Ara
Toplam kayıt 15, listelenen: 11-15
First Observation of Hemoglobin Kansas [beta 102(G4)Asn -> Thr, AAC > ACC] in the Turkish Population
(Galenos Yayincilik, 2015)
[No Abstract Available]
Investigation of alpha globin gene mutations by complementary methods in Antalya
(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 ...
Effects of idiopathic erythrocytosis on the left ventricular diastolic functions and the spectrum of genetic mutations: A case control study
(Lippincott Williams & Wilkins, 2022)
Background: We have aimed at exposing left ventricular diastolic functions and the presence of known genetic mutations for familial erythrocytosis, in patients who exhibit idiopathic erythrocytosis. Methods: Sixty-four ...
In Silico Analysis of the Structural and Functional Consequences of Polymorphic Amino Acid Substitutions in the Cattle HSF1 Protein
(Kafkas Univ, Veteriner Fakultesi Dergisi, 2022)
Heat stress causes a decrease in the productivity of livestock by negatively affecting some important economic features such as fertility, growth and milk production. The heat shock transcription factor 1 (HSF1) gene plays ...
FMR1 Gene Mutation Analysis and CGG Repeat Number Distribution from a Single Center
(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 ...