Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Lorraine A. Everett"'
Autor:
Truyen D. Pham, Vladimir Pech, Lorraine A. Everett, Alan M. Weinstein, Young-Hee Kim, Susan M. Wall
Publikováno v:
American Journal of Physiology-Renal Physiology. 292:F914-F920
Pendrin ( Slc26a4) localizes to type B and non-A, non-B intercalated cells in the distal convoluted tubule, the connecting tubule, and the cortical collecting duct (CCD), where it mediates apical Cl−/HCO3−exchange. The purpose of this study was t
Autor:
Young-Hee Kim, Susan M. Wall, William H. Beierwaltes, Eric D. Green, Truyen D. Pham, Lorraine A. Everett, Kathryn A. Hassell, Jill W. Verlander, Wonkyong Shin, Sharon W. Matthews
Publikováno v:
American Journal of Physiology-Renal Physiology. 291:F833-F839
Pendrin, encoded by Slc26a4, is a Cl−/HCO3−exchanger expressed in the apical region of type B and non-A, non-B intercalated cells, which regulates renal NaCl excretion. Dietary Cl−restriction upregulates total pendrin protein expression. Whethe
Autor:
Kathryn A. Hassell, Susan M. Wall, Ines E. Royaux, Eric D. Green, Lorraine A. Everett, Mou-Er Wang, Jill W. Verlander, Dawn M. Glapion
Publikováno v:
Hypertension. 42:356-362
Pendrin is an anion exchanger expressed along the apical plasma membrane and apical cytoplasmic vesicles of type B and of non-A, non-B intercalated cells of the distal convoluted tubule, connecting tubule, and cortical collecting duct. Thus, Pds ( Sl
Autor:
Tong Wang, Peter S. Aronson, Gerhard Giebisch, Lawrence P. Karniski, Eric D. Green, Lorraine A. Everett
Publikováno v:
American Journal of Physiology-Renal Physiology. 283:F952-F956
A significant fraction of active chloride reabsorption across the apical membrane of the proximal tubule is mediated by a chloride/formate exchange process, whereby intracellular formate drives the transport of chloride into the cell. When chloride/f
Autor:
Eric D. Green, Mark A. Knepper, Koichi Suzuki, Lorraine A. Everett, Susan M. Wall, Lawrence P. Karniski, Ines E. Royaux
Publikováno v:
Proceedings of the National Academy of Sciences. 98:4221-4226
Pendrin is an anion transporter encoded by the PDS / Pds gene. In humans, mutations in PDS cause the genetic disorder Pendred syndrome, which is associated with deafness and goiter. Previous studies have shown that this gene has a relatively restrict
Autor:
S. Srisailapathy, Arabandi Ramesh, N.L. Dietrich, Eric D. Green, Agnete Parving, Carrie Ris-Stalpers, Lorraine A. Everett, C.H.H.M. Bolder, P. van Hauwe, M.L. Kraft, Barto J. Otten, G. Van Camp, Daryl A. Scott, C.W.R.J. Cremers, J. J. M. De Vijlder, Paul Coucke, P.H.G.M. Willems, Richard J.H. Smith
Publikováno v:
Human Molecular Genetics, 7, pp. 1099-1104
Human molecular genetics
Human molecular genetics, 7(7), 1099-1104. Oxford University Press
Human Molecular Genetics, 7, 1099-1104
Human molecular genetics
Human molecular genetics, 7(7), 1099-1104. Oxford University Press
Human Molecular Genetics, 7, 1099-1104
Pendred syndrome is an autosomal recessive disorder characterized by early childhood deafness and goiter. A century after its recognition as a syndrome by Vaughan Pendred, the disease gene ( PDS ) was mapped to chromosome 7q22-q31.1 and, recently, fo
Autor:
Lorraine A. Everett
Publikováno v:
Epithelial Anion Transport in Health and Disease: The Role of the SLC26 Transporters Family: Novartis Foundation Symposium 273
For over 100 years after the first description of the disorder, the molecular pathology underlying the deafness and thyroid pathology in Pendred syndrome (PS) remained unknown. In 1997, early progress towards understanding the molecular basis of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5819e59a35bb2b2c5ff3917300d29d6
https://doi.org/10.1002/0470029579.ch14
https://doi.org/10.1002/0470029579.ch14
Reduced ENaC protein abundance contributes to the lower blood pressure observed in pendrin-null mice
Autor:
Jill W. Verlander, Vladimir Pech, Susan M. Wall, Eric D. Green, Lorraine A. Everett, Roy L. Sutliff, William H. Beierwaltes, Kathryn B. Spencer, Wonkyong Shin, Young-Hee Kim
Publikováno v:
American journal of physiology. Renal physiology. 293(4)
Pendrin (encoded by Pds, Slc26a4) is a Cl−/HCO3−exchanger expressed in the apical regions of type B and non-A, non-B intercalated cells of kidney and mediates renal Cl−absorption, particularly when upregulated. Aldosterone increases blood press
Autor:
Wonkyong Shin, Kathryn B. Spencer, Young-Hee Kim, Vladimir Pech, Eric D. Green, Susan M. Wall, Lorraine A Everett, William H. Beierwaltes, Roy L. Sutliff
Publikováno v:
The FASEB Journal. 21
Autor:
Lorraine A, Everett
Publikováno v:
Novartis Foundation symposium. 273
For over 100 years after the first description of the disorder, the molecular pathology underlying the deafness and thyroid pathology in Pendred syndrome (PS) remained unknown. In 1997, early progress towards understanding the molecular basis of the