Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Hüseyin Avcılar"'
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:
Ahmet Eken, Hüseyin Avcılar
Publikováno v:
Medical Hypotheses
Toll-like receptor 7 is critical in recognition of single strand RNA viruses, including SARS CoV-2, and generation of anti-viral immunity. Coronaviruses evolved strategies to dampen the host immunity. Herein, we discuss the potential use of TLR7 agon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b2a7f5b665c39ae695226107a33c42f
https://doi.org/10.1016/j.mehy.2020.110202
https://doi.org/10.1016/j.mehy.2020.110202
Autor:
Aydin Unal, Eray Eroglu, Oktay Oymak, Aydın Tunçay, Hüseyin Avcılar, Mustafa Yavuz Köker, Berkay Saraymen, Ertuğrul Mavili, Ismail Kocyigit
Publikováno v:
International urology and nephrology. 48(6)
Arteriovenous fistula (AVF) failure is one of the most important clinical problems in end-stage renal disease. Endothelial progenitor cells (EPCs) have a role on vascular angiogenesis and endothelialization. We aimed to investigate the association ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::636079901a285970666d010ba876f2e6
https://pubmed.ncbi.nlm.nih.gov/27068816
https://pubmed.ncbi.nlm.nih.gov/27068816
Publikováno v:
Volume: 36, Issue: 3 415-421
Cumhuriyet Medical Journal
Cumhuriyet Medical Journal
The physical morphology of bone marrow and peripheral blood cells has to be well known to achieve more accurate results with flow cytometric analysis. In flow cytometry; FS, SS and through the gate of CD45, it is possible to obtain a good knowledge a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b723cccdfaf4ce33ba641c7d4e16356f
https://dergipark.org.tr/tr/pub/cmj/issue/4231/56438
https://dergipark.org.tr/tr/pub/cmj/issue/4231/56438
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
Autor:
M. Yavuz Köker, Hüseyin Avcılar
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 nicotinamide adenine dinucleotide phosphate (NAD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25e9573ab5f2782d062a0b859573def0
https://doi.org/10.5772/35758
https://doi.org/10.5772/35758