O.3
Shiloni, E.4
Nassir, E.5
Hazani, E.6
Glaser, B.7
-
22
-
-
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., and Bidart J.M. Na(+)/I(-) symporter and Pendred syndrome gene and protein expressions in human extra-thyroidal tissues. Eur. J. Endocrinol. 144 (2001) 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
-
23
-
-
0034672636
-
Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger
-
Lohi H., Kujala M., Kerkela E., Saarialho-Kere U., Kestila M., and Kere J. Mapping of five new putative anion transporter genes in human and characterization of SLC26A6, a candidate gene for pancreatic anion exchanger. Genomics 70 (2000) 102-112
-
(2000)
Genomics
, vol.70
, pp. 102-112
-
-
Lohi, H.1
Kujala, M.2
Kerkela, E.3
Saarialho-Kere, U.4
Kestila, M.5
Kere, J.6
-
24
-
-
0037134440
-
Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9
-
Lohi H., Kujala M., Makela S., Lehtonen E., Kestila M., Saarialho-Kere U., Markovich D., and Kere J. Functional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9. J. Biol. Chem. 277 (2002) 14246-14254
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 14246-14254
-
-
Lohi, H.1
Kujala, M.2
Makela, S.3
Lehtonen, E.4
Kestila, M.5
Saarialho-Kere, U.6
Markovich, D.7
Kere, J.8
-
25
-
-
0037369278
-
Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domains
-
Lohi H., Lamprecht G., Markovich D., Heil A., Kujala M., Seidler U., and Kere J. Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domains. Am. J. Physiol. Cell. Physiol. 284 (2003) C769-C779
-
(2003)
Am. J. Physiol. Cell. Physiol.
, vol.284
-
-
Lohi, H.1
Lamprecht, G.2
Markovich, D.3
Heil, A.4
Kujala, M.5
Seidler, U.6
Kere, J.7
-
26
-
-
0035957373
-
Reciprocal electromechanical properties of rat prestin: the motor molecule from rat outer hair cells
-
Ludwig J., Oliver D., Frank G., Klocker N., Gummer A.W., and Fakler B. Reciprocal electromechanical properties of rat prestin: the motor molecule from rat outer hair cells. Proc. Natl. Acad. Sci. U. S. A. 98 (2001) 4178-4183
-
(2001)
Proc. Natl. Acad. Sci. U. S. A.
, vol.98
, pp. 4178-4183
-
-
Ludwig, J.1
Oliver, D.2
Frank, G.3
Klocker, N.4
Gummer, A.W.5
Fakler, B.6
-
27
-
-
0344528790
-
Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea
-
Moseley R.H., Hoglund P., Wu G.D., Silberg D.G., Haila S., de la Chapelle A., Holmberg C., and Kere J. Downregulated in adenoma gene encodes a chloride transporter defective in congenital chloride diarrhea. Am. J. Physiol. 276 (1999) G185-G192
-
(1999)
Am. J. Physiol.
, vol.276
-
-
Moseley, R.H.1
Hoglund, P.2
Wu, G.D.3
Silberg, D.G.4
Haila, S.5
de la Chapelle, A.6
Holmberg, C.7
Kere, J.8
-
28
-
-
0035933514
-
Intracellular anions as the voltage sensor of prestin, the outer hair cell motor protein
-
Oliver D., He D.Z., Klocker N., Ludwig J., Schulte U., Waldegger S., Ruppersberg J.P., Dallos P., and Fakler B. Intracellular anions as the voltage sensor of prestin, the outer hair cell motor protein. Science 292 (2001) 2340-2343
-
(2001)
Science
, vol.292
, pp. 2340-2343
-
-
Oliver, D.1
He, D.Z.2
Klocker, N.3
Ludwig, J.4
Schulte, U.5
Waldegger, S.6
Ruppersberg, J.P.7
Dallos, P.8
Fakler, B.9
-
29
-
-
0037215185
-
Regulation of the apical Cl-/HCO- 3 exchanger pendrin in rat cortical collecting duct in metabolic acidosis
-
Petrovic S., Wang Z., Ma L., and Soleimani M. Regulation of the apical Cl-/HCO- 3 exchanger pendrin in rat cortical collecting duct in metabolic acidosis. Am. J. Physiol. Renal. Physiol. 284 (2003) F103-F112
-
(2003)
Am. J. Physiol. Renal. Physiol.
, vol.284
-
-
Petrovic, S.1
Wang, Z.2
Ma, L.3
Soleimani, M.4
-
31
-
-
1842607847
-
-
R Foundation for Statistical Computing, Vienna, Austria. 3-900051-07-0 URL http://www.R-project.org
-
R Development Core Team. R: a Language and Environment for Statistical Computing (2004), R Foundation for Statistical Computing, Vienna, Austria. 3-900051-07-0. http://www.R-project.org. URL http://www.R-project.org
-
(2004)
R: a Language and Environment for Statistical Computing
-
-
R Development Core Team1
-
32
-
-
0037225536
-
Prolactin regulation of the pendrin-iodide transporter in the mammary gland
-
Rillema J.A., and Hill M.A. Prolactin regulation of the pendrin-iodide transporter in the mammary gland. Am. J. Physiol. Endocrinol. Metab. 284 (2003) E25-E28
-
(2003)
Am. J. Physiol. Endocrinol. Metab.
, vol.284
-
-
Rillema, J.A.1
Hill, M.A.2
-
33
-
-
0141864361
-
Pendrin transporter carries out iodide uptake into MCF-7 human mammary cancer cells
-
Rillema J.A., and Hill M.A. Pendrin transporter carries out iodide uptake into MCF-7 human mammary cancer cells. Exp. Biol. Med. (Maywood) 228 (2003) 1078-1082
-
(2003)
Exp. Biol. Med. (Maywood)
, vol.228
, pp. 1078-1082
-
-
Rillema, J.A.1
Hill, M.A.2
-
34
-
-
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., and 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 141 (2000) 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
-
35
-
-
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., and 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. 98 (2001) 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
-
36
-
-
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., and Filetti S. Sodium/iodide symporter (NIS) and pendrin are expressed differently in hot and cold nodules of thyroid toxic multinodular goiter. Eur. J. Endocrinol. 145 (2001) 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
-
37
-
-
0033956476
-
Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange
-
Scott D.A., and Karniski L.P. Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange. Am. J. Physiol. Cell Physiol. 278 (2000) C207-C211
-
(2000)
Am. J. Physiol. Cell Physiol.
, vol.278
-
-
Scott, D.A.1
Karniski, L.P.2
-
38
-
-
0032901865
-
The Pendred syndrome gene encodes a chloride-iodide transport protein
-
Scott D.A., Wang R., Kreman T.M., Sheffield V.C., and Karniski L.P. The Pendred syndrome gene encodes a chloride-iodide transport protein. Nat. Genet. 21 (1999) 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
-
39
-
-
0029963073
-
Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification
-
Sheffield V.C., Kraiem Z., Beck J.C., Nishimura D., Stone E.M., Salameh M., Sadeh O., and Glaser B. Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification. Nat. Genet. 12 (1996) 424-426
-
(1996)
Nat. Genet.
, vol.12
, pp. 424-426
-
-
Sheffield, V.C.1
Kraiem, Z.2
Beck, J.C.3
Nishimura, D.4
Stone, E.M.5
Salameh, M.6
Sadeh, O.7
Glaser, B.8
-
41
-
-
0029917537
-
A chondrodysplasia family produced by mutations in the diastrophic dysplasia sulfate transporter gene: genotype/phenotype correlations
-
Superti-Furga A., Rossi A., Steinmann B., and Gitzelmann R. A chondrodysplasia family produced by mutations in the diastrophic dysplasia sulfate transporter gene: genotype/phenotype correlations. Am. J. Med. Genet. 63 (1996) 144-147
-
(1996)
Am. J. Med. Genet.
, vol.63
, pp. 144-147
-
-
Superti-Furga, A.1
Rossi, A.2
Steinmann, B.3
Gitzelmann, R.4
-
42
-
-
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., and Kohn L.D. Expression of PDS/Pds, the Pendred syndrome gene, in endometrium. J. Clin. Endocrinol. Metab. 87 (2002) 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
-
43
-
-
0034885192
-
The relative roles of passive surface forces and active ion transport in the modulation of airway surface liquid volume and composition
-
Tarran R., Grubb B.R., Gatzy J.T., Davis C.W., and Boucher R.C. The relative roles of passive surface forces and active ion transport in the modulation of airway surface liquid volume and composition. J. Gen. Physiol. 118 (2001) 223-236
-
(2001)
J. Gen. Physiol.
, vol.118
, pp. 223-236
-
-
Tarran, R.1
Grubb, B.R.2
Gatzy, J.T.3
Davis, C.W.4
Boucher, R.C.5
-
44
-
-
0042333487
-
Deoxycorticosterone upregulates PDS (Slc26a4) in mouse kidney: role of pendrin in mineralocorticoid-induced hypertension
-
Verlander J.W., Hassell K.A., Royaux I.E., Glapion D.M., Wang M.E., Everett L.A., Green E.D., and Wall S.M. Deoxycorticosterone upregulates PDS (Slc26a4) in mouse kidney: role of pendrin in mineralocorticoid-induced hypertension. Hypertension 42 (2003) 356-362
-
(2003)
Hypertension
, vol.42
, pp. 356-362
-
-
Verlander, J.W.1
Hassell, K.A.2
Royaux, I.E.3
Glapion, D.M.4
Wang, M.E.5
Everett, L.A.6
Green, E.D.7
Wall, S.M.8
-
45
-
-
0036436278
-
Regulation of the expression of the Cl-/anion exchanger pendrin in mouse kidney by acid-base status
-
Wagner C.A., Finberg K.E., Stehberger P.A., Lifton R.P., Giebisch G.H., Aronson P.S., and Geibel J.P. Regulation of the expression of the Cl-/anion exchanger pendrin in mouse kidney by acid-base status. Kidney Int. 62 (2002) 2109-2117
-
(2002)
Kidney Int.
, vol.62
, pp. 2109-2117
-
-
Wagner, C.A.1
Finberg, K.E.2
Stehberger, P.A.3
Lifton, R.P.4
Giebisch, G.H.5
Aronson, P.S.6
Geibel, J.P.7
-
46
-
-
0035864964
-
Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family
-
Waldegger S., Moschen I., Ramirez A., Smith R.J., Ayadi H., Lang F., and Kubisch C. Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family. Genomics 72 (2001) 43-50
-
(2001)
Genomics
, vol.72
, pp. 43-50
-
-
Waldegger, S.1
Moschen, I.2
Ramirez, A.3
Smith, R.J.4
Ayadi, H.5
Lang, F.6
Kubisch, C.7
-
47
-
-
0037216245
-
Localization of pendrin in mouse kidney
-
Wall S.M., Hassell K.A., Royaux I.E., Green E.D., Chang J.Y., Shipley G.L., and Verlander J.W. Localization of pendrin in mouse kidney. Am. J. Physiol. Renal. Physiol. 284 (2003) F229-F241
-
(2003)
Am. J. Physiol. Renal. Physiol.
, vol.284
-
-
Wall, S.M.1
Hassell, K.A.2
Royaux, I.E.3
Green, E.D.4
Chang, J.Y.5
Shipley, G.L.6
Verlander, J.W.7
-
48
-
-
9644300806
-
NaCl restriction upregulates renal Slc26a4 through subcellular redistribution: role in Cl-conservation
-
Wall S.M., Kim Y.H., Stanley L., Glapion D.M., Everett L.A., Green E.D., and Verlander J.W. NaCl restriction upregulates renal Slc26a4 through subcellular redistribution: role in Cl-conservation. Hypertension 44 (2004) 982-987
-
(2004)
Hypertension
, vol.44
, pp. 982-987
-
-
Wall, S.M.1
Kim, Y.H.2
Stanley, L.3
Glapion, D.M.4
Everett, L.A.5
Green, E.D.6
Verlander, J.W.7
-
50
-
-
0036324859
-
Pendrin is an iodide-specific apical porter responsible for iodide efflux from thyroid cells
-
Yoshida A., Taniguchi S., Hisatome I., Royaux I.E., Green E.D., Kohn L.D., and Suzuki K. Pendrin is an iodide-specific apical porter responsible for iodide efflux from thyroid cells. J. Clin. Endocrinol. Metab. 87 (2002) 3356-3361
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 3356-3361
-
-
Yoshida, A.1
Taniguchi, S.2
Hisatome, I.3
Royaux, I.E.4
Green, E.D.5
Kohn, L.D.6
Suzuki, K.7
-
51
-
-
0036713174
-
Dynamic expression of mRNAs and proteins for matrix metalloproteinases and their tissue inhibitors in the primate corpus luteum during the menstrual cycle
-
Young K.A., Hennebold J.D., and Stouffer R.L. Dynamic expression of mRNAs and proteins for matrix metalloproteinases and their tissue inhibitors in the primate corpus luteum during the menstrual cycle. Mol. Hum. Reprod. 8 (2002) 833-840
-
(2002)
Mol. Hum. Reprod.
, vol.8
, pp. 833-840
-
-
Young, K.A.1
Hennebold, J.D.2
Stouffer, R.L.3
-
52
-
-
0034636553
-
Prestin is the motor protein of cochlear outer hair cells
-
Zheng J., Shen W., He D.Z., Long K.B., Madison L.D., and Dallos P. Prestin is the motor protein of cochlear outer hair cells. Nature 405 (2000) 149-155
-
(2000)
Nature
, vol.405
, pp. 149-155
-
-
Zheng, J.1
Shen, W.2
He, D.Z.3
Long, K.B.4
Madison, L.D.5
Dallos, P.6
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