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Human Molecular Genetics|May 24, 2007
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathwaysYuhei Nishimura, Christa L Martin, Araceli Vazquez-Lopez, et al.
NPJ Regenerative Medicine|October 1, 2022
Clinically relevant small-molecule promotes nerve repair and visual function recoveryNgan Pan Bennett Au, Gajendra Kumar, Pallavi Asthana, et al.
Neuron|December 21, 2021
Oxytocin normalizes altered circuit connectivity for social rescue of the Cntnap2 knockout mouseKatrina Y Choe, Richard A I Bethlehem, Martin Safrin, et al.
Nature|March 22, 2018
De novo mutations in regulatory elements in neurodevelopmental disordersPatrick J Short, Jeremy F McRae, Giuseppe Gallone, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 3, 2008
The HDAC inhibitor 4b ameliorates the disease phenotype and transcriptional abnormalities in Huntington's disease transgenic miceElizabeth A Thomas, Giovanni Coppola, Paula A Desplats, et al.
Science (New York, N.Y.)|February 27, 2025
4D marmoset brain map reveals MRI and molecular signatures for onset of multiple sclerosis-like lesionsJing-Ping Lin, Alexis Brake, Maxime Donadieu, et al.
Experimental Neurology|April 1, 2023
Nav1.7 gain-of-function mutation I228M triggers age-dependent nociceptive insensitivity and C-LTMR dysregulationNivanthika K Wimalasena, Daniel G Taub, Jaehoon Shim, et al.
Medrxiv : the Preprint Server for Health Sciences|July 9, 2020
Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health SystemTimothy S Chang, Yi Ding, Malika K Freund, et al.
Cerebral Cortex (New York, N.Y. : 1991)|September 13, 2022
A neural stem cell paradigm of pediatric hydrocephalusPhan Q Duy, Pasko Rakic, Seth L Alper, et al.
Cancer Research Communications|October 10, 2022
Pathway-based approach reveals differential sensitivity to E2F1 inhibition in glioblastomaAlvaro G Alvarado, Kaleab Tessema, Sree Deepthi Muthukrishnan, et al.
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