Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Arsham Banisadr"'
Autor:
Mahboobeh Ramezani, Bita Javan, Mohammad Hasan Jafari, Arsham Banisadr, Mahdieh pourafshar, seyedeh Sara Raeissadati, Pardis Mokhtary, Mohammad Arefi, Azizeh Karimian, Morteza Oladnabi
Publikováno v:
Journal of Clinical and Basic Research, Vol 5, Iss 4, Pp 31-43 (2021)
Background and objectives: In gene expression studies, to validate and obtain reliable results, normalization of qRT-PCR data by housekeeping genes (HKGs) is required. However, the expression level of these genes may vary in tissues or cells and may
Externí odkaz:
https://doaj.org/article/08d56e7cd52d4f7ca5c438a44397ef3a
Publikováno v:
Human Vaccines & Immunotherapeutics, Vol 14, Iss 4, Pp 856-863 (2018)
The aim of this study was to produce a humanized single chain antibody (scFv) as a potential improved product design to target EGFR (Epidermal Growth Factor Receptor) overexpressing cancer cells. To this end, CDR loops of cetuximab (an FDA-approved a
Externí odkaz:
https://doaj.org/article/c8d24c5e0b5e45f1bac83b230912538d
Publikováno v:
Metabolic Brain Disease. 37:2669-2675
Sandhoff disease is a rare neurodegenerative and autosomal recessive disorder, which is characterized by a defect in ganglioside metabolism. Also, it is caused by mutations in the HEXB gene for the β-subunit isoform 1 of β-N-acetyl hexosaminidase.
Autor:
Atena Farahpour, Navid Ramezanian, Leila Gholami, Saeedeh Askarian, Arsham Banisadr, Reza Kazemi Oskuee
Publikováno v:
Pharmaceutical development and technology. 27(5)
Cationic polymers endowed with a flexible system for condensing DNA, are regarded as effective materials for gene delivery. The synthesis of poly(β-amino esters) (pBAEs) based on 1,4-butanediol diacrylate-ethanolamine monomer (1.2:1 molar ratio) and
Novel homozygous HEXB mutation identified in a consanguineous Iranian pedigree with Sandhoff disease
Background Sandhoff disease is a rare neurodegenerative and autosomal recessive disorder, characterized by a defect in ganglioside metabolism. It is caused by mutations in the HEXB gene for the β-subunit of β-N-acetyl hexosaminidase. Results In the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de4d528b3c1859cf2ba3a9072d87f0b1
https://doi.org/10.21203/rs.2.21720/v1
https://doi.org/10.21203/rs.2.21720/v1
Publikováno v:
Human Vaccines & Immunotherapeutics. 14:856-863
The aim of this study was to produce a humanized single chain antibody (scFv) as a potential improved product design to target EGFR (Epidermal Growth Factor Receptor) overexpressing cancer cells. To this end, CDR loops of cetuximab (an FDA-approved a
Autor:
Mahdieh Pourafshar, Safoura Khajeniazi, Arsham Banisadr, Yaghoub Yazdani, Yaghoub Safdari, Kamal Veisi
Publikováno v:
International Journal of Peptide Research and Therapeutics. 24:171-178
Recombinant expression and EGFR-binding activity assay of single chain nimotuzumab (nimotuzumab scFv) is reported in this study. The scFv was produced in VH-linker-VL format in Origami™ 2(DE3)pLysS bacterial cells and purified using Ni-TNA resin co
Autor:
Farahpour, Atena1 (AUTHOR), Ramezanian, Navid1 (AUTHOR) ramezanian@um.ac.ir, Gholami, Leila2 (AUTHOR), Askarian, Saeedeh3 (AUTHOR), Banisadr, Arsham4 (AUTHOR), Kazemi Oskuee, Reza5 (AUTHOR) OskueeKR@mums.ac.ir
Publikováno v:
Pharmaceutical Development & Technology. Jun2022, Vol. 27 Issue 5, p606-614. 9p.
Autor:
Pourafshar, Mahdieh1, Safdari, Yaghoub1,2 Safdari_14@yahoo.com, Khajeniazi, Safoura2, Yazdani, Yaghoub3, Banisadr, Arsham1, Veisi, Kamal4
Publikováno v:
International Journal of Peptide Research & Therapeutics. Mar2018, Vol. 24 Issue 1, p171-178. 8p.
Publikováno v:
Metabolic Brain Disease; Dec2022, Vol. 37 Issue 8, p2669-2675, 7p