Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Hamid Reza, Khorramkhorshid"'
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:
Asghar Ebadifar, Nazila Ameli, Hamid Reza Khorramkhorshid, Mehdi Salehi Zeinabadi, Kourosh Kamali, Tayyebeh Khoshbakht
Publikováno v:
Journal of Dental Research, Dental Clinics, Dental Prospects, Vol 9, Iss 2, Pp 101-104 (2015)
Background and aims. The aim of the present study is to determine the incidence of MTHFR C677 T and A1298C muta-tions in Iranian patients with cleft lip and/or cleft palate. Materials and methods. We screened 61 Iranian patients with cleft lip and/o
Externí odkaz:
https://doaj.org/article/0c64865fa4674981bce51bd5d60ae4fa
Autor:
Reza Morvaridi Farimani, Mohsen Azimi-Nezhad, Hamid Reza KhorramKhorshid, Asghar Ebadifar, Saba Tohidkhah, Zahra Jafarian, Koorosh Kamali, Zeinab Nazari, Reza Ebrahimzadeh-Vesal
Publikováno v:
Avicenna Journal of Medical Biotechnology.
Background: Non-Syndromic Cleft Lip with or without cleft Palate (NSCL/P) is a common developmental disorder of the head and neck with a multifactorial etiology. The current study aimed to evaluate the potential association of PTCH1 (rs10512248) and
Autor:
Reza, Morvaridi Farimani, Mohsen, Azimi-Nezhad, Hamid Reza, KhorramKhorshid, Asghar, Ebadifar, Saba, Tohidkhah, Zahra, Jafarian, Koorosh, Kamali, Zeinab, Nazari, Reza, Ebrahimzadeh-Vesal
Publikováno v:
Avicenna journal of medical biotechnology. 14(4)
Non-Syndromic Cleft Lip with or without cleft Palate (NSCL/P) is a common developmental disorder of the head and neck with a multifactorial etiology. The current study aimed to evaluate the potential association ofIn the present study, blood samples
Autor:
Asghar Ebadifar, Nazila Ameli, Hamid Reza KhorramKhorshid, Koorosh Kamali, Mehdi Salehi Zeinabadi
Publikováno v:
Journal of Research in Medical Sciences, Vol 21, Iss 1, Pp 59-59 (2016)
Background: We studied the role of maternal folic acid supplementation in modifying the effects of methylenetetrahydrofolate reductase (MTHFR C677T and A1298C) gene polymorphisms in Iranian children with oral clefts. Materials and Methods: Forty-seve
Externí odkaz:
https://doaj.org/article/a547a53e197d4660adf1650e921488a1
Publikováno v:
Journal of reproductioninfertility. 20(2)
The purpose of this study was to analyze the expression level of CRISP2, CATSPER1, PATE1 and SEMG1 genes in the sperm of men with asthenozoospermia (AZS). AZS is a cause of infertility in men in which the motility of the sperm is reduced. So far, a f