Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Yavuz Köker"'
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
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:
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:
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:
Semiha Bahceci Erdem, Canan Sule Unsal Karkiner, İlker Devrim, Nesrin Gulez, Hikmet Tekin Nacaroğlu, Ferah Genel, Demet Can, Mustafa Yavuz Köker
Chronic granulomatous disease (CGD) is a genetically heterogeneous primary immunodeficiency that is characterized by recurrent and life-threatening infections resulting from defects in phagocyte nicotinamide adenine dinucleotide phosphate (NADPH) oxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c387a69855fe3bff38a1ce267b1a1f74
https://avesis.erciyes.edu.tr/publication/details/a2dd6e88-a89a-4eef-ab51-114631325010/oai
https://avesis.erciyes.edu.tr/publication/details/a2dd6e88-a89a-4eef-ab51-114631325010/oai
Autor:
Ayse Metin, Hüseyin Avcılar, Mustafa Yavuz Köker, Mustafa Yilmaz, Isil Barlan, Yildiz Camcioglu, Alisan Yildiran, Sara Sebnem Kilic, Olcay Yegin, Ilhan Tezcan, Dirk Roos, Karin van Leeuwen, Ozden Sanal, Martin de Boer, Turkan Patiroglu
Publikováno v:
Journal of allergy and clinical immunology, 132(5), 1156-1163.e5. Mosby Inc.
Background: Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder of phagocytes resulting in impaired killing of bacteria and fungi. A mutation in one of the 4 genes encoding the components p22(phox), p47(phox), p67(phox), a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccb0c2bb71bf12fe075a53c32aae2c70
http://hdl.handle.net/11452/28932
http://hdl.handle.net/11452/28932