Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yavuz Köker"'
Autor:
Deniz Cagdas, Halil Tuna Akar, Karin van Leeuwen, Cagman Tan, Ilhan Tezcan, Yavuz Köker, Saliha Esenboga, Dirk Roos, Begum Ozbek, Sevil Oskay Halacli, Martin de Boer
Publikováno v:
Journal of clinical immunology, 41(5), 992-1003. Springer New York
Background: Chronic granulomatous disease (CGD), one of the phagocytic system defects, is the primary immunodeficiency caused by dysfunction of the NADPH oxidase complex which generates reactive oxygen species (ROS), which are essential for killing p
Autor:
Amber Begtrup, Mohammad Shahrooei, Deniz Cagdas, Douglas B. Kuhns, Juan Luis Valdivieso Shephard, Nezihe Köker, Joachim Roesler, Amy P. Hsu, Marie José Stasia, Antonio Condino-Neto, Harry L. Malech, Jacinta Bustamante, Esmaeil Mortaz, Ilhan Tezcan, Pandiarajan Vignesh, Baruch Wolach, Dirk Roos, María Bravo García-Morato, Marianne Antonius Jakobsen, Steven M. Holland, Roya Sherkat, Rhonda Brandon, Hirokazu Kanegane, Mauno Vihinen, Faris G. Bakri, Lizbeth Blancas-Galicia, Abbas Fayezi, Amit Rawat, Karin van Leeuwen, John I. Gallin, Toshinao Kawai, M. Yavuz Köker, Christa S. Zerbe, Martin de Boer, Manesha Madkaikar, Debra A. Long Priel
Publikováno v:
Roos, D, van Leeuwen, K, Hsu, A P, Priel, D L, Begtrup, A, Brandon, R, Rawat, A, Vignesh, P, Madkaikar, M, Stasia, M J, Bakri, F G, de Boer, M, Roesler, J, Köker, N, Köker, M Y, Jakobsen, M, Bustamante, J, Garcia-Morato, M B, Shephard, J L V, Cagdas, D, Tezcan, I, Sherkat, R, Mortaz, E, Fayezi, A, Shahrooei, M, Wolach, B, Blancas-Galicia, L, Kanegane, H, Kawai, T, Condino-Neto, A, Vihinen, M, Zerbe, C S, Holland, S M, Malech, H L, Gallin, J I & Kuhns, D B 2021, ' Hematologically important mutations : The autosomal forms of chronic granulomatous disease (third update) ', Blood Cells, Molecules and Diseases, vol. 92, 102596 . https://doi.org/10.1016/j.bcmd.2021.102596
Blood Cells, Molecules and Diseases
Blood Cells, Molecules and Diseases, 2021, 92, pp.102596. ⟨10.1016/j.bcmd.2021.102596⟩
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Blood Cells, Molecules and Diseases, Elsevier, 2021, 92, pp.102596. ⟨10.1016/j.bcmd.2021.102596⟩
Blood cells, molecules & diseases, 92:102596. Academic Press Inc.
Blood Cells, Molecules and Diseases
Blood Cells, Molecules and Diseases, 2021, 92, pp.102596. ⟨10.1016/j.bcmd.2021.102596⟩
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Blood Cells, Molecules and Diseases, Elsevier, 2021, 92, pp.102596. ⟨10.1016/j.bcmd.2021.102596⟩
Blood cells, molecules & diseases, 92:102596. Academic Press Inc.
Chronic granulomatous disease (CGD) is an immunodeficiency disorder affecting about 1 in 250,000 individuals. CGD patients suffer from severe, recurrent bacterial and fungal infections. The disease is caused by mutations in the genes encoding the com
Autor:
Dirk Roos, Karin van Leeuwen, Amy P. Hsu, Debra Long Priel, Amber Begtrup, Rhonda Brandon, Marie José Stasia, Faris Ghalib Bakri, Nezihe Köker, M. Yavuz Köker, Manisha Madkaika, Martin de Boer, Maria Bravo Garcia-Morato, Juan Luis Valdivieso Shephard, Joachim Roesler, Hirokazu Kanegane, Toshinao Kawai, Gigliola Di Matteo, Mohammad Shahrooei, Jacinta Bustamante, Amit Rawat, Pandiarajan Vignesh, Esmaeil Mortaz, Abbas Fayezi, Deniz Cagdas, Ilhan Tezcan, Maleewan Kitcharoensakkul, Mary C. Dinauer, Isabelle Meyts, Baruch Wolach, Antonio Condino-Neto, Christa S. Zerbe, Steven M. Holland, Harry L. Malech, John I. Gallin, Douglas B. Kuhns
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Blood Cells, Molecules and Diseases
Blood Cells, Molecules and Diseases, Elsevier, 2021, 90, pp.102587. ⟨10.1016/j.bcmd.2021.102587⟩
Blood cells, molecules & diseases, 90:102587. Academic Press Inc.
Blood Cells, Molecules and Diseases, 2021, 90, pp.102587. ⟨10.1016/j.bcmd.2021.102587⟩
Universidade de São Paulo (USP)
instacron:USP
Blood Cells, Molecules and Diseases
Blood Cells, Molecules and Diseases, Elsevier, 2021, 90, pp.102587. ⟨10.1016/j.bcmd.2021.102587⟩
Blood cells, molecules & diseases, 90:102587. Academic Press Inc.
Blood Cells, Molecules and Diseases, 2021, 90, pp.102587. ⟨10.1016/j.bcmd.2021.102587⟩
International audience; Chronic granulomatous disease (CGD) is an immunodeficiency disorder affecting about 1 in 250,000 individuals. CGD patients suffer from severe bacterial and fungal infections. The disease is caused by a lack of superoxide produ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e3250be50520e2ec9033c351c42615b
Autor:
Şeyhan Kutluğ, Asuman Birinci, Mustafa Yavuz Köker, Gulnar Sensoy, Alişan Yιldιran, Berkay Saraymen
Publikováno v:
Asian Pacific Journal of Allergy and Immunology.
Background Chronic granulomatous disease (CGD) is a rare primary immunodeficiency caused by defects in the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase enzyme system. This disease causes the disordered functioning of phagocytic cells.
Autor:
Selma Gokahmetoglu, Leylagül Kaynar, Esra Ermiş Turak, Serdar Sivgin, Musa Solmaz, Yavuz Köker, Mustafa Cetin, Koray Demir, Ali Ünal, Zeynep Burçin Gönen, Çiğdem Pala Öztürk, Gokmen Zararsiz, Bulent Eser
The use of αβ+ T-cell-depleted grafts is a novel approach to prevent graft failure, graft-versus-host disease (GVHD), and non-relapse mortality (NRM) in patients undergoing haploidentical hematopoietic stem cell transplantation.Thirty-four patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::296b010251cffd24f20f03ce2243c2d4
https://avesis.erciyes.edu.tr/publication/details/0ed44074-fb27-4783-90c2-471db67896c4/oai
https://avesis.erciyes.edu.tr/publication/details/0ed44074-fb27-4783-90c2-471db67896c4/oai
Publikováno v:
Dicle Medical Journal, Vol 43, Iss 1, Pp 33-38 (2016)
Objective: Determination the expression of P-glycoprotein is especially problematic for normal tissues because immunological methods are limited in terms of sensitivity. We aimed to determine the expression of P-glycoprotein and CD34 by flow cytometr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff8660e5f54cafec868e312b1f1f4d8a
https://avesis.erciyes.edu.tr/publication/details/a3e9981f-694c-4d62-b54b-0509b14899ec/oai
https://avesis.erciyes.edu.tr/publication/details/a3e9981f-694c-4d62-b54b-0509b14899ec/oai
Autor:
Irina Kondratenko, Baruch Wolach, Harry L. Malech, Jianxin He, John I. Gallin, László Maródi, Tadej Avcin, Anne Maddalena, Martin de Boer, Gigliola Di Matteo, Douglas B. Kuhns, Karin van Leeuwen, Dirk Roos, Steven M. Holland, Caroline Kannengiesser, Anna Maria Ventura, Marie José Stasia, Jacinta Bustamante, Juan Álvaro López, Joachim Roesler, Antonio Condino-Neto, Harry R. Hill, Tadashi Ariga, Carl T. Witwer, M. Yavuz Köker, Hiroyuki Nunoi
Publikováno v:
Blood Cells, Molecules and Diseases
Blood Cells, Molecules and Diseases, Elsevier, 2010, 45 (3), pp.246-65. ⟨10.1016/j.bcmd.2010.07.012⟩
Blood cells, molecules & diseases, 45(3), 246-265. Academic Press Inc.
Blood Cells, Molecules and Diseases, Elsevier, 2010, 45 (3), pp.246-65. ⟨10.1016/j.bcmd.2010.07.012⟩
Blood cells, molecules & diseases, 45(3), 246-265. Academic Press Inc.
Chronic granulomatous disease (CGD) is an immunodeficiency disorder affecting about 1 in 250,000 individuals. The disease is caused by a lack of superoxide production by the leukocyte enzyme NADPH oxidase. Superoxide is used to kill phagocytosed micr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd5d09d723f3a34e8f7c7ff3605815e1