Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Mutlu Karkucak"'
Publikováno v:
Perinatal Journal, Vol 30, Iss 3, Pp 320-325 (2022)
Objective: Jacobsen syndrome is an infrequent contiguous gene syndrome that involves the deletion of the long arm of chromosome 11. It is mostly accompanied by intellectual disability and other abnormalities. The majority of the patients are hospital
Externí odkaz:
https://doaj.org/article/45cecad6539b490ca1bd1afe09808db1
Publikováno v:
Journal of Infection and Public Health, Vol 10, Iss 6, Pp 774-777 (2017)
Objective: MBL acts as a binding protein that enables uptake of mycobacteria into macrophages. And, TNF-alpha is an important cytokine that is involved in control of mycobacterial infections both in-vivo and in-vitro. A large number of genetic factor
Externí odkaz:
https://doaj.org/article/88adc58d21c04147ae0bf6ac1ceca059
Autor:
Sevil Toka, Tahsin Yakut, Hakan Turan, Emel Başkan Bülbül, Mutlu Karkucak, Hayriye Sarıcaoğlu
Publikováno v:
Balkan Medical Journal, Vol 29, Iss 3, Pp 310-313 (2012)
Objective: Monnose-Binding lectin (MBL) appears to play an important role in the immune system. The genetic polymorphisms in the MBL2 gene can result in a reduction of serum levels, leading to a predisposition to recurrent infection. The aim of this
Externí odkaz:
https://doaj.org/article/034bce7e15fa4fed8454aebe7eff1a0b
Autor:
Mustafa Ferhat Öksuz, Mutlu Karkucak, Orhan Görukmez, Gökhan Ocakoğlu, Abdulmecit Yıldız, Mehmet Ture, Tahsin Yakut, Kamil Dilek
Publikováno v:
Revista Brasileira de Reumatologia, Vol 57, Iss 6, Pp 501-506
Abstract Aim: Various mutations have been identified in the Mediterranean fever (MEFV) gene which is reported to be responsible from Familial Mediterranean fever (FMF). In our study, we aimed to determine the frequency of the MEFV mutations in our re
Externí odkaz:
https://doaj.org/article/e9df650824be4705a663d07ac8d72b56
Autor:
Duygu Övünç Hacıhamdioğlu, Zeynep Altan Ferhatoğlu, Mutlu Karkucak, Neslihan Müge Fişek İzci, Tahsin Yakut
Publikováno v:
Pediatrics International. 64
No Abstract Aviable 35438212
Autor:
Mutlu Karkucak, Ozen Oz Gul, Adem Deligonul, Nizameddin Koca, Soner Cander, Pinar Sisman, Canan Ersoy
Publikováno v:
Volume: 7, Issue: 5 447-456
The European Research Journal
The European Research Journal
Objectives: Glutathione S-transferase (GST) polymorphism may play a role in the etiology of type 1 diabetes, as GST is involved to detoxification of reactive oxygen radicals and synthesis of proinflammatory mediators. Genetic polymorphisms in the ren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebc2d7ebde7e856f3614a45c06b59013
https://dergipark.org.tr/tr/pub/eurj/issue/64737/827173
https://dergipark.org.tr/tr/pub/eurj/issue/64737/827173
Autor:
Mustafa Ferhat Öksüz, Orhan Gorukmez, Mehmet Ture, Gokhan Ocakoglu, Kamil Dilek, Tahsin Yakut, Mutlu Karkucak, Abdulmecit Yildiz
Publikováno v:
Revista Brasileira de Reumatologia. 57:501-506
ResumoObjetivoIdentificaram‐se mutações no gene da febre mediterrânica (MEFV) relatadas como responsáveis pela febre mediterrânica familiar (FMF). Este estudo teve como objetivo determinar a frequência de mutações no MEFV na região sul do
Autor:
Jesús María Hernández-Rivas, Margarida Lima, Mutlu Karkucak, José Padilla, Maria Luisa Lozano, Maria Trapero-Marugan, José Ramón González-Porras, Rosário Santos, Catarina Lau, Juan Francisco Ruiz-Pividal, Eduarda Couto, Verónica Palma-Barqueros, Rocío Benito, Kamila Janusz, Vicente Vicente, Nuria Bermejo, Jorge Oliveira, Marta Martín-Izquierdo, José Rivera, José María Bastida, Ana Marín-Quílez, Natalia Bohdan, Yusuf Yucel, Mónica Pereira, Sara Morais
Publikováno v:
Ann Med
Hermansky-Pudlak syndrome (HPS) is a rare inherited platelet disorder characterized by bleeding diathesis, oculocutaneous albinism (OCA) and a myriad of often-serious clinical complications. We established the clinical and laboratory phenotype and ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b792d1428d9d3aa3dfa57c78b8711c7
https://hdl.handle.net/20.500.12619/71497
https://hdl.handle.net/20.500.12619/71497
Publikováno v:
International Journal of Human Genetics. 15:183-189
The aim of the present study is to investigate the relationship between angiotensin-converting enzyme (ACE) gene polymorphism and pulmonary embolism by comparing the frequency of ACE gene polymorphism between cases diagnosed with pulmonary embolism w
Autor:
Mutlu Karkucak, Esma Uslu, Teoman Erdem, Hakan Turan, Sebnem Ozemri Sag, Tahsin Yakut, Gokhan Ocakoglu, Berna Solak
Publikováno v:
Medical Principles and Practice
Objective: To determine the role of glutathione S-transferase (GST) isoenzyme polymorphisms as susceptibility factors in patients with psoriasis in a Turkish cohort. Subjects and Methods: In this case-control study, 105 patients with plaque-type psor