Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Marziyeh Mojbafan"'
Autor:
Azita Tavasoli, Khadije Arjmandi Rafsanjani, Saba Hemmati, Marziyeh Mojbafan, Elham Zarei, Soudabeh Hosseini
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-6 (2019)
Abstract Background Manganese is a critical trace element that not only has antioxidant properties, but also is essential for various metabolic pathways and neurotransmitters production. However, it can be toxic at high levels, particularly in the ce
Externí odkaz:
https://doaj.org/article/27010929c87b44c9b3dcb3e2e2081938
Autor:
Marziyeh Mojbafan, Kamran Ghaedi, Shahnaz Razavi, Fereshteh Karamali, Khadijeh Karbalaii, Somayeh Tanhaie, Farzaneh Rabiee, Mohammad Hossein Nasr Esfahani, Hossein Baharvand
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 28, Iss 110 (2010)
Background: P19 cells are mouse embryonic carcinoma cells which contain pluripotent ability, like stem cells, to differentiate into different cell lines. There are several properties for this cell line that make it a valuable cell model for study of
Externí odkaz:
https://doaj.org/article/9d4bc5d8683e4972a390b5084c898bf5
Autor:
Marziyeh Mojbafan, Soudabeh Hosseini, Elham Zarei, Saba Hemmati, Azita Tavasoli, Khadije Arjmandi Rafsanjani
Publikováno v:
BMC Pediatrics
BMC Pediatrics, Vol 19, Iss 1, Pp 1-6 (2019)
BMC Pediatrics, Vol 19, Iss 1, Pp 1-6 (2019)
Background Manganese is a critical trace element that not only has antioxidant properties, but also is essential for various metabolic pathways and neurotransmitters production. However, it can be toxic at high levels, particularly in the central ner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f6a439f9869eede21950e2e72682ffb
http://europepmc.org/articles/PMC6615235
http://europepmc.org/articles/PMC6615235
Autor:
Sirous Zeinali, Mohammad Reza Noori-Daloii, Morteza Karimipoor, Marziyeh Mojbafan, Maryam Abiri, Masomeh Safi, Atefeh Jodaki, Soodeh Kianfar, Mohammad Reza Alaei, Ameneh Bandehi Sarhaddi, Razieh Karamzadeh
Publikováno v:
Metabolic Brain Disease. 32:105-113
Maple Syrup Urine Disease (MSUD) is a rare autosomal recessive disorder of branched-chain amino acid (BCAA) metabolism. The disease is mainly caused by mutations either in the BCKDHA, BCKDHB, DBT or DLD genes encoding components of the E1α, E1β, E2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59db4f39a13e9e67ddb3da2ff5c589bc
https://doi.org/10.1007/s11011-016-9867-1
https://doi.org/10.1007/s11011-016-9867-1