Zobrazeno 1 - 10
of 120
pro vyhledávání: '"E. Sadowski"'
Autor:
Shazia Ashraf, Hiroki Kudo, Jia Rao, Atsuo Kikuchi, Eugen Widmeier, Jennifer A. Lawson, Weizhen Tan, Tobias Hermle, Jillian K. Warejko, Shirlee Shril, Merlin Airik, Tilman Jobst-Schwan, Svjetlana Lovric, Daniela A. Braun, Heon Yung Gee, David Schapiro, Amar J. Majmundar, Carolin E. Sadowski, Werner L. Pabst, Ankana Daga, Amelie T. van der Ven, Johanna M. Schmidt, Boon Chuan Low, Anjali Bansal Gupta, Brajendra K. Tripathi, Jenny Wong, Kirk Campbell, Kay Metcalfe, Denny Schanze, Tetsuya Niihori, Hiroshi Kaito, Kandai Nozu, Hiroyasu Tsukaguchi, Ryojiro Tanaka, Kiyoshi Hamahira, Yasuko Kobayashi, Takumi Takizawa, Ryo Funayama, Keiko Nakayama, Yoko Aoki, Naonori Kumagai, Kazumoto Iijima, Henry Fehrenbach, Jameela A. Kari, Sherif El Desoky, Sawsan Jalalah, Radovan Bogdanovic, Nataša Stajić, Hildegard Zappel, Assel Rakhmetova, Sharon-Rose Wassmer, Therese Jungraithmayr, Juergen Strehlau, Aravind Selvin Kumar, Arvind Bagga, Neveen A. Soliman, Shrikant M. Mane, Lewis Kaufman, Douglas R. Lowy, Mohamad A. Jairajpuri, Richard P. Lifton, York Pei, Martin Zenker, Shigeo Kure, Friedhelm Hildebrandt
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-14 (2018)
Nephrotic syndrome is the second most common chronic kidney disease but there are no targeted treatment strategies available. Here the authors identify mutations of six genes codifying for proteins involved in cytoskeleton remodelling and modulation
Externí odkaz:
https://doaj.org/article/5fa7365ce28f4895a98f2773a190db3e
Akademický článek
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Autor:
Heon Yung Gee, Carolin E. Sadowski, Pardeep K. Aggarwal, Jonathan D. Porath, Toma A. Yakulov, Markus Schueler, Svjetlana Lovric, Shazia Ashraf, Daniela A. Braun, Jan Halbritter, Humphrey Fang, Rannar Airik, Virginia Vega-Warner, Kyeong Jee Cho, Timothy A. Chan, Luc G. T. Morris, Charles ffrench-Constant, Nicholas Allen, Helen McNeill, Rainer Büscher, Henriette Kyrieleis, Michael Wallot, Ariana Gaspert, Thomas Kistler, David V. Milford, Moin A. Saleem, Wee Teik Keng, Stephen I. Alexander, Rudolph P. Valentini, Christoph Licht, Jun C. Teh, Radovan Bogdanovic, Ania Koziell, Agnieszka Bierzynska, Neveen A. Soliman, Edgar A. Otto, Richard P. Lifton, Lawrence B. Holzman, Nicholas E. S. Sibinga, Gerd Walz, Alda Tufro, Friedhelm Hildebrandt
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-11 (2016)
Steroid-sensitive nephrotic syndrome (SRNS) can cause CKD and necessitate kidney transplant. Here the authors identify FAT1 mutations by homozygosity mapping and whole-exome sequencing in families with SRNS and provide functional mouse and zebrafish
Externí odkaz:
https://doaj.org/article/28d36207928640028a9a892d5c32fd4f
Akademický článek
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Autor:
E. Sadowski, S. Szydlowski
Publikováno v:
Clinical Social Work and Health Intervention. 10:59-63
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::184d78a49d8c43d482b3426c3d011704
https://doi.org/10.22359/cswhi_10_1_09
https://doi.org/10.22359/cswhi_10_1_09
Autor:
E. Fourniols, Alexandra Aubry, Crioac Pitié-Salpêtrière, F. Devriese, E Sadowski, E. Lafeuille, S. Jauréguiberry
Publikováno v:
Médecine et Maladies Infectieuses
Médecine et Maladies Infectieuses, Elsevier Masson, 2020, ⟨10.1016/j.medmal.2020.09.010⟩
Médecine et Maladies Infectieuses, Elsevier Masson, 2020, ⟨10.1016/j.medmal.2020.09.010⟩
Objective Conventional microbiological methods (CMM), including long-term culture, for the diagnosis of osteo-articular infections (OAI) fail in at least 5% of all cases. Only one IOA dedicated molecular method has been commercialized, and only the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6947e0e9225477b7a378f18c508f5b37
https://hal.archives-ouvertes.fr/hal-03125202
https://hal.archives-ouvertes.fr/hal-03125202
Autor:
Frank E. Sadowski
Publikováno v:
Serials Librarianship in Transition ISBN: 9780367816674
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d8ae771753bc7ae3661fb38ee215510
https://doi.org/10.4324/9780367816674-12
https://doi.org/10.4324/9780367816674-12
Akademický článek
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Autor:
Heon Yung Gee, Richard P. Lifton, Aytül Noyan, Stefan Kohl, Weizhen Tan, Michael A. J. Ferguson, Neveen A. Soliman, Deborah R. Stein, Jing Chen, Svjetlana Lovric, J. Magdalena Schmidt, Jameela A. Kari, Avram Z. Traum, Jia Rao, Gil Chernin, Sherif El Desoky, Radovan Bogdanovic, Nadine Benador, Werner L. Pabst, Hanan M. Fathy, Jeffrey B. Kopp, Jillian K. Warejko, Asaf Vivante, Henry Fehrenbach, Detlef Bockenhauer, Carolin E. Sadowski, Velibor Tasic, Robert B. Ettenger, Amelie T. van der Ven, Shrikant Mane, Ankana Daga, Jeffrey Hopcian, Martin Zenker, Markus J. Kemper, Amar J. Majmundar, Erkin Serdaroglu, Ronen Schneider, Fatih Ozaltin, Ghaleb Daouk, Natasa Stajic, Nancy Rodig, Jennifer A. Lawson, Reyner Loza Munarriz, Melissa A. Cadnapaphornchai, Hadas Ityel, Shazia Ashraf, Rainer Büscher, Dominik N. Müller, Makiko Nakayama, Michelle A. Baum, Seema Hashmi, Ludmila Podracka, David Schapiro, Daniela A. Braun, Shirlee Shril, Michael J. Somers, Eugen Widmeier, Tilman Jobst-Schwan, Friedhelm Hildebrandt, Sevcan A. Bakkaloglu, Tobias Hermle
Publikováno v:
Clinical Journal of the American Society of Nephrology. 13:53-62
Background and objectives Steroid-resistant nephrotic syndrome overwhelmingly progresses to ESRD. More than 30 monogenic genes have been identified to cause steroid-resistant nephrotic syndrome. We previously detected causative mutations using target
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d15411e30c773cf5cd62db0ecbe78cbb
https://doi.org/10.2215/cjn.04120417
https://doi.org/10.2215/cjn.04120417
Publikováno v:
Gynecologic Oncology. 159:104-105
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aba2d7ea0514a6f559c1f205595af6a9
https://doi.org/10.1016/j.ygyno.2020.05.105
https://doi.org/10.1016/j.ygyno.2020.05.105