Бібліотека Вінницького національного медичного університету ім. М.І.Пирогова

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Шифр: УУ60/2018/90/4
Журнал

The Ukrainian biochemical journal [Текст]. - Выходит раз в два месяца
2018г. Т. 90 № 4

Содержание:
Veklich, T. O. Pathways and mechanisms of transmembrane calcium ions exchange in the cell nucleus / T. O. Veklich, Yu. V. Nikonishyna, S. O. Kosterin. - P.5-24
Zaiets, I. V. The P60-S6K1 isoform of ribosomal protein S6 kinaze 1 is a product of alternative mRNA translation / I. V. Zaiets [et al.]. - P.25-35
Другие авторы: Sivchenko A. S., Khoruzhenko A. I., Savinska L. O., Filonenko V. V.
Shymanskyi, I. O. Liver cytochrome P450-hydroxylation system of tumor-bearing rats under the influence of ?-3 polyunsaturated fatty acids and vitamin D3 / I. O. Shymanskyi [et al.]. - P.36-44
Другие авторы: Ketsa O. V., Marchenko M. M., Veliky M. M.
Ajilore, B. S. Gentamicin and magnesium chloride normalizes cholinesterase and ATPase activities in rats acutely exposed to dichlorvos (DDVP) pesticide / B. S. Ajilore, A. E. Adewuyi, T. O. Oluwadairo. - P.45-51
Makarchikov, A. F. Adenosine thiamine triphosphate and adenosine thiamine triphosphate hydrolase activity in animal tissues / A. F. Makarchikov [et al.]. - P.52-63
Другие авторы: Saroka T. V., Kudyrka T. G., Kolas I. K., Luchko T. A., Rusina I. M., Gurinovich V. A.
Kaplia, A. A. Assessment of the effect of monohydroxy alcohols, unsaturated fatty acids, organophosphate compounds on the enzymatic ATP-hydrolysis in the cell membranes of the smooth muscle of the rat colon / A. A. Kaplia, S. V. Midyk, S. V. Khyzhnyak. - P.64-73
Yukalo, V. G. Isolation of к-CN-1P and β-CN-5P fractions from native casein micelles / V. G. Yukalo, L. A. Storozh. - P.74-79
Bobrovnik, S. A. Effect of trifluoroethanol on antibody reactivity against corresponding and nonrealated antigens / S. A. Bobrovnik, M. O. Demchenko, S. V. Komisarenko. - P.80-89
Sierra-Campos, E. Nitrate and nitrite in drinking water affect antioxidant enzymes in erythrocytes of rats / E. Sierra-Campos [et al.]. - P.90-101
Другие авторы: Valdez-Solana M. A., Campos-Almazan M. I., Avitia-Dominguez C., Hernandez-Rivera J. L., de Lira-Sanchez J. A., Garcia-Arenas G., Tellez-Valencia A.
Salyha, N. O. Effects of L-glutamic acid and pyridoxine on glutathione depletion and lipid peroxidation generated by epinephrine-induced stress in rats / N. O. Salyha. - P.102-110
Asadi, A. Evaluation of serum adenosine deainase and its isoenzymes in patients with ovarian cancer / A. Asadi [et al.]. - P.111-114
Другие авторы: Atyabi S. M., Sadeghi S., Khatami S., Ebrahimi-Rad M., Valadbeigi S., Saghiri R.
Ozbolat, Guluzar. Hematologic features of beta-globin gene mutation type (??) with homozygous beta thalassemia / Guluzar Ozbolat, Abdullah Tuli. - P.115-120
Данилова, В. М. Альфред Бернгард Нобель і Нобелівська премія / В. М. Данилова, Р. П. Виноградова, С. В. Комісаренко. - P.121-134
Danylova, T. V. Scientific investigation of Nobel prize winner Emil Fischer as a launching pad for the development of biochemistry: a brief overview / T. V. Danylova, S. V. Komisarenko. - P.135-142
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(03.10.2018г. Экз. 1 - Б.ц.) (свободен)

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Ozbolat, Guluzar.
Hematologic features of beta-globin gene mutation type (??) with homozygous beta thalassemia / Guluzar Ozbolat, Abdullah Tuli // The Ukrainian Biochemical Journal. - 2018. - Том 90, N 4. - P115-120

MeSH-главная:
БЕТА-ТАЛАССЕМИЯ -- BETA-THALASSEMIA (генетика, диагностика, этиология)
СЕКВЕНИРОВАНИЕ ДНК -- SEQUENCE ANALYSIS, DNA (использование, методы)
ГЕНЕТИЧЕСКАЯ ИЗМЕНЧИВОСТЬ -- GENETIC VARIATION
Аннотация: β-Tthalassemia is common genetic disorders in Turkey that characterized by the reduced synthesis (β+) or absence (βo) of the β-globin chains in the HbA molecule. In this study, we aimed to determine the effect of the mutation type of the β-globin gene on hematological values in homozygous β-thalassemia. This retrospective study was undertaken by Prenatal Diagnosis Centres of Cukurova University Medical Biochemistry at Adana. We evaluated 60 homozygous by implementing DNA sequencing analysis for mutations undetectable by conventional methods. 30 patients with βo [FSC 44/ C-A] mutations and the other 30 patients with βo [(IVS-II-1(GA), CD39 (CT), Cd8 (-AA) Cd39 C T and CD36/37 (–T)] mutations, totally 60 patients were included in the study. Erythrocyte indices, HbF, HbA2 levels were compared between the two groups. FSC 44/(-C) mutations were detected in patients. Hb, Hct, MCV in this group values were statistically lower than in patients with other detected mutations (P 0.05). Between the two groups, there is no statistically different RBC, MCH, MCHC, HbF, HbA2 levels (P ˃ 0.05). For the first time in this study, it was found that the Hb, Hct and MCV value of the persons who carried the FSC 44/(-C) mutation were significantly lower than the persons who carrying other mutations. Between the two groups, there was no statistical difference in RBC, MCH, MCHC, HbF and HbA2 levels. Awareness of FSC/44 mutation, which may have a heterogeneous clinical presentation, is required. We herein present the hematologic findings of a Turkish population carrying this mutation. This will also help to make a diagnosis
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Tuli, Abdullah

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