Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Saeedeh Ghazaey"'
Autor:
Arefe Edalatian Kharrazi, Forough Forghani, Danial Jahantigh, Saeedeh Ghazaey Zidanloo, Mahnaz Rezaei, Mohsen Taheri
Publikováno v:
International Journal of Reproductive BioMedicine, Vol 22, Iss 6, Pp 451-462 (2024)
Abstract Background: Endometriosis is a chronic, gynecological disorder, and the disease's pathogenesis is still debatable. Genes related to apoptosis have been revealed to be deregulated in endometriosis. Objective: This study investigates the relat
Externí odkaz:
https://doaj.org/article/d6908b24d138490da27c9087831fd5ac
Publikováno v:
Clinical and Experimental Hypertension, Vol 44, Iss 3, Pp 280-290 (2022)
Background and aim Preeclampsia (PE), a multifactorial disorder, is the main cause of maternal mortality and morbidity. Genetic polymorphisms in key proteins involved in the immune system may change the risk of PE risk. In this study, we examined the
Externí odkaz:
https://doaj.org/article/2cd7eca126ba44459b0a88c7c64c88b4
Autor:
Saeedeh Ghazaey, Fatemeh Keify, Farzaneh Mirzaei, Masumeh Maleki, Semiramis Tootian, Mitra Ahadian, Mohammad Reza Abbaszadegan
Publikováno v:
International Journal of Fertility and Sterility, Vol 9, Iss 1, Pp 47-54 (2015)
Background Cytogenetic study of reproductive wastage is an important aspect in determining the genetic background of early embryogenesis. Approximately 15 to 20% of all pregnancies in humans are terminated as recurrent spontaneous abortions (RSAs). T
Externí odkaz:
https://doaj.org/article/d2fc5527021f4a1483ca4d4833aab31d
Geographic Heterogeneity of the AML1-ETO Fusion Gene in Iranian Patients with Acute Myeloid Leukemia
Publikováno v:
Reports of Biochemistry and Molecular Biology, Vol 3, Iss 1, Pp 7-13 (2014)
Background: The human AML1 gene, located on chromosome 21, can be fused to the AML1- eight-twenty-one (ETO) oncoprotein on chromosome eight, resulting in a t(8;21)(q22;q22) translocation. Acute myeloid leukemia (AML) associated with this translocatio
Externí odkaz:
https://doaj.org/article/420c8ac065dc4e9b99fb7b9af674786d
Autor:
Saeedeh Ghazaey, Farzaneh Mirzaei, Mitra Ahadian, Fatemeh Keifi, Semiramis Tootian, Mohammad Reza Abbaszadegan
Publikováno v:
Cell Journal, Vol 15, Iss 3, Pp 258-262 (2013)
Objective: Chromosomal aberrations are common causes of multiple anomaly syndromes. Recurrent chromosomal aberrations have been identified by conventional cytogenetic methods used widely as one of the most important clinical diagnostic techniques.Mat
Externí odkaz:
https://doaj.org/article/1f2a43f6adc14ae68482ef553e0538d3
Publikováno v:
Reports of Biochemistry and Molecular Biology, Vol 1, Iss 1, Pp 9-13 (2012)
Background: Multidrug resistance in Salmonella enteritidis isolates is a public health problem worldwide; the present study, therefore, was designed for antimicrobial-resistance determination in this strain. Methods: Salmonella strains isolated fr
Externí odkaz:
https://doaj.org/article/8212b24aaafc46db9c9b5ba4ac26cf14
Akademický článek
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Autor:
Zidanloo, Saeedeh Ghazaey
Publikováno v:
Journal of Genetic Resources; 2024, Vol. 10 Issue 1, p1-8, 8p
Akademický článek
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Publikováno v:
Nutrition and cancer.
Genetic variations in the vitamin D-binding protein (VDBP) may be associated with the plasma level of serum 25-hydroxyvitamin D. Furthermore, vitamin D deficiency increases the risk of acute myeloid leukemia (AML). This study aimed to examine the pot