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Cell Genomics|July 9, 2024
Crosstalk between epitranscriptomic and epigenomic modifications and its implication in human diseasesChengyu Li, Kexuan Chen, Qianchen Fang, et al.Cell Genomics|July 17, 2024
Rare variation in non-coding regions with evolutionary signatures contributes to autism spectrum disorder riskTaehwan Shin, Janet H T Song, Michael Kosicki, et al.Cell Genomics|January 26, 2024
Multiplex single-cell chemical genomics reveals the kinase dependence of the response to targeted therapyJosé L McFaline-Figueroa, Sanjay Srivatsan, Andrew J Hill, et al.Cell Genomics|August 29, 2024
Isotype-aware inference of B cell clonal lineage trees from single-cell sequencing dataLeah L Weber, Derek Reiman, Mrinmoy S Roddur, et al.Cell Genomics|August 28, 2024
Rhinovirus infection of airway epithelial cells uncovers the non-ciliated subset as a likely driver of genetic risk to childhood-onset asthmaSarah Djeddi, Daniela Fernandez-Salinas, George X Huang, et al.Cell Genomics|August 31, 2024
ABCA7-dependent induction of neuropeptide Y is required for synaptic resilience in Alzheimer's disease through BDNF/NGFR signalingHüseyin Tayran, Elanur Yilmaz, Prabesh Bhattarai, et al.Cell Genomics|September 17, 2024
Functional and dynamic profiling of transcript isoforms reveals essential roles of alternative splicing in interferon responseMahoko Takahashi Ueda, Jun Inamo, Fuyuki Miya, et al.Cell Genomics|September 12, 2024
Long genetic and social isolation in Neanderthals before their extinctionLudovic Slimak, Tharsika Vimala, Andaine Seguin-Orlando, et al.Cell Genomics|September 12, 2024
Overcoming drug-resistant tumors with selection gene drivesHui Wang, Mingqi XieCell Genomics|September 12, 2024
Ribosomes unraveled: The path from variant to impactPaxton Kostos, Anna Galligos, Jennifer L GertonPageof 68