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Michael D Wilson

Showing results (191-200 of 215) with videos related to

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NPJ Genomic Medicine|July 2, 2025
Assessing the diagnostic impact of blood transcriptome profiling in a pediatric cohort previously assessed by genome sequencingHuayun Hou, Kyoko E Yuki, Gregory Costain, et al.
Nature Communications|November 12, 2024
Inter-chromosomal contacts demarcate genome topology along a spatial gradientMilad Mokhtaridoost, Jordan J Chalmers, Marzieh Soleimanpoor, et al.
Nature Communications|October 30, 2024
Inhibiting EZH2 targets atypical teratoid rhabdoid tumor by triggering viral mimicry via both RNA and DNA sensing pathwaysShengrui Feng, Sajid A Marhon, Dustin J Sokolowski, et al.
Annals of Clinical and Translational Neurology|July 8, 2016
A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsyNaim Panjwani, Michael D Wilson, Laura Addis, et al.
Molecular Cell|January 19, 2020
Candidate Cancer Driver Mutations in Distal Regulatory Elements and Long-Range Chromatin Interaction NetworksHelen Zhu, Liis Uusküla-Reimand, Keren Isaev, et al.
Elife|October 4, 2014
Multi-species, multi-transcription factor binding highlights conserved control of tissue-specific biological pathwaysBenoit Ballester, Alejandra Medina-Rivera, Dominic Schmidt, et al.
JCI Insight|October 22, 2024
Autosomal-dominant macular dystrophy linked to a chromosome 17 tandem duplicationRabiat Adele, Rowaida Hussein, Erika Tavares, et al.
Circulation Research|October 12, 2020
Genome-Wide Analysis Identifies an Essential Human TBX3 Pacemaker EnhancerVincent W W van Eif, Stephanie I Protze, Fernanda M Bosada, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 9, 2022
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndromeRachel Youjin Oh, Ashish R Deshwar, Ashish Marwaha, et al.
Developmental Cell|December 18, 2018
Dual Regulatory Functions of SUFU and Targetome of GLI2 in SHH Subgroup MedulloblastomaWen-Chi Yin, Thevagi Satkunendran, Rong Mo, et al.
Pageof 22

Showing results (191-200 of 215) with videos related to

Sort By:
Pageof 22
NPJ Genomic Medicine|July 2, 2025
Assessing the diagnostic impact of blood transcriptome profiling in a pediatric cohort previously assessed by genome sequencingHuayun Hou, Kyoko E Yuki, Gregory Costain, et al.
Nature Communications|November 12, 2024
Inter-chromosomal contacts demarcate genome topology along a spatial gradientMilad Mokhtaridoost, Jordan J Chalmers, Marzieh Soleimanpoor, et al.
Nature Communications|October 30, 2024
Inhibiting EZH2 targets atypical teratoid rhabdoid tumor by triggering viral mimicry via both RNA and DNA sensing pathwaysShengrui Feng, Sajid A Marhon, Dustin J Sokolowski, et al.
Annals of Clinical and Translational Neurology|July 8, 2016
A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsyNaim Panjwani, Michael D Wilson, Laura Addis, et al.
Molecular Cell|January 19, 2020
Candidate Cancer Driver Mutations in Distal Regulatory Elements and Long-Range Chromatin Interaction NetworksHelen Zhu, Liis Uusküla-Reimand, Keren Isaev, et al.
Elife|October 4, 2014
Multi-species, multi-transcription factor binding highlights conserved control of tissue-specific biological pathwaysBenoit Ballester, Alejandra Medina-Rivera, Dominic Schmidt, et al.
JCI Insight|October 22, 2024
Autosomal-dominant macular dystrophy linked to a chromosome 17 tandem duplicationRabiat Adele, Rowaida Hussein, Erika Tavares, et al.
Circulation Research|October 12, 2020
Genome-Wide Analysis Identifies an Essential Human TBX3 Pacemaker EnhancerVincent W W van Eif, Stephanie I Protze, Fernanda M Bosada, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 9, 2022
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndromeRachel Youjin Oh, Ashish R Deshwar, Ashish Marwaha, et al.
Developmental Cell|December 18, 2018
Dual Regulatory Functions of SUFU and Targetome of GLI2 in SHH Subgroup MedulloblastomaWen-Chi Yin, Thevagi Satkunendran, Rong Mo, et al.
Pageof 22