Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mohammad H, Sanati"'
Autor:
Yeganeh, Eshaghkhani, Mohammad H, Sanati, Manouchehr, Nakhjavani, Reza, Safari, Alireza, Khajavi, Mitra, Ataei, Zohreh, Jadali
Publikováno v:
Minerva endocrinologica. 41(1)
Graves' disease (GD) is a common autoimmune disorder that is primarily driven by malfunction of T lymphocytes, which influences the production of antibodies reacting with cellular and tissue components of the thyroid gland. The aim of this study was
Autor:
Reyhaneh, Lahmy, Masoud, Soleimani, Mohammad H, Sanati, Mehrdad, Behmanesh, Fatemeh, Kouhkan, Naser, Mobarra
Publikováno v:
Journal of tissue engineering and regenerative medicine. 10(6)
Development of stem cell-based therapies for the treatment of type 1 diabetes would provide a renewable supply of human β-cells. Human embryonic stem cells (ESCs) are considered to be one of the stem cell populations with sufficient proliferative ca
Autor:
Behnaz, Bayat, Shahin, Yazdani, Afagh, Alavi, Mohsen, Chiani, Fereshteh, Chitsazian, Betsabeh Khoramian, Tusi, Fatemeh, Suri, Mehrnaz, Narooie-Nejhad, Mohammad H, Sanati, Elahe, Elahi
Publikováno v:
Molecular Vision
Purpose To investigate the role of MYOC and CYP1B1 in Iranian juvenile open angle glaucoma (JOAG) patients. Methods Twenty-three JOAG probands, their available affected and unaffected family members, and 100 ethnically matched control individuals wit
Autor:
Seyed A, Mesbah-Namin, Mohammad H, Sanati, Alireza, Mowjoodi, Philip J, Mason, Tom J, Vulliamy, Mohammad R, Noori-Daloii
Publikováno v:
British journal of haematology. 117(3)
We report the first investigation of glucose- 6-phosphate dehydrogenase (G6PD) deficiency among the Mazandaranians in the north of Iran. We analysed the G6PD gene in 74 unrelated G6PD-deficient men with a history of favism. Molecular analysis reveale