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Experimental Eye Research|February 8, 2020
The pathogenicity of SLC38A8 in five families with foveal hypoplasia and congenital nystagmusChen Weiner, Idan Hecht, Ygal Rotenstreich, et al.
Proceedings of Machine Learning Research|September 27, 2021
Marginal Contribution Feature Importance - an Axiomatic Approach for Explaining DataAmnon Catav, Boyang Fu, Yazeed Zoabi, et al.
Journal of Medical Genetics|May 20, 2015
Rare genetic variants in Tunisian Jewish patients suffering from age-related macular degenerationEran Pras, Dana Kristal, Nadav Shoshany, et al.
Plos One|May 23, 2018
Analysis of microRNAs in familial Mediterranean feverGil Amarilyo, Nir Pillar, Ilan Ben-Zvi, et al.
Human Genetics|April 27, 2017
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidismNir Pillar, Oren Pleniceanu, Mingyan Fang, et al.
Iscience|September 11, 2023
mRNA splicing is modulated by intronic microRNAsLuba Farberov, Daphna Weissglas-Volkov, Guy Shapira, et al.
Bioorganic & Medicinal Chemistry|March 31, 2004
Bioactivation of carbamate-based 20(S)-camptothecin prodrugsNeta Pessah, Mika Reznik, Marina Shamis, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|April 20, 2020
The black sheep of the family- whole-exome sequencing in family of lithium response discordant bipolar monozygotic twinsAsaf Jacobs, Michal Hagin, Miraz Shugol, et al.
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