Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Afet Akdag-Kose"'
Autor:
Armagan Kutlay, Afet Akdag Kose
Publikováno v:
Indian Journal of Dermatology, Vol 68, Iss 4, Pp 372-376 (2023)
Background: Elafin is a serine protease inhibitor with anti-inflammatory properties. It is expressed in various epithelial tissues with increased production under inflammatory conditions. Increased tissue elafin expression in Behçet's disease (BD) l
Externí odkaz:
https://doaj.org/article/38f8ac029b1149cea8dbfd9ab91439d4
Autor:
Murat Erdugan, Suzan Çinar, Esin Aktas Cetin, Ahmet Gül, Goncagul Babuna-kobaner, Metin Yusuf Gelmez, Gulce Ozcit-Gurel, Afet Akdag-Kose, Günnur Deniz
Publikováno v:
Immunology Letters. 235:1-8
Innate lymphoid cells (ILCs) are lymphoid cells that have important effector and regulatory functions in innate immunity and tissue remodeling. Uncontrolled activation and proliferation of ILCs can contribute to inflammatory autoimmune diseases. Behc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5415d89f71fc30c4bc2eff0afb0f5fc5
https://doi.org/10.1016/j.imlet.2021.04.008
https://doi.org/10.1016/j.imlet.2021.04.008
Autor:
Murat Kürtüncü, Ates Kadioglu, Huseyin Oflaz, Mehmet Barburoglu, Selcuk Erdem, Artur Salmaslioglu, Erkingül Shugaiv, Yasemin Erdem, Ekrem Bilal Karaayvaz, Afet Akdag Kose
Publikováno v:
Advances in Dermatology and Allergology, Vol 38, Iss 4, Pp 622-628 (2021)
Advances in Dermatology and Allergology/Postȩpy Dermatologii i Alergologii
Advances in Dermatology and Allergology/Postȩpy Dermatologii i Alergologii
Introduction Behçet’s disease (BD) is a chronic inflammatory disease which can be limited to only mucocutaneous tissues or can affect different systems of the body. Aim To investigate the association of endothelial and erectile dysfunctions with B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e24b6fc36346b95cd0bd6f3c0693a10
https://doi.org/10.5114/ada.2021.108931
https://doi.org/10.5114/ada.2021.108931
Autor:
Esma Erbudak, Derya Aydin, Meric Yilmaz, Bahar Akgun-Karapinar, Melike Omeroglu, Afet Akdag-Kose
Publikováno v:
Klimik Dergisi/Klimik Journal. 31:115-119
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b78a01a6d08e0b9422c2a51344792131
https://doi.org/10.5152/kd.2018.28
https://doi.org/10.5152/kd.2018.28
Autor:
Suzan Çinar, Goncagul Babuna-kobaner, Esin Aktas, Afet Akdag Kose, Metin Yusuf Gelmez, Fatma Betul Oktelik, Murat Erdugan, Ahmet Gül, Günnur Deniz
Publikováno v:
Turkish Journal of Immunology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0d55d77717a02699d992c831a9737dd
https://doi.org/10.5222/tji.2021.03521
https://doi.org/10.5222/tji.2021.03521
Autor:
Marwen Ghabra, Farida Fortune, Neslihan Abaci, Phaedon G. Kaklamanis, Oznur Aglar, Oliver J. Brand, John M O'Shea, Ahmet Gül, Benjamin D. Korman, Miles Stanford, Hulya Azakli, Colleen Satorius, Dongsik Bang, Young-Hun Cho, Ilknur Tugal-Tutkun, Elaine F. Remmers, Virginia G. Kaklamani, Gulsen Akman-Demir, Michael B. Dizon, Afet Akdag Kose, Burak Erer, Graham R. Wallace, Daniel L. Kastner, Duran Ustek, Massimo Gadina, Wei-Wei Chen, William E R Ollier, Christopher I. Amos, Aris Cakiris, Julie M. Le, Eldad Ben-Chetrit, Fulya Cosan, Michael J. Ombrello, Yohei Kirino, Zeliha Emrence, Gülsevim Azizlerli, Barbara Yang
Publikováno v:
Nature genetics
Behçet's disease is a genetically complex disease of unknown etiology characterized by recurrent inflammatory attacks affecting the orogenital mucosa, eyes and skin. We performed a genome-wide association study with 311,459 SNPs in 1,215 individuals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5be1fd6ac9b45f9ffccab1cd283931b1
https://doi.org/10.1038/ng.625
https://doi.org/10.1038/ng.625
Autor:
Afet Akdag-Kose, Kurtuluş Didem Yazganoğlu, Dilek Erzengin, Rifkiye Sarica-Kucukoglu, Gülsevim Azizlerli, Murat Kayabali, Rian Disci
Publikováno v:
International journal of dermatology. 45(8)
Background Vascular lesions can be the presenting sign of Behcet's disease (BD) preceding classical symptoms. The aim of this study was to evaluate the prevalence and types of vascular involvement in BD. Methods Among 2319 patients diagnosed with BD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f6a88180ee949631f5b54b7258f7cb2
https://pubmed.ncbi.nlm.nih.gov/16911374
https://pubmed.ncbi.nlm.nih.gov/16911374
Publikováno v:
Scopus-Elsevier
Background. Behcet's disease is a chronic, relapsing disease, about which information on its clinical course in juveniles is only available from small groups of patients. Materials and Methods. Patients suffering from Behcet's disease who had their f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf0e1a3bf3f42e8e0859d1e019f6784d
https://doi.org/10.1111/j.1365-4362.1996.tb03272.x
https://doi.org/10.1111/j.1365-4362.1996.tb03272.x
Autor:
Meri Urgancioglu, Rian Disci, Rifkiye Sarica, Afet Akdag Kose, İlknur Tuğal Tutkun, Recep Tunc, Gülsevim Azizlerli, Ahmet Gül, Mustafa Kulaç
Publikováno v:
International journal of dermatology. 42(10)
Background The prevalence of Behcet's disease (BD) is much higher in countries along the ancient Silk Route, extending from Japan to Mediterranean countries including Turkey, than in northern Europe and the USA. Three previous epidemiologic surveys h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c0407a7c70587c07f655571f501682f
https://pubmed.ncbi.nlm.nih.gov/14521694
https://pubmed.ncbi.nlm.nih.gov/14521694
Autor:
Afet Akdag Kose
Publikováno v:
Yonsei Medical Journal
Purpose: Behcet’s disease (BD) is a disease of unknown etiology, which has multisystemic involvement. This multisystemic involvement might be the clue for an autoimmune pathogenesis. In order to evaluate an autoimmune pathogenesis, we examined immu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::904e4c4c95c8b7078afc4c849e8486de
https://doi.org/10.3349/ymj.2009.50.4.505
https://doi.org/10.3349/ymj.2009.50.4.505