Skip to main content

Umbrella menu

  • SfN.org
  • eNeuro
  • The Journal of Neuroscience
  • Neuronline
  • BrainFacts.org

Main menu

  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Latest Articles
    • Issue Archive
    • Editorials
    • Research Highlights
  • TOPICS
    • Cognition and Behavior
    • Development
    • Disorders of the Nervous System
    • History, Teaching and Public Awareness
    • Integrative Systems
    • Neuronal Excitability
    • Novel Tools and Methods
    • Sensory and Motor Systems
  • ALERTS
  • FOR AUTHORS
  • EDITORIAL BOARD
  • BLOG
  • ABOUT
    • Overview
    • For the Media
    • Privacy Policy
    • Contact Us
    • Feedback
  • SfN.org
  • eNeuro
  • The Journal of Neuroscience
  • Neuronline
  • BrainFacts.org

User menu

  • My alerts

Search

  • Advanced search
eNeuro
  • My alerts

eNeuro

Advanced Search

Submit a Manuscript
  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Latest Articles
    • Issue Archive
    • Editorials
    • Research Highlights
  • TOPICS
    • Cognition and Behavior
    • Development
    • Disorders of the Nervous System
    • History, Teaching and Public Awareness
    • Integrative Systems
    • Neuronal Excitability
    • Novel Tools and Methods
    • Sensory and Motor Systems
  • ALERTS
  • FOR AUTHORS
  • EDITORIAL BOARD
  • BLOG
  • ABOUT
    • Overview
    • For the Media
    • Privacy Policy
    • Contact Us
    • Feedback
PreviousNext
Research ArticleResearch Article: New Research, Sensory and Motor Systems

The Neural Representation of Force across Grasp Types in Motor Cortex of Humans with Tetraplegia

Anisha Rastogi, Francis R. Willett, Jessica Abreu, Douglas C. Crowder, Brian A. Murphy, William D. Memberg, Carlos E. Vargas-Irwin, Jonathan P. Miller, Jennifer Sweet, Benjamin L. Walter, Paymon G. Rezaii, Sergey D. Stavisky, Leigh R. Hochberg, Krishna V. Shenoy, Jaimie M. Henderson, Robert F. Kirsch and A. Bolu Ajiboye
eNeuro 25 January 2021, 8 (1) ENEURO.0231-20.2020; DOI: https://doi.org/10.1523/ENEURO.0231-20.2020
Anisha Rastogi
1Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Anisha Rastogi
Francis R. Willett
2Department of Neurosurgery, Stanford University, Stanford, CA 94035
3Department of Electrical Engineering, Stanford University, Stanford, CA 94035
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Jessica Abreu
1Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106
4Louis Stokes Cleveland Department of VA Medical Center, Cleveland, OH 44106
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Douglas C. Crowder
1Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106
4Louis Stokes Cleveland Department of VA Medical Center, Cleveland, OH 44106
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Brian A. Murphy
1Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106
4Louis Stokes Cleveland Department of VA Medical Center, Cleveland, OH 44106
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
William D. Memberg
1Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Carlos E. Vargas-Irwin
5Department of Neuroscience, Brown University, Providence, RI 02912
6Robert J. and Nancy D. Carney Institute for Brain Sciences, Brown University, Providence, RI 02912
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Jonathan P. Miller
4Louis Stokes Cleveland Department of VA Medical Center, Cleveland, OH 44106
8Department of Neurological Surgery, University Hospitals Cleveland Medical Center, Cleveland, OH 44106
9Department of Neurological Surgery, Case Western Reserve School of Medicine School of Medicine, Cleveland, OH 44106
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Jennifer Sweet
8Department of Neurological Surgery, University Hospitals Cleveland Medical Center, Cleveland, OH 44106
9Department of Neurological Surgery, Case Western Reserve School of Medicine School of Medicine, Cleveland, OH 44106
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Benjamin L. Walter
4Louis Stokes Cleveland Department of VA Medical Center, Cleveland, OH 44106
10Department of Neurology, University Hospitals Cleveland Medical Center, Cleveland, OH 44106
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Paymon G. Rezaii
2Department of Neurosurgery, Stanford University, Stanford, CA 94035
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Sergey D. Stavisky
2Department of Neurosurgery, Stanford University, Stanford, CA 94035
3Department of Electrical Engineering, Stanford University, Stanford, CA 94035
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Sergey D. Stavisky
Leigh R. Hochberg
6Robert J. and Nancy D. Carney Institute for Brain Sciences, Brown University, Providence, RI 02912
7VA RR&D Center for Neurorestoration and Neurotechnology, Providence, RI 02912
11School of Engineering, Brown University, Providence, RI 02912
12Center for Neurotechnology and Neurorecovery, Department of Neurology, Massachusetts General Hospital, Boston, MA 02114
13Department of Neurology, Harvard Medical School, Boston, MA 02114
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Leigh R. Hochberg
Krishna V. Shenoy
3Department of Electrical Engineering, Stanford University, Stanford, CA 94035
14Department of Bioengineering, Stanford University, Stanford, CA 94035
15Department of Neurobiology, Stanford University, Stanford, CA 94035
16Howard Hughes Medical Institute at Stanford University, Stanford, CA 94035
17Wu Tsai Neuroscience Institute, Stanford University, Stanford, CA 94035
18Bio-X Program, Stanford University, Stanford, CA 94035
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for Krishna V. Shenoy
Jaimie M. Henderson
2Department of Neurosurgery, Stanford University, Stanford, CA 94035
17Wu Tsai Neuroscience Institute, Stanford University, Stanford, CA 94035
18Bio-X Program, Stanford University, Stanford, CA 94035
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Robert F. Kirsch
1Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106
4Louis Stokes Cleveland Department of VA Medical Center, Cleveland, OH 44106
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
A. Bolu Ajiboye
1Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106
4Louis Stokes Cleveland Department of VA Medical Center, Cleveland, OH 44106
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for A. Bolu Ajiboye
  • Article
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF
Loading

Article Figures & Data

Figures

  • Tables
  • Extended Data
  • Figure 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 1.

    Data collection scheme for research sessions. A, Experimental setup (adapted from Rastogi et al., 2020). Participants had two 96-channel microelectrode arrays placed chronically in motor cortex, which recorded neural activity while participants completed a force task. TC and SBP features were extracted from these recordings. Figure 1A is reprinted by permission from Springer Nature as indicated in the Terms and Conditions of a Creative Commons Attribution 4.0 International license (https://www.nature.com/srep/). B, Research session architecture. Each session consisted of 12–21 blocks, each of which contained ∼20 trials (see Table 1). In each trial, participants attempted to generate one of three visually-cued forces with one of four grasps: power, closed pinch, open pinch, ring pinch. During session 5, participant T8 also attempted force production using elbow extension. Each trial contained a preparatory (prep) phase, a go phase where forces were actively embodied, and a stop phase where neural activity was allowed to return to baseline. Participants were prompted with both audio and visual cues, in which a researcher squeezed or lifted an object associated with each force level. During pinch blocks, the researcher squeezed the pinchable objects (cotton ball, eraser, nasal aspirator tip) using the particular pinch grip dictated by the block (ring pinch, open pinch, closed pinch). Here, only closed pinches of objects are shown.

  • Figure 2.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 2.

    Exemplary TC and SBP features tuned to task parameters of interest in participant T8 (TC and SBP features in participant T5 are illustrated in Extended Data Fig. 2-1). Rows indicate average per-condition activity (PSTH) of four exemplary features tuned to force, grasp, both factors, and an interaction between force and grasp, recorded during session 5 from participant T8 (two-way Welch-ANOVA, corrected p < 0.05, Benjamini–Hochberg method). Bolded, starred p values indicate significant tuning to force (Rows 1 and 3), grasp (Rows 2 and 3), or a force-grasp interaction (Row 4). Neural activity was normalized by subtracting block-specific mean feature activity within each recording block, and then smoothed with a 100-ms Gaussian kernel to aid in visualization. Column 1 contains PSTHs averaged within individual force levels (across multiple grasps), such that observable differences between data traces are because of force alone. Similarly, column 2 shows PSTHs averaged within individual grasps (across multiple forces). Column 3 shows a graphical representation of the simple main effects as normalized mean neural deviations from baseline activity during force trials within each of the five grasps. (cp, c-pinch = closed pinch; op, o-pinch = open pinch; rp, r-pinch = ring pinch, pow = power, elb = elbow extension). Mean neural deviations were computed over the go phase of each trial and subsequently averaged within each force-grasp pair. Error bars indicate 95% confidence intervals.

  • Figure 3.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 3.

    Summary of neural feature population tuning to force and grasp. Row 1, Fraction of neural features significantly tuned to force, grasp, both force, and grasp and an interaction between force and grasp in participants T8 and T5 (two-way Welch-ANOVA, corrected p < 0.05). Row 2, Fraction of neural features significantly tuned to an interaction between force and grasp, subdivided into force-tuned features within each individual grasp (c-pinch = closed pinch, o-pinch = open pinch, r-pinch = ring pinch). Note that the number of grasp types differed between sessions (see Table 1).

  • Figure 4.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 4.

    Simulated models of independent and interacting (grasp-dependent) neural representations of force. Row 1, Equations corresponding to the independent and interacting models of force representation. Here, xij represents neural feature activity generated during a particular grasp i and force j, gi represents baseline feature activity during grasp i, f represents force-related neural feature activity, and sj is a discrete force level. Row 2, Simulated population neural activity projected into a two-dimensional PCA space. Estimated force axes within the low-dimensional spaces are shown as blue lines. Row 3, Summary of variances accounted for by the top 20 dPCs extracted from the simulated neural data from each model. Here, the variance of each individual component is separated by marginalization (force, grasp, and interaction between force and grasp). Pie charts indicate the percentage of total signal variance due to these marginalizations.

  • Figure 5.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 5.

    Neural population-level activity patterns. A, Demixed principal components (dPCs) isolated from all force-grasp conditions from T8 session 5, all force-grasp conditions from T5 session 7, and power versus elbow conditions from T8 session 5 neural data. dPCs were tuned to four marginalizations of interest: Condition-Independent (CI) tuning (i.e., time), Force, Grasp, and an interaction between force and grasp (FxGrasp). dPCs that account for the highest amount of variance in the per-marginalization neural activity are shown here. These variances are included in brackets next to each component number. Vertical bars indicate the start and end of the go phase. Horizontal bars indicate time points at which the decoder axes of the pictured components classified forces (row 2), grasps (row 3), or force-grasp pairs (row 4) significantly above chance. B, Summary of variances accounted for by the top 20 dPCs and PCs from each session. Here, the variance accounted for by the dPCs approaches the variance accounted for by traditional PCs. Horizontal dashed lines indicate total signal variance, excluding noise. Row 2 shows the variance of each individual component, separated by marginalization. C, Go-phase activity within a two-dimensional PCA space. Estimated force axes within the low-dimensional PCA spaces are shown as blue lines. Here, c-pinch = closed pinch, o-pinch = open pinch, r-pinch = ring pinch. D, Encoding model performances. The task-dependent components of neural feature activity were fit to the additive, scalar, and combined encoding models via cross-validated ordinary least squares regression. Tables contain the fit model coefficients for each session. Bar graphs indicate mean R2 values for each model over 100 iterations of Monte Carlo leave-group-out cross-validation. Error bars indicate SDs across iterations. Stars indicate statistically significant differences between model R2 values; **p < 0.01 and ***p < 0.001.

  • Figure 6.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 6.

    Time-dependent classification accuracies for force (rows 1–2) and grasp (row 3). Data traces were smoothed with a 100-ms boxcar filter to aid in visualization. Shaded areas surrounding each data trace indicate the SD across 240 session-runs for most trials in participant T8, 40 session-runs for elbow extension trials in participant T8, and 40 session-runs in participant T5. Gray shaded areas indicate the upper and lower bounds of chance performance over S × 100 shuffles of trial data, where S is the number of sessions per participant. Time points at which force or grasp is decoded above the upper bound of chance are deemed to contain significant force-related or grasp-related information. Blue shaded regions indicate the time points used to compute go-phase confusion matrices in Figure 7. Here, c-pinch = closed pinch, o-pinch = open pinch, r-pinch = ring pinch. Time-dependent classification accuracies for individual force levels and grasp types are shown in Extended Data Figure 6-1. Grasp classification accuracies, separated by number of attempted grasp types, are presented in Extended Data Figure 6-2. Force classification accuracies, separated by individual session, are presented in Extended Data Figure 6-3.

  • Figure 7.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 7.

    Go-phase confusion matrices. A, Time-dependent classification accuracies (shown in Fig. 6) were averaged over go-phase time windows that commenced when performance exceeded 90% of maximum and ended with the end of the go phase. These yielded mean trial accuracies, which were then averaged over all session-runs in each participant. Overall force and grasp classification accuracies are indicated above each confusion matrix. SDs across multiple session-runs are indicated next to mean accuracies (cp = closed pinch, op = open pinch, rp = ring pinch, pow = power, elb = elbow extension). Statistical comparisons between the achieved classification accuracies are shown in Extended Data Figure 7-1. B, Confusion matrices, now separated by the grasps (c-pinch = closed pinch, o-pinch = open pinch, r-pinch = ring pinch, power, elbow) that participants T8 (row 1) and T5 (row 2) used to attempt producing forces. Statistical comparisons between the achieved force accuracies are shown in Extended Data Figures 7-2, 7-3.

  • Figure 8.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 8.

    Go-phase force classification accuracy for novel (test) grasps. Within each session (rows), dPCA force decoders were trained on neural data generated during all grasps, excluding a single leave-out grasp type (columns). The force decoder was then evaluated over the set of training grasps (gray bars), as well as the novel leave-out grasp type (white bars). Stars indicate statistically significant differences in performance between training and novel grasps; **p < 0.01, ***p < 0.001. Error bars indicate the 95% confidence intervals. The horizontal dotted line in each panel indicates upper bound of the empirical chance distribution for force classification. Here, c-pinch = closed pinch, o-pinch = open pinch, r-pinch = ring pinch.

Tables

  • Figures
  • Extended Data
    • View popup
    Table 1.

    Session information

    Session NumberParticipantPost-Implant DayNumber of Blocks per Grasp
    Closed PinchOpen PinchRing PinchPowerElbow
    1T8Day 73511——10—
    2T8Day 7715555—
    3T8Day 7746555—
    4T8Day 7885555—
    5T8Day 80244445
    6T8Day 9564444—
    7T5Day 3904444—
    • Session information for participants T8 and T5, including the number of blocks per grasp type.

Extended Data

  • Figures
  • Tables
  • Extended Data Figure 2-1

    Exemplary TC and SBP features tuned to task parameters of interest in participant T5, presented as in Figure 2. Note the presence of sharp activity peaks during the prep and stop phases of the trial, which were due to the presence of visual cues (Rastogi et al, 2020). Download Figure 2-1, TIF file.

  • Extended Data Figure 5-1

    Neural population-level activity patterns for all sessions, presented as in Figure 5A–C. A, dPCs isolated from all individual sessions of neural data. B, Summary of variances accounted for by the top 20 dPCs from each exemplary session. Pie charts indicate the percentage of total signal variance accounted for by each marginalization. Total signal variance was computed with (left) and without (right) the condition-independent portion of the signal, as a basis of comparison to Figure 4 of the main text. C, Go-phase activity within two-dimensional PCA space. This figure shows dPCs, variances, and PCA plots for all recorded sessions. Corresponding encoding model performances for all recorded sessions appear in Extended Data Figure 5-2. Download Figure 5-1, TIF file.

  • Extended Data Figure 5-2

    Encoding model performances, presented as in Figure 5D. Download Figure 5-2, TIF file.

  • Extended Data Figure 6-1

    Time-dependent classification accuracies for individual force levels and grasp types. A, Time-dependent classification accuracies for force (row 1) and grasp (row 2), separated by force class and grasp class, respectively. Data traces were smoothed with a 100-ms boxcar filter to aid in in visualization. Shaded areas surrounding each data trace indicate the SD across 240 session-runs during most trials in participant T8, 40 session-runs during elbow extension trials in participant T8, and 40-session runs in participant T5. Gray shaded regions indicate the upper and lower bounds of chance performance over S × 100 shuffles of trial data, where S is the number of sessions per participant. Blue shaded regions indicate the time points used to compute go-phase confusion matrices. B, Time-dependent force classification accuracies during individual grasps in participants T8 (row 1) and T5 (row 2). Blue shaded regions indicate the time points used to compute go-phase confusion matrices. Decoding performances were averaged over S × 40 session runs, where S is the number of sessions per participant. Download Figure 6-1, TIF file.

  • Extended Data Figure 6-2

    Time-dependent grasp classification accuracies by number of grasps attempted per session in participant T8. Data traces were smoothed with a 100-ms boxcar filter to aid in in visualization. Shaded areas surrounding each data trace indicate the SD across 40 runs during each session in participant T8. Gray shaded regions indicate the upper and lower bounds of chance performance over 100 shuffles of trial data per session. Intended grasp is classified above chance performance at all trial time points, regardless of the number of grasps to be decoded. Download Figure 6-2, TIF file.

  • Extended Data Figure 6-3

    Time-dependent force classification accuracies by force level, per session, in participant T8. Data traces were smoothed with a 100-ms boxcar filter to aid in in visualization. Shaded areas surrounding each data trace indicate the SD across 40 runs during each session in participant T8. Gray shaded regions indicate the upper and lower bounds of chance performance over 100 shuffles of trial data per session. Intended grasp is classified above chance performance at all trial time points, regardless of the number of grasps to be decoded. Download Figure 6-3, TIF file.

  • Extended Data Figure 7-1

    Statistics for go-phase force and grasp classifications accuracies. A, Force classification accuracy histograms (row 1) and corrected p values (row 2). Hard and light forces are classified significantly more accurately than medium forces across all sessions (p < 0.05). B, Grasp classification accuracy histograms (row 1) and corrected p values (row 2). Decoding performance differed significantly between grasps across all sessions. Download Figure 7-1, TIF file.

  • Extended Data Figure 7-2

    Statistics for go-phase force classification accuracies within individual grasp types. A one-way ANOVA was implemented on force classification accuracies achieved during different grasp types. A, Force classification accuracy histograms. B, p values between force pairs, corrected for multiple comparisons across grasps and sessions using the Benjamini–Hochberg procedure. Within each grasp, hard and light forces were classified more accurately than medium forces across all sessions (p < 0.05). Download Figure 7-2, TIF file.

  • Extended Data Figure 7-3

    Statistics for go-phase force classification accuracies within individual force levels. A one-way ANOVA was implemented on the force classification accuracies achieved during different grasp types. A, Force classification accuracy histograms, color-coded by the grasp type used to produce each force level. B, p values between pairs of grasps used to produce each individual force level, corrected for multiple comparisons across forces and sessions using the Benjamini–Hochberg procedure. The decoding performance for each discrete force level was significantly different across grasps (p < 0.05), indicating that grasp type affected force decoding performance. Download Figure 7-3, TIF file.

Back to top

In this issue

eneuro: 8 (1)
eNeuro
Vol. 8, Issue 1
January/February 2021
  • Table of Contents
  • Index by author
Email

Thank you for sharing this eNeuro article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
The Neural Representation of Force across Grasp Types in Motor Cortex of Humans with Tetraplegia
(Your Name) has forwarded a page to you from eNeuro
(Your Name) thought you would be interested in this article in eNeuro.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Print
View Full Page PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Citation Tools
The Neural Representation of Force across Grasp Types in Motor Cortex of Humans with Tetraplegia
Anisha Rastogi, Francis R. Willett, Jessica Abreu, Douglas C. Crowder, Brian A. Murphy, William D. Memberg, Carlos E. Vargas-Irwin, Jonathan P. Miller, Jennifer Sweet, Benjamin L. Walter, Paymon G. Rezaii, Sergey D. Stavisky, Leigh R. Hochberg, Krishna V. Shenoy, Jaimie M. Henderson, Robert F. Kirsch, A. Bolu Ajiboye
eNeuro 25 January 2021, 8 (1) ENEURO.0231-20.2020; DOI: 10.1523/ENEURO.0231-20.2020

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Respond to this article
Share
The Neural Representation of Force across Grasp Types in Motor Cortex of Humans with Tetraplegia
Anisha Rastogi, Francis R. Willett, Jessica Abreu, Douglas C. Crowder, Brian A. Murphy, William D. Memberg, Carlos E. Vargas-Irwin, Jonathan P. Miller, Jennifer Sweet, Benjamin L. Walter, Paymon G. Rezaii, Sergey D. Stavisky, Leigh R. Hochberg, Krishna V. Shenoy, Jaimie M. Henderson, Robert F. Kirsch, A. Bolu Ajiboye
eNeuro 25 January 2021, 8 (1) ENEURO.0231-20.2020; DOI: 10.1523/ENEURO.0231-20.2020
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Significance Statement
    • Introduction
    • Materials and Methods
    • Results
    • Discussion
    • Acknowledgments
    • Footnotes
    • References
    • Synthesis
    • Author Response
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF

Keywords

  • brain-computer interface
  • force
  • grasp
  • kinetic
  • motor cortex

Responses to this article

Respond to this article

Jump to comment:

No eLetters have been published for this article.

Related Articles

Cited By...

More in this TOC Section

Research Article: New Research

  • Using Cortical Neuron Markers to Target Cells in the Dorsal Cochlear Nucleus
  • Parvalbumin Interneurons Are Differentially Connected to Principal Cells in Inhibitory Feedback Microcircuits along the Dorsoventral Axis of the Medial Entorhinal Cortex
  • Traumatic brain injury broadly affects GABAergic signaling in dentate gyrus granule cells
Show more Research Article: New Research

Sensory and Motor Systems

  • Otoacoustic emissions evoked by the time-varying harmonic structure of speech
  • Robustness to Noise in the Auditory System: A Distributed and Predictable Property
  • Interlimb transfer of reach adaptation does not require an intact corpus callosum:Evidence from patients with callosal lesions and agenesis
Show more Sensory and Motor Systems

Subjects

  • Sensory and Motor Systems
  • Home
  • Alerts
  • Visit Society for Neuroscience on Facebook
  • Follow Society for Neuroscience on Twitter
  • Follow Society for Neuroscience on LinkedIn
  • Visit Society for Neuroscience on Youtube
  • Follow our RSS feeds

Content

  • Early Release
  • Current Issue
  • Latest Articles
  • Issue Archive
  • Blog
  • Browse by Topic

Information

  • For Authors
  • For the Media

About

  • About the Journal
  • Editorial Board
  • Privacy Policy
  • Contact
  • Feedback
(eNeuro logo)
(SfN logo)

Copyright © 2021 by the Society for Neuroscience.
eNeuro eISSN: 2373-2822

The ideas and opinions expressed in eNeuro do not necessarily reflect those of SfN or the eNeuro Editorial Board. Publication of an advertisement or other product mention in eNeuro should not be construed as an endorsement of the manufacturer’s claims. SfN does not assume any responsibility for any injury and/or damage to persons or property arising from or related to any use of any material contained in eNeuro.