Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Tahsin, Yakut"'
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:
Mustafa Kemal Demir, Ozlem Yapıcıer, Turker Kilic, Serkan Celik, Bala Basak Oven, Umut Ozdamarlar, Naz Ece Kundak, Duaa Kanan, Alp Dincer, Onder Ertem, Tahsin Yakut, Baran Yılmaz, Sebnem Safi
Publikováno v:
Current Medical Imaging Formerly Current Medical Imaging Reviews. 19
Background and Purpose: Diffuse leptomeningeal glioneuronal tumors (DL-GNT) are rare glioneuronal neoplasms with oligodendroglioma-like cells. These tumors can present as a dominant intracranial mass or as a solitary spinal cord mass without leptomen
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:
Sahin Erdol MD, Mehmet Ture MD, Tahsin Yakut PhD, Halil Saglam PhD, Hideo Sasai MD, Elsayed Abdelkreem MD, Hiroki Otsuka MD, Toshiyuki Fukao MD, PhD
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 4 (2016)
Succinyl-CoA:3-oxoacid CoA transferase (SCOT) deficiency is an autosomal recessive disorder of ketone body utilization that is clinically characterized with intermittent ketoacidosis crises. We report here the second Turkish case with SCOT deficiency
Externí odkaz:
https://doaj.org/article/1f6beff17898491787ca450ad33d0315
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
Publikováno v:
Volume: 16, Issue: 1 29-34
Güncel Pediatri
Güncel Pediatri
GIRIS ve AMAC: Processus vaginalisin (PV) kapanmasinin, testisin inisini saglamak icin gecici olarak bulunan duz kas hucrelerinin, devamliligina bagli oldugu ileri surulmustur. Bu amacla, inguinal herni keseleri, PV kapanmasi ve duz kas hucre varligi
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:
Mehmet Ture, Emine Tuna Gülten, Şebnem Özemri Sağ, Betul Eser, Serdar Şahintürk, Tahsin Yakut, Bilge Çetinkaya Demir
Publikováno v:
Turkiye Klinikleri Journal of Gynecology and Obstetrics. 26:125-128
Partial trisomy of distal 17q is rare. Until now, 32 cases of partial trisomy for the distal region of 17q were reported. Our case has multiple anomalies, such as increased nuchal translucency, hypoplastic left heart syndrome and cerebral anomalies b
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
Publikováno v:
Balkan Journal of Medical Genetics, Vol 18, Iss 2, Pp 43-48 (2015)
Carpal tunnel syndrome (CTS) is the most common entrapment neuropathy of the upper extremity. In this study, we aimed to clarify the relationships between the catechol-O-methyltransferase (COMT) gene Val158Met (rs4680) polymorphism and development, f