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Sruti Rayaprolu

Showing results (31-40 of 44) with videos related to

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Neurobiology of Aging|April 2, 2014
Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's diseaseBarbara Shannon, Alexandra Soto-Ortolaza, Sruti Rayaprolu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 12, 2026
Laterally spreading AAV.SPR enables safe and efficient RS1 delivery to the macula after peripheral subretinal injectionEva Andres-Mateos, Christopher Kozlowski, Hangning Zhang, et al.
Neurobiology of Disease|June 20, 2026
Robust tauopathy and memory deficits in a mouse model constitutively overexpressing human P301L MAPTMatthew J Hamm, Kevin McNaught, Christopher Janus, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 2, 2021
Unique molecular characteristics and microglial origin of Kv1.3 channel-positive brain myeloid cells in Alzheimer's diseaseSupriya Ramesha, Sruti Rayaprolu, Christine A Bowen, et al.
Plos One|May 4, 2017
A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR traffickingSwati Khare, Jerelyn A Nick, Yalan Zhang, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|January 19, 2026
Factors associated with discordant visual and quantitative amyloid PET resultsJasmin E Guevara, Emily F Matusz, Wei-En Wang, et al.
Elife|May 12, 2023
APOE expression and secretion are modulated by mitochondrial dysfunctionMeghan E Wynne, Oluwaseun Ogunbona, Alicia R Lane, et al.
Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.
Neurology. Genetics|July 27, 2016
TREM2 p.R47H substitution is not associated with dementia with Lewy bodiesRonald L Walton, Alexandra I Soto-Ortolaza, Melissa E Murray, et al.
Neurobiology of Aging|July 31, 2012
Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotypeNicola J Rutherford, Michael G Heckman, Mariely Dejesus-Hernandez, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Neurobiology of Aging|April 2, 2014
Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's diseaseBarbara Shannon, Alexandra Soto-Ortolaza, Sruti Rayaprolu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 12, 2026
Laterally spreading AAV.SPR enables safe and efficient RS1 delivery to the macula after peripheral subretinal injectionEva Andres-Mateos, Christopher Kozlowski, Hangning Zhang, et al.
Neurobiology of Disease|June 20, 2026
Robust tauopathy and memory deficits in a mouse model constitutively overexpressing human P301L MAPTMatthew J Hamm, Kevin McNaught, Christopher Janus, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 2, 2021
Unique molecular characteristics and microglial origin of Kv1.3 channel-positive brain myeloid cells in Alzheimer's diseaseSupriya Ramesha, Sruti Rayaprolu, Christine A Bowen, et al.
Plos One|May 4, 2017
A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR traffickingSwati Khare, Jerelyn A Nick, Yalan Zhang, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|January 19, 2026
Factors associated with discordant visual and quantitative amyloid PET resultsJasmin E Guevara, Emily F Matusz, Wei-En Wang, et al.
Elife|May 12, 2023
APOE expression and secretion are modulated by mitochondrial dysfunctionMeghan E Wynne, Oluwaseun Ogunbona, Alicia R Lane, et al.
Neurology|November 8, 2014
LRRK2 exonic variants and risk of multiple system atrophyMichael G Heckman, Lucia Schottlaender, Alexandra I Soto-Ortolaza, et al.
Neurology. Genetics|July 27, 2016
TREM2 p.R47H substitution is not associated with dementia with Lewy bodiesRonald L Walton, Alexandra I Soto-Ortolaza, Melissa E Murray, et al.
Neurobiology of Aging|July 31, 2012
Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotypeNicola J Rutherford, Michael G Heckman, Mariely Dejesus-Hernandez, et al.
Pageof 5