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Biological Psychiatry|September 22, 2019
Synaptic Dysfunction in Human Neurons With Autism-Associated Deletions in PTCHD1-ASP Joel Ross, Wen-Bo Zhang, Rebecca S F Mok, et al.
International Journal of Molecular Sciences|October 14, 2023
Transcriptional Dysregulation and Impaired Neuronal Activity in FMR1 Knock-Out and Fragile X Patients' iPSC-Derived ModelsGilles Maussion, Cecilia Rocha, Narges Abdian, et al.
Brain Communications|October 11, 2021
Midbrain organoids with an SNCA gene triplication model key features of synucleinopathyNguyen-Vi Mohamed, Julien Sirois, Janani Ramamurthy, et al.
Autophagy|July 8, 2025
Activation of endogenous PRKN by structural derepression is linked to increased turnover of the E3 ubiquitin ligaseFabienne C Fiesel, Bernardo A Bustillos, Jens O Watzlawik, et al.
Nature Medicine|January 27, 2015
Whole-genome sequencing of quartet families with autism spectrum disorderRyan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, et al.
NPJ Genomic Medicine|August 16, 2016
Genome-wide characteristics of de novo mutations in autismRyan K C Yuen, Daniele Merico, Hongzhi Cao, et al.
Nature|May 13, 2026
An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autismClarrisa A Bradley, Sangyoon Y Ko, Meng Tian, et al.
Nature Neuroscience|March 7, 2017
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorderRyan K C Yuen, Daniele Merico, Matt Bookman, et al.
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