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Results: 1-8 |
Results: 8
Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome
Authors: Everett, LA Belyantseva, IA Noben-Trauth, K Cantos, R Chen, A Thakkar, SI Hoogstraten-Miller, SL Kachar, B Wu, DK Green, ED
Citation: La. Everett et al., Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome, HUM MOL GEN, 10(2), 2001, pp. 153-161
Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion
Authors: Royaux, IE Wall, SM Karniski, LP Everett, LA Suzuki, K Knepper, MA Green, ED
Citation: Ie. Royaux et al., Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion, P NAS US, 98(7), 2001, pp. 4221-4226
The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4
Authors: Wilcox, ER Everett, LA Li, XYC Lalwani, AK Green, ED
Citation: Er. Wilcox et al., The PDS gene, Pendred syndrome and non-syndromic deafness DFNB4, ADV OTO-RH, 56, 2000, pp. 145-151
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
Authors: Royaux, IE Suzuki, K Mori, A Katoh, R Everett, LA Kohn, LD Green, ED
Citation: Ie. Royaux et al., 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, ENDOCRINOL, 141(2), 2000, pp. 839-845
A family of mammalian anion transporters and their involvement in human genetic diseases
Authors: Everett, LA Green, ED
Citation: La. Everett et Ed. Green, A family of mammalian anion transporters and their involvement in human genetic diseases, HUM MOL GEN, 8(10), 1999, pp. 1883-1891
Exploring a hydrological concept through children's drawings
Authors: Dove, JE Everett, LA Preece, PFW
Citation: Je. Dove et al., Exploring a hydrological concept through children's drawings, INT J SCI E, 21(5), 1999, pp. 485-497
Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear
Authors: Everett, LA Morsli, H Wu, DK Green, ED
Citation: La. Everett et al., Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear, P NAS US, 96(17), 1999, pp. 9727-9732
Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome
Authors: Coucke, PJ Van Hauwe, P Everett, LA Demirhan, O Kabakkaya, Y Dietrich, NL Smith, RJH Coyle, E Reardon, W Trembath, R Willems, PJ Green, ED Van Camp, G
Citation: Pj. Coucke et al., Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome, J MED GENET, 36(6), 1999, pp. 475-477
Risultati: 1-8 |