Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Tayebeh Oghabi Bakhshaiesh"'
Autor:
Rasoul Motahari, Mohammad Amin Boshagh, Setareh Moghimi, Fariba Peytam, Zaman Hasanvand, Tayebeh Oghabi Bakhshaiesh, Roham Foroumadi, Hamidreza Bijanzadeh, Loghman Firoozpour, Ali Khalaj, Rezvan Esmaeili, Alireza Foroumadi
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-17 (2022)
Abstract The novel derivatives of tetrahydropyridothienopyrimidine-based compounds have been designed and efficiently synthesized with good yields through seven steps reaction. The anticancer activity of compounds 11a-y has been evaluated against MCF
Externí odkaz:
https://doaj.org/article/07d7a0f7d0774faaab270e0b593877c1
Publikováno v:
Cell Cycle
Radiotherapy has an essential role in breast cancer treatment. However, tumor cells may be resistant to radiotherapy. Noncoding RNAs are considered regulators of different pathways which modulate radiotherapy. This systematic review classifies long n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d8eca64e4d5abdea78c25656de51d4a
https://doi.org/10.1080/15384101.2022.2035915
https://doi.org/10.1080/15384101.2022.2035915
Autor:
Alireza Vajhi, Amir Darbandi-Azar, Rezvan Esmaeili, Leila Eini, Anita Sadeghpour, Narges Jafarbeik-Iravani, Farzad Masoudkabir, Parisa Hoseinpour, Tayebeh Oghabi Bakhshaiesh, Majid Sadeghizadeh, Keivan Majidzadeh-A
Publikováno v:
The American Journal of the Medical Sciences. 361:765-775
Background Stem cell therapy is among the novel approaches for the treatment of post-myocardial infarction cardiomyopathy. This study aims to compare the effect of stromal-derived factor 1 α (SDF1α), mesenchymal stem cells (MSCs) in combination wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::801a2e8c6f1bc8e883500d7731fb22bd
https://doi.org/10.1016/j.amjms.2021.01.025
https://doi.org/10.1016/j.amjms.2021.01.025
Autor:
Zaman Hasanvand, Tayebeh Oghabi Bakhshaiesh, Fariba Peytam, Loghman Firoozpour, Elaheh Hosseinzadeh, Rasoul Motahari, Setareh Moghimi, Elaheh Nazeri, Mahsa Toolabi, Farhad Momeni, Hamidreza Bijanzadeh, Ali Khalaj, Blandine Baratte, Béatrice Josselin, Thomas Robert, Stéphane Bach, Rezvan Esmaeili, Alireza Foroumadi
Publikováno v:
Bioorganic Chemistry. 133:106383
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ff9bcfa76e07a5e9cce353da089f3fb
https://doi.org/10.1016/j.bioorg.2023.106383
https://doi.org/10.1016/j.bioorg.2023.106383
Autor:
Tayebeh Oghabi Bakhshaiesh, Elahe Nazeri, Narges Jafarbeik-Iravani, Zainab Shirvani-Farsani, Rezvan Esmaeili
Publikováno v:
Annals of medicine and surgery (2012). 80
•BsmI and TaqI have association with breast cancer risk in Iranian women.•No significant associations were identified between the FokI and ApaI and breast cancer risk in Iranian women.•No association was detected between Vitamin D level and bre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf4a5c2cce946e36500b525a1c9c2303
https://pubmed.ncbi.nlm.nih.gov/36045810
https://pubmed.ncbi.nlm.nih.gov/36045810
Autor:
Adileh Ayati, Tayebeh Oghabi Bakhshaiesh, Mahsa Toolabi, Rezvan Esmaeili, Elahe Nazeri, Loghman Firoozpour, Alireza Foroumadi, Ayoub Aghcheli, Maryam Norouzbahari, Setareh Moghimi
Publikováno v:
Medicinal Chemistry Research. 29:2000-2010
A novel series of 1-(5-(benzylthio)-1,3,4-thiadiazol-2-yl)-3-phenylurea derivatives (5a–l) were designed and synthesized as sorafenib analogs. The in vitro cytotoxicity effects of synthesized compounds were evaluated against four different human ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84bfec1c3526e0d5780f813bac51c82c
https://doi.org/10.1007/s00044-020-02616-2
https://doi.org/10.1007/s00044-020-02616-2
Autor:
Esmaeil Mohammadian, Tayebeh Oghabi Bakhshaiesh, Abolghasem Jouyban, Elahe Nazeri, Zaman Hasanvand, Setareh Moghimi, Rasoul Motahari, Loghman Firoozpour, Hamidreza Bijanzadeh, Mahmood Alizadeh Sani, Elaheh Hosseinzadeh, Rezvan Esmaeili, Alireza Foroumadi
Publikováno v:
Archiv der Pharmazie. 356:2200349
An important role has been considered for the vascular endothelial growth factor receptor 2 (VEGFR-2) in the angiogenesis process, so that its inhibition is an important scientific way for cancer treatment. In this work, new thienopyrimidine derivati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa138397349bd332d72660e1694ea484
https://doi.org/10.1002/ardp.202200349
https://doi.org/10.1002/ardp.202200349
Autor:
Saeed Emami, Tayebeh Oghabi Bakhshaiesh, Loghman Firoozpour, Adileh Ayati, Keivan Majidzadeh-A, Rezvan Esmaeili, Setareh Moghimi, Maliheh Safavi, Alireza Foroumadi
Publikováno v:
European Journal of Medicinal Chemistry. 155:483-491
A series of new coumarin-containing compounds 3a-l and 4a-c was designed and synthesized based on the chalcone-type 4-amino-5-cinnamoylthiazole scaffold 2, and screened for their in vitro anticancer and antioxidant activities. Representatively, the 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f169470e894fea4e7ab97a3efb59303
https://doi.org/10.1016/j.ejmech.2018.06.015
https://doi.org/10.1016/j.ejmech.2018.06.015
Autor:
Tayebeh Oghabi Bakhshaiesh, Keivan Majidzadeh-A, Saeed Emami, Setareh Moghimi, Rezvan Esmaeili, Zahra Eslami-S, Alireza Foroumadi, Adileh Ayati, Maliheh Safavi
Publikováno v:
European Journal of Medicinal Chemistry. 145:404-412
A series of 4-amino-5-cinnamoylthiazoles 3a-p were designed and synthesized as chalcone-like anticancer agents. The synthesized derivatives 3a-p were evaluated for their in vitro antiproliferative activities against three different human cancer cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9003f63187f61afdedc9d970e751c6e1
https://doi.org/10.1016/j.ejmech.2018.01.015
https://doi.org/10.1016/j.ejmech.2018.01.015
Autor:
Tayebeh Oghabi Bakhshaiesh, Zaman Hasanvand, Rezvan Esmaeili, Ali Khalaj, Mahsa Toolabi, Ayoub Aghcheli, Setareh Moghimi, Somayeh Salarinejad, Elahe Nazeri, Alireza Foroumadi
Publikováno v:
European journal of medicinal chemistry. 185
In this paper, we described the synthesis and cytotoxic activities of two new series of thieno[2,3-d]pyrimidine and thieno[3,2-d] pyrimidine derivatives. Most of the synthesized compounds had significant antiproliferative activities against PC3, MDA-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b34742bf2376a16e667702e18019cda
https://pubmed.ncbi.nlm.nih.gov/31671308
https://pubmed.ncbi.nlm.nih.gov/31671308