Showing results (91-100 of 179) with videos related to
Sort By:
Pageof 18
Clinical Laboratory|October 3, 2015
Frequencies of Six (Five Novel) STR Markers Linked to TUSC3 (MRT7) or NSUN2 (MRT5) Genes Used for Homozygosity Mapping of Recessive Intellectual DisabilityShirin Ghadami, Hossein Malek Mohammadi, Jamileh Malbin, et al.Molecular Biology Reports|October 20, 2021
The role of miRNA-377 as a tumor suppressor in lung cancer by negative regulation of genes belonging to ErbB signaling pathwaySaba Hashemi, Naghmeh Yari, Fatemeh Rahimi Jamnani, et al.Journal of Molecular Neuroscience : MN|June 6, 2016
Linkage Study Revealed Complex Haplotypes in a Multifamily due to Different Mutations in CAPN3 Gene in an Iranian Ethnic GroupMarzieh Mojbafan, Seyed Hassan Tonekaboni, Maryam Abiri, et al.Iranian Journal of Basic Medical Sciences|January 27, 2018
Novel frameshift mutation in the <i>KCNQ1</i> gene responsible for Jervell and Lange-Nielsen syndromeAzam Amirian, Seyed Mohammad Dalili, Zahra Zafari, et al.Therapeutic Advances in Respiratory Disease|June 21, 2024
Identification and <i>in silico</i> structural analysis for the first <i>de novo</i> mutation in the cystic fibrosis transmembrane conductance regulator protein in Iran: case report and developmental insight using microsatellite markersAmin Hosseini Nami, Mahboubeh Kabiri, Fatemeh Zafarghandi Motlagh, et al.Journal of Arrhythmia|June 29, 2018
Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange-Nielsen syndrome in 2 Iranian familiesAzam Amirian, Zahra Zafari, Mohammad Dalili, et al.Archives of Iranian Medicine|January 4, 2011
First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in IranAzam Amirian, Morteza Karimipoor, Masoumeh Jafarinejad, et al.BMC Infectious Diseases|October 13, 2017
G allele at -924 A > G position of FoxP3 gene promoter as a risk factor for tuberculosisElham Beiranvand, Saeid Abediankenari, Soghra Khani, et al.Molecular Biology Reports|December 11, 2025
Genetic variability in maple syrup urine disease: novel mutations and their pathogenicity in the Iranian populationMansooreh Jafari, Fatemeh Karami, Iman Salahshourifar, et al.Hemoglobin|December 24, 2005
The IVS-II-1 (G-->a) beta0-thalassemia mutation in cis with HbA2-Troodos [delta116(G18)Arg-->Cys (CGC-->TGC)] causes a complex prenatal diagnosis in an Iranian familyS Mohammad Eram, Babak Azimifar, Hassan Abolghasemi, et al.Pageof 18