Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Majid, Yavarian"'
Autor:
Arghavan Kavosi, Saeideh Hosseini Ghale Noei, Samaneh Madani, Solmaz Khalighfard, Saeed Khodayari, Hamid Khodayari, Malihe Mirzaei, Mohammad Reza Kalhori, Majid Yavarian, Ali Mohammad Alizadeh, Mojtaba Falahati
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/d264b2f83487443f80bfff8bd17c5c03
Autor:
Ali Amanati, Parisa Badiee, Mehrzad Lotfi, Ahmad Monabati, Mohammad Ali Faghihi, Majid Yavarian, Nazafarin Hatami-Mazinani
Publikováno v:
Current Medical Mycology, Vol 6, Iss 3, Pp 73-78 (2020)
Background and Purpose: Skin rashes, mostly seen in children and adolescents, are considered among the most common side effects of azole antifungals. Although therapeutic concentrations of voriconazole (VCZ) have been documented for infected skin, th
Externí odkaz:
https://doaj.org/article/97adbbd76b7245cea00450e1dfb4ca62
Autor:
Farzaneh Ardeshir, Leila Keshavarz, Fatemeh Asadian, Gohar Omidmokhtarkhanloo, Majid Yavarian
Publikováno v:
International Journal of Reproductive BioMedicine, Vol 18, Pp 747-754 (2020)
Background: Insulin-like growth factor-2 (IGF-2) is a polypeptide growth factor and one of the first genes expressed prior to the implantation of the embryo, with its highest expression in the placental cells. Its activity strongly depends on the gen
Externí odkaz:
https://doaj.org/article/139490961b3e450d95353f2c053f0861
Autor:
Malihe Mirzaei, Arghavan Kavosi, Mahboobeh Sharifzadeh, Ghazale Mahjoub, Mohammad Ali Faghihi, Parham Habibzadeh, Majid Yavarian
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Abstract Background Dihidropyrimidinase (DHP) deficiency is an inherited inborn error of pyrimidine metabolism with a variable clinical presentation and even asymptomatic subjects. Dihydropyrimidinase is encoded by the DPYS gene, thus pathogenic muta
Externí odkaz:
https://doaj.org/article/869381773d4e409f843b18e28ac102ba
Autor:
Parham Habibzadeh, Mohammad Silawi, Hassan Dastsooz, Shima Bahramjahan, Shahrokh Ezzatzadegan Jahromi, Vahid Reza Ostovan, Majid Yavarian, Mohammad Mofatteh, Mohammad Ali Faghihi
Publikováno v:
BMC Gastroenterology, Vol 20, Iss 1, Pp 1-7 (2020)
Abstract Background Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is a rare autosomal recessive disorder caused by mutations in TYMP gene, encoding nuclear thymidine phosphorylase (TP). MNGIE mainly presents with gastrointestinal symp
Externí odkaz:
https://doaj.org/article/1ad67086578c4d8dbcb568d201b04d92
Autor:
Leila Keshavarz, Majid Yavarian
Publikováno v:
International Journal of Reproductive BioMedicine, Vol 17, Pp 473-480 (2019)
Background Recurrent spontaneous abortion (RSA) often remains unclear and can be burden for the patient and time consuming for clinician. RSA may initiates from a genetic or non-genetic factors. It is well known that the quality of placental cir
Externí odkaz:
https://doaj.org/article/eb66b821304c4eeabbf2fe7cb00bce5b
Publikováno v:
Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, Vol 24, Iss 11, Pp 861-867 (2017)
Introduction: Sirtuin 1 is a protein deacetylase that plays an important role in many cellular processes. The serum sirtuin 1 levels are higher in the polycystic ovary syndrome (PCOS) patients than the healthy subjects. The aim of this study was to a
Externí odkaz:
https://doaj.org/article/8d41923187744a2c86c8317eef2a179c
Autor:
Parham Habibzadeh, Soroor Inaloo, Mohammad Silawi, Hassan Dastsooz, Mohammad Ali Farazi Fard, Forough Sadeghipour, Zahra Faghihi, Mohaddeseh Rezaeian, Majid Yavarian, Johann Böhm, Mohammad Ali Faghihi
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Mitochondrial complex III deficiency nuclear type 2 is an autosomal-recessive disorder caused by mutations in TTC19 gene. TTC19 is involved in the preservation of mitochondrial complex III, which is responsible for transfer of electrons from reduced
Externí odkaz:
https://doaj.org/article/d312bc71ba574865a1c9b67a15653618
Autor:
Fatemeh Asadian, Majid Yavarian, Leila Keshavarz, Gohar Omidmokhtarkhanloo, Farzaneh Ardeshir
Publikováno v:
International Journal of Reproductive BioMedicine, Vol 18, Pp 747-754 (2020)
International Journal of Reproductive Biomedicine
International Journal of Reproductive Biomedicine
Background: Insulin-like growth factor-2 (IGF-2) is a polypeptide growth factor and one of the first genes expressed prior to the implantation of the embryo, with its highest expression in the placental cells. Its activity strongly depends on the gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1db5e7d1d5fdc197cabb6b03e5a37f9c
https://doaj.org/article/139490961b3e450d95353f2c053f0861
https://doaj.org/article/139490961b3e450d95353f2c053f0861
Autor:
Majid Yavarian, Parisa Badiee, Ali Amanati, Mohammad Ali Faghihi, Ahmad Monabati, Nazafarin Hatami Mazinani, Mehrzad Lotfi
Publikováno v:
Current Medical Mycology
Current Medical Mycology, Vol 6, Iss 3, Pp 73-78 (2020)
Current Medical Mycology, Vol 6, Iss 3, Pp 73-78 (2020)
Background and Purpose: Skin rashes, mostly seen in children and adolescents, are considered among the most common side effects of azole antifungals. Although therapeutic concentrations of voriconazole (VCZ) have been documented for infected skin, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5716763c13cba3c5e6e436e4a9543bb1
http://europepmc.org/articles/PMC8018824
http://europepmc.org/articles/PMC8018824