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Nature Neuroscience
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August 20, 2021
A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies
Yunhee Kang, Ying Zhou, Yujing Li, et al.
Biorxiv : the Preprint Server for Biology
|
May 13, 2026
Convergent effects of neurodevelopmental disorder-associated variants at mitochondria
Maxine I Robinette, Jada B Gundy, Xinyan Leng, et al.
Molecular Cell
|
June 28, 2020
Robust Hi-C Maps of Enhancer-Promoter Interactions Reveal the Function of Non-coding Genome in Neural Development and Diseases
Leina Lu, Xiaoxiao Liu, Wei-Kai Huang, et al.
Biorxiv : the Preprint Server for Biology
|
February 12, 2026
Cell type-resolved proteomics reveals intra- and intercellular signaling in Alzheimer's disease
Xue Zhang, Kaiwen Yu, Him K Shrestha, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 15, 2021
Mitochondrial Proteostasis Requires Genes Encoded in a Neurodevelopmental Syndrome Locus
Avanti Gokhale, Chelsea E Lee, Stephanie A Zlatic, et al.
Cell Reports
|
April 14, 2021
Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis
Nisha Raj, Zachary T McEachin, William Harousseau, et al.
Biorxiv : the Preprint Server for Biology
|
February 7, 2023
Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
Ryan H Purcell, Esra Sefik, Erica Werner, et al.
Science Advances
|
November 23, 2022
Expression of expanded GGC repeats within <i>NOTCH2NLC</i> causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease
Qiong Liu, Kailin Zhang, Yunhee Kang, et al.
Science Advances
|
August 16, 2023
Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
Ryan H Purcell, Esra Sefik, Erica Werner, et al.
Nature Communications
|
March 4, 2021
Pharmacological rescue in patient iPSC and mouse models with a rare DISC1 mutation
Nam-Shik Kim, Zhexing Wen, Jing Liu, et al.
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of 11
Search research articles
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Showing results (81-90 of 102) with videos related to
Sort By:
Page
of 11
Nature Neuroscience
|
August 20, 2021
A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies
Yunhee Kang, Ying Zhou, Yujing Li, et al.
Biorxiv : the Preprint Server for Biology
|
May 13, 2026
Convergent effects of neurodevelopmental disorder-associated variants at mitochondria
Maxine I Robinette, Jada B Gundy, Xinyan Leng, et al.
Molecular Cell
|
June 28, 2020
Robust Hi-C Maps of Enhancer-Promoter Interactions Reveal the Function of Non-coding Genome in Neural Development and Diseases
Leina Lu, Xiaoxiao Liu, Wei-Kai Huang, et al.
Biorxiv : the Preprint Server for Biology
|
February 12, 2026
Cell type-resolved proteomics reveals intra- and intercellular signaling in Alzheimer's disease
Xue Zhang, Kaiwen Yu, Him K Shrestha, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 15, 2021
Mitochondrial Proteostasis Requires Genes Encoded in a Neurodevelopmental Syndrome Locus
Avanti Gokhale, Chelsea E Lee, Stephanie A Zlatic, et al.
Cell Reports
|
April 14, 2021
Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis
Nisha Raj, Zachary T McEachin, William Harousseau, et al.
Biorxiv : the Preprint Server for Biology
|
February 7, 2023
Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
Ryan H Purcell, Esra Sefik, Erica Werner, et al.
Science Advances
|
November 23, 2022
Expression of expanded GGC repeats within <i>NOTCH2NLC</i> causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease
Qiong Liu, Kailin Zhang, Yunhee Kang, et al.
Science Advances
|
August 16, 2023
Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
Ryan H Purcell, Esra Sefik, Erica Werner, et al.
Nature Communications
|
March 4, 2021
Pharmacological rescue in patient iPSC and mouse models with a rare DISC1 mutation
Nam-Shik Kim, Zhexing Wen, Jing Liu, et al.
Page
of 11