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Disease Models & Mechanisms|September 1, 2025
The importance of imperfect pre-clinical models in adolescent idiopathic scoliosisDiane S Sepich, Ryan S Gray, Nadav Ahituv, et al.Journal of Lipid Research|July 18, 2008
A new mouse mutant for the LDL receptor identified using ENU mutagenesisKaren L Svenson, Nadav Ahituv, Rebecca S Durgin, et al.Communications Medicine|August 21, 2025
Leveraging sequences missing from the human genome to diagnose cancerIlias Georgakopoulos-Soares, Ofer Yizhar-Barnea, Ioannis Mouratidis, et al.Science (New York, N.Y.)|December 15, 2018
CRISPR-mediated activation of a promoter or enhancer rescues obesity caused by haploinsufficiencyNavneet Matharu, Sawitree Rattanasopha, Serena Tamura, et al.Plos Genetics|October 26, 2019
Dysregulation of STAT3 signaling is associated with endplate-oriented herniations of the intervertebral disc in Adgrg6 mutant miceZhaoyang Liu, Garrett W D Easson, Jingjing Zhao, et al.Plos Computational Biology|June 27, 2014
Integrating diverse datasets improves developmental enhancer predictionGenevieve D Erwin, Nir Oksenberg, Rebecca M Truty, et al.Biorxiv : the Preprint Server for Biology|June 19, 2023
Impaired cerebellar plasticity hypersensitizes sensory reflexes in SCN2A-associated ASDChenyu Wang, Kimberly D Derderian, Elizabeth Hamada, et al.American Journal of Human Genetics|September 9, 2017
Variant Interpretation: Functional Assays to the RescueLea M Starita, Nadav Ahituv, Maitreya J Dunham, et al.Nature Communications|August 10, 2019
Saturation mutagenesis of twenty disease-associated regulatory elements at single base-pair resolutionMartin Kircher, Chenling Xiong, Beth Martin, et al.Human Molecular Genetics|January 13, 2022
Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysisHélène Choquet, Weiyu Li, Jie Yin, et al.Pageof 18