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Sruti Rayaprolu

Showing results (11-20 of 44) with videos related to

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Acta Neuropathologica Communications|December 20, 2018
Analysis of spinal and muscle pathology in transgenic mice overexpressing wild-type and ALS-linked mutant MATR3Christina Moloney, Sruti Rayaprolu, John Howard, et al.
The Journal of Comparative Neurology|February 16, 2016
Heterogeneity of Matrin 3 in the developing and aging murine central nervous systemSruti Rayaprolu, Simon D'Alton, Keith Crosby, et al.
Parkinsonism & Related Disorders|April 23, 2013
Investigating the role of FUS exonic variants in essential tremorCatherine Labbé, Alexandra I Soto-Ortolaza, Sruti Rayaprolu, et al.
Neurology. Clinical Practice|October 10, 2025
Development and Clinical Validation of Blood-Based Multibiomarker Models for the Evaluation of Brain Amyloid PathologyDarren M Weber, Matthew A Stroh, Steven W Taylor, et al.
Medrxiv : the Preprint Server for Health Sciences|May 2, 2025
Development and clinical validation of blood-based multibiomarker models for the evaluation of brain amyloid pathologyDarren M Weber, Matthew A Stroh, Steven W Taylor, et al.
Parkinsonism & Related Disorders|December 3, 2015
Association of Parkinson disease age of onset with DRD2, DRD3 and GRIN2B polymorphismsAnhar Hassan, Michael G Heckman, J E Ahlskog, et al.
Acta Neuropathologica Communications|November 20, 2016
Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotypeChristina Moloney, Sruti Rayaprolu, John Howard, et al.
Acta Neuropathologica Communications|December 15, 2017
Retraction Note: Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotypeChristina Moloney, Sruti Rayaprolu, John Howard, et al.
Molecular & Cellular Proteomics : MCP|April 15, 2023
Cellular Proteomic Profiling Using Proximity Labeling by TurboID-NES in Microglial and Neuronal Cell LinesSydney Sunna, Christine Bowen, Hollis Zeng, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
VPS35 and DNAJC13 disease-causing variants in essential tremorAlex Rajput, Jay P Ross, Cecily Q Bernales, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Acta Neuropathologica Communications|December 20, 2018
Analysis of spinal and muscle pathology in transgenic mice overexpressing wild-type and ALS-linked mutant MATR3Christina Moloney, Sruti Rayaprolu, John Howard, et al.
The Journal of Comparative Neurology|February 16, 2016
Heterogeneity of Matrin 3 in the developing and aging murine central nervous systemSruti Rayaprolu, Simon D'Alton, Keith Crosby, et al.
Parkinsonism & Related Disorders|April 23, 2013
Investigating the role of FUS exonic variants in essential tremorCatherine Labbé, Alexandra I Soto-Ortolaza, Sruti Rayaprolu, et al.
Neurology. Clinical Practice|October 10, 2025
Development and Clinical Validation of Blood-Based Multibiomarker Models for the Evaluation of Brain Amyloid PathologyDarren M Weber, Matthew A Stroh, Steven W Taylor, et al.
Medrxiv : the Preprint Server for Health Sciences|May 2, 2025
Development and clinical validation of blood-based multibiomarker models for the evaluation of brain amyloid pathologyDarren M Weber, Matthew A Stroh, Steven W Taylor, et al.
Parkinsonism & Related Disorders|December 3, 2015
Association of Parkinson disease age of onset with DRD2, DRD3 and GRIN2B polymorphismsAnhar Hassan, Michael G Heckman, J E Ahlskog, et al.
Acta Neuropathologica Communications|November 20, 2016
Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotypeChristina Moloney, Sruti Rayaprolu, John Howard, et al.
Acta Neuropathologica Communications|December 15, 2017
Retraction Note: Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotypeChristina Moloney, Sruti Rayaprolu, John Howard, et al.
Molecular & Cellular Proteomics : MCP|April 15, 2023
Cellular Proteomic Profiling Using Proximity Labeling by TurboID-NES in Microglial and Neuronal Cell LinesSydney Sunna, Christine Bowen, Hollis Zeng, et al.
European Journal of Human Genetics : EJHG|August 14, 2014
VPS35 and DNAJC13 disease-causing variants in essential tremorAlex Rajput, Jay P Ross, Cecily Q Bernales, et al.
Pageof 5