Virtual signals of head rotation induce gravity‐dependent inferences of linear acceleration
Key points Considerable debate exists regarding whether electrical vestibular stimuli encoded by vestibular afferents induce a net signal of linear acceleration, rotation or a combination of the two. This debate exists because an isolated signal of head rotation encoded by the vestibular afferents c...
Saved in:
Published in | The Journal of physiology Vol. 597; no. 21; pp. 5231 - 5246 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
Wiley Subscription Services, Inc
01.11.2019
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Key points
Considerable debate exists regarding whether electrical vestibular stimuli encoded by vestibular afferents induce a net signal of linear acceleration, rotation or a combination of the two.
This debate exists because an isolated signal of head rotation encoded by the vestibular afferents can cause perceptions of both linear and angular motion.
We recorded participants' perceptions in different orientations relative to gravity and predicted their responses by modelling the effect of electrical vestibular stimuli on vestibular afferents and a current model of central vestibular processing.
We show that, even if electrical vestibular stimuli are encoded as a net signal of head rotation, participants perceive both linear acceleration and rotation motions, provided the electrical stimulation‐induced rotational vector has a component orthogonal to gravity.
The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying electrical vestibular stimulation.
Electrical vestibular stimulation (EVS) is an increasingly popular biomedical tool for generating sensations of virtual motion in humans, for which the mechanism of action is a topic of considerable debate. Contention surrounds whether the evoked vestibular afferent activity encodes a signal of net rotation and/or linear acceleration. Central processing of vestibular self‐motion signals occurs through an internal representation of gravity that can lead to inferred linear accelerations in absence of a true inertial acceleration. Applying this model to virtual signals of rotation evoked by EVS, we predict that EVS will induce behaviours attributed to both angular and linear motion, depending on the head orientation relative to gravity. To demonstrate this, 18 subjects indicated their perceived motion during sinusoidal EVS when in one of four head/body positions orienting the gravitational vector parallel or orthogonal to the EVS rotation vector. During stimulation, participants selected one simulated movement from seven that corresponded best to what they perceived. Participants' responses in each orientation were predicted by a model combining the influence of EVS on vestibular afferents with known mechanisms of vestibular processing. When the EVS rotation vector had a component orthogonal to gravity, human perceptual responses were consistent with a non‐zero central estimate of interaural or superior‐inferior linear acceleration. The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying EVS, which has important implications for its use in human biomedical or sensory augmentation applications.
Key points
Considerable debate exists regarding whether electrical vestibular stimuli encoded by vestibular afferents induce a net signal of linear acceleration, rotation or a combination of the two.
This debate exists because an isolated signal of head rotation encoded by the vestibular afferents can cause perceptions of both linear and angular motion.
We recorded participants' perceptions in different orientations relative to gravity and predicted their responses by modelling the effect of electrical vestibular stimuli on vestibular afferents and a current model of central vestibular processing.
We show that, even if electrical vestibular stimuli are encoded as a net signal of head rotation, participants perceive both linear acceleration and rotation motions, provided the electrical stimulation‐induced rotational vector has a component orthogonal to gravity.
The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying electrical vestibular stimulation. |
---|---|
AbstractList | Key points
Considerable debate exists regarding whether electrical vestibular stimuli encoded by vestibular afferents induce a net signal of linear acceleration, rotation or a combination of the two.
This debate exists because an isolated signal of head rotation encoded by the vestibular afferents can cause perceptions of both linear and angular motion.
We recorded participants' perceptions in different orientations relative to gravity and predicted their responses by modelling the effect of electrical vestibular stimuli on vestibular afferents and a current model of central vestibular processing.
We show that, even if electrical vestibular stimuli are encoded as a net signal of head rotation, participants perceive both linear acceleration and rotation motions, provided the electrical stimulation‐induced rotational vector has a component orthogonal to gravity.
The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying electrical vestibular stimulation.
Electrical vestibular stimulation (EVS) is an increasingly popular biomedical tool for generating sensations of virtual motion in humans, for which the mechanism of action is a topic of considerable debate. Contention surrounds whether the evoked vestibular afferent activity encodes a signal of net rotation and/or linear acceleration. Central processing of vestibular self‐motion signals occurs through an internal representation of gravity that can lead to inferred linear accelerations in absence of a true inertial acceleration. Applying this model to virtual signals of rotation evoked by EVS, we predict that EVS will induce behaviours attributed to both angular and linear motion, depending on the head orientation relative to gravity. To demonstrate this, 18 subjects indicated their perceived motion during sinusoidal EVS when in one of four head/body positions orienting the gravitational vector parallel or orthogonal to the EVS rotation vector. During stimulation, participants selected one simulated movement from seven that corresponded best to what they perceived. Participants' responses in each orientation were predicted by a model combining the influence of EVS on vestibular afferents with known mechanisms of vestibular processing. When the EVS rotation vector had a component orthogonal to gravity, human perceptual responses were consistent with a non‐zero central estimate of interaural or superior‐inferior linear acceleration. The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying EVS, which has important implications for its use in human biomedical or sensory augmentation applications.
Key points
Considerable debate exists regarding whether electrical vestibular stimuli encoded by vestibular afferents induce a net signal of linear acceleration, rotation or a combination of the two.
This debate exists because an isolated signal of head rotation encoded by the vestibular afferents can cause perceptions of both linear and angular motion.
We recorded participants' perceptions in different orientations relative to gravity and predicted their responses by modelling the effect of electrical vestibular stimuli on vestibular afferents and a current model of central vestibular processing.
We show that, even if electrical vestibular stimuli are encoded as a net signal of head rotation, participants perceive both linear acceleration and rotation motions, provided the electrical stimulation‐induced rotational vector has a component orthogonal to gravity.
The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying electrical vestibular stimulation. Electrical vestibular stimulation (EVS) is an increasingly popular biomedical tool for generating sensations of virtual motion in humans, for which the mechanism of action is a topic of considerable debate. Contention surrounds whether the evoked vestibular afferent activity encodes a signal of net rotation and/or linear acceleration. Central processing of vestibular self‐motion signals occurs through an internal representation of gravity that can lead to inferred linear accelerations in absence of a true inertial acceleration. Applying this model to virtual signals of rotation evoked by EVS, we predict that EVS will induce behaviours attributed to both angular and linear motion, depending on the head orientation relative to gravity. To demonstrate this, 18 subjects indicated their perceived motion during sinusoidal EVS when in one of four head/body positions orienting the gravitational vector parallel or orthogonal to the EVS rotation vector. During stimulation, participants selected one simulated movement from seven that corresponded best to what they perceived. Participants' responses in each orientation were predicted by a model combining the influence of EVS on vestibular afferents with known mechanisms of vestibular processing. When the EVS rotation vector had a component orthogonal to gravity, human perceptual responses were consistent with a non‐zero central estimate of interaural or superior‐inferior linear acceleration. The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying EVS, which has important implications for its use in human biomedical or sensory augmentation applications. Considerable debate exists regarding whether electrical vestibular stimuli encoded by vestibular afferents induce a net signal of linear acceleration, rotation or a combination of the two. This debate exists because an isolated signal of head rotation encoded by the vestibular afferents can cause perceptions of both linear and angular motion. We recorded participants' perceptions in different orientations relative to gravity and predicted their responses by modelling the effect of electrical vestibular stimuli on vestibular afferents and a current model of central vestibular processing. We show that, even if electrical vestibular stimuli are encoded as a net signal of head rotation, participants perceive both linear acceleration and rotation motions, provided the electrical stimulation-induced rotational vector has a component orthogonal to gravity. The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying electrical vestibular stimulation. Electrical vestibular stimulation (EVS) is an increasingly popular biomedical tool for generating sensations of virtual motion in humans, for which the mechanism of action is a topic of considerable debate. Contention surrounds whether the evoked vestibular afferent activity encodes a signal of net rotation and/or linear acceleration. Central processing of vestibular self-motion signals occurs through an internal representation of gravity that can lead to inferred linear accelerations in absence of a true inertial acceleration. Applying this model to virtual signals of rotation evoked by EVS, we predict that EVS will induce behaviours attributed to both angular and linear motion, depending on the head orientation relative to gravity. To demonstrate this, 18 subjects indicated their perceived motion during sinusoidal EVS when in one of four head/body positions orienting the gravitational vector parallel or orthogonal to the EVS rotation vector. During stimulation, participants selected one simulated movement from seven that corresponded best to what they perceived. Participants' responses in each orientation were predicted by a model combining the influence of EVS on vestibular afferents with known mechanisms of vestibular processing. When the EVS rotation vector had a component orthogonal to gravity, human perceptual responses were consistent with a non-zero central estimate of interaural or superior-inferior linear acceleration. The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying EVS, which has important implications for its use in human biomedical or sensory augmentation applications. Considerable debate exists regarding whether electrical vestibular stimuli encoded by vestibular afferents induce a net signal of linear acceleration, rotation or a combination of the two. This debate exists because an isolated signal of head rotation encoded by the vestibular afferents can cause perceptions of both linear and angular motion. We recorded participants' perceptions in different orientations relative to gravity and predicted their responses by modelling the effect of electrical vestibular stimuli on vestibular afferents and a current model of central vestibular processing. We show that, even if electrical vestibular stimuli are encoded as a net signal of head rotation, participants perceive both linear acceleration and rotation motions, provided the electrical stimulation-induced rotational vector has a component orthogonal to gravity. The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying electrical vestibular stimulation.KEY POINTSConsiderable debate exists regarding whether electrical vestibular stimuli encoded by vestibular afferents induce a net signal of linear acceleration, rotation or a combination of the two. This debate exists because an isolated signal of head rotation encoded by the vestibular afferents can cause perceptions of both linear and angular motion. We recorded participants' perceptions in different orientations relative to gravity and predicted their responses by modelling the effect of electrical vestibular stimuli on vestibular afferents and a current model of central vestibular processing. We show that, even if electrical vestibular stimuli are encoded as a net signal of head rotation, participants perceive both linear acceleration and rotation motions, provided the electrical stimulation-induced rotational vector has a component orthogonal to gravity. The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying electrical vestibular stimulation.Electrical vestibular stimulation (EVS) is an increasingly popular biomedical tool for generating sensations of virtual motion in humans, for which the mechanism of action is a topic of considerable debate. Contention surrounds whether the evoked vestibular afferent activity encodes a signal of net rotation and/or linear acceleration. Central processing of vestibular self-motion signals occurs through an internal representation of gravity that can lead to inferred linear accelerations in absence of a true inertial acceleration. Applying this model to virtual signals of rotation evoked by EVS, we predict that EVS will induce behaviours attributed to both angular and linear motion, depending on the head orientation relative to gravity. To demonstrate this, 18 subjects indicated their perceived motion during sinusoidal EVS when in one of four head/body positions orienting the gravitational vector parallel or orthogonal to the EVS rotation vector. During stimulation, participants selected one simulated movement from seven that corresponded best to what they perceived. Participants' responses in each orientation were predicted by a model combining the influence of EVS on vestibular afferents with known mechanisms of vestibular processing. When the EVS rotation vector had a component orthogonal to gravity, human perceptual responses were consistent with a non-zero central estimate of interaural or superior-inferior linear acceleration. The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying EVS, which has important implications for its use in human biomedical or sensory augmentation applications.ABSTRACTElectrical vestibular stimulation (EVS) is an increasingly popular biomedical tool for generating sensations of virtual motion in humans, for which the mechanism of action is a topic of considerable debate. Contention surrounds whether the evoked vestibular afferent activity encodes a signal of net rotation and/or linear acceleration. Central processing of vestibular self-motion signals occurs through an internal representation of gravity that can lead to inferred linear accelerations in absence of a true inertial acceleration. Applying this model to virtual signals of rotation evoked by EVS, we predict that EVS will induce behaviours attributed to both angular and linear motion, depending on the head orientation relative to gravity. To demonstrate this, 18 subjects indicated their perceived motion during sinusoidal EVS when in one of four head/body positions orienting the gravitational vector parallel or orthogonal to the EVS rotation vector. During stimulation, participants selected one simulated movement from seven that corresponded best to what they perceived. Participants' responses in each orientation were predicted by a model combining the influence of EVS on vestibular afferents with known mechanisms of vestibular processing. When the EVS rotation vector had a component orthogonal to gravity, human perceptual responses were consistent with a non-zero central estimate of interaural or superior-inferior linear acceleration. The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying EVS, which has important implications for its use in human biomedical or sensory augmentation applications. Considerable debate exists regarding whether electrical vestibular stimuli encoded by vestibular afferents induce a net signal of linear acceleration, rotation or a combination of the two. This debate exists because an isolated signal of head rotation encoded by the vestibular afferents can cause perceptions of both linear and angular motion. We recorded participants' perceptions in different orientations relative to gravity and predicted their responses by modelling the effect of electrical vestibular stimuli on vestibular afferents and a current model of central vestibular processing. We show that, even if electrical vestibular stimuli are encoded as a net signal of head rotation, participants perceive both linear acceleration and rotation motions, provided the electrical stimulation‐induced rotational vector has a component orthogonal to gravity. The emergence of a perception of linear acceleration from a single rotational input signal clarifies the origins of the neural mechanisms underlying electrical vestibular stimulation. |
Author | Dakin, Christopher J. Blouin, Jean‐Sébastien Khosravi‐Hashemi, Navid Forbes, Patrick A. |
Author_xml | – sequence: 1 givenname: Navid orcidid: 0000-0001-6957-6567 surname: Khosravi‐Hashemi fullname: Khosravi‐Hashemi, Navid organization: University of British Columbia – sequence: 2 givenname: Patrick A. orcidid: 0000-0002-0230-9971 surname: Forbes fullname: Forbes, Patrick A. organization: University Medical Center Rotterdam – sequence: 3 givenname: Christopher J. orcidid: 0000-0002-6781-0281 surname: Dakin fullname: Dakin, Christopher J. email: chris.dakin@usu.edu organization: Utah State University – sequence: 4 givenname: Jean‐Sébastien surname: Blouin fullname: Blouin, Jean‐Sébastien organization: University of British Columbia |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31483492$$D View this record in MEDLINE/PubMed |
BookMark | eNp9kctKxTAQhoMoeryATyAFN26qmSRtkqWIt8MBXRzcSUnbiUZ60mPSKmfnI_iMPon1DoKuZjHf_8_MP-tk2bceCdkGug8A_GB8yaTKBVsiIxC5TqXUfJmMKGUs5TKDNbIe4x2lwKnWq2SNg1BcaDYi11cudL1pkuhuvGli0trkFk2dhLYznWt94nzdV5jcBPPgusXL03ONc_Q1-m5oWQzoK3yXNc6jCYmpKmwwvIs3yYodTHHrs26Q6cnx9OgsnVycnh8dTtKKK5GneU61sZniBmhpJQO0pUGptbA5FyJjmZW1EHlmtYKSlWCUZKhLCVIACr5B9j5s56G97zF2xczFYYvGeGz7WDCmRJapQTygu7_Qu7YPb5cXjANVVEjKB2rnk-rLGdbFPLiZCYviK7efiVVoYwxovxGgxdtLiq-XDOj-L7RyH9F2wbjmH8Gja3Dxp3ExHV8Clzrnrzx7mj8 |
CitedBy_id | crossref_primary_10_3389_fneur_2019_01270 crossref_primary_10_1016_j_jneumeth_2022_109709 crossref_primary_10_3233_VES_220075 crossref_primary_10_1016_j_gaitpost_2024_12_026 crossref_primary_10_1089_neu_2020_7432 crossref_primary_10_1093_pnasnexus_pgac174 crossref_primary_10_1038_s41598_021_87485_4 crossref_primary_10_1152_jn_00276_2019 crossref_primary_10_3389_fnhum_2021_631782 crossref_primary_10_3389_fnsys_2022_886284 crossref_primary_10_1371_journal_pcbi_1012601 crossref_primary_10_1371_journal_pone_0231334 crossref_primary_10_1523_JNEUROSCI_0987_22_2023 crossref_primary_10_1007_s00221_024_06905_9 crossref_primary_10_1007_s00421_022_05043_w crossref_primary_10_7554_eLife_65085 crossref_primary_10_1523_JNEUROSCI_1463_19_2020 crossref_primary_10_1097_WCO_0000000000001228 crossref_primary_10_1109_ACCESS_2022_3206047 crossref_primary_10_1152_jn_00171_2023 |
Cites_doi | 10.1152/japplphysiol.00008.2004 10.1016/0006-8993(82)90990-8 10.3233/VES-1993-3203 10.3389/fneur.2012.00148 10.1007/s002210050533 10.1016/S0013-4694(98)00056-X 10.1145/3139131.3141219 10.1523/JNEUROSCI.19-01-00316.1999 10.1016/j.brainresbull.2004.07.008 10.3233/VES-2003-122-303 10.1152/jn.01029.2011 10.1523/JNEUROSCI.23-28-09265.2003 10.1007/s00221-011-2568-4 10.1007/978-3-540-79007-5_12 10.1088/1741-2560/2/3/S02 10.3389/fneur.2012.00117 10.1152/jn.00485.2001 10.1109/51.827403 10.1111/j.1469-7793.1999.0931s.x 10.1097/00001756-200212200-00001 10.1159/000046815 10.1145/1178823.1178881 10.3389/fneur.2012.00104 10.1016/j.jneumeth.2017.11.012 10.1007/s00221-012-3302-6 10.1038/19303 10.3389/fnint.2014.00004 10.1113/jphysiol.2010.195222 10.1007/s00221-002-1038-4 10.1007/s10162-005-0003-x 10.1007/s00422-006-0133-1 10.1016/j.neuropsychologia.2015.03.004 10.1152/jn.1976.39.5.970 10.1007/BF00279665 10.1007/s00221-002-1067-z 10.1007/s00221-009-2054-4 10.1152/jn.1984.51.6.1236 10.1152/jn.90677.2008 10.3389/fnint.2014.00094 10.1038/s41467-019-09738-1 10.1113/jphysiol.1997.sp022051 10.1111/j.1749-6632.2008.03732.x 10.1016/j.cub.2018.09.049 10.1152/jn.00114.2015 10.1523/JNEUROSCI.1902-16.2016 10.1038/nn.3530 10.1152/jn.00558.2001 10.1152/jn.1995.73.2.896 10.1152/jn.01234.2003 10.1007/s00221-006-0792-0 10.1113/jphysiol.2010.197053 10.1145/2967934.2968080 10.1038/nature02754 10.1113/jphysiol.2004.079525 10.1002/ana.410420616 10.1113/jphysiol.2005.092544 10.1101/087692 |
ContentType | Journal Article |
Copyright | 2019 The Authors. The Journal of Physiology © 2019 The Physiological Society 2019 The Authors. The Journal of Physiology © 2019 The Physiological Society. Journal compilation © 2019 The Physiological Society |
Copyright_xml | – notice: 2019 The Authors. The Journal of Physiology © 2019 The Physiological Society – notice: 2019 The Authors. The Journal of Physiology © 2019 The Physiological Society. – notice: Journal compilation © 2019 The Physiological Society |
DBID | AAYXX CITATION NPM 7QP 7QR 7TK 7TS 8FD FR3 P64 7X8 |
DOI | 10.1113/JP278642 |
DatabaseName | CrossRef PubMed Calcium & Calcified Tissue Abstracts Chemoreception Abstracts Neurosciences Abstracts Physical Education Index Technology Research Database Engineering Research Database Biotechnology and BioEngineering Abstracts MEDLINE - Academic |
DatabaseTitle | CrossRef PubMed Technology Research Database Chemoreception Abstracts Engineering Research Database Calcium & Calcified Tissue Abstracts Neurosciences Abstracts Physical Education Index Biotechnology and BioEngineering Abstracts MEDLINE - Academic |
DatabaseTitleList | Technology Research Database PubMed MEDLINE - Academic CrossRef |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Anatomy & Physiology |
EISSN | 1469-7793 |
EndPage | 5246 |
ExternalDocumentID | 31483492 10_1113_JP278642 TJP13796 |
Genre | article Research Support, Non-U.S. Gov't Journal Article |
GrantInformation_xml | – fundername: Netherlands Organization for Scientific Research funderid: NWO #016.Veni.188.049 – fundername: Natural Sciences and Engineering Research Council of Canada funderid: RGPIN: 356026‐13 |
GroupedDBID | --- -DZ -~X .3N .GA 05W 0R~ 10A 123 18M 1OC 24P 29L 2WC 33P 36B 3SF 4.4 50Y 50Z 51W 51X 52M 52N 52O 52P 52R 52S 52T 52U 52V 52W 52X 53G 5GY 5HH 5LA 5RE 5VS 66C 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A01 A03 AAESR AAEVG AAFWJ AAHHS AAHQN AAIPD AAMNL AANLZ AAONW AASGY AAXRX AAYCA AAZKR ABCQN ABCUV ABEML ABITZ ABIVO ABJNI ABOCM ABPPZ ABPVW ABQWH ABXGK ACAHQ ACCFJ ACCZN ACFBH ACGFO ACGFS ACGOF ACIWK ACMXC ACNCT ACPOU ACPRK ACSCC ACXBN ACXQS ADBBV ADBTR ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN AEEZP AEGXH AEIGN AEIMD AEQDE AEUQT AEUYR AFBPY AFEBI AFFPM AFGKR AFPWT AFWVQ AFZJQ AHBTC AI. AIACR AIAGR AITYG AIURR AIWBW AJBDE ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN ALVPJ AMBMR AMYDB AOIJS ATUGU AZBYB AZVAB BAFTC BAWUL BFHJK BHBCM BMXJE BROTX BRXPI BY8 C45 CS3 D-6 D-7 D-E D-F DCZOG DIK DPXWK DR2 DRFUL DRMAN DRSTM E3Z EBS EMOBN EX3 F00 F01 F04 F5P FIJ FUBAC G-S G.N GODZA GX1 H.X HGLYW HZI HZ~ IHE IX1 J0M K48 KBYEO LATKE LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LYRES MEWTI MK4 MRFUL MRMAN MRSTM MSFUL MSMAN MSSTM MXFUL MXMAN MXSTM N04 N05 N9A NF~ O66 O9- OIG OK1 OVD P2P P2W P2X P2Z P4B P4D Q.N Q11 QB0 R.K ROL RPM RX1 SUPJJ TEORI TLM TN5 TR2 UB1 UPT V8K VH1 W8F W8V W99 WBKPD WH7 WIH WIJ WIK WIN WNSPC WOHZO WOQ WOW WQJ WRC WXI WXSBR WYISQ XG1 YBU YHG YKV YQT YSK YZZ ZZTAW ~IA ~WT .55 .GJ .Y3 0YM 31~ 3EH 3O- AAYJJ AAYXX ADXHL AEYWJ AFFNX AGHNM AGYGG C1A CAG CHEAL CITATION COF EJD FA8 H13 HF~ H~9 LW6 MVM NEJ OHT RIG UKR WHG X7M XOL YXB YYP ZGI ZXP 1OB IPNFZ NPM PKN SAMSI 7QP 7QR 7TK 7TS 8FD FR3 P64 7X8 |
ID | FETCH-LOGICAL-c3846-6609af583a10bf721efbae7994f6344525f7d4465f981b2b1a872e9b71741e43 |
IEDL.DBID | DR2 |
ISSN | 0022-3751 1469-7793 |
IngestDate | Fri Jul 11 05:14:43 EDT 2025 Fri Jul 25 12:19:21 EDT 2025 Wed Feb 19 02:29:57 EST 2025 Thu Apr 24 23:04:19 EDT 2025 Tue Jul 01 04:29:28 EDT 2025 Wed Jan 22 16:37:41 EST 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 21 |
Keywords | gravito-inertial ambiguity internal model spatial orientation electrical vestibular stimulation vestibular system |
Language | English |
License | 2019 The Authors. The Journal of Physiology © 2019 The Physiological Society. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c3846-6609af583a10bf721efbae7994f6344525f7d4465f981b2b1a872e9b71741e43 |
Notes | Edited by: Richard Carson & Janet Taylor These authors contributed equally to this work. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0002-0230-9971 0000-0001-6957-6567 0000-0002-6781-0281 |
OpenAccessLink | https://physoc.onlinelibrary.wiley.com/doi/pdfdirect/10.1113/JP278642 |
PMID | 31483492 |
PQID | 2310804703 |
PQPubID | 1086388 |
PageCount | 16 |
ParticipantIDs | proquest_miscellaneous_2284558981 proquest_journals_2310804703 pubmed_primary_31483492 crossref_primary_10_1113_JP278642 crossref_citationtrail_10_1113_JP278642 wiley_primary_10_1113_JP278642_TJP13796 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 1 November 2019 2019-11-00 20191101 |
PublicationDateYYYYMMDD | 2019-11-01 |
PublicationDate_xml | – month: 11 year: 2019 text: 1 November 2019 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | England |
PublicationPlace_xml | – name: England – name: London |
PublicationTitle | The Journal of physiology |
PublicationTitleAlternate | J Physiol |
PublicationYear | 2019 |
Publisher | Wiley Subscription Services, Inc |
Publisher_xml | – name: Wiley Subscription Services, Inc |
References | 1995; 73 2004; 64 1997; 42 2019; 10 2002; 12 2002; 13 2010; 588 2015; 74 1988; 73 2008; 100 2009; 1164 2016; 36 1993; 3 1984; 51 1997; 500 2007; 179 2000; 19 2018; 294 2013; 16 1999; 19 2002; 144 2002; 87 2002; 145 1982; 252 1998; 122 1976; 39 2014; 8 2018; 28 2011; 2 2010; 200 2008 2013; 224 2006 2005 2007; 96 2015; 8 2011; 210 2012; 108 2011; 589 2004; 430 2004; 96 2012; 3 2004; 92 2001; 6 2005; 563 2015; 114 2005; 567 1995; 106 1998; 107 2005; 6 2017 2016 2005; 2 1999; 398 1999; 517 2003; 23 e_1_2_5_27_1 e_1_2_5_25_1 Merfeld DM (e_1_2_5_43_1) 1995; 106 e_1_2_5_48_1 e_1_2_5_23_1 e_1_2_5_46_1 e_1_2_5_21_1 e_1_2_5_44_1 e_1_2_5_29_1 e_1_2_5_61_1 e_1_2_5_40_1 e_1_2_5_15_1 e_1_2_5_38_1 e_1_2_5_17_1 e_1_2_5_36_1 e_1_2_5_59_1 e_1_2_5_9_1 Cohen B (e_1_2_5_6_1) 2011; 2 e_1_2_5_11_1 e_1_2_5_34_1 e_1_2_5_57_1 e_1_2_5_7_1 e_1_2_5_13_1 e_1_2_5_32_1 e_1_2_5_55_1 e_1_2_5_5_1 e_1_2_5_3_1 e_1_2_5_19_1 e_1_2_5_30_1 e_1_2_5_53_1 e_1_2_5_51_1 e_1_2_5_28_1 e_1_2_5_49_1 e_1_2_5_26_1 e_1_2_5_47_1 e_1_2_5_24_1 e_1_2_5_45_1 e_1_2_5_22_1 Merfeld DM (e_1_2_5_42_1) 1995; 106 e_1_2_5_60_1 e_1_2_5_62_1 e_1_2_5_20_1 e_1_2_5_41_1 e_1_2_5_14_1 e_1_2_5_39_1 e_1_2_5_16_1 e_1_2_5_37_1 e_1_2_5_58_1 e_1_2_5_8_1 e_1_2_5_10_1 e_1_2_5_35_1 e_1_2_5_56_1 e_1_2_5_12_1 e_1_2_5_33_1 e_1_2_5_54_1 e_1_2_5_4_1 e_1_2_5_2_1 e_1_2_5_18_1 e_1_2_5_31_1 e_1_2_5_52_1 e_1_2_5_50_1 |
References_xml | – volume: 28 start-page: 3589 year: 2018 end-page: 3598.e3583 article-title: Cerebellar degeneration increases visual influence on dynamic estimates of verticality publication-title: Curr Biol – volume: 1164 start-page: 116 year: 2009 end-page: 118 article-title: Galvanic vestibular stimulation combines with Earth‐horizontal rotation in roll to induce the illusion of translation publication-title: Ann NY Acad Sci – volume: 23 start-page: 9265 year: 2003 end-page: 9275 article-title: Resolution of sensory ambiguities for gaze stabilization requires a second neural integrator publication-title: J Neurosci – volume: 12 start-page: 77 year: 2002 end-page: 85 article-title: The effects of stochastic monopolar galvanic vestibular stimulation on human postural sway publication-title: J Vestib Res – volume: 114 start-page: 264 year: 2015 end-page: 273 article-title: Gain and phase of perceived virtual rotation evoked by electrical vestibular stimuli publication-title: J Neurophysiol – volume: 430 start-page: 560 year: 2004 end-page: 564 article-title: Neurons compute internal models of the physical laws of motion publication-title: Nature – volume: 16 start-page: 1701 year: 2013 end-page: 1708 article-title: Computation of linear acceleration through an internal model in the macaque cerebellum publication-title: Nat Neurosci – volume: 252 start-page: 156 year: 1982 end-page: 160 article-title: Responses of vestibular‐nerve afferents in the squirrel monkey to externally applied galvanic currents publication-title: Brain Res – volume: 8 start-page: 94 year: 2015 article-title: Task, muscle and frequency dependent vestibular control of posture publication-title: Front Integr Neurosci – volume: 398 start-page: 615 year: 1999 end-page: 618 article-title: Humans use internal models to estimate gravity and linear acceleration publication-title: Nature – start-page: 279 year: 2008 end-page: 300 – volume: 19 start-page: 35 year: 2000 end-page: 42 article-title: A spatial disorientation survey of experienced instructor pilots publication-title: IEEE Eng Med Biol Mag – volume: 8 start-page: 4 year: 2014 article-title: Galvanic vestibular stimulation in hemi‐spatial neglect publication-title: Front Integr Neurosci – volume: 36 start-page: 11510 year: 2016 end-page: 11520 article-title: Transformation of vestibular signals for the control of standing in humans publication-title: J Neurosci – volume: 6 start-page: 191 year: 2005 end-page: 206 article-title: Orientation of human semicircular canals measured by three‐dimensional multiplanar CT reconstruction publication-title: J Assoc Res Otolaryngol – volume: 3 start-page: 148 year: 2012 end-page: 148 article-title: What does galvanic vestibular stimulation actually activate: response publication-title: Front Neurol – volume: 122 start-page: 453 year: 1998 end-page: 458 article-title: Maintained ocular torsion produced by bilateral and unilateral galvanic (DC) vestibular stimulation in humans publication-title: Exp Brain Res – volume: 200 start-page: 197 year: 2010 end-page: 222 article-title: Internal models and neural computation in the vestibular system publication-title: Exp Brain Res – volume: 64 start-page: 265 year: 2004 end-page: 271 article-title: Responses of primary vestibular neurons to galvanic vestibular stimulation (GVS) in the anaesthetised guinea pig publication-title: Brain Res Bull – volume: 96 start-page: 389 year: 2007 end-page: 404 article-title: Bayesian processing of vestibular information publication-title: Biol Cybern – volume: 10 start-page: 1904 year: 2019 article-title: Neural substrates, dynamics and thresholds of galvanic vestibular stimulation in the behaving primate publication-title: Nat Commun – volume: 13 start-page: 2379 year: 2002 end-page: 2383 article-title: Galvanic vestibular stimulation evokes sensations of body rotation publication-title: Neuroreport – volume: 92 start-page: 905 year: 2004 end-page: 925 article-title: An integrative neural network for detecting inertial motion and head orientation publication-title: J Neurophysiol – volume: 106 start-page: 111 year: 1995 end-page: 122 article-title: The vestibulo‐ocular reflex of the squirrel monkey during eccentric rotation and roll tilt publication-title: Exp Brain Res – volume: 3 start-page: 117 year: 2012 end-page: 117 article-title: What galvanic vestibular stimulation actually activates publication-title: Front Neurol – volume: 144 start-page: 69 year: 2002 end-page: 78 article-title: Between‐subject variability and within‐subject reliability of the human eye‐movement response to bilateral galvanic (DC) vestibular stimulation publication-title: Exp Brain Res – volume: 108 start-page: 1511 year: 2012 end-page: 1520 article-title: Spatial and temporal properties of eye movements produced by electrical stimulation of semicircular canal afferents publication-title: J Neurophysiol – volume: 100 start-page: 2981 year: 2008 end-page: 2996 article-title: Computational approaches to spatial orientation: from transfer functions to dynamic Bayesian inference publication-title: J Neurophysiol – volume: 563 start-page: 229 year: 2005 end-page: 234 article-title: Otolith and canal reflexes in human standing publication-title: J Physiol – volume: 107 start-page: 200 year: 1998 end-page: 205 article-title: Effects of galvanic vestibular stimulation on otolithic and semicircular canal eye movements and perceived vertical publication-title: Electroencephalogr Clin Neurophysiol – volume: 567 start-page: 591 year: 2005 end-page: 597 article-title: Virtual head rotation reveals a process of route reconstruction from human vestibular signals publication-title: J Physiol – volume: 39 start-page: 970 year: 1976 end-page: 984 article-title: Physiology of peripheral neurons innervating otolith organs of squirrel‐monkey I. Response to static tilts and to long‐duration centrifugal force publication-title: J Neurophysiol – volume: 51 start-page: 1236 year: 1984 end-page: 1256 article-title: Relation between discharge regularity and responses to externally applied galvanic currents in vestibular nerve afferents of the squirrel‐monkey publication-title: J Neurophysiol – volume: 96 start-page: 2301 year: 2004 end-page: 2316 article-title: Probing the human vestibular system with galvanic stimulation publication-title: J Appl Physiol – volume: 87 start-page: 2064 year: 2002 end-page: 2073 article-title: Comparison of human ocular torsion patterns during natural and galvanic vestibular stimulation publication-title: J Neurophysiol – volume: 19 start-page: 316 year: 1999 end-page: 327 article-title: Computation of inertial motion: neural strategies to resolve ambiguous otolith information publication-title: J Neurosci – volume: 500 start-page: 661 year: 1997 end-page: 672 article-title: Human body‐segment tilts induced by galvanic stimulation: a vestibularly driven balance protection mechanism publication-title: J Physiol – volume: 589 start-page: 843 year: 2011 end-page: 853 article-title: Adaptation of vestibular signals for self‐motion perception publication-title: J Physiol – volume: 517 start-page: 931 year: 1999 end-page: 939 article-title: Effects of galvanic vestibular stimulation during human walking publication-title: J Physiol – volume: 294 start-page: 116 year: 2018 end-page: 121 article-title: Ocular torsion responses to sinusoidal electrical vestibular stimulation publication-title: J Neurosci Methods – volume: 106 start-page: 123 year: 1995 end-page: 134 article-title: Modeling the vestibulo‐ocular reflex of the squirrel monkey during eccentric rotation and roll tilt publication-title: Exp Brain Res – volume: 73 start-page: 106 year: 1988 end-page: 114 article-title: Motion perceptions induced by off‐vertical axis rotation (OVAR) at small angles of tilt publication-title: Exp Brain Res – volume: 210 start-page: 407 year: 2011 end-page: 422 article-title: The functional significance of velocity storage and its dependence on gravity publication-title: Exp Brain Res – volume: 2 start-page: S164 year: 2005 end-page: 179 article-title: Sensory vestibular contributions to constructing internal models of self‐motion publication-title: J Neural Eng – volume: 588 start-page: 4441 year: 2010 end-page: 4451 article-title: Lack of otolith involvement in balance responses evoked by mastoid electrical stimulation publication-title: J Physiol – start-page: 1 year: 2017 end-page: 2 – volume: 179 start-page: 263 year: 2007 end-page: 290 article-title: A Bayesian model of the disambiguation of gravitoinertial force by visual cues publication-title: Exp Brain Res – volume: 87 start-page: 819 year: 2002 end-page: 833 article-title: Neural processing of gravitoinertial cues in humans. III. Modeling tilt and translation responses publication-title: J Neurophysiol – year: 2016 – volume: 2 start-page: 90 year: 2011 article-title: What does galvanic vestibular stimulation actually activate? publication-title: Front Neurol – volume: 42 start-page: 933 year: 1997 end-page: 950 article-title: Spinocerebellar ataxia type 6: gaze‐evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset publication-title: Ann Neurol – volume: 74 start-page: 178 year: 2015 end-page: 183 article-title: Subliminal galvanic‐vestibular stimulation recalibrates the distorted visual and tactile subjective vertical in right‐sided stroke publication-title: Neuropsychologia – volume: 145 start-page: 1 year: 2002 end-page: 27 article-title: The vestibulo‐ocular reflex in three dimensions publication-title: Exp Brain Res – volume: 224 start-page: 233 year: 2013 end-page: 241 article-title: Galvanic vestibular stimulation influences randomness of number generation publication-title: Exp Brain Res – volume: 3 start-page: 104 year: 2012 end-page: 104 article-title: Galvanic vestibular stimulation produces sensations of rotation consistent with activation of semicircular canal afferents publication-title: Front Neurol – volume: 6 start-page: 98 year: 2001 end-page: 107 article-title: Directional sensitivity of the human macula utriculi based on morphological characteristics publication-title: Audiol Neurootol – start-page: 289 year: 2005 end-page: 290 – year: 2006 – volume: 3 start-page: 123 year: 1993 end-page: 139 article-title: Three dimensional eye movements of squirrel monkeys following postrotatory tilt publication-title: J Vestib Res – volume: 73 start-page: 896 year: 1995 end-page: 901 article-title: Effect of galvanic vestibular stimulation on human postural responses during support surface translations publication-title: J Neurophysiol – ident: e_1_2_5_16_1 doi: 10.1152/japplphysiol.00008.2004 – ident: e_1_2_5_21_1 doi: 10.1016/0006-8993(82)90990-8 – volume: 106 start-page: 123 year: 1995 ident: e_1_2_5_42_1 article-title: Modeling the vestibulo‐ocular reflex of the squirrel monkey during eccentric rotation and roll tilt publication-title: Exp Brain Res – ident: e_1_2_5_46_1 doi: 10.3233/VES-1993-3203 – ident: e_1_2_5_7_1 doi: 10.3389/fneur.2012.00148 – ident: e_1_2_5_60_1 doi: 10.1007/s002210050533 – ident: e_1_2_5_62_1 doi: 10.1016/S0013-4694(98)00056-X – ident: e_1_2_5_57_1 doi: 10.1145/3139131.3141219 – ident: e_1_2_5_3_1 doi: 10.1523/JNEUROSCI.19-01-00316.1999 – ident: e_1_2_5_29_1 doi: 10.1016/j.brainresbull.2004.07.008 – ident: e_1_2_5_55_1 doi: 10.3233/VES-2003-122-303 – ident: e_1_2_5_35_1 doi: 10.1152/jn.01029.2011 – ident: e_1_2_5_24_1 doi: 10.1523/JNEUROSCI.23-28-09265.2003 – ident: e_1_2_5_33_1 doi: 10.1007/s00221-011-2568-4 – ident: e_1_2_5_32_1 doi: 10.1007/978-3-540-79007-5_12 – ident: e_1_2_5_27_1 doi: 10.1088/1741-2560/2/3/S02 – ident: e_1_2_5_8_1 doi: 10.3389/fneur.2012.00117 – ident: e_1_2_5_44_1 doi: 10.1152/jn.00485.2001 – ident: e_1_2_5_56_1 doi: 10.1109/51.827403 – ident: e_1_2_5_17_1 doi: 10.1111/j.1469-7793.1999.0931s.x – ident: e_1_2_5_18_1 doi: 10.1097/00001756-200212200-00001 – ident: e_1_2_5_59_1 doi: 10.1159/000046815 – ident: e_1_2_5_48_1 doi: 10.1145/1178823.1178881 – ident: e_1_2_5_52_1 doi: 10.3389/fneur.2012.00104 – ident: e_1_2_5_37_1 doi: 10.1016/j.jneumeth.2017.11.012 – ident: e_1_2_5_40_1 – ident: e_1_2_5_15_1 doi: 10.1007/s00221-012-3302-6 – ident: e_1_2_5_45_1 doi: 10.1038/19303 – ident: e_1_2_5_61_1 doi: 10.3389/fnint.2014.00004 – ident: e_1_2_5_47_1 doi: 10.1113/jphysiol.2010.195222 – ident: e_1_2_5_36_1 doi: 10.1007/s00221-002-1038-4 – ident: e_1_2_5_12_1 doi: 10.1007/s10162-005-0003-x – volume: 2 start-page: 90 year: 2011 ident: e_1_2_5_6_1 article-title: What does galvanic vestibular stimulation actually activate? publication-title: Front Neurol – ident: e_1_2_5_31_1 doi: 10.1007/s00422-006-0133-1 – ident: e_1_2_5_49_1 doi: 10.1016/j.neuropsychologia.2015.03.004 – ident: e_1_2_5_14_1 doi: 10.1152/jn.1976.39.5.970 – ident: e_1_2_5_13_1 doi: 10.1007/BF00279665 – ident: e_1_2_5_51_1 doi: 10.1007/s00221-002-1067-z – ident: e_1_2_5_26_1 doi: 10.1007/s00221-009-2054-4 – ident: e_1_2_5_22_1 doi: 10.1152/jn.1984.51.6.1236 – ident: e_1_2_5_38_1 doi: 10.1152/jn.90677.2008 – ident: e_1_2_5_19_1 doi: 10.3389/fnint.2014.00094 – ident: e_1_2_5_30_1 doi: 10.1038/s41467-019-09738-1 – ident: e_1_2_5_11_1 doi: 10.1113/jphysiol.1997.sp022051 – ident: e_1_2_5_54_1 doi: 10.1111/j.1749-6632.2008.03732.x – ident: e_1_2_5_9_1 doi: 10.1016/j.cub.2018.09.049 – ident: e_1_2_5_50_1 doi: 10.1152/jn.00114.2015 – ident: e_1_2_5_20_1 doi: 10.1523/JNEUROSCI.1902-16.2016 – ident: e_1_2_5_34_1 doi: 10.1038/nn.3530 – ident: e_1_2_5_53_1 doi: 10.1152/jn.00558.2001 – ident: e_1_2_5_28_1 doi: 10.1152/jn.1995.73.2.896 – volume: 106 start-page: 111 year: 1995 ident: e_1_2_5_43_1 article-title: The vestibulo‐ocular reflex of the squirrel monkey during eccentric rotation and roll tilt publication-title: Exp Brain Res – ident: e_1_2_5_25_1 doi: 10.1152/jn.01234.2003 – ident: e_1_2_5_39_1 doi: 10.1007/s00221-006-0792-0 – ident: e_1_2_5_58_1 doi: 10.1113/jphysiol.2010.197053 – ident: e_1_2_5_4_1 doi: 10.1145/2967934.2968080 – ident: e_1_2_5_2_1 doi: 10.1038/nature02754 – ident: e_1_2_5_5_1 doi: 10.1113/jphysiol.2004.079525 – ident: e_1_2_5_23_1 doi: 10.1002/ana.410420616 – ident: e_1_2_5_10_1 doi: 10.1113/jphysiol.2005.092544 – ident: e_1_2_5_41_1 doi: 10.1101/087692 |
SSID | ssj0013099 |
Score | 2.4348397 |
Snippet | Key points
Considerable debate exists regarding whether electrical vestibular stimuli encoded by vestibular afferents induce a net signal of linear... Considerable debate exists regarding whether electrical vestibular stimuli encoded by vestibular afferents induce a net signal of linear acceleration, rotation... Electrical vestibular stimulation (EVS) is an increasingly popular biomedical tool for generating sensations of virtual motion in humans, for which the... |
SourceID | proquest pubmed crossref wiley |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 5231 |
SubjectTerms | electrical vestibular stimulation gravito‐inertial ambiguity internal model Motion detection Sensory neurons spatial orientation Vestibular system |
Title | Virtual signals of head rotation induce gravity‐dependent inferences of linear acceleration |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1113%2FJP278642 https://www.ncbi.nlm.nih.gov/pubmed/31483492 https://www.proquest.com/docview/2310804703 https://www.proquest.com/docview/2284558981 |
Volume | 597 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NTtwwELbQnrhAKdBuochICE5Z4rWT2EeEukJ7QCu0ICSEIjuxpVXbbJXuHuDEI_CMfZLO2EmqpVSquEWKf-J4ZvyNPf6GkCOA0C4pVRKxNI0j4RLMBqiLSJSZYdylyGiO0RaX6cW1GN8mt01UJd6FCfwQ3YYbaoa316jg2jRZSBiSDYwnw0wCegbzi6FaiIeuhn8OEGKlOqLwLGEN7yxUPW0rrq5Ef8HLVbTql5vRJrlrPzREmXwdLBdmUDy-4HB820jekY0GhdKzIDZbZM1W78n2WQUe-PcHekx9XKjfcN8m9zezGi-ZUAz1AGGlc0fBgpe0nodjfApuPQgIxUxGgOl_PT23mXUXdNbeJ_TV8FN1TXVRwGIXRG-HTEdfpucXUZOUISo4YJUIplRpl0iuWWwc-I_WGW0zpYRLucBTUpeVyMLmFCDioWFaZkOrDLiNglnBd0mvmlf2I6HCSsB3GU-1MqIURhYeT8XwLAvJ4j45aecnLxrCcsyb8S0PjgvP2x_XJ4ddyR-BpOOVMvvtFOeNmv7MEdzKWIDVgya616BgeGqiKztfQhlYwJNEwmj65EMQja4TznAvVkHjJ36C_9l7Ph1PGM9U-um_S-6RdQBnKtx73Ce9Rb20nwEALcyBF_UDvzP1G6DC_t0 |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NTtwwEB5RemgvlEKBLbQ1UlVOgXjtJLY4oVK0XShC1bbi0CqyE1tCQBZtdw_l1EfoM_ZJOhMnQfRHQtwixT9xPOP5xmN_A_AaIbRPSp1EPE3jSPqEsgGaIpJlZrnwKTGa02mL43TwSQ5Pk9M52G3vwgR-iG7DjTSjXq9JwWlDutFyYhsYnvQzhfD5ATykhN5EnL__sX8TQoi17qjCs4Q3zLNYd6etedsW_QUwb-PV2uAcPIEv7aeGcybn27Op3S6u_2BxvOdYFmGhAaJsL0jOU5hz1RIs71XohF9-Z29YfTS03nNfhq-fzyZ0z4TRaQ-UVzb2DBfxkk3GIZLP0LNHGWGUzAhh_a8fP9vkulN21l4prKvRt5oJM0WB9i5I3zMYHbwbvR1ETV6GqBAIVyKcVW18ooThsfXoQjpvjcu0lj4VkgKlPiuJiM1rBMV9y43K-k5b9Bwld1KswHw1rtwaMOkUQrxMpEZbWUqrihpSxfisCsXjHmy1E5QXDWc5pc64yIPvIvL2x_Vgsyt5FXg6_lFmo53jvNHUbznhWxVLXPiwie416hgFTkzlxjMsgzY8SRSOpgerQTa6TgSn7ViNjW_VM_zf3vPR8ISLTKfP71zyFTwajD4c5Ufvjw_X4TFiNR2uQW7A_HQycy8QD03ty1rufwOKfAH4 |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NTtwwEB61VEK9FFr6s5QWV0JwCo3XTmIfUemKbiu0qhaEVKHITmxpBc2i7e4BTn2EPmOfhJk4SUUpUsUtUvwTxzP2N_bMNwBbCKF9Uuok4mkaR9InlA3QFJEsM8uFT4nRnLwtDtODIzk8SU4ar0qKhQn8EN2BG2lGvV6Tgl-UvlFyIhsYjvqZQvT8EB7JNNaUtmH_a__PDUKsdccUniW8IZ7Fuu_bmje3olv48iZcrfebwQp8a780uJmc7S7mdre4-ovE8X5DWYUnDQxle0FunsIDVz2Dtb0KTfDvl2yb1Y6h9Yn7GpweT2YUZcLI1wOllU09wyW8ZLNpuMdnaNejhDBKZYSg_vfPX21q3TmbtAGFdTX6VDNjpihwtwuy9xzGg4_jDwdRk5UhKgSClQjnVBufKGF4bD0akM5b4zKtpU-FpGtSn5VEw-Y1QuK-5UZlfact2o2SOylewFI1rdwrYNIpBHiZSI22spRWFTWgivFZFYrHPdhp5ycvGsZySpxxngfLReTtj-vBu67kRWDp-EeZjXaK80ZPf-SEblUscdnDJrrXqGF0bWIqN11gGdzBk0ThaHrwMohG14ngdBirsfGdeoLv7D0fD0dcZDpd_--Sm7A82h_kXz4dfn4NjxGo6RADuQFL89nCvUEwNLdva6m_BoDHAKc |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Virtual+signals+of+head+rotation+induce+gravity%E2%80%90dependent+inferences+of+linear+acceleration&rft.jtitle=The+Journal+of+physiology&rft.au=Navid+Khosravi%E2%80%90Hashemi&rft.au=bes%2C+Patrick+A&rft.au=Dakin%2C+Christopher+J&rft.au=Jean%E2%80%90S%C3%A9bastien+Blouin&rft.date=2019-11-01&rft.pub=Wiley+Subscription+Services%2C+Inc&rft.issn=0022-3751&rft.eissn=1469-7793&rft.volume=597&rft.issue=21&rft.spage=5231&rft.epage=5246&rft_id=info:doi/10.1113%2FJP278642&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0022-3751&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0022-3751&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0022-3751&client=summon |