Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Anzel Bahadır"'
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:
Turkish Journal of Hematology, Vol 26, Iss 01, Pp 17-20 (2009)
Objective: The aim of this study was to determine the laboratory diagnosis and genetic origins of the hemoglobin (Hb) variants, Hb D-Los Angeles and Hb Beograd observed frequently in our region.Material and Methods: Hb variants were investigated in o
Externí odkaz:
https://doaj.org/article/d7e8a53bb86a4944bfd43888945101f9
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:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 25(1)
Hb D-Ouled Rabah [beta19(B1)AsnLys] is a rare hemoglobin (Hb) beta chain variant reported from Tuareg tribes in Algeria and once from China. It was suggested that Hb D-Ouled Rabah might be specific of Berber-speaking populations. Our report describes
Autor:
Anzel, Bahadır, Aylin, Köseler, Ayfer, Atalay, Hasan, Koyuncu, Ece, Akar, Nejat, Akar, Erol Ömer, Atalay
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 26(1)
The aim of this study was to determine the laboratory diagnosis and genetic origins of the hemoglobin (Hb) variants, Hb D-Los Angeles and Hb Beograd observed frequently in our region.Hb variants were investigated in one Hb D-Los Angeles and two Hb Be
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 26(3)
Our aim is to identify the beta globin gene cluster haplotypes for the beta thalassemia mutations in Turkey at regional basis. Beta thalassemia mutations included in this study were IVS-I-110 (GA), FSC 8/9 (+G), IVS-II-1 (GA), IVS-I-5 (GC), IVS-I-1 (
Autor:
Aylin, Köseler, Ayfer, Atalay, Hasan, Koyuncu, Berna, Turgut, Anzel, Bahadır, Erol Ömer, Atalay
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 23(3)
Hb J-Iran [beta77(EF1)His-Asp], a rare hemoglobin variant that does not present health problems, was reported for the first time in the Turkish population in 1986. Our case is the fourth case reported in Turkey and the first case from the Denizli pro
Autor:
Havva Erdem, Nilüfer Kadıoğlu, Hasan Rıza Aydın, Feyza Başar, Anzel Bahadır, Murat Oktay, Abdullah Belada, Hilal Balta
Publikováno v:
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 119:e138
Publikováno v:
Czech Journal of Genetics and Plant Breeding, Vol 55, Iss 1, Pp 20-27 (2019)
This study was conducted to determine the effects of magnetic field (MF) strength on shoot regeneration and Agrobacterium tumefaciens-mediated gene transfer in flax (Linum usitatissimum L.). Seeds of flax cv. Madaras were exposed to different MF stre
Externí odkaz:
https://doaj.org/article/e5dfbebe4d18480387661063a1478876