Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Halimeh Rezaei"'
Publikováno v:
Cell Journal, Vol 23, Iss 3, Pp 341-348 (2021)
Objective: Hemophilia-A is a common genetic abnormality resulted from decreased or lack of factor VIII (FVIII) pro-coagulant protein function caused by mutations in the F8 gene. Majority of molecular studies consider screening of mutations and their
Externí odkaz:
https://doaj.org/article/3649018d25124f7bb50301ddde63dc52
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 36, Iss 475, Pp 366-371 (2018)
Background: Colorectal cancer is the third cancer which results in death in western countries. Some of the risk factors of this cancer are age, inadequate diet, obesity, inactivity, genetic changes, etc. Considering the relationship between genetic c
Externí odkaz:
https://doaj.org/article/076a40c35b064f8fb7bb5b31c022a850
Publikováno v:
Iranian Journal of Reproductive Medicine, Vol 13, Iss 9, Pp 563-570 (2015)
Background: Infertility is a health problem which affects about 10-20% of married couples. Male factor infertility is involved approximately 50% of infertile couples. Most of male infertility is regarding to deletions in the male-specific region of t
Externí odkaz:
https://doaj.org/article/fadefd6365a047afaddf68a37f38bb3c
Publikováno v:
Cell Journal, Vol 16, Iss 3, Pp 309-314 (2014)
Objective: People are usually susceptible to carcinogenic aromatic amines, present in cigarrette smoke and polluted environment, which can cause DNA damage. Therefore, maintenance of genomic DNA integrity is a direct result of proper function of DN
Externí odkaz:
https://doaj.org/article/68d6b730ec084c6ba212b3e891004ed2
Publikováno v:
تاکسونومی و بیوسیستماتیک, Vol 5, Iss 14, Pp 35-40 (2013)
GJB2 gene encodes connexin 26 which is an important skin-expressed gap junction protein. Connexin 26 is a transmembrane protein that is involved in the potassium ion recycling pathway in the inner ear. In this study, the neutrality tests were perform
Externí odkaz:
https://doaj.org/article/eb4cfe878e5b48999e8d338e365ebdcb
Autor:
Setareh Taghipour Kamalabad, Zahra Zamanzadeh, Halimeh Rezaei, Maryam Tabatabaeian, Morteza Abkar
Publikováno v:
Breast Disease. 42:45-58
BACKGROUND: Multiple lines of evidence suggest that single nucleotide polymorphisms (SNPs) in genes encoding components of the microRNA processing machinery may underlie susceptibility to various human diseases, including cancer. OBJECTIVE: The prese
Autor:
Reza Ghanbari, Ali Attaripour Isfahani, Sina Pirmoradian, Halimeh Rezaei, Sasan Radfar, Majid Kheirollahi
Publikováno v:
Analytical Biochemistry. 665:115052
Publikováno v:
Iranian Journal of Biotechnology
Background: Hemophilia A is an X-linked bleeding disorder resulting in a deficiency of plasma clotting factor VIII and caused by mutations in the FVIII gene (F8 gene). MicroRNAs (miRNAs) in body fluids are promising biomarker candidates for Hemophili
Publikováno v:
Molecular Biology Research Communications
Hemophilia A is an X-linked bleeding disorder that occurs due to the deficiency of Factor VIII (FVIII) protein clotting activity. The mutations in the F8 gene, which encodes FVIII coagulating protein have been widely reviewed. However, there is a wid
Publikováno v:
Bioelectrochemistry. 145:108087
Determination of microRNAs (miRNAs) as valuable blood-borne biomarkers has attracted many scientific attentions. However, analytical methods are still restricted by miRNAs intrinsic characteristics. In this study, for the first time, novel blackberry