Author

Megan C. Rich

University of Alabama at Birmingham

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Neuroscience· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:drug response / drug discovery· 2 Organism:rat· 2 Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Organism:human· 1 Organism:mouse· 1 Assay:proteomics· 1

Frequent Co-Authors

Farah D. LubiniD· 3 shared Mark BoldingiD· 2 shared Alistair J. Jenkins· 1 shared Ashley Dickey· 1 shared Aundrea F. BartleyiD· 1 shared Devin R. BroadwateriD· 1 shared Eric ZhangiD· 1 shared Haley W. JonesiD· 1 shared

Activity by Year

2019-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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3 shared papersNeuroscience

Farah D. LubinORCID

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3 papers

Recent·Most cited

A Noninvasive Approach to Optogenetics Using Focused Ultrasound Blood Brain Barrier Disruption for the Delivery of Radioluminescent Particles

Megan C. Rich, Eric Zhang, Ashley Dickey, Haley W. Jones, Kelli E Cannon, Yuriy P. Bandera, Stephen H. Foulger, Farah D. Lubin, Mark Bolding

This paper develops a noninvasive optogenetic system using radioluminescent particles and focused ultrasound to deliver light-sensitive proteins to brain regions without invasive procedures.

bioRxiv · Aug 20, 2020 · PreprintNeuroscience

Focused ultrasound blood brain barrier opening mediated delivery of MRI-visible albumin nanoclusters to the rat brain for localized drug delivery with temporal control

Megan C. Rich, Jennifer A. Sherwood, Aundrea F. Bartley, Quentin A. Whitsitt, Magdelene Lee, William Ryan Willoughby, Lynn E. Dobrunz, Yuping Bao, Farah D. Lubin, Mark Bolding

This paper demonstrates a method for noninvasive, temporally controlled drug delivery to the rat brain using focused ultrasound and MRI-visible albumin nanoclusters.

Journal of Controlled Release · May 5, 2020Peer-reviewedNeuroscience

Human and Rodent Temporal Lobe Epilepsy is Characterized by Changes in O-GlcNAc Homeostasis that can be Reversed to Dampen Epileptiform Activity

Richard G. Sánchez, R. Ryley Parrish, Megan C. Rich, William M. Webb, Roxanne M. Lockhart, Kazuhito Nakao, Lara Ianov, Susan C. Buckingham, Devin R. Broadwater, Alistair J. Jenkins, Nihal C. de Lanerolle, Mark O. Cunningham, Tore Eid, Kristen Owen Riley, Farah D. Lubin

This study shows that O-GlcNAc homeostasis is disrupted in TLE and that inhibiting OGA can reverse these changes and reduce seizures.

Neurobiology of Disease · Jan 6, 2019Peer-reviewedNeuroscience