Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yavuz Köker"'
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
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