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American Journal of Human Genetics|September 29, 2021
ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomaliesGabrielle Lemire, Yoko A Ito, Aren E Marshall, et al.
Annals of Neurology|November 19, 2025
Pathogenic Variants in RNU2-2, a Non-coding Spliceosomal RNA, Cause a Distinctive Developmental and Epileptic EncephalopathyAnnie T G Chiu, Mark F Bennett, Harshini Thiyagarajah, et al.
Biorxiv : the Preprint Server for Biology|May 7, 2024
An integrated single-cell RNA-seq map of human neuroblastoma tumors and preclinical models uncovers divergent mesenchymal-like gene expression programsRichard H Chapple, Xueying Liu, Sivaraman Natarajan, et al.
Neuron|March 7, 2024
Multimodal sensory control of motor performance by glycinergic interneurons of the mouse spinal cord deep dorsal hornMark A Gradwell, Nofar Ozeri-Engelhard, Jaclyn T Eisdorfer, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Genome sequencing boosts diagnostic yield for the developmental and epileptic encephalopathiesJacob E Munro, Harshini Thiyagarajah, Mark F Bennett, et al.
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