Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Yavuz Köker"'
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 8, Iss 1 (2009)
Mutations in any of four known NADPH-oxidase components lead to CGD. X-linked CGD (X-CGD) is caused by defects in CYBB, the gene that encodes gp91-phox. Autosomal recessive (AR) CGD is caused by defects in the genes for p47 phox, p22-phox or p67-phox
Externí odkaz:
https://doaj.org/article/76fbf677835d4704baee06e5a972a220
Autor:
Nezihe Köker, İhsan Deveci, Karin van Leeuwen, Sinan Akbayram, Dirk Roos, Taco W. Kuijpers, Mustafa Yavuz Köker
Publikováno v:
K?ker, N, Deveci, van Leeuwen, K, Akbayram, S, Roos, D, Kuijpers, T W & K?ker, M Y 2023, ' A Novel Deletion in FERMT3 Causes LAD-III in a Turkish Family ', Journal of clinical immunology, vol. 43, no. 4, pp. 741-746 . https://doi.org/10.1007/s10875-022-01420-4
Journal of clinical immunology, 43(4), 741-746. Springer New York
Journal of clinical immunology, 43(4), 741-746. Springer New York
Leukocyte adhesion deficiency-III (LAD-III) is an extremely rare autosomal recessive syndrome caused by mutations in FERMT3, the gene encoding kindlin-3. The genetic alterations in this gene lead to abnormal expression or activity of kindlin-3 in leu
Publikováno v:
Erciyes Medical Journal, Vol 42, Iss 2, Pp 229-232 (2020)
Chronic granulomatous disease (CGD) is a rare inherited immunodeficiency that arises from defects in the NADPH oxidase complex, primarily affecting the respiratory burst in neutrophils. Kabuki syndrome (KS) is a rare genetic syndrome and often presen
Externí odkaz:
https://doaj.org/article/7d38b4ed13cd4d1893ff62825f9125ef
Publikováno v:
International Journal of Rheumatic Diseases. 26:764-768
Publikováno v:
Journal of Pediatric Infection. 16:114-117
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:
Robin van Bruggen, Anton T.J. Tool, Xi Wen Zhao, Taco W. Kuijpers, Nezihe Köker, Michel van Houdt, Mustafa Yavuz Köker, Paul Verkuijlen, Timo K. van den Berg, Panagiota Bouti, Hanke L. Matlung, Sinan Akbayram, Ozlem Keskin
Publikováno v:
Cancer immunology research, 9(2), 147-155. American Association for Cancer Research Inc.
The CD47–signal regulatory protein-alpha (SIRPα) immune checkpoint constitutes a therapeutic target in cancer, and initial clinical studies using inhibitors of CD47–SIRPα interactions in combination with tumor-targeting antibodies show promisin
Autor:
Canan Albayrak, B Koc, Davut Albayrak, F Bianchi, Berkay Saraymen, Emine Zengin, Christophe Chenet, Mustafa Yavuz Köker, Musa Karakukcu, Bulent Zulfikar, Nazan Sarper, V. Jallu, R Petermann, Hüseyin Avcılar, A.G. de Brevern
Publikováno v:
Platelets
Platelets, Taylor & Francis, 2022, 33 (4), pp.551-561. ⟨10.1080/09537104.2021.1947481⟩
Platelets, Taylor & Francis, 2022, 33 (4), pp.551-561. ⟨10.1080/09537104.2021.1947481⟩
Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding disorder characterized by impaired platelet aggregation due to defects in integrin alpha IIb beta 3, a fibrinogen receptor. Platelet phenotypes and allelic variations in 28 Turkish
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1de0f6dd347b725a48b111d27b16324
https://avesis.kayseri.edu.tr/publication/details/0c61e85d-cb1c-4134-b43d-3ca233af65f3/oai
https://avesis.kayseri.edu.tr/publication/details/0c61e85d-cb1c-4134-b43d-3ca233af65f3/oai
Autor:
Mustafa Yavuz Köker, Sevil Ozsoy, Mehmet Halil Çeliksoy, Alper Gezdirici, Baris Malbora, Songul Gungor
Leukocyte adhesion deficiency is an autosomal recessive primary immunodeficiency that has been divided into three types: LAD1 (beta-2 integrin (CD18) family deficiency/defect), LAD2 (absence of fucosylated carbonhydrate ligands for selectins) and LAD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41905b0ec089433a345101ccc0ae5ae4
https://avesis.erciyes.edu.tr/publication/details/69b5e52c-f886-47b0-9f93-6c73383ace9f/oai
https://avesis.erciyes.edu.tr/publication/details/69b5e52c-f886-47b0-9f93-6c73383ace9f/oai
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