Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mohammadarian, Akbari"'
Autor:
Mohammadarian Akbari, Reyhane Eghtedarian, Bashdar Mahmud Hussen, Solat Eslami, Mohammad Taheri, Soudeh Ghafouri-Fard
Publikováno v:
BMC Psychiatry, Vol 22, Iss 1, Pp 1-7 (2022)
Abstract Angiotensin-converting enzyme (ACE) as an important enzyme in the renin-angiotensin system facilitates biogenesis of the functionally active product angiotensin II from angiotensin I. ACE gene contains a number of functional polymorphisms wh
Externí odkaz:
https://doaj.org/article/791336e454034cb7a2f00dbbc15af921
Autor:
Mohammadarian Akbari, Bashdar Mahmud Hussen, Solat Eslami, Seyedeh Morvarid Neishabouri, Soudeh Ghafouri-Fard
Publikováno v:
Heliyon, Vol 9, Iss 3, Pp e14081- (2023)
Obsessive-compulsive disorder (OCD) is a disorder in which genetic factors participate. ANRIL is an example of long non-coding RNAs with crucial roles in the pathoetiology of multifactorial disorders, including neuropsychiatric conditions. We apprais
Externí odkaz:
https://doaj.org/article/103aa8de1d7e42588bd19c01d63a305b
Autor:
Mohammadarian Akbari, Reyhane Eghtedarian, Bashdar Mahmud Hussen, Solat Eslami, Mohammad Taheri, Seyedeh Morvarid Neishabouri, Soudeh Ghafouri-Fard
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
Dysfunction of regulatory T cells (Tregs) has been shown to affect the etiology of autism spectrum disorder (ASD). Differentiation of this group of T cells has been found to be regulated by a group of long non-coding RNAs (lncRNAs). In this study, we
Externí odkaz:
https://doaj.org/article/358a8e992e8e4edbbabfda45ede58f5c
Autor:
Mohammadarian Akbari, Mahdi Gholipour, Bashdar Mahmud Hussen, Mohammad Taheri, Solat Eslami, Arezou Sayad, Soudeh Ghafouri-Fard
Publikováno v:
Metabolic Brain Disease. 37:901-909
Autor:
Mohammadarian Akbari, Mahdi Gholipour, Hedyeh Davoudikianersi, Bashdar Mahmud Hussen, Atefe Abak, Solat Eslami, Soudeh Ghafouri-Fard, Arezou Sayad
Publikováno v:
Acta neurologica Belgica.
NF-κB partakes in the pathophysiology of neurologic conditions. We quantified levels of NF-κB-associated genes in 119 patients with migraine versus healthy controls.We measured levels of NF-κB-associated genes in 42 patients with migraine compared
Autor:
Mohammadarian Akbari, Fatemeh Eshghyar, Mahdi Gholipour, Solat Eslami, Bashdar Mahmud Hussen, Mohammad Taheri, Mir Davood Omrani, Soudeh Ghafouri-Fard
Publikováno v:
Metabolic brain diseaseReferences. 37(6)
mTOR has been shown to be involved in the regulation of immune responses and differentiation of immune cells. This protein is a candidate molecule for unraveling the molecular mechanisms of autoimmune disorders such as multiple sclerosis (MS). We des
Autor:
Mohammadarian Akbari, Reyhane Eghtedarian, Bashdar Mahmud Hussen, Solat Eslami, Mohammad Taheri, Soudeh Ghafouri-Fard
Publikováno v:
BMC psychiatry. 22(1)
Angiotensin-converting enzyme (ACE) as an important enzyme in the renin-angiotensin system facilitates biogenesis of the functionally active product angiotensin II from angiotensin I. ACE gene contains a number of functional polymorphisms which modul
Autor:
Soudeh Ghafouri-Fard, Bashdar Mahmud Hussen, N M Arefian, Golbarg Mehrpoor, Mohammad Taheri, Solat Eslami, Mohammadarian Akbari
Publikováno v:
Vascular Pharmacology
Contribution of the renin-angiotensinogen system in the risk of COVID-19 and related complications have been assessed by several groups. However, the results are not consistent. We examined levels of ACE1 and ACE2 in the circulation of two groups of
Autor:
Reyhane, Eghtedarian, Mohammadarian, Akbari, Elham, Badrlou, Bashdar, Mahmud Hussen, Solat, Eslami, Mehdi, Akhavan-Bahabadi, Mohammad, Taheri, Soudeh, Ghafouri-Fard, Seyedeh Morvarid, Neishabouri
Publikováno v:
European Journal of Pharmacology. 932:175205
Schizophrenia is a neuropsychiatric disorder characterized by a variety of clinical manifestations. This disorder has a complex inheritance. Oxytocinegic system has been shown to be implicated in the pathophysiology of schizophrenia. This system can
Autor:
Mohammadarian Akbari, Elham Badrlou, Solat Eslami, Bashdar Mahmud Hussen, Mohammad Taheri, Seyedeh Morvarid Neishabouri, Soudeh Ghafouri-Fard
Publikováno v:
Human Gene. 33:201046