Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Israel, Zelikovic"'
Publikováno v:
Cellular Physiology and Biochemistry, Vol 33, Iss 3, Pp 605-620 (2014)
Background: Molecular dynamics (MD) simulations provide valuable information on the conformational changes that accompany time-dependent motions in proteins. The reported crystal structure of rat prestin (PDB 3LLO) is remarkable for an α1-α2 inter-
Externí odkaz:
https://doaj.org/article/1dbab14c22b947d992539ab80c1304a9
Autor:
Julia Rozenfeld, Osnat Tal, Orly Kladnitsky, Lior Adler, Edna Efrati, Stephen L. Carrithers, Seth L. Alper, Israel Zelikovic
Publikováno v:
Cellular Physiology and Biochemistry, Vol 32, Iss 1, Pp 221-237 (2013)
Guanylin (GN) and uroguanylin (UGN) are low-molecular-weight peptide hormones produced mainly in the intestinal mucosa in response to oral salt load. GN and UGN (guanylin peptides) induce secretion of electrolytes and water in both intestine and kidn
Externí odkaz:
https://doaj.org/article/bd148e1e341a49558d196f2ac8034a97
Autor:
Israel Zelikovic, Aude Servais
Publikováno v:
Pediatric Nephrology ISBN: 9783642278433
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d2a05b8f3ca129670d55440c318ef83
https://doi.org/10.1007/978-3-030-52719-8_33
https://doi.org/10.1007/978-3-030-52719-8_33
Autor:
Israel Eisenstein, Shirley Pollack, Amir Hadash, Danny Eytan, Ori Attias, Michael Halberthal, Josef Ben-Ari, Gad Bar-Joseph, Israel Zelikovic, Hanna Mandel, Galit Tal, Daniella Magen
Publikováno v:
Pediatric nephrology (Berlin, Germany). 37(11)
Inborn errors of metabolism (IEM), including organic acidemias and urea cycle defects, are characterized by systemic accumulation of toxic metabolites with deleterious effect on the developing brain. While hemodialysis (HD) is most efficient in clear
Autor:
Russell W. Chesney, Israel Zelikovic
Publikováno v:
Absorption and Utilization of Amino Acids ISBN: 9780429487514
Absorption and Utilization of Amino Acids
Absorption and Utilization of Amino Acids
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96b73d702bd4cd56b2dfd5d8133724ad
https://doi.org/10.1201/9780429487514-10
https://doi.org/10.1201/9780429487514-10
Autor:
Sharon P. Andreoli, Timur Azhibekov, Carlton Bates, Michel Baum, Stephen Baumgart, Marie H. Beall, Martine TP Besouw, Richard D. Bland, Detlef Bockenhauer, Melvin Bonilla-Felix, Debora Malta Cerqueira, Andrew Thomas Costarino, Nilka de Jesús-González, Joseph Flynn, Jyothsna Gattineni, Jean-Bernard Gouyon, Jean-Pierre Guignard, Jacqueline Ho, Lucky Jain, Pedro A. Jose, Sarah D. Keene, Myda Khalid, Yosef Levenbrown, Douglas G. Matsell, Ran Namgung, Aruna Natarajan, William Oh, Pawan Puri, Raymond Quigley, Michael G. Ross, Jeffrey Segar, Istvan Seri, Reginald C. Tsang, Jeroen P.H.M. van den Wijngaard, Martin van Gemert, Van Anthony M. Villar, Matthias Tilmann Wolf, Israel Zelikovic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d2f9b35fa1cd66cc8fe8fc3a8a8c10f
https://doi.org/10.1016/b978-0-323-53367-6.00025-x
https://doi.org/10.1016/b978-0-323-53367-6.00025-x
Publikováno v:
Biochemistry and Biophysics Reports
Mutations in the human SLC26A4/Pendrin polypeptide (hPDS) cause Pendred Syndrome /DFNB4, syndromic deafness with enlargement of the vestibular aqueduct and low-penetrance goiter. Here we present data on cloning, protein overexpression and purificatio
Publikováno v:
The Role of Pendrin in Health and Disease ISBN: 9783319432854
The SLC26A4 gene’s 21 exons on chromosome 7q31.1 encode the pendrin (SLC26A4) Cl−/anion exchanger. SLC26A4 is highly expressed in the epithelial cells of kidney, thyroid, inner ear and airways, in which the pendrin polypeptide is essential for no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe5482abe5c029b89529568f52ff6a74
https://doi.org/10.1007/978-3-319-43287-8_10
https://doi.org/10.1007/978-3-319-43287-8_10
Publikováno v:
Experimental Physiology. 100:79-94
New Findings What is the central question of this study? In the kidney, the bulk of the filtered Mg2+ is reabsorbed in the thick ascending limb by paracellular conductance, mediated by the tight junction protein, claudin-16, which is encoded by the g
Autor:
Israel Zelikovic, Seth L. Alper, Edna Efrati, Orly Kladnitsky, Stephen L. Carrithers, Julia Rozenfeld, Osnat Tal, Lior Adler
Publikováno v:
American Journal of Physiology-Renal Physiology. 302:F614-F624
The pendrin/SLC26A4 Cl−/HCO3− exchanger, encoded by the PDS gene, is expressed in cortical collecting duct (CCD) non-A intercalated cells. Pendrin is essential for CCD bicarbonate secretion and is also involved in NaCl balance and blood pressure