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Nature Genetics|June 15, 2026
Decoding common and rare noncoding variant effects across cellular and developmental contextsAndrew R Marderstein, Soumya Kundu, Evin M Padhi, et al.Genome Research|May 20, 2025
Integrated single-cell multiome analysis reveals muscle fiber-type gene regulatory circuitry modulated by endurance exerciseAliza B Rubenstein, Gregory R Smith, Zidong Zhang, et al.Blood Advances|September 10, 2021
Lymphoid blast transformation in an MPN with BCR-JAK2 treated with ruxolitinib: putative mechanisms of resistanceJustin Anthony Chen, Yanli Hou, Krishna M Roskin, et al.Biorxiv : the Preprint Server for Biology|June 4, 2026
Building an Interoperable Rare Disease Multi-omic Resource: The GREGoR Data Model and DatasetBenjamin D Heavner, Marsha M Wheeler, Jesse D Bengtsson, et al.Genome Research|March 13, 2013
The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomesStephen B Montgomery, David L Goode, Erika Kvikstad, et al.Nature Medicine|July 31, 2019
Atheroprotective roles of smooth muscle cell phenotypic modulation and the TCF21 disease gene as revealed by single-cell analysisRobert C Wirka, Dhananjay Wagh, David T Paik, et al.Nature Medicine|July 15, 2025
Disruption of the cerebrospinal fluid-plasma protein balance in cognitive impairment and agingAmelia Farinas, Jarod Rutledge, Veronica Augustina Bot, et al.American Journal of Epidemiology|October 6, 2017
Current Challenges and New Opportunities for Gene-Environment Interaction Studies of Complex DiseasesKimberly McAllister, Leah E Mechanic, Christopher Amos, et al.Nature Communications|March 21, 2020
FAM13A affects body fat distribution and adipocyte functionMohsen Fathzadeh, Jiehan Li, Abhiram Rao, et al.Genome Research|May 9, 2015
The landscape of genomic imprinting across diverse adult human tissuesYael Baran, Meena Subramaniam, Anne Biton, et al.Pageof 20