Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Erol Ömer, Atalay"'
Although the etiopathogenesis of Behcet's disease is not known, studies conducted in different populations show that it is a multifactorial disease that is thought to develop as a result of the interaction of environmental and genetic factors. IL-17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7ae6e3ca4147f06152684112cc5c701
https://hdl.handle.net/11499/50379
https://hdl.handle.net/11499/50379
Publikováno v:
Clinical and Experimental Dermatology. 46:1462-1470
Background Behcet disease (BD) is associated with the immune system, especially neutrophilic activity. The CXCR1, CXCR2 and CXCL5 genes mediate the activation and migration of neutrophils. Aim To investigate CXCR1, CXCR2 and CXCL5 single nucleotide p
Publikováno v:
Turkish Journal of Hematology, Vol 26, Iss 03, Pp 129-137 (2009)
Objective: Our aim was to identify the beta globin gene cluster haplotypes for the beta thalassemia mutations in Turkey on a regional level. Beta thalassemia mutations included in this study were IVS-I-110 (G>A), FSC 8/9 (+G), IVS-II-1 (G>A), IVS-I-5
Externí odkaz:
https://doaj.org/article/a0cc4f3ac1d44525805ff85b0cf3e941
Publikováno v:
Acta Medica, Vol 47, Iss 2, Pp 133-136 (2004)
Summary: The angiotensin converting enzyme (ACE) gene is located on human chromosome 17 expressing three genotypes within the intron 16 of the related gene structure. These genotypes are classified as I and D alleles which are termed as insertion and
Externí odkaz:
https://doaj.org/article/3c0971b36ba346d8a553ec834863cfce
Autor:
Aylin Köseler, Hasan Koyuncu, Onur Öztürk, Anzel Bahadır, Sanem Demirtepe, Ayfer Atalay, Erol Ömer Atalay
Publikováno v:
Turkish Journal of Hematology, Vol 27, Iss 02, Pp 120-122 (2010)
Hb Tunis [beta124(H2)Pro>Ser] was reported from Tunisia in 1988. This hemoglobin variant was detected by isoelectric focusing moving just ahead of Hb A. It cannot be identified by standard hemoglobin electrophoresis due to its similar mobility to Hb
Externí odkaz:
https://doaj.org/article/c3a24d15689740dc9eecc347ca5c41bb
Publikováno v:
Molecular Genetics & Genomic Medicine
Background: ß-Globin gene cluster haplotypes associated with the Hb D-Los Angeles mutation have been reported in many different locations in different populations including Italy, Iran, Thailand, Belgium, Mexico, Holland, and Turkey. In this study,
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 30:2658-2664
Objective: In the present study, we investigated the effects of promoter polymorphism and an exon-1 mutation (G71R) in the UGT1A1 gene in neonates with unexplained hyperbilirubinemia and direct Coombs-negative [DC(-)] ABO incompatibility. Methods: Tw
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 3, Pp 289-290 (2012)
Externí odkaz:
https://doaj.org/article/a6a2e61a33754398b8d5fdf9662777b5
Publikováno v:
Adli Tıp Bülteni, Vol 2, Iss 1 (1997)
Son yıllarda adli tıp alanında, elde edilen materyalin kimliklendirilmesinde, DNA parmak izi büyük bir potansiyel göstermiştir. Bu çalışma: DNA parmak izi tekniğinde farklı biyolojik örneklerin kullanılması ve sonuçların yorumlanmas
Externí odkaz:
https://doaj.org/article/d8328824f3344444bec21de43eee9ccb
Publikováno v:
Molecular Genetics & Genomic Medicine
Background: Hb G-Coushatta variant was reported from various populations’ parts of the world such as Thai, Korea, Algeria, Thailand, China, Japan and Turkey. In our study, we aimed to discuss the possible historical relationships of the Hb G-Cousha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c55e0fff8a6628600a2e89fdc126628e
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/10726
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/10726