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Genes & Diseases|December 18, 2020
Whole-exome sequencing identified a novel mutation of MLH1 in an extended family with lynch syndromeHamid Ghaedi, Samira Molaei Ramsheh, Maryam Erfanian Omidvar, et al.Journal of Medical Biochemistry|December 21, 2018
Association of MiR-149 (RS2292832) Variant with the Risk of Coronary Artery DiseaseMaryam Ghaffarzadeh, Hamid Ghaedi, Behnam Alipoor, et al.Clinical Laboratory|March 9, 2017
The pre-mir-499 Variant rs3746444 May Contribute to Coronary Artery Disease Susceptibility: a Case-Control and Meta-Analysis StudyAfsaneh Labbaf, Hamid Ghaedi, Behnam Alipoor, et al.Biological Chemistry|February 28, 2023
Characterization of Kv1.2-mediated outward current in TRIP8b-deficient miceAfsaneh Labbaf, Maurice Dellin, Marlene Komadowski, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 25, 2025
TREK1 Channels Shape Spindle-Like Oscillations, Neuronal Activity, and Short-Term Synaptic Plasticity in Thalamocortical CircuitsAfsaneh Labbaf, Valérie Krauth, Nicole Rychlik, et al.Pageof 1