Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yavuz Köker"'
Autor:
İhsan Çetin, Leyla Cimen, Ahmet Öztürk, Behzat Çimen, Aysun Çetin, Göktug Savas, Ahmet Sen, Mustafa Yavuz Köker
Publikováno v:
Turkish Journal of Biochemistry. 43:540-548
BackgroundAlthough majority of the previous studies have shown a good correlation between enzyme linked immuno sorbent assay (ELISA) and flow cytometry in terms of cytokines, two laboratory methods usually were compared with the regression analysis a
Autor:
Edgar Selzer, Mustafa Yavuz Köker, Elisabetta Bobbioni-Harsch, Valeria Cernaro, Michele Buemi, Michael Hoffmann, Agnès Vinet, Robin P. F. Dullaart, Majed Abed, Je-Ken Chang, Kathryn Boyle, Yoshitaka Minami, Michael Willmann, Jose Antonio Amado Señarís, Juan Ybarra, Ville Kytö, Zu-Yau Lin, Christa Buechler, Reza Rahimian, Juan Sztajzel, Jasmin Amighi, Jose R. de Berrazueta, Michael Lichtenauer, Martin A. Walter, Christopher Adlbrecht, Jeroni Jurado, Alberto Cuocolo, Kou-Gi Shyu, Andrzej Wykretowicz, David Montero, Chung-Hwan Chen, Pekka Saukko, Wen-Ping Cheng, Mamoru Satoh, Farouk Mookadam, Pedram Ghafourifar, Florian Lang, Karl Winkler, Przemysław Guzik, Emanuele Nicolai, Richard Pacher, Hendrik Jan Ankersmit
Publikováno v:
European Journal of Clinical Investigation. 41:1149-1163
Autor:
M de Boer, Ahmet Metin, Ozden Sanal, Ilhan Tezcan, Dirk Roos, Tuba Turul Ozgur, K. van Leeuwen, Mustafa Yavuz Köker, Fatih Celmeli
Publikováno v:
European journal of clinical investigation, 39(4), 311-319. Wiley-Blackwell
Background One of the rarest forms of autosomal recessive chronic granulomatous disease (AR-CGD) is attributable to mutations in the CYBA gene, which encodes the alpha polypeptide of cytochrome b558, (also known as p22-phox), a key transmembrane prot
Background Despite major advances in the management of newborn infants, neonatal sepsis (NS) remain important causes of neonatal morbidity and mortality in the newborn, mainly among preterm and low birth weight infants. Objective: The aim of this stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ceda4dc5c3b90fd52338b71fedaa62b5
https://avesis.erciyes.edu.tr/publication/details/3d3b44c9-5956-43f4-a3f9-011bc5c212f0/oai
https://avesis.erciyes.edu.tr/publication/details/3d3b44c9-5956-43f4-a3f9-011bc5c212f0/oai
Autor:
Ozden Sanal, K. van Leeuwen, Mustafa Yavuz Köker, Tuba Turul Ozgur, Ahmet Metin, Ilhan Tezcan, Dirk Roos, M de Boer, Turkan Patiroglu
Publikováno v:
European journal of clinical investigation, 39(10), 942-951. Wiley-Blackwell
Background One of the rarest forms of autosomal recessive chronic granulomatous disease (AR-CGD) is attributable to mutations in the NCF2 gene, which encodes the polypeptide p67phox, a key cytoplasmic protein in the phagocyte NADPH oxidase system. NC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef07234197ba10517fa89fc3e4d34a8c
https://avesis.erciyes.edu.tr/publication/details/c2b7bb86-c148-4137-aaaa-a88c6f5ba9e9/oai
https://avesis.erciyes.edu.tr/publication/details/c2b7bb86-c148-4137-aaaa-a88c6f5ba9e9/oai
Publikováno v:
European journal of clinical investigation, 37(7), 589-595. Wiley-Blackwell
Background Chronic granulomatous disease (CGD) is an inherited disorder of the innate immune system characterized by impairment of intracellular microbicidal activity of phagocytes. Mutations in one of four known NADPH-oxidase components preclude gen
Autor:
Cagman Tan, M de Boer, Mustafa Yavuz Köker, Ilhan Tezcan, Dirk Roos, Ahmet Metin, Fügen Ersoy, Ozden Sanal
Publikováno v:
European journal of clinical investigation, 36(4), 257-264. Wiley-Blackwell
Background Chronic granulomatous disease (CGD) is an inherited disorder of the innate immune system characterized by impairment of intracellular microbicidal activity of phagocytes. Mutations in one of the four known NADPH-oxidase components preclude