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Rachel M Bailey

Showing results (21-30 of 34) with videos related to

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Brain Communications|December 22, 2025
Neurological, metabolic and inflammatory phenotypes in a mouse model of ECHS1 deficiencyMeghan M Eller, Aamir R Zuberi, Xiaorong Fu, et al.
Communications Medicine|January 27, 2025
Preclinical use of a clinically-relevant scAAV9/SUMF1 vector for the treatment of multiple sulfatase deficiencyMaximiliano Presa, Rachel M Bailey, Somdatta Ray, et al.
Genes|September 23, 2022
SLC13A5 Deficiency Disorder: From Genetics to Gene TherapyKimberly Goodspeed, Judy S Liu, Kimberly L Nye, et al.
The Journal of Clinical Investigation|February 19, 2026
AAV-mediated gene therapy in a SLC13A5 citrate transporter disorder model rescues epileptic and metabolic phenotypesLauren E Bailey, Raegan M Adams, Morgan K Schackmuth, et al.
Gene Therapy|May 6, 2025
Nitrous oxide enhances MR-guided focused ultrasound delivery of gene therapy to the murine hippocampusDeepshikha Bhardwaj, Ibrahim Youssef, Darren Imphean, et al.
Acta Neuropathologica|October 12, 2013
LRRK2 phosphorylates novel tau epitopes and promotes tauopathyRachel M Bailey, Jason P Covy, Heather L Melrose, et al.
The Journal of Clinical Investigation|April 20, 2021
AAV9-mediated FIG4 delivery prolongs life span in Charcot-Marie-Tooth disease type 4J mouse modelMaximiliano Presa, Rachel M Bailey, Crystal Davis, et al.
Parkinsonism & Related Disorders|April 3, 2007
Identification of potential protein interactors of Lrrk2Justus C Dächsel, Julie P Taylor, Su San Mok, et al.
Muscle & Nerve|August 29, 2025
T2 Hyperintensities in Gracile Tracts of Cervical Spinal Cord in Giant Axonal Neuropathy (GAN)Diane Armao, Thomas W Bouldin, Diana X Bharucha-Goebel, et al.
Genes|October 26, 2024
Sleep Abnormalities in SLC13A5 Citrate Transporter DisorderRaegan M Adams, Can Ozlu, Lauren E Bailey, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Brain Communications|December 22, 2025
Neurological, metabolic and inflammatory phenotypes in a mouse model of ECHS1 deficiencyMeghan M Eller, Aamir R Zuberi, Xiaorong Fu, et al.
Communications Medicine|January 27, 2025
Preclinical use of a clinically-relevant scAAV9/SUMF1 vector for the treatment of multiple sulfatase deficiencyMaximiliano Presa, Rachel M Bailey, Somdatta Ray, et al.
Genes|September 23, 2022
SLC13A5 Deficiency Disorder: From Genetics to Gene TherapyKimberly Goodspeed, Judy S Liu, Kimberly L Nye, et al.
The Journal of Clinical Investigation|February 19, 2026
AAV-mediated gene therapy in a SLC13A5 citrate transporter disorder model rescues epileptic and metabolic phenotypesLauren E Bailey, Raegan M Adams, Morgan K Schackmuth, et al.
Gene Therapy|May 6, 2025
Nitrous oxide enhances MR-guided focused ultrasound delivery of gene therapy to the murine hippocampusDeepshikha Bhardwaj, Ibrahim Youssef, Darren Imphean, et al.
Acta Neuropathologica|October 12, 2013
LRRK2 phosphorylates novel tau epitopes and promotes tauopathyRachel M Bailey, Jason P Covy, Heather L Melrose, et al.
The Journal of Clinical Investigation|April 20, 2021
AAV9-mediated FIG4 delivery prolongs life span in Charcot-Marie-Tooth disease type 4J mouse modelMaximiliano Presa, Rachel M Bailey, Crystal Davis, et al.
Parkinsonism & Related Disorders|April 3, 2007
Identification of potential protein interactors of Lrrk2Justus C Dächsel, Julie P Taylor, Su San Mok, et al.
Muscle & Nerve|August 29, 2025
T2 Hyperintensities in Gracile Tracts of Cervical Spinal Cord in Giant Axonal Neuropathy (GAN)Diane Armao, Thomas W Bouldin, Diana X Bharucha-Goebel, et al.
Genes|October 26, 2024
Sleep Abnormalities in SLC13A5 Citrate Transporter DisorderRaegan M Adams, Can Ozlu, Lauren E Bailey, et al.
Pageof 4