Yazar "Keser, İbrahim" için listeleme
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First Observation of Hemoglobin Kansas [beta 102(G4)Asn -> Thr, AAC > ACC] in the Turkish Population
Keser, İbrahim; Öztaş, Alev; Bilgen, Türker; Canatan, Duran (Galenos Yayincilik, 2015)[No Abstract Available] -
FMR1 Gene Mutation Analysis and CGG Repeat Number Distribution from a Single Center
Arıkan, Yunus; Bilgen, Türker; Mıhcı, Ercan; Duman, Özgür; Karaman, Tuğba; Keser, İbrahim (Gazi Univ, Fac Med, 2022)Background: Mutation occurring in fragile X mental retardation 1 (FMR1) gene is acknowledged as the most common cause for X chromosome linked intellectual disability/mental retardation (XLID/XLMR). This gene harbors unstable ... -
Gap-PCR Screening for Common Large Deletional Mutations of beta-Globin Gene Cluster Revealed a Higher Prevalence of the Turkish Inversion/Deletion (delta beta)(0) Mutation in Antalya
Bilgen, Türker; Clark, Özden Altıok; Öztürk, Zeynep; Yesilipek, M. Akif; Keser, İbrahim (Galenos Yayincilik, 2016)Objective: Although the calculated carrier frequency for point mutations of the beta-globin gene is around 10% for Antalya Province, nothing is known about the profile of large deletional mutations involving the beta-globin ... -
Induction of fetal hemoglobin by modulation of epigenetic and genetic factors in beta thalassemia major patients
Keser, İbrahim; Arikan, Y.; Kupesiz, A.; Bilgen, Türker; Kurtoglu, E. (Nature Publishing Group, 2018)[No Abstract Available] -
Investigation of alpha globin gene mutations by complementary methods in Antalya
Keser, İbrahim; Mercan, T.K.; Bilgen, Türker; Kupesiz, O.A.; Arikan, Y.; Canatan, D. (Yuzuncu Yil Universitesi Tip Fakultesi, 2021)Alpha (?) thalassemia is one of the hemoglobinopaties that is inherited by autosomal recessive mode. It is caused by mutations on alpha-1 and alpha-2 globin genes. Deletional type mutations of globin genes have commonly ... -
A Novel Mutation in the Promoter Region of the -Globin Gene: HBB: c.-127G > C
Bilgen, Türker; Canatan, Duran; Delibas, Serpil; Keser, İbrahim (Taylor & Francis Ltd, 2016)Novel -globin gene mutations are still occasionally being reported, especially when evaluating milder phenotypes. We report here a novel putative mutation in the promoter region of the -globin gene and assess its clinical ...