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Biswarathan Ramani

Showing results (11-20 of 24) with videos related to

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Biorxiv : the Preprint Server for Biology|February 6, 2026
In vivo Proximity & Spatial Proteomics with CRISPR Screening Identify STXBP1 as a Protective Modifier of α-synuclein Toxicity in Dopamine NeuronsDaichi Shonai, Julie Kent, Arinze Okafor, et al.
Journal of Pediatric Hematology/Oncology|February 2, 2023
Patterns of Extraneural Metastases in Children With EpendymomaPriya P Chan, Nicholas S Whipple, Biswarathan Ramani, et al.
Nature Neuroscience|August 22, 2025
CRISPR screening by AAV episome-sequencing (CrAAVe-seq): a scalable cell-type-specific in vivo platform uncovers neuronal essential genesBiswarathan Ramani, Indigo V L Rose, Noam Teyssier, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
CRISPR screening by AAV episome-sequencing (CrAAVe-seq) is a highly scalable cell type-specific <i>in vivo</i> screening platformBiswarathan Ramani, Indigo V L Rose, Noam Teyssier, et al.
Neurobiology of Disease|July 5, 2015
Differential recruitment of UBQLN2 to nuclear inclusions in the polyglutamine diseases HD and SCA3Li Zeng, Bo Wang, Sean A Merillat, et al.
Human Molecular Genetics|October 17, 2014
A knockin mouse model of spinocerebellar ataxia type 3 exhibits prominent aggregate pathology and aberrant splicing of the disease gene transcriptBiswarathan Ramani, Ginny M Harris, Rogerio Huang, et al.
Human Molecular Genetics|June 13, 2017
A knockin mouse model of spinocerebellar ataxia type 3 exhibits prominent aggregate pathology and aberrant splicing of the disease gene transcriptBiswarathan Ramani, Ginny M Harris, Rogerio Huang, et al.
Ophthalmology|July 14, 2022
Iris and Ciliary Body Melanocytomas Are Defined by Solitary GNAQ Mutation Without Additional Oncogenic AlterationsDavid A Solomon, Biswarathan Ramani, Maya Eiger-Moscovich, et al.
Acta Neuropathologica|September 6, 2020
The immunohistochemical, DNA methylation, and chromosomal copy number profile of cauda equina paraganglioma is distinct from extra-spinal paragangliomaBiswarathan Ramani, Rohit Gupta, Jasper Wu, et al.
Journal of Neuropathology and Experimental Neurology|June 15, 2022
Targeted Next-Generation Sequencing Reveals Divergent Clonal Evolution in Components of Composite Pleomorphic Xanthoastrocytoma-GangliogliomaCalixto-Hope G Lucas, Christian J Davidson, Mouied Alashari, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Biorxiv : the Preprint Server for Biology|February 6, 2026
In vivo Proximity & Spatial Proteomics with CRISPR Screening Identify STXBP1 as a Protective Modifier of α-synuclein Toxicity in Dopamine NeuronsDaichi Shonai, Julie Kent, Arinze Okafor, et al.
Journal of Pediatric Hematology/Oncology|February 2, 2023
Patterns of Extraneural Metastases in Children With EpendymomaPriya P Chan, Nicholas S Whipple, Biswarathan Ramani, et al.
Nature Neuroscience|August 22, 2025
CRISPR screening by AAV episome-sequencing (CrAAVe-seq): a scalable cell-type-specific in vivo platform uncovers neuronal essential genesBiswarathan Ramani, Indigo V L Rose, Noam Teyssier, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
CRISPR screening by AAV episome-sequencing (CrAAVe-seq) is a highly scalable cell type-specific <i>in vivo</i> screening platformBiswarathan Ramani, Indigo V L Rose, Noam Teyssier, et al.
Neurobiology of Disease|July 5, 2015
Differential recruitment of UBQLN2 to nuclear inclusions in the polyglutamine diseases HD and SCA3Li Zeng, Bo Wang, Sean A Merillat, et al.
Human Molecular Genetics|October 17, 2014
A knockin mouse model of spinocerebellar ataxia type 3 exhibits prominent aggregate pathology and aberrant splicing of the disease gene transcriptBiswarathan Ramani, Ginny M Harris, Rogerio Huang, et al.
Human Molecular Genetics|June 13, 2017
A knockin mouse model of spinocerebellar ataxia type 3 exhibits prominent aggregate pathology and aberrant splicing of the disease gene transcriptBiswarathan Ramani, Ginny M Harris, Rogerio Huang, et al.
Ophthalmology|July 14, 2022
Iris and Ciliary Body Melanocytomas Are Defined by Solitary GNAQ Mutation Without Additional Oncogenic AlterationsDavid A Solomon, Biswarathan Ramani, Maya Eiger-Moscovich, et al.
Acta Neuropathologica|September 6, 2020
The immunohistochemical, DNA methylation, and chromosomal copy number profile of cauda equina paraganglioma is distinct from extra-spinal paragangliomaBiswarathan Ramani, Rohit Gupta, Jasper Wu, et al.
Journal of Neuropathology and Experimental Neurology|June 15, 2022
Targeted Next-Generation Sequencing Reveals Divergent Clonal Evolution in Components of Composite Pleomorphic Xanthoastrocytoma-GangliogliomaCalixto-Hope G Lucas, Christian J Davidson, Mouied Alashari, et al.
Pageof 3