Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Sevil Oskay Halacli"'
Autor:
Saliha ESENBOĞA, Hande UCLER, Sevil OSKAY HALACLI, Cagman TAN, Nergis KENDIRCI, Yu ZHANG, Helen SU, Deniz CAGDAS, Ilhan TEZCAN
Publikováno v:
Asthma Allergy Immunology. 20:197-201
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5725778d052632348799a390d3354617
https://doi.org/10.21911/aai.033
https://doi.org/10.21911/aai.033
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4b2c36446478e79601414e6fbc8b073
https://doi.org/10.1007/s10875-021-01002-w
https://doi.org/10.1007/s10875-021-01002-w
Autor:
Hacer Neslihan Bildik, Şükrü Çekiç, Ozlem Keskin, Saliha Esenboga, Karin van Leeuwen, Ilhan Tezcan, Ismail Yaz, Dirk Roos, Deniz Cagdas, Begum Ozbek, Cagman Tan, Elif Soyak Aytekin, Sara Sebnem Kilic, Sevil Oskay Halacli
Publikováno v:
Clinical and experimental immunology, 206(1), 47-55. Wiley-Blackwell
Clin Exp Immunol
Clin Exp Immunol
Leukocyte adhesion deficiency type I is a rare primary immunodeficiency disorder characterized by mutations in the ITGB2 gene encoding CD18. We present clinical and immunological features of 15 patients with leukocyte adhesion deficiency type 1 (LAD-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36bcfcc9962bd7eff2908337d9737524
https://pure.amc.nl/en/publications/clinical-and-laboratory-findings-in-patients-with-leukocyte-adhesion-deficiency-type-i-a-multicenter-study-in-turkey(f554e3a6-6dff-4005-b041-a0739e6fc2ec).html
https://pure.amc.nl/en/publications/clinical-and-laboratory-findings-in-patients-with-leukocyte-adhesion-deficiency-type-i-a-multicenter-study-in-turkey(f554e3a6-6dff-4005-b041-a0739e6fc2ec).html
Autor:
Deniz Cagdas, Sevil Oskay Halacli, Hacer Neslihan Bildik, Ilhan Tezcan, Aysenur Ozturk Kura, Ozden Sanal
Publikováno v:
Immunological investigations. 51(5)
Wiskott Aldrich Syndrome is an X-linked primary immunodeficiency disorder characterized by microthrombocytopenia, severe immunodeficiency, and eczema. To define clinical-laboratory features, genetic defects (known/novel) of 23 patients of Wiskott Ald
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5899dbda65ef2489e3962004ab04a186
https://pubmed.ncbi.nlm.nih.gov/34098853
https://pubmed.ncbi.nlm.nih.gov/34098853
Autor:
Nalan Yakici, Ilhan Tezcan, Pınar Gur Cetinkaya, Deniz Cagdas, Busra Cavdarli, Sevil Oskay Halacli, Cagman Tan, Begum Ozbek, Halil Tuna Akar
Purpose: Chronic mucocutaneous candidiasis (CMC) is characterized by persistent or recurrent fungal infections involving the nails, skin, oral and genital mucosa. Impaired IL17 mediated immunity is a cause for CMC. Patient and Methods: After the next
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e69bd9cd8e38b491e4b61be5e8021b0f
https://doi.org/10.21203/rs.3.rs-186598/v1
https://doi.org/10.21203/rs.3.rs-186598/v1
Autor:
Sevil Oskay Halacli
Publikováno v:
Immunologic research. 70(1)
In the diagnosis of primary immunodeficiencies which are heterogeneous groups of genetic disorders, next-generation sequencing strategies take an important place. Protein expression analyses and some functional studies which are fundamental to determ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e182e241984dfa44fa9b9c86793a9b7
https://pubmed.ncbi.nlm.nih.gov/34622368
https://pubmed.ncbi.nlm.nih.gov/34622368
Autor:
Sevil Oskay Halacli
Primary Immunodeficiencies (PIDs) compose of a large spectrum of diseases characterized by abrogated or dysregulated functions of innate and adaptive immune system components that cause susceptibility to recurrent infections, autoimmunity, neoplasia/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c4393b78b2ee35e28598587054ec142
https://doi.org/10.5772/intechopen.96004
https://doi.org/10.5772/intechopen.96004
Autor:
Saliha Esenboga, Ilhan Tezcan, Diclehan Orhan, Pınar Gur Cetinkaya, Deniz Cagdas, Rezan Topaloglu, Kaan Boztug, Betul Karaatmaca, Ozden Sanal, Cagman Tan, Aysegul Uner, Sevil Oskay Halacli, Seza Ozen, Burcu Balci-Hayta, Arzu Saglam Ayhan
Background Serine/threonine kinase-4 (STK4) deficiency is an autosomal recessive combined immunodeficiency. Objective We aimed to define characteristic clinical and laboratory features to aid the differential diagnosis and determine the most suitable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea9e1be38099b520215b44d669b2b95a
https://aperta.ulakbim.gov.tr/record/230554
https://aperta.ulakbim.gov.tr/record/230554
Autor:
Sevil Oskay Halacli, Begum Ozbek, Cagman Tan, Elif Soyak Aytekin, Deniz Cagdas Ayvaz, Ilhan Tezcan, Ismail Yaz
Publikováno v:
Turkish Journal of Immunology.
Objective: TCR (T Cell Receptor) which is expressed on T cells is responsible for recognizing antigens presented by HLA molecules of the APCs (Antigen Presenting Cells) and initiation of the immune response. It has been reported that TACI (Transmembr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7add3a57828acdd6caf12acbc8791f8a
https://doi.org/10.5222/tji.2021.43531
https://doi.org/10.5222/tji.2021.43531
Publikováno v:
Asthma Allergy Immunology.
Objective: STK4 (serine-threonine protein kinase 4) deficiency is categorized under combined immunodeficiencies, which are a subgroup of primary immunodeficiencies that profoundly affect T cells. Autosomal recessive STK4 deficiency is characterized b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79cd1a7a7aa29da6a135a1180efa4a71
https://doi.org/10.21911/aai.518
https://doi.org/10.21911/aai.518