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Medical Oncology (Northwood, London, England)|December 11, 2013
HE4 combined with CA125: favorable screening tool for ovarian cancerNasrin Ghasemi, Samira Ghobadzadeh, Mahnaz Zahraei, et al.
Genetic Testing and Molecular Biomarkers|March 10, 2016
An Association Study of the SLC19A1 Gene Polymorphisms/Haplotypes with Idiopathic Recurrent Pregnancy Loss in an Iranian PopulationShirin Mohtaram, Mohammad Hasan Sheikhha, Negar Honarvar, et al.
Journal of Immunotoxicology|August 14, 2015
Association between lower frequency of R381Q variant (rs11209026) in IL-23 receptor gene and increased risk of recurrent spontaneous abortion (RSA)Elham Abdollahi, Fataneh Tavasolian, Nasrin Ghasemi, et al.
International Journal of Reproductive Biomedicine|October 31, 2017
Frequency of <i>TNFR1 36 A/G</i> gene polymorphism in azoospermic infertile men: A case-control studyHamid Reza Ashrafzadeh, Tahere Nazari, Masoud Dehghan Tezerjani, et al.
International Journal of Reproductive Biomedicine|April 29, 2026
Meiotic gene expression of <i>STAG3</i> and <i>DMC1</i> in blood: A novel non-invasive biomarker approach for diminished ovarian reserve: A case-control studyKhosro Namjoo, Farzaneh Iravani, Fateme Montazeri, et al.
International Journal of Molecular and Cellular Medicine|June 27, 2020
Utilization of Whole Exome Sequencing in Lethal Form of Multiple Pterygium Syndrome: Identification of Mutations in Embryonal Subunit of Acetylcholine ReceptorTahere Nazari, Ali Rashidi-Nezhad, Maziar Ganji, et al.
Experimental Eye Research|August 14, 2021
Homozygous females for a X-linked RPGR-ORF15 mutation in an Iranian family with retinitis pigmentosaFahimeh Beigi, Marta Del Pozo-Valero, Inmaculada Martin-Merida, et al.
Clinical and Experimental Reproductive Medicine|April 18, 2018
Variable localization of Toll-like receptors in human fallopian tube epithelial cellsFatemehsadat Amjadi, Zahra Zandieh, Ensieh Salehi, et al.
Journal of Assisted Reproduction and Genetics|December 11, 2013
The association of arylendosulfatase 1 (SULF1) gene polymorphism with recurrent miscarriageMahnaz Zahraei, Mohammad Hasan Sheikhha, Seyed Mehdi Kalantar, et al.
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