Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Yuya Sugano"'
Autor:
Viktoria Fisi, Agnieszka Wengi, Dominique Loffing-Cueni, Robert A. Fenton, Marta Mariniello, James A. McCormick, Sandra Moser, Yuya Sugano, Johannes Loffing, Lena Lindtoft Rosenbaek
Publikováno v:
Moser, S, Sugano, Y, Wengi, A, Fisi, V, Lindtoft Rosenbaek, L, Mariniello, M, Loffing-Cueni, D, McCormick, J A, Fenton, R A & Loffing, J 2021, ' A five amino acids deletion in NKCC2 of C57BL/6 mice affects analysis of NKCC2 phosphorylation but does not impact kidney function ', Acta Physiologica
, vol. 233, no. 1, e13705 . https://doi.org/10.1111/apha.13705
Acta Physiologica (Oxford, England)
, vol. 233, no. 1, e13705 . https://doi.org/10.1111/apha.13705
Acta Physiologica (Oxford, England)
Aim: The phosphorylation level of the furosemide-sensitive Na +-K +-2Cl − cotransporter (NKCC2) in the thick ascending limb (TAL) is used as a surrogate marker for NKCC2 activation and TAL function. However, in mice, analyses of NKCC2 phosphorylati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96c42f9acd9ff97476045a353660fa8e
https://pure.au.dk/portal/da/publications/a-five-amino-acids-deletion-in-nkcc2-of-c57bl6-mice-affects-analysis-of-nkcc2-phosphorylation-but-does-not-impact-kidney-function(3db88d28-8d8c-4c74-967b-c92ddbc167bb).html
https://pure.au.dk/portal/da/publications/a-five-amino-acids-deletion-in-nkcc2-of-c57bl6-mice-affects-analysis-of-nkcc2-phosphorylation-but-does-not-impact-kidney-function(3db88d28-8d8c-4c74-967b-c92ddbc167bb).html
Autor:
Magdalena Cardenas-Rodriguez, Elisa Molinari, Yuya Sugano, Iain A. Drummond, Ruxandra Bachmann-Gagescu, John A. Sayer, Judith G.M. Bergboer, Christina Austin-Tse
Publikováno v:
Journal of Cell Science
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Mutations in CEP290 (also known as NPHP6), a large multidomain coiled coil protein, are associated with multiple cilia-associated syndromes. Over 130 CEP290 mutations have been linked to a wide spectrum of human ciliopathies, raising the question of
Publikováno v:
Zebrafish. 17:153-155
Reactive oxygen species (ROS) are important regulators of intracellular signaling pathways in health and disease. It is implicated that ROS may play critical roles in pathogenesis of a number of kidney diseases including diabetic nephropathy. However
Publikováno v:
Zebrafish
Reactive oxygen species (ROS) are important regulators of intracellular signaling pathways in health and disease. It is implicated that ROS may play critical roles in pathogenesis of a number of kidney diseases including diabetic nephropathy. However
Autor:
Cardenas-Rodriguez, Magdalena, Austin-Tse, Christina, Bergboer, Judith G. M., Molinari, Elisa, Yuya Sugano, Bachmann-Gagescu, Ruxandra, Sayer, John A., Drummond, Iain A.
Publikováno v:
Journal of Cell Science; Jul2021, Vol. 134 Issue 14, p1-13, 13p
Autor:
Johannes Loffing, Dominique Loffing-Cueni, Chiara Cianciolo Cosentino, Yuya Sugano, Stephan C.F. Neuhauss
Understanding the molecular basis of the complex regulatory networks controlling renal ion transports is of major physiological and clinical importance. In this study, we aimed to identify evolutionarily conserved critical players in the function of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6713f11ed35a75821f24da2e92a0fe19
https://www.zora.uzh.ch/id/eprint/139007/
https://www.zora.uzh.ch/id/eprint/139007/
Autor:
Yuya Sugano, Stephan C.F. Neuhauss
Publikováno v:
General and comparative endocrinology
The zebrafish is a powerful genetic model organism. In recent years, zebrafish has been increasingly used to model human diseases. Due to a number of recent technological advancements, the genetic tool box is now also stocked with sophisticated trans
Autor:
Stephan Segerer, Stephan C.F. Neuhauss, Johannes Loffing, Maja T. Lindenmeyer, Clemens D. Cohen, Urs Ziegler, Yuya Sugano, Ines Auberger
Publikováno v:
Kidney International
Podocyte dysfunction impairs the size selectivity of the glomerular filter, leading to proteinuria, hypoalbuminuria, and edema, clinically defined as nephrotic syndrome. Hereditary forms of nephrotic syndrome are linked to mutations in podocyte-speci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae67d5f659a8710f06c558883007ed1e
https://doi.org/10.5167/uzh-115850
https://doi.org/10.5167/uzh-115850
Autor:
Christian Thiel, Andreas Giessl, Steffen Uebe, Kristin Kessler, Heinrich Sticht, Helmuth-Günther Dörr, Arif B. Ekici, Holger Blessing, Stephan C.F. Neuhauss, Yuya Sugano, Diana Zahnleiter, André Reis, Nadine N. Hauer
Numerous genes are involved in human growth regulation. Recently, autosomal-recessive inherited variants in centrosomal proteins have been identified in Seckel syndrome, primary microcephaly, or microcephalic osteodysplastic primary dwarfism. Common
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::762649a0e12c4edc2e2b2509a398a446
https://www.zora.uzh.ch/id/eprint/104947/
https://www.zora.uzh.ch/id/eprint/104947/
Autor:
Yuya Sugano, Ines Auberger, Maja T. Lindenmeyer, Johannes Loffing, Stephan C.F. Neuhauss, Urs Ziegler, Stephan Segerer, Clemens D. Cohen
Publikováno v:
Kidney International