Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ali Kowsari"'
Publikováno v:
Research in Molecular Medicine, Vol 8, Iss 2, Pp 93-102 (2020)
Background: Cell viability and apoptosis are two crucial factors that may determine cell fate. There are several factors, such as hypoxia, which may be effective in cell processes. Because of its unique features, such as its antioxidant, anti-inflamm
Externí odkaz:
https://doaj.org/article/55e335e5a3e44ea8befe9abf11e246e2
Autor:
Tahereh Zarei Taher, Ali Kowsari, Mohsen Sheykhhasan, Hamed Manoochehri, Naser Kalhor, Leila Naserpour
Publikováno v:
Journal of Advanced Biomedical Sciences, Vol 9, Iss 4, Pp 1758-1773 (2019)
The widespread use of effective vaccines against infectious diseases has been one of the most important public health progresses in the 21st century. Early vaccines containing weakened or inactivated pathogens or toxins may elicit robust, protective
Externí odkaz:
https://doaj.org/article/f0a8ad6b4b4a4f8d88469a3dbeed62e3
Publikováno v:
Sālmand, Vol 11, Iss 3, Pp 440-447 (2016)
Objectives GSTs are detoxification enzymes that remove excess reactive oxygen species (ROS) from cells. Evidence suggests that oxidative stress plays a role in several stages of the neurodegenarative disease like Alzheimer disease. Free radicals and
Externí odkaz:
https://doaj.org/article/733409e30aec4a6a908f2b27d87593bb
Publikováno v:
Acta Medica Iranica, Vol 47, Iss 3 (2009)
The deciduous teeth play a very important role in proper alignment, placing and occlusion of permanent teeth. Calcification of deciduous teeth begins during the fourth month of fetal life, and by the end of sixth month all of the deciduous teeth have
Externí odkaz:
https://doaj.org/article/e71d311cee9346fb977289b864a82580
Publikováno v:
Clinical Medicine And Health Research Journal. 2:165-168
Background: Pycnodysostosis is a rare autosomal recessive skeletal dysplasia, which is characterized by various skeletal malformations and distinctive facial characteristics. The disorder is caused by mutations in CTSK gene at chromosomal region 1q21
Publikováno v:
Clinical Medicine And Health Research Journal. 2:99-102
Introduction: Argininemia is an autosomal recessive uncommon metabolic condition, caused by mutations in arginase enzyme. Variable clinical symptoms of argininemia might bring about a delayed diagnosis. In order to prove an argininemia condition, a g
Autor:
Seyedeh Saeideh Sahraei, Ali Kowsari, Faezeh Davoodi Asl, Mohsen Sheykhhasan, Leila Naserpoor, Azar Sheikholeslami
Publikováno v:
Anatomy & Cell Biology. 55:100-108
Endometriosis is a common, benign gynecological disease which is determined as an overspreading of endometrial tissue in exterior region of the uterine cavity. Evidence suggests that retrograde menstrual blood which contains mesenchymal stem cells wi
Publikováno v:
International Journal of English Language and Translation Studies, Vol 08, Iss 04, Pp 69-76 (2021)
This study examined the effect of negative evidence on young learners’ performance on grammar test. Gass (1997) asserted that negative evidence, also known as “negative feedback”, offers the learner with information about the inaccuracy of a se
Publikováno v:
Research in Molecular Medicine, Vol 8, Iss 2, Pp 93-102 (2020)
Background: Cell viability and apoptosis are two crucial factors that may determine cell fate. There are several factors, such as hypoxia, which may be effective in cell processes. Because of its unique features, such as its antioxidant, anti-inflamm
Autor:
Safoura Khamse, Hossein Afshar, Mina Ohadi, Fatemeh Adelirad, Ahmad Delbari, Ali Kowsari, Reza Najafipour, Ali Bozorgmehr, Naser Kalhor, Mahshid Foroughan, Neda Nazaripanah
Publikováno v:
Gerontology. 66:514-522
Background: Approximately 2% of the human core promoter short tandem repeats (STRs) reach lengths of ≥6 repeats, which may in part be a result of adaptive evolutionary processes and natural selection. A single-exon transcript of the human nescient