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Joanna Mattis

Researcher at Stanford University

Publications -  21
Citations -  6255

Joanna Mattis is an academic researcher from Stanford University. The author has contributed to research in topics: Optogenetics & Channelrhodopsin. The author has an hindex of 15, co-authored 20 publications receiving 5368 citations. Previous affiliations of Joanna Mattis include Yale University & University of Pennsylvania.

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Structural and molecular interrogation of intact biological systems

TL;DR: It is shown that CLARITY enables fine structural analysis of clinical samples, including non-sectioned human tissue from a neuropsychiatric-disease setting, establishing a path for the transmutation of human tissue into a stable, intact and accessible form suitable for probing structural and molecular underpinnings of physiological function and disease.
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Molecular and Cellular Approaches for Diversifying and Extending Optogenetics

TL;DR: Subcellular and transcellular trafficking strategies now permit increased potency of optical inhibition without increased light power requirement, and generalizable strategies for targeting cells based not only on genetic identity, but also on morphology and tissue topology, to allow versatile targeting when promoters are not known or in genetically intractable organisms.
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Principles for applying optogenetic tools derived from direct comparative analysis of microbial opsins

TL;DR: This work systematically compared microbial opsins under matched experimental conditions to extract essential principles and identify key parameters for the conduct, design and interpretation of experiments involving optogenetic techniques.
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Red-shifted optogenetic excitation: a tool for fast neural control derived from Volvox carteri

TL;DR: A cation-conducting channelrhodopsin (VChR1) from Volvox carteri that can drive spiking at 589 nm, with excitation maximum red-shifted ∼70 nm compared with ChR2 is described, thereby defining a functionally distinct third category of microbial rhodopin proteins.
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Diverging neural pathways assemble a behavioural state from separable features in anxiety

TL;DR: It is demonstrated that distinct BNST subregions exert opposite effects in modulating anxiety, separable anxiolytic roles for different anterodorsal BN ST projections are established, and circuit mechanisms underlying selection of features for the assembly of the anxious state are illustrated.