Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tohid Naderi"'
Autor:
Tohid Naderi, Samira Mohammadi Yeganeh, Neda Mohammadi-Hezaveh, Razie Hadavi, Ahmad Gharehbaghian, Nader Vazifeh Shiran, Vahid Fallah Azad, Mahdi Paryan
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 23, Iss 3, Pp 376-382 (2020)
Objective(s): microRNAs are small non-coding molecules that regulate gene expression in various biological processes. T-cell acute lymphoblastic leukemia (T-ALL) is a malignancy accompanied with genetic aberrations and accounts for 20% of children’
Externí odkaz:
https://doaj.org/article/b36f1cb61e1345ce8b0ff3767e108813
Autor:
Pedram Torabian, Hassan Yousefi, Aysan Fallah, Zahra Moradi, Tohid Naderi, Mahsa Rostamian Delavar, Yavuz Nuri Ertas, Ali Zarrabi, Amir Reza Aref
Breast cancer is the most frequently diagnosed malignancy in women and a major public health concern. In the current report, differential expression of the breast cancer resistance promoting genes with a focus on breast cancer stem cell related eleme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da20871cde554482963d57de4986dba6
https://avesis.erciyes.edu.tr/publication/details/a75971da-78b6-46ca-9d32-0e0fc7892098/oai
https://avesis.erciyes.edu.tr/publication/details/a75971da-78b6-46ca-9d32-0e0fc7892098/oai
Autor:
Aysan Fallah, Mahmood Shams, Elnaz Agi, Mohammad Jazebi, Mohammad R. Baghaipoor, Tohid Naderi, Mohammad R. Rezvany
Publikováno v:
Blood Coagulation & Fibrinolysis. 33:75-82
Factor X deficiency is a rare bleeding disorder that affects almost 1 : 1000 000 people worldwide. It derives from multiple mutational changes in the factor X gene (F10). The main objective of the present study was to determine a consistent correlati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f4f79726286e2c424f6fab921f7a33b
https://doi.org/10.1097/mbc.0000000000001101
https://doi.org/10.1097/mbc.0000000000001101
Autor:
Akbar Dorgalaleh, Mehran Bahraini, Mahmood Shams, Fereshteh Parhizkari, Ali Dabbagh, Tohid Naderi, Aysan Fallah, Alieh Fazeli, Seyed Esmaeil Ahmadi, Amir Samii, Maryam Daneshi, Farshad Heydari, Shadi Tabibian, Behnaz Tavasoli, Ali Noroozi-Aghideh, Tahere Tabatabaei, Mohammad Saeed Gholami
Publikováno v:
Blood Reviews. 59:101029
Rare bleeding disorders (RBDs), including factor (F) I, FII, FV, FVII, combined FV and FVIII (CF5F8), FXI, FXIII and vitamin-K dependent coagulation factors (VKCF) deficiencies, are a heterogeneous group of hemorrhagic disorder with a variable bleedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aec7312a45aa456c6763db91753ef95e
https://doi.org/10.1016/j.blre.2022.101029
https://doi.org/10.1016/j.blre.2022.101029
Autor:
Negin Soghli, Hassan Yousefi, Tohid Naderi, Aysan Fallah, Amin Moshksar, Farzaneh Darbeheshti, Cecilia Vittori, Mahsa Rostamian Delavar, Ali Zare, Habib Sadeghi Rad, Abtin Kazemi, Amirreza Bitaraf, Bashdar Mahmud Hussen, Mohammad Taheri, Elena Jamali
Publikováno v:
Pathology - Research and Practice. 243:154341
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd59049cf2ff660d0b7c11c4449ea30e
https://doi.org/10.1016/j.prp.2023.154341
https://doi.org/10.1016/j.prp.2023.154341
Autor:
Maryam Daneshi, Tohid Naderi, Shadi Tabibian, Mahmood Shams, Jamal Rashidpanah, Akbar Dorgalaleh
Publikováno v:
Journal of Cellular and Molecular Anesthesia, Vol 3, Iss 4, Pp 146-154 (2019)
Congenital prothrombin deficiency is an extremely rare hemorrhagic disorder with estimated prevalence of 1 per 2,000,000 in the general population. Since the disorder is an autosomal recessive disorder, the disorder is more frequent in areas with hig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::23bfcec81931f962ac8eeac7f3c4d29c
http://journals.sbmu.ac.ir/jcma/article/view/23494
http://journals.sbmu.ac.ir/jcma/article/view/23494