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Cellular and Molecular Life Sciences : CMLS|April 20, 2020
Pathogenic mechanisms underlying spinocerebellar ataxia type 1Leon Tejwani, Janghoo Lim
Cell Research|November 15, 2017
Hunting for the mutant without the MAP(K)Leon Tejwani, Janghoo Lim
JCI Insight|October 7, 2021
Microglia regulate brain progranulin levels through the endocytosis/lysosomal pathwayTingting Dong, Leon Tejwani, Youngseob Jung, et al.
The Journal of Clinical Investigation|May 11, 2026
Oligodendrocyte dysfunction contributes to motor deficits and Purkinje cell axonopathy in spinocerebellar ataxia type 1Changwoo Lee, Rosalie M Grijalva, Leon Tejwani, et al.
The Journal of Clinical Investigation|August 28, 2025
Peripherally administered androgen receptor-targeted antisense oligonucleotide rescues spinal pathology in a murine SBMA modelChangwoo Lee, Zhigang Yu, Curtis J Kuo, et al.
Genes|October 20, 2020
Genetic Risk of Autism Spectrum Disorder in a Pakistani PopulationMadiha Khalid, Hashim Raza, Terri M Driessen, et al.
Cell Stem Cell|August 15, 2017
Modeling of TREX1-Dependent Autoimmune Disease using Human Stem Cells Highlights L1 Accumulation as a Source of NeuroinflammationCharles A Thomas, Leon Tejwani, Cleber A Trujillo, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2022
Differential effects of Wnt-β-catenin signaling in Purkinje cells and Bergmann glia in spinocerebellar ataxia type 1Kimberly Luttik, Leon Tejwani, Hyoungseok Ju, et al.
Cells|October 14, 2022
A Novel Missense Mutation in ERCC8 Co-Segregates with Cerebellar Ataxia in a Consanguineous Pakistani FamilyZeeshan Gauhar, Leon Tejwani, Uzma Abdullah, et al.
Gene|April 24, 2018
Association of CACNA1C with bipolar disorder among the Pakistani populationMadiha Khalid, Terri M Driessen, Jong Seo Lee, et al.
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