Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Morteza Karimipour"'
Autor:
Mahdi Mohammadi Ghanbarlou, Shahriyar Abdoli, Hamed Omid, Leila Qazizadeh, Hadi Bamehr, Mozhgan Raigani, Hosein Shahsavarani, Morteza Karimipour, Mohammad Ali Shokrgozar
Publikováno v:
Magnetochemistry, Vol 9, Iss 3, p 71 (2023)
The overexpression of stem cell-related genes such as octamer-binding transcription factor 4 (OCT4) and (sex determining region Y)-box 2 (SOX2) has been indicated to play several critical roles in stem cell self-renewal; moreover, the elevation of th
Externí odkaz:
https://doaj.org/article/ee85c465e5ca47b194ab0dc134972d28
Autor:
Venus Vatankhah, Arash Mirabzadeh, Hamidreza Iranpour, Bahman Dieji, Mehdi Norouzi, Morteza Karimipour, Jaleh Nobakht, Elham Esmaeili, Maryam Ayazi
Publikováno v:
Iranian Rehabilitation Journal, Vol 17, Iss 4, Pp 369-376 (2019)
Objectives: Schizophrenia is a chronic psychiatric disorder, which reduces the patient’s quality of life. Although a minimum dose of medications has been recommended for treating this disorder, antipsychotic polypharmacy has been used experimentall
Externí odkaz:
https://doaj.org/article/c00aafe64ffc4d408e2e3307e17fd6c3
Autor:
Azam Amirian, Seyed Mohammad Dalili, Zahra Zafari, Siamak Saber, Morteza Karimipour, Vahid Akbari, Amirfarjam Fazelifar, Sirous Zeinali
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 21, Iss 1, Pp 108-111 (2018)
Objective(s): Jervell and Lange–Nielsen syndrome is an autosomal recessive disorder caused by mutations in KCNQ1 or KCNE1 genes. The disease is characterized by sensorineural hearing loss and long QT syndrome. Methods: Here we present a 3.5-year-ol
Externí odkaz:
https://doaj.org/article/9b38e1cfd6d8411fa5820575c3cae96c
Autor:
Shamseddin Yousef-Amoli, Leila Kokabee, Keyvan Majidzadeh-Ardebili, Rezvan Esmaeili, Hamzeh Rahimi, Fahimeh Maryami, Morteza Karimipour
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 32, Iss 273, Pp 50-58 (2014)
Background: Cancer-Testis genes (CT-genes) are a gene family that only expressed in normal testis tissue and some of them are randomly expressed in some types of cancers. These genes can be promising cases for immunotherapy of breast cancer. This res
Externí odkaz:
https://doaj.org/article/d03bc4e564324bcc885ccda5c90720d2
Publikováno v:
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum, Vol 7, Iss 5, Pp 28-34 (2013)
Background and Objectives: Hemophilia A (HA) is an X-linked recessive bleeding disorder. The disease is caused by mutations in the F8 gene. Inversion of intron 22 is the most common causative mutation of severe hemophilia A, which is detectable by so
Externí odkaz:
https://doaj.org/article/e05ede2cb973430aa5281b8ae61cf3f2
Autor:
Sadegh Yoosefee, Esmaeil Shahsavand Ananloo, Mohammad-Taghi Joghataei, Morteza Karimipour, Mahmoudreza Hadjighassem, Hoorie Mohaghghegh, Mehdi Tehrani-Doost, Amir-Abbas Rahimi, Hamid Mostafavi Abdolmaleky, Maryam Hatami
Publikováno v:
Iranian Journal of Psychiatry, Vol 11, Iss 3 (2016)
Objective: Although the etiology of schizophrenia is unknown, it has a significant genetic component. A number of studies have indicated that neuregulin-1 (NRG1) gene may play a role in the pathogenesis of schizophrenia. In this study, we exami
Externí odkaz:
https://doaj.org/article/f88643ba93d643a583c04c0165a051b7
Autor:
Mahin Hashemipour, Fahimeh Soheilipour, Sakineh Karimizare, Hossein Khanahmad, Morteza Karimipour, Sepideh Aminzadeh, Leila Kokabee, Massoud Amini, Silva Hovsepian, Rezvaneh Hadian
Publikováno v:
International Journal of Endocrinology, Vol 2012 (2012)
Background. Thyroid peroxidase gene (TPO) mutations are one of the most common causes of thyroid dyshormonogenesis in patients with congenital hypothyroidism (CH). In this study, the prevalence of TPO gene mutations in patients with thyroid dyshormon
Externí odkaz:
https://doaj.org/article/d528decbb8514d4c864c49b97ad88d2f
Autor:
Mahdi Behdani, Sirous Zeinali, Morteza Karimipour, Hossein Khanahmad, Nader Asadzadeh, Kayhan Azadmanesh, Negar Seyed, Seyed Farzad Baniahmad, Mahdi Habibi Anbouhi
Publikováno v:
Advanced Biomedical Research, Vol 1, Iss 1, Pp 34-34 (2012)
Antibodies and their derivative fragments have long been used as tools in a variety of applications, in fundamental research work, biotechnology, diagnosis, and therapy. Camels produce single heavy-chain antibodies (VHH) in addition to usual antibodi
Externí odkaz:
https://doaj.org/article/998a5a6a56a946d1b0bb2b89e7512d24
Publikováno v:
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum, Vol 1, Iss 4, Pp 28-0 (2008)
Background and Objectives: Hemophilia A (HA) is an X-linked recessive bleeding disorder. The disease is caused by mutations in the F8 gene. Inversion of intron 22 is the most common causative mutation of severe hemophilia A, which is detectable by so
Externí odkaz:
https://doaj.org/article/fbc6d3e2f9ab439e8b55f0f7356a6cd8
Autor:
Hoorie Mohaghghegh, Esmaeil Shahsavand Ananloo, Mahmoudreza Hadjighasem, Morteza Karimipour, Shiva Hashemizadeh, Seyyed Ali Ahmadi Abhari
Publikováno v:
Journal of Molecular Neuroscience. 72:1670-1681
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c190e9563ca3be8bc2a1b69aa871428e
https://doi.org/10.1007/s12031-021-01879-7
https://doi.org/10.1007/s12031-021-01879-7