Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Fatemeh Aghakhani Moghadam"'
Autor:
Behnoosh Soghani, Asghar Ebadifar, Hamid Reza Khorram Khorshid, Koorosh Kamali, Roya Hamedi, Fatemeh Aghakhani Moghadam
Publikováno v:
BioImpacts, Vol 7, Iss 4, Pp 263-268 (2017)
Introduction: Cleft lip/palate is one of the most common congenital defects and is supposed to have multifactorial etiology, including a complex interaction between genetics and environment. Reduced folate carrier 1 (RFC1) gene takes part in folate t
Externí odkaz:
https://doaj.org/article/a176eee01911403c9ebebaa6c2111b63
Autor:
Asghar Ebadifar, Roya Hamedi, Hamid Reza KhorramKhorshid, Koorosh Kamali, Fatemeh Aghakhani Moghadam
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 19, Iss 4, Pp 366-373 (2016)
Objective(s):We investigated the influence of genetic variation of the transforming growth-factor alpha (TGFA) locus on the relationship between smoking and oral clefts. Materials and methods:In this study 105 Iranian infants with non-syndromic cleft
Externí odkaz:
https://doaj.org/article/aeb4937f6f4945fcbaf3f9ba2dd14f50
Autor:
Gholam Abbas Kaydani, Seyedeh Elham Mortazavi, Seyed Amir Momeni, Talat Mokhtari-Azad, Fatemeh Aghakhani Moghadam, Hanieh Behravan, Mohammad Khazeni, Azarakhsh Azaran, Zakiye Mokhames, Farhad Jeddi, Ebrahim Kord, Seyed Mohammad Hashemi-Shahri, Azam Ghaziasadi, Alijan Tabarraei, Fatemeh Ghodratpour, Masood Ziaee, Ali Jafarpour, Jila Yavarian, Abdolvahab Moradi, Azar Hadadi, Zohreh Fattahi, Hossein Najmabadi, Shokouh Ghafari, Issa Jahanzad, Reza Malekzadeh, Marzieh Mohseni, Farid Yousefi, Shahram Habibzadeh, Seyed Mohammad Jazayeri, Khadijeh Jalalvand, Saber Soltani, Kimia Kahrizi, Alireza Soleimani, Sadegh Ali Azimi, Reza Najafipour, Alireza Abdollahi, Fatemeh Keshavarzi
Publikováno v:
Transboundary and Emerging Diseases
The SARS‐CoV‐2 virus has been rapidly spreading globally since December 2019, triggering a pandemic, soon after its emergence. While Iran was among the first countries confronted with rapid spread of virus in February 2020, no real‐time SARS‐
Autor:
Reza Najafipour, Kord E, Zohreh Fattahi, Zakiye Mokhames, Fatemeh Ghodratpour, Azarakhsh Azaran, Alireza Abdollahi, Issa Jahanzad, Fatemeh Keshavarzi, Mohammad Khazeni, Talat Mokhtari-Azad, Khadijeh Jalalvand, Seyed Mohammad Hashemi-Shahri, Seyed Mohammad Jazayeri, Shokouh Ghafari, Farid Yousefi, Abdolvahab Moradi, Alireza Soleimani, Gholam Abbas Kaydani, Alijan Tabarraei, Marzieh Mohseni, Farhad Jeddi, Shahram Habibzadeh, Azam Ghaziasadi, Fatemeh Aghakhani Moghadam, Ali Jafarpour, Hossein Najmabadi, Kimia Kahrizi, Saber Soltani, Mortazavi Se, Jila Yavarian, Reza Malekzadeh, Momeni Sa, Azar Hadadi, Hanieh Behravan, Sadegh Ali Azimi, Masoud Ziaee
The SARS-CoV-2 virus has been rapidly spreading globally since December 2019, triggering a pandemic, soon after its emergence, with now more than one million deaths around the world. While Iran was among the first countries confronted with rapid spre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40d504d10ed2f1872ded4b9b35e02c6a
https://doi.org/10.1101/2020.11.16.20229047
https://doi.org/10.1101/2020.11.16.20229047
Autor:
Koorosh Kamali, Mitra Saket, Kioomars Saliminejad, Nazanin Esmaeili Anvar, Fatemeh Aghakhani Moghadam, Hamid Reza Khorram Khorshid
Publikováno v:
Archives of Oral Biology. 72:134-137
Objective Non-syndromic cleft lip with or without cleft palate (CL/P) is one of the most common congenital anomalies and arises from the interaction of environmental and genetic factors. The objective of this study was to investigate the association
Autor:
Mohsen, Soosanabadi, Reza, Mirfakhraie, Lilit, Atanesyan, Akbar, Biglarian, Fatemeh, Aghakhani Moghadam, Maryam, Rahimi, Farkhondeh, Behjati, Elaheh, Keyhani
Publikováno v:
Reports of biochemistrymolecular biology. 8(1)
BACKGROUND: The aim of this study was to assess the usability of multiplex ligation-dependent probe amplification (MLPA) for copy number determination of HER gene family members (ERBB1-4) in invasive breast carcinoma and to explore the association of
Autor:
Reza Pazhoomand, Elahe Keyhan, Mehdi Banan, Hossein Najmabad, Masoud Karimlou, Faranak Khodadad, Alireza Iraniparast, Farnaz Feiz, Keivan Majidzadeh, Ideh Bahman, Fatemeh Aghakhani Moghadam, Atoosa Madadkar Sobhani, Seyedeh Sedigheh Abedin, Ahad Muhammadnejad, Farkhondeh Behjat
Publikováno v:
Asian Pacific Journal of Cancer Prevention. 14:7621-7628
Human epidermal growth factor receptor (HER) status is an important prognostic factor in breast cancer. There is no globally accepted method for determining its status, and which method is most precise is still a matter of debate. We here analyzed HE
Autor:
Asghar, Ebadifar, Roya, Hamedi, Hamid Reza, Khorram Khorshid, Kioomars, Saliminejad, Koorosh, Kamali, Fatemeh, Aghakhani Moghadam, Nazanin, Esmaeili Anvar, Nazilla, Ameli
Publikováno v:
Avicenna Journal of Medical Biotechnology
Background: Cleft lip with or without cleft palate (CL/P) is one of the most common congenital anomalies and the etiology of orofacial clefts is multifactorial. Transforming growth factor alpha (TGFA) is expressed at the medial edge epithelium of fus
Autor:
Reza, Pazhoomand, Elahe, Keyhani, Mehdi, Banan, Hossein, Najmabadi, Faranak, Khodadadi, Alireza, Iraniparast, Farnaz, Feiz, Keivan, Majidzadeh, Ideh, Bahman, Fatemeh Aghakhani, Moghadam, Atoosa Madadkar, Sobhani, Ahad, Muhammadnejad, Seyedeh Sedigheh, Abedini, Farkhondeh, Behjati
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 14(12)
Human epidermal growth factor receptor (HER) status is an important prognostic factor in breast cancer. There is no globally accepted method for determining its status, and which method is most precise is still a matter of debate. We here analyzed HE
Autor:
Haruo, Shimazaki, Reza, Vazifehmand, Mohhamad-Hassan, Heidari, Hamid-Reza, Khorram-Khorshid, Sassan, Saber, Shamsodin, Hejazi, Fatemeh, Aghakhani-Moghadam, Yi, Ouyang, Junko, Honda, Imaharu, Nakano, Yoshihisa, Takiyama
Publikováno v:
Archives of Iranian medicine. 11(4)
The authors describe a large Iranian family with autosomal dominant cerebellar ataxia, which included 14 patients in four generations. We examined seven patients who had expanded CAG repeats in the CACNA1A gene with repeat instability (24 and 25 repe