Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Shohre Zare Karizi"'
Publikováno v:
Journal of Kerman University of Medical Sciences, Vol 30, Iss 1, Pp 17-24 (2023)
Background: It is expected that the expression of key enzymes of the glycolysis pathway, specially PFK-1, increases tumor cells and so enhances the function of this pathway. The p53 and HIF-1 proteins are regulators of the expression of PFK-1 and LDH
Externí odkaz:
https://doaj.org/article/6a986233cc5c4c1faeb89aea2f0c8953
Autor:
Shohre Zare Karizi, Gholamreza Javadi, Nadia Mirzaei Gisomi, Parvaneh Keshavarz, Mohammad Miryounesi
Publikováno v:
Transfusion Clinique et Biologique. 27:243-252
Objective Invasive biopsy during the pregnancy is associated with an abortion risk of approximately 1% for the fetus. Free fetal DNA in maternal plasma is an excellent source of genetic material for prenatal molecular diagnoses. This study was conduc
Autor:
Reza Shiari, Shirin Farivar, Shohre Zare Karizi, Mohammad Esmaeil Akbari, Helal Nemat Farahzadi
Publikováno v:
Journal of Human Genetics and Genomics. 3
Background: Familial Mediterranean fever (FMF) is the most common type of periodic fever syndrome. The disease is most prevalent in the western Mediterranean population, but today it is widespread in the world due to the large ethnic migrations of Tu
Publikováno v:
Gene Reports. 26:101466
Publikováno v:
Gene Reports. 26:101450
Publikováno v:
Journal of Research in Medical and Dental Science, Vol 6, Iss 1, Pp 295-300 (2018)
Introduction: lung cancer is a disease that is characterized by an uncontrolled growth of the cell in the lung tissue. This cancer is the most common cause of cancer death worldwide. The SOX2, OCT4 and NANOG transcription factor are the main regulato
Autor:
Mohammad Esmaeil Akbari, Faravareh Khordadpoor Deilamani, Shohre Zare Karizi, Sara Khatamianfar
Publikováno v:
Journal of Human Genetics and Genomics. 3
Background: Chronic myeloproliferative disorders (CMPD) occur due toclonal proliferation of the single hematopoietic stem cells and result in an increased number of mature and immature cells in the peripheral blood. The mutations in JAK2 gene are ide
Autor:
Shokouholsadat Mahdavi, Fatemeh Omrani Tabarestani, Shohre Zare Karizi, Mohammad Esmaeil Akbari, Faravareh Khordadpoor Deilamani, Farzane Bahari, Gholam Reza Babamohamadi
Publikováno v:
Journal of Neurology & Neurophysiology.
Background: Mental retardation is a relatively frequent disorder and occurs in 1-3% of the general population. Chromosomal rearrangements involving microdeletion and microduplication particularly in subtelomeric regions are involved as a significant