Modulation of 7 T fMRI Signal in the Cerebellar Cortex and Nuclei During Acquisition, Extinction, and Reacquisition of Conditioned Eyeblink Responses
Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction and savings of conditioned eyeblink responses (CRs). Saving effects, which are reflected in a reacquisition after extinction that is faster tha...
Saved in:
Published in | Human brain mapping Vol. 38; no. 8; pp. 3957 - 3974 |
---|---|
Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
John Wiley & Sons, Inc
01.08.2017
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
ISSN | 1065-9471 1097-0193 1097-0193 |
DOI | 10.1002/hbm.23641 |
Cover
Abstract | Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction and savings of conditioned eyeblink responses (CRs). Saving effects, which are reflected in a reacquisition after extinction that is faster than the initial acquisition, suggest that learned associations are at least partly preserved during extinction. In this study, we tested the hypothesis that acquisition‐related plasticity is nihilated during extinction in the cerebellar cortex, but retained in the cerebellar nuclei, allowing for faster reacquisition. Changes of 7 T functional magnetic resonance imaging (fMRI) signals were investigated in the cerebellar cortex and nuclei of young and healthy human subjects. Main effects of acquisition, extinction, and reacquisition against rest were calculated in conditioned stimulus‐only trials. First‐level β values were determined for a spherical region of interest (ROI) around the acquisition peak voxel in lobule VI, and dentate and interposed nuclei ipsilateral to the unconditioned stimulus. In the cerebellar cortex and nuclei, fMRI signals were significantly lower in extinction compared to acquisition and reacquisition, but not significantly different between acquisition and reacquisition. These findings are consistent with the theory of bidirectional learning in both the cerebellar cortex and nuclei. It cannot explain, however, why conditioned responses reappear almost immediately in reacquisition following extinction. Although the present data do not exclude that part of the initial memory remains in the cerebellum in extinction, future studies should also explore changes in extracerebellar regions as a potential substrate of saving effects. Hum Brain Mapp 38:3957–3974, 2017. © 2017 Wiley Periodicals, Inc. |
---|---|
AbstractList | Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction and savings of conditioned eyeblink responses (CRs). Saving effects, which are reflected in a reacquisition after extinction that is faster than the initial acquisition, suggest that learned associations are at least partly preserved during extinction. In this study, we tested the hypothesis that acquisition‐related plasticity is nihilated during extinction in the cerebellar cortex, but retained in the cerebellar nuclei, allowing for faster reacquisition. Changes of 7 T functional magnetic resonance imaging (fMRI) signals were investigated in the cerebellar cortex and nuclei of young and healthy human subjects. Main effects of acquisition, extinction, and reacquisition against rest were calculated in conditioned stimulus‐only trials. First‐level β values were determined for a spherical region of interest (ROI) around the acquisition peak voxel in lobule VI, and dentate and interposed nuclei ipsilateral to the unconditioned stimulus. In the cerebellar cortex and nuclei, fMRI signals were significantly lower in extinction compared to acquisition and reacquisition, but not significantly different between acquisition and reacquisition. These findings are consistent with the theory of bidirectional learning in both the cerebellar cortex and nuclei. It cannot explain, however, why conditioned responses reappear almost immediately in reacquisition following extinction. Although the present data do not exclude that part of the initial memory remains in the cerebellum in extinction, future studies should also explore changes in extracerebellar regions as a potential substrate of saving effects.
Hum Brain Mapp 38:3957–3974, 2017
. ©
2017 Wiley Periodicals, Inc. Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction and savings of conditioned eyeblink responses (CRs). Saving effects, which are reflected in a reacquisition after extinction that is faster than the initial acquisition, suggest that learned associations are at least partly preserved during extinction. In this study, we tested the hypothesis that acquisition‐related plasticity is nihilated during extinction in the cerebellar cortex, but retained in the cerebellar nuclei, allowing for faster reacquisition. Changes of 7 T functional magnetic resonance imaging (fMRI) signals were investigated in the cerebellar cortex and nuclei of young and healthy human subjects. Main effects of acquisition, extinction, and reacquisition against rest were calculated in conditioned stimulus‐only trials. First‐level β values were determined for a spherical region of interest (ROI) around the acquisition peak voxel in lobule VI, and dentate and interposed nuclei ipsilateral to the unconditioned stimulus. In the cerebellar cortex and nuclei, fMRI signals were significantly lower in extinction compared to acquisition and reacquisition, but not significantly different between acquisition and reacquisition. These findings are consistent with the theory of bidirectional learning in both the cerebellar cortex and nuclei. It cannot explain, however, why conditioned responses reappear almost immediately in reacquisition following extinction. Although the present data do not exclude that part of the initial memory remains in the cerebellum in extinction, future studies should also explore changes in extracerebellar regions as a potential substrate of saving effects. Hum Brain Mapp 38:3957–3974, 2017. © 2017 Wiley Periodicals, Inc. Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction and savings of conditioned eyeblink responses (CRs). Saving effects, which are reflected in a reacquisition after extinction that is faster than the initial acquisition, suggest that learned associations are at least partly preserved during extinction. In this study, we tested the hypothesis that acquisition-related plasticity is nihilated during extinction in the cerebellar cortex, but retained in the cerebellar nuclei, allowing for faster reacquisition. Changes of 7 T functional magnetic resonance imaging (fMRI) signals were investigated in the cerebellar cortex and nuclei of young and healthy human subjects. Main effects of acquisition, extinction, and reacquisition against rest were calculated in conditioned stimulus-only trials. First-level β values were determined for a spherical region of interest (ROI) around the acquisition peak voxel in lobule VI, and dentate and interposed nuclei ipsilateral to the unconditioned stimulus. In the cerebellar cortex and nuclei, fMRI signals were significantly lower in extinction compared to acquisition and reacquisition, but not significantly different between acquisition and reacquisition. These findings are consistent with the theory of bidirectional learning in both the cerebellar cortex and nuclei. It cannot explain, however, why conditioned responses reappear almost immediately in reacquisition following extinction. Although the present data do not exclude that part of the initial memory remains in the cerebellum in extinction, future studies should also explore changes in extracerebellar regions as a potential substrate of saving effects. Hum Brain Mapp 38:3957-3974, 2017. © 2017 Wiley Periodicals, Inc.Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction and savings of conditioned eyeblink responses (CRs). Saving effects, which are reflected in a reacquisition after extinction that is faster than the initial acquisition, suggest that learned associations are at least partly preserved during extinction. In this study, we tested the hypothesis that acquisition-related plasticity is nihilated during extinction in the cerebellar cortex, but retained in the cerebellar nuclei, allowing for faster reacquisition. Changes of 7 T functional magnetic resonance imaging (fMRI) signals were investigated in the cerebellar cortex and nuclei of young and healthy human subjects. Main effects of acquisition, extinction, and reacquisition against rest were calculated in conditioned stimulus-only trials. First-level β values were determined for a spherical region of interest (ROI) around the acquisition peak voxel in lobule VI, and dentate and interposed nuclei ipsilateral to the unconditioned stimulus. In the cerebellar cortex and nuclei, fMRI signals were significantly lower in extinction compared to acquisition and reacquisition, but not significantly different between acquisition and reacquisition. These findings are consistent with the theory of bidirectional learning in both the cerebellar cortex and nuclei. It cannot explain, however, why conditioned responses reappear almost immediately in reacquisition following extinction. Although the present data do not exclude that part of the initial memory remains in the cerebellum in extinction, future studies should also explore changes in extracerebellar regions as a potential substrate of saving effects. Hum Brain Mapp 38:3957-3974, 2017. © 2017 Wiley Periodicals, Inc. |
Author | Thürling, Markus Schlamann, Marc De Zeeuw, Chris I. Ladd, Mark E. Koekkoek, Sebastiaan K. E. Kahl, Fabian Boele, Henk‐Jan Timmann, Dagmar Müller, Sarah Diedrichsen, Jörn Ernst, Thomas M. Maderwald, Stefan |
AuthorAffiliation | 6 Department for Computer Science University of Western Ontario London Ontario Canada 5 Department of Neuroscience Erasmus MC Rotterdam The Netherlands 1 Department of Neurology Essen University Hospital Essen Germany 4 Department of Neuroradiology University Hospital of Giessen, Justus‐Liebig‐University of Giessen Giessen Germany 3 Department for Diagnostic and Interventional Radiology and Neuroradiology Essen University Hospital, University of Duisburg‐Essen Essen Germany 8 Division of Medical Physics in Radiology German Cancer Research Center Heidelberg Germany 2 Erwin L. Hahn Institute for MRI, University of Duisburg‐Essen Essen Germany 7 The Netherlands Institute for Neuroscience, Royal Academy of Arts & Sciences Amsterdam The Netherlands |
AuthorAffiliation_xml | – name: 6 Department for Computer Science University of Western Ontario London Ontario Canada – name: 1 Department of Neurology Essen University Hospital Essen Germany – name: 8 Division of Medical Physics in Radiology German Cancer Research Center Heidelberg Germany – name: 5 Department of Neuroscience Erasmus MC Rotterdam The Netherlands – name: 4 Department of Neuroradiology University Hospital of Giessen, Justus‐Liebig‐University of Giessen Giessen Germany – name: 2 Erwin L. Hahn Institute for MRI, University of Duisburg‐Essen Essen Germany – name: 3 Department for Diagnostic and Interventional Radiology and Neuroradiology Essen University Hospital, University of Duisburg‐Essen Essen Germany – name: 7 The Netherlands Institute for Neuroscience, Royal Academy of Arts & Sciences Amsterdam The Netherlands |
Author_xml | – sequence: 1 givenname: Thomas M. orcidid: 0000-0002-2170-9241 surname: Ernst fullname: Ernst, Thomas M. email: thomas.m.ernst@uni-duisburg-essen.de organization: Erwin L. Hahn Institute for MRI, University of Duisburg‐Essen – sequence: 2 givenname: Markus surname: Thürling fullname: Thürling, Markus organization: Erwin L. Hahn Institute for MRI, University of Duisburg‐Essen – sequence: 3 givenname: Sarah surname: Müller fullname: Müller, Sarah organization: Essen University Hospital – sequence: 4 givenname: Fabian surname: Kahl fullname: Kahl, Fabian organization: Essen University Hospital – sequence: 5 givenname: Stefan surname: Maderwald fullname: Maderwald, Stefan organization: Erwin L. Hahn Institute for MRI, University of Duisburg‐Essen – sequence: 6 givenname: Marc surname: Schlamann fullname: Schlamann, Marc organization: University Hospital of Giessen, Justus‐Liebig‐University of Giessen – sequence: 7 givenname: Henk‐Jan surname: Boele fullname: Boele, Henk‐Jan organization: Erasmus MC – sequence: 8 givenname: Sebastiaan K. E. surname: Koekkoek fullname: Koekkoek, Sebastiaan K. E. organization: Erasmus MC – sequence: 9 givenname: Jörn surname: Diedrichsen fullname: Diedrichsen, Jörn organization: University of Western Ontario – sequence: 10 givenname: Chris I. surname: De Zeeuw fullname: De Zeeuw, Chris I. organization: The Netherlands Institute for Neuroscience, Royal Academy of Arts & Sciences – sequence: 11 givenname: Mark E. surname: Ladd fullname: Ladd, Mark E. organization: German Cancer Research Center – sequence: 12 givenname: Dagmar surname: Timmann fullname: Timmann, Dagmar organization: Essen University Hospital |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28474470$$D View this record in MEDLINE/PubMed |
BookMark | eNp1ks1uEzEQxy1URD_gwAsgS1xAYlt7vbuOL5XKNtBKDUilnC3vepK4OHZq79LmRTjzLDwZ3iTlo4KTx57f_D2a_-yjHecdIPSckkNKSH40bxaHOasK-gjtUSJ4RqhgO0NclZkoON1F-zFeE0JpSegTtJuPCl4UnOyhbxOve6s64x32U8x_fL_C08nlOf5kZk5ZbBzu5oBrCNCAtSrg2ocO7rByGn_oWwsGn_bBuBk-aW96E80g9QaP7zrj2k08oJegfqeHn2rv9PoCGo9X0FjjviQqLr2LEJ-ix1NlIzzbngfo87vxVX2WXXx8f16fXGQtK0c0KyutpjnRwBsmRNlQzlrFBRDGipJASytdihI0VYJoxgnLKShdQHptCgKCHaDjje6ybxagW3BdUFYug1mosJJeGfl3xpm5nPmvshpVFa94Eni1FQj-pofYyYWJ7TApB76Pko5ERVhV0gF9-QC99n1IQ06UoCUvklN5ol782dGvVu4tS8DRBmiDjzHAVLamWxuYGjRWUiKHpZBpKeR6KVLF6wcV96L_Yrfqt8bC6v-gPHs72VT8BIk9yBg |
CitedBy_id | crossref_primary_10_1016_j_euroneuro_2018_11_464 crossref_primary_10_1523_JNEUROSCI_2133_17_2017 crossref_primary_10_3389_fnbeh_2019_00256 crossref_primary_10_1016_j_nlm_2019_107137 crossref_primary_10_1093_schizbullopen_sgab040 crossref_primary_10_7554_eLife_46831 crossref_primary_10_1515_nf_2020_0015 crossref_primary_10_1016_j_bbr_2019_111947 crossref_primary_10_1016_j_neuropharm_2023_109444 crossref_primary_10_1016_j_pscychresns_2020_111133 crossref_primary_10_3389_fnsys_2023_1160083 crossref_primary_10_1002_hbm_25317 crossref_primary_10_1111_acer_14288 crossref_primary_10_1007_s12311_018_0945_2 crossref_primary_10_1007_s12311_018_0973_y crossref_primary_10_1016_j_neuroimage_2022_119080 crossref_primary_10_3389_fnsys_2023_1166166 crossref_primary_10_1016_j_bbr_2018_11_030 |
Cites_doi | 10.1101/lm.80004 10.1126/science.280.5360.77 10.1111/j.1460-9568.1992.tb00123.x 10.1016/j.neuroimage.2010.11.028 10.1016/0028-3932(71)90067-4 10.1007/s00221-004-2181-x 10.1101/lm.2023011 10.1016/j.nlm.2015.07.009 10.1016/j.acra.2011.10.004 10.1007/BF00232192 10.1523/JNEUROSCI.2061-08.2008 10.1016/j.neuroimage.2006.05.056 10.1038/nrn728 10.1016/0959-4388(93)90133-J 10.3109/00016482709120085 10.1523/JNEUROSCI.0784-06.2006 10.1093/brain/awt107 10.1002/ar.22515 10.1038/76606 10.1006/nimg.1999.0459 10.1126/science.6701513 10.1101/cshperspect.a021683 10.1037/0097-7403.18.2.182 10.1016/j.neuron.2016.01.008 10.1037/0735-7044.114.6.1058 10.1016/j.neuropsychologia.2016.03.027 10.1007/s12311-012-0377-3 10.1016/j.bbr.2010.04.007 10.1073/pnas.92.16.7500 10.1016/j.neuron.2011.02.044 10.1016/j.celrep.2015.10.057 10.1016/j.celrep.2015.10.047 10.1523/JNEUROSCI.23-37-11753.2003 10.1016/j.neuroimage.2009.01.045 10.1523/JNEUROSCI.4202-06.2007 10.1097/WNR.0b013e3282e326e8 10.1002/mrm.23108 10.1073/pnas.91.17.8122 10.1152/jn.00381.2011 10.1523/JNEUROSCI.0511-13.2013 10.1146/annurev.neuro.31.060407.125606 10.1037/0097-7403.9.3.248 10.1152/jn.1997.77.4.2153 10.1016/j.ypmed.2014.06.010 10.1006/nlme.1996.0003 10.1016/j.neuroimage.2012.01.040 10.1016/j.neuroimage.2010.10.035 10.1016/j.neuroimage.2014.01.060 10.1111/j.1601-183X.2008.00417.x 10.1523/JNEUROSCI.0266-05.2005 10.1007/s12311-015-0711-7 10.1038/nrn3312 10.1016/S0006-8993(01)02111-4 10.1113/jphysiol.1996.sp021581 10.1016/S0074-7742(08)60359-1 10.1002/hbm.10056 10.1146/annurev.psych.121208.131631 10.1006/nimg.2002.1199 10.1016/B978-0-444-63356-9.00004-2 10.1038/416330a 10.1523/JNEUROSCI.04-11-02811.1984 10.1523/JNEUROSCI.21-15-05715.2001 10.1101/lm.59603 10.1016/j.neubiorev.2015.09.019 10.1152/jn.2000.84.6.3026 10.1523/JNEUROSCI.21-11-04081.2001 10.1523/JNEUROSCI.16-12-04032.1996 10.1007/BF00241372 10.1016/j.nlm.2013.08.012 10.1523/JNEUROSCI.2492-14.2015 10.3389/neuro.03.019.2009 10.1016/B978-0-12-420247-4.00002-6 10.1016/j.neubiorev.2011.12.014 |
ContentType | Journal Article |
Copyright | 2017 Wiley Periodicals, Inc. |
Copyright_xml | – notice: 2017 Wiley Periodicals, Inc. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7QR 7TK 7U7 8FD C1K FR3 K9. P64 7X8 5PM |
DOI | 10.1002/hbm.23641 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Chemoreception Abstracts Neurosciences Abstracts Toxicology Abstracts Technology Research Database Environmental Sciences and Pollution Management Engineering Research Database ProQuest Health & Medical Complete (Alumni) Biotechnology and BioEngineering Abstracts MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Technology Research Database Toxicology Abstracts ProQuest Health & Medical Complete (Alumni) Chemoreception Abstracts Engineering Research Database Neurosciences Abstracts Biotechnology and BioEngineering Abstracts Environmental Sciences and Pollution Management MEDLINE - Academic |
DatabaseTitleList | CrossRef Technology Research Database MEDLINE MEDLINE - Academic |
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 – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine Anatomy & Physiology |
DocumentTitleAlternate | Cerebellar 7 T fMRI of Eyeblink Conditioning |
EISSN | 1097-0193 |
EndPage | 3974 |
ExternalDocumentID | PMC6866767 28474470 10_1002_hbm_23641 HBM23641 |
Genre | article Journal Article |
GrantInformation_xml | – fundername: German Research Foundation funderid: DFG TI 239/10‐1, 10‐2 – fundername: Dutch Organization for Medical Sciences, Life Sciences, and Social and Behavioral Sciences – fundername: ERC‐adv and ERC Poc – fundername: ; grantid: DFG TI 239/10‐1, 10‐2 |
GroupedDBID | --- .3N .GA .Y3 05W 0R~ 10A 1L6 1OB 1OC 1ZS 24P 31~ 33P 3SF 3WU 4.4 4ZD 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 53G 5GY 5VS 66C 702 7PT 7X7 8-0 8-1 8-3 8-4 8-5 8FI 8FJ 8UM 930 A03 AAESR AAEVG AAHHS AANHP AAONW AAYCA AAZKR ABCQN ABCUV ABEML ABIJN ABIVO ABJNI ABPVW ABUWG ACBWZ ACCFJ ACCMX ACGFS ACIWK ACPOU ACPRK ACRPL ACSCC ACXQS ACYXJ ADBBV ADEOM ADIZJ ADMGS ADNMO ADPDF ADXAS ADZOD AEEZP AEIMD AENEX AEQDE AEUQT AFBPY AFGKR AFKRA AFPWT AFRAH AFZJQ AHMBA AIURR AIWBW AJBDE AJXKR ALAGY ALIPV ALMA_UNASSIGNED_HOLDINGS ALUQN AMBMR ASPBG ATUGU AUFTA AVWKF AZBYB AZFZN AZVAB BAFTC BDRZF BENPR BFHJK BHBCM BMNLL BMXJE BNHUX BROTX BRXPI BY8 C45 CCPQU CS3 D-E D-F DCZOG DPXWK DR1 DR2 DU5 EBD EBS EJD EMOBN F00 F01 F04 F5P FEDTE FYUFA G-S G.N GAKWD GNP GODZA GROUPED_DOAJ H.T H.X HBH HF~ HHY HHZ HMCUK HVGLF HZ~ IAO IHR ITC IX1 J0M JPC KQQ L7B LAW LC2 LC3 LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES M6M MK4 MRFUL MRSTM MSFUL MSSTM MXFUL MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG OK1 OVD OVEED P2P P2W P2X P4D PALCI PIMPY PQQKQ Q.N Q11 QB0 QRW R.K RIWAO RJQFR ROL RPM RWD RWI RX1 RYL SAMSI SUPJJ SV3 TEORI UB1 UKHRP V2E W8V W99 WBKPD WIB WIH WIK WIN WJL WNSPC WOHZO WQJ WRC WUP WXSBR WYISQ XG1 XSW XV2 ZZTAW ~IA ~WT AAFWJ AAMMB AAYXX AEFGJ AFPKN AGQPQ AGXDD AIDQK AIDYY AIQQE CITATION PHGZM PHGZT PUEGO CGR CUY CVF ECM EIF NPM 7QR 7TK 7U7 8FD C1K FR3 K9. P64 7X8 5PM |
ID | FETCH-LOGICAL-c3581-56daf20de7b3995b173ca79e033450ec16d595ed1a90d370321ead4ed59b40e93 |
IEDL.DBID | DR2 |
ISSN | 1065-9471 1097-0193 |
IngestDate | Tue Sep 30 16:44:27 EDT 2025 Sat Sep 27 19:27:57 EDT 2025 Sat Jul 26 02:21:13 EDT 2025 Mon Jul 21 06:05:18 EDT 2025 Thu Apr 24 23:06:55 EDT 2025 Wed Oct 01 01:55:34 EDT 2025 Wed Jan 22 16:57:28 EST 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 8 |
Keywords | delay conditioning deep cerebellar nuclei cerebellar imaging associative learning human |
Language | English |
License | http://onlinelibrary.wiley.com/termsAndConditions#vor 2017 Wiley Periodicals, Inc. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c3581-56daf20de7b3995b173ca79e033450ec16d595ed1a90d370321ead4ed59b40e93 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0002-2170-9241 |
OpenAccessLink | https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/hbm.23641 |
PMID | 28474470 |
PQID | 1915749472 |
PQPubID | 996345 |
PageCount | 18 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_6866767 proquest_miscellaneous_1896036517 proquest_journals_1915749472 pubmed_primary_28474470 crossref_citationtrail_10_1002_hbm_23641 crossref_primary_10_1002_hbm_23641 wiley_primary_10_1002_hbm_23641_HBM23641 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | August 2017 |
PublicationDateYYYYMMDD | 2017-08-01 |
PublicationDate_xml | – month: 08 year: 2017 text: August 2017 |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States – name: San Antonio – name: Hoboken |
PublicationTitle | Human brain mapping |
PublicationTitleAlternate | Hum Brain Mapp |
PublicationYear | 2017 |
Publisher | John Wiley & Sons, Inc John Wiley and Sons Inc |
Publisher_xml | – name: John Wiley & Sons, Inc – name: John Wiley and Sons Inc |
References | 2015; 35 2002; 17 1998; 280 2009; 46 2006; 33 2000; 3 1997; 41 1975 1992; 18 2008; 7 2014; 68 1983; 9 2011; 54 2012; 19 1972 2012; 13 2014; 210 2011; 18 2012; 11 1993; 3 2003; 10 2005; 25 1971; 9 2012; 295 2011; 70 2008; 28 2006; 26 2016; 85 1999; 10 1996; 495 2010; 3 2012; 67 1996; 65 2016; 89 1992; 4 2012; 63 2007; 27 2012; 62 2001; 897 2015; 13 2007; 18 2015; 59 2002a; 416 2014; 117 2014; 92 1995; 92 2015; 126 2000; 114 2002b; 3 1984a; 223 2012; 36 2015; 9 1996; 16 2016; 15 2015; 7 2012; 107 2001; 21 1990; 83 2004; 11 2014; 108 2005; 162 2009; 32 1984b; 4 2013; 33 1997; 77 2010; 212 2000; 84 2013; 136 1996; 110 1994; 91 1927 2003; 23 e_1_2_6_51_1 e_1_2_6_74_1 e_1_2_6_53_1 e_1_2_6_76_1 Rescorla RA (e_1_2_6_60_1) 1972 e_1_2_6_32_1 e_1_2_6_70_1 e_1_2_6_30_1 e_1_2_6_72_1 Gormezano I (e_1_2_6_25_1) 1975 e_1_2_6_19_1 e_1_2_6_13_1 e_1_2_6_36_1 e_1_2_6_59_1 e_1_2_6_11_1 e_1_2_6_34_1 e_1_2_6_17_1 e_1_2_6_55_1 e_1_2_6_15_1 e_1_2_6_38_1 e_1_2_6_57_1 D'Angelo E (e_1_2_6_12_1) 2015; 9 e_1_2_6_62_1 e_1_2_6_64_1 e_1_2_6_43_1 e_1_2_6_20_1 e_1_2_6_41_1 e_1_2_6_9_1 e_1_2_6_5_1 e_1_2_6_7_1 e_1_2_6_24_1 e_1_2_6_49_1 e_1_2_6_3_1 e_1_2_6_22_1 e_1_2_6_66_1 e_1_2_6_28_1 e_1_2_6_45_1 e_1_2_6_26_1 e_1_2_6_47_1 e_1_2_6_68_1 e_1_2_6_52_1 e_1_2_6_73_1 e_1_2_6_54_1 e_1_2_6_75_1 e_1_2_6_10_1 e_1_2_6_31_1 e_1_2_6_50_1 e_1_2_6_71_1 e_1_2_6_14_1 e_1_2_6_35_1 e_1_2_6_33_1 e_1_2_6_18_1 e_1_2_6_39_1 e_1_2_6_56_1 e_1_2_6_77_1 e_1_2_6_16_1 e_1_2_6_37_1 e_1_2_6_58_1 e_1_2_6_63_1 e_1_2_6_42_1 e_1_2_6_65_1 e_1_2_6_21_1 e_1_2_6_40_1 e_1_2_6_61_1 e_1_2_6_8_1 e_1_2_6_4_1 e_1_2_6_6_1 e_1_2_6_48_1 e_1_2_6_23_1 e_1_2_6_2_1 e_1_2_6_29_1 e_1_2_6_44_1 e_1_2_6_67_1 e_1_2_6_27_1 e_1_2_6_46_1 e_1_2_6_69_1 |
References_xml | – volume: 36 start-page: 1773 year: 2012 end-page: 1802 article-title: Neural and cellular mechanisms of fear and extinction memory formation publication-title: Neurosci Biobehav Rev – volume: 416 start-page: 330 year: 2002a end-page: 333 article-title: Inhibition of climbing fibres is a signal for the extinction of conditioned eyelid responses publication-title: Nature – volume: 21 start-page: 4081 year: 2001 end-page: 4089 article-title: A mechanism for savings in the cerebellum publication-title: J Neurosci – volume: 77 start-page: 2153 year: 1997 end-page: 2163 article-title: Lateralization and behavioral correlation of changes in regional cerebral blood flow with classical conditioning of the human eyeblink response publication-title: J Neurophysiol – volume: 92 start-page: 381 year: 2014 end-page: 397 article-title: Permutation inference for the general linear model publication-title: Neuroimage – volume: 18 start-page: 1479 year: 2007 end-page: 1482 article-title: Extinction of conditioned blink responses by cerebello‐olivary pathway stimulation publication-title: Neuroreport – volume: 212 start-page: 143 year: 2010 end-page: 151 article-title: Evaluation of multiple‐session delay eyeblink conditioning comparing patients with focal cerebellar lesions and cerebellar degeneration publication-title: Behav Brain Res – volume: 33 start-page: 17897 year: 2013 end-page: 17907 article-title: Axonal sprouting and formation of terminals in the adult cerebellum during associative motor learning publication-title: J Neurosci – volume: 10 start-page: 233 year: 1999 end-page: 260 article-title: Three‐dimensional MRI atlas of the human cerebellum in proportional stereotaxic space publication-title: Neuroimage – volume: 117 start-page: 21 year: 2014 end-page: 37 article-title: Cerebellar mechanisms of learning and plasticity revealed by delay eyelid conditioning publication-title: Int Rev Neurobiol – volume: 21 start-page: 5715 year: 2001 end-page: 5722 article-title: Acquisition of eyeblink conditioning is critically dependent on normal function in cerebellar cortical lobule HVI publication-title: J Neurosci – volume: 3 start-page: 122 year: 2002b end-page: 131 article-title: Parallels between cerebellum‐ and amygdala‐dependent conditioning publication-title: Nat Rev Neurosci – volume: 54 start-page: 1786 year: 2011 end-page: 1794 article-title: Imaging the deep cerebellar nuclei: A probabilistic atlas and normalization procedure publication-title: Neuroimage – year: 1927 – volume: 83 start-page: 44 year: 1990 end-page: 54 article-title: Activity of deep cerebellar nuclear cells during classical conditioning of nictitating membrane extension in rabbits publication-title: Exp Brain Res – volume: 91 start-page: 8122 year: 1994 end-page: 8126 article-title: A functional anatomical study of associative learning in humans publication-title: Proc Natl Acad Sci U S A – volume: 35 start-page: 1228 year: 2015 end-page: 1239 article-title: Cerebellar cortex and cerebellar nuclei are concomitantly activated during eyeblink conditioning: A 7T fMRI study in humans publication-title: J Neurosci – volume: 85 start-page: 287 year: 2016 end-page: 300 article-title: Pronounced reduction of acquisition of conditioned eyeblink responses in young adults with focal cerebellar lesions impedes conclusions on the role of the cerebellum in extinction and savings publication-title: Neuropsychologia – volume: 23 start-page: 11753 year: 2003 end-page: 11758 article-title: fMRI of the conscious rabbit during unilateral classical eyeblink conditioning reveals bilateral cerebellar activation publication-title: J Neurosci – volume: 4 start-page: 2811 year: 1984b end-page: 2822 article-title: Neuronal responses of the rabbit cerebellum during acquisition and performance of a classically conditioned nictitating membrane‐eyelid response publication-title: J Neurosci – volume: 7 start-page: 770 year: 2008 end-page: 777 article-title: Savings and extinction of conditioned eyeblink responses in fragile X syndrome publication-title: Genes Brain Behav – volume: 108 start-page: 52 year: 2014 end-page: 64 article-title: Behavioral and neurobiological mechanisms of extinction in Pavlovian and instrumental learning publication-title: Neurobiol Learn Mem – volume: 7 start-page: a021683 year: 2015 article-title: Motor learning and the cerebellum publication-title: Cold Spring Harb Perspect Biol – volume: 84 start-page: 3026 year: 2000 end-page: 3035 article-title: Learning‐ and expectation‐related changes in the human brain during motor learning publication-title: J Neurophysiol – volume: 54 start-page: 2612 year: 2011 end-page: 2622 article-title: Evidence for a motor and a non‐motor domain in the human dentate nucleus ‐ an fMRI study publication-title: Neuroimage – volume: 9 start-page: 1 year: 2015 end-page: 3 article-title: Editorial: The olivo‐cerebellar system publication-title: Front Neural Circuits – volume: 897 start-page: 150 year: 2001 end-page: 156 article-title: Two‐stage theory of conditioning: Involvement of the cerebellum and the amygdala publication-title: Brain Res – volume: 13 start-page: 619 year: 2012 end-page: 635 article-title: Distributed synergistic plasticity and cerebellar learning publication-title: Nat Rev Neurosci – volume: 495 start-page: 159 year: 1996 end-page: 168 article-title: Reversible inactivations of the cerebellum prevent the extinction of conditioned nictitating membrane responses in rabbits publication-title: J Physiol – volume: 33 start-page: 127 year: 2006 end-page: 138 article-title: A spatially unbiased atlas template of the human cerebellum publication-title: Neuroimage – start-page: 64 year: 1972 end-page: 99 – volume: 27 start-page: 2493 year: 2007 end-page: 2502 article-title: Acquisition, extinction, and reacquisition of a cerebellar cortical memory trace publication-title: J Neurosci – volume: 63 start-page: 129 year: 2012 end-page: 151 article-title: Fear extinction as a model for translational neuroscience: Ten years of progress publication-title: Annu Rev Psychol – volume: 28 start-page: 10549 year: 2008 end-page: 10560 article-title: Mechanisms of potentiation of mossy fiber EPSCs in the cerebellar nuclei by coincident synaptic excitation and inhibition publication-title: J Neurosci – volume: 126 start-page: 78 year: 2015 end-page: 86 article-title: Neurosubstrates and mechanisms underlying the extinction of associative motor memory publication-title: Neurobiol Learn Mem – volume: 19 start-page: 172 year: 2012 end-page: 178 article-title: Caudal image contrast inversion in MPRAGE at 7 Tesla: Problem and solution publication-title: Acad Radiol – volume: 223 start-page: 296 year: 1984a end-page: 299 article-title: Cerebellum: Essential involvement in the classically conditioned eyelid response publication-title: Science – volume: 65 start-page: 17 year: 1996 end-page: 34 article-title: Changes in rabbit cerebellar cortical and interpositus nucleus activity during acquisition, extinction, and backward classical eyelid conditioning publication-title: Neurobiol Learn Mem – volume: 15 start-page: 139 year: 2016 end-page: 151 article-title: Distributed circuit plasticity: New clues for the cerebellar mechanisms of learning publication-title: Cerebellum – volume: 110 start-page: 36 year: 1996 end-page: 46 article-title: Inhibition of the inferior olive during conditioned responses in the decerebrate ferret publication-title: Exp Brain Res – volume: 136 start-page: 2063 year: 2013 end-page: 2076 article-title: Storage of a naturally acquired conditioned response is impaired in patients with cerebellar degeneration publication-title: Brain – volume: 62 start-page: 1040 year: 2012 end-page: 1050 article-title: Neuronal inhibition and excitation, and the dichotomic control of brain hemodynamic and oxygen responses publication-title: Neuroimage – volume: 41 start-page: 341 year: 1997 end-page: 366 article-title: Classical conditioning publication-title: Int Rev Neurobiol – volume: 9 start-page: 248 year: 1983 end-page: 265 article-title: Contextual control of the extinction of conditioned fear: Tests for the associative value of the context publication-title: J Exp Psychol Anim Behav Process – volume: 11 start-page: 946 year: 2012 end-page: 956 article-title: Eyeblink conditioning in healthy adults: A positron emission tomography study publication-title: Cerebellum – volume: 68 start-page: 29 year: 2014 end-page: 36 article-title: Why behavior change is difficult to sustain publication-title: Prev Med – volume: 17 start-page: 977 year: 2002 end-page: 987 article-title: Electromyography as a recording system for eyeblink conditioning with functional magnetic resonance imaging publication-title: Neuroimage – volume: 3 start-page: 401 year: 1993 end-page: 406 article-title: Cellular mechanisms of long‐term depression in the cerebellum publication-title: Curr Opin Neurobiol – volume: 162 start-page: 332 year: 2005 end-page: 345 article-title: Eyeblink conditioning in patients with hereditary ataxia: A one‐year follow‐up study publication-title: Exp Brain Res – volume: 59 start-page: 83 year: 2015 end-page: 91 article-title: The anatomy of fear learning in the cerebellum: A systematic meta‐analysis publication-title: Neurosci Biobehav Rev – volume: 92 start-page: 7500 year: 1995 end-page: 7504 article-title: Functional anatomy of human eyeblink conditioning determined with regional cerebral glucose metabolism and positron‐emission tomography publication-title: Proc Natl Acad Sci U S A – volume: 210 start-page: 79 year: 2014 end-page: 101 article-title: Distribution of neural plasticity in cerebellum‐dependent motor learning publication-title: Prog Brain Res – volume: 32 start-page: 413 year: 2009 end-page: 434 article-title: Cerebellum and nonmotor function publication-title: Annu Rev Neurosci – volume: 26 start-page: 6935 year: 2006 end-page: 6944 article-title: Long‐term depression at the mossy fiber‐deep cerebellar nucleus synapse publication-title: J Neurosci – volume: 16 start-page: 4032 year: 1996 end-page: 4040 article-title: Functional mapping of human learning: A positron emission tomography activation study of eyeblink conditioning publication-title: J Neurosci – volume: 11 start-page: 517 year: 2004 end-page: 524 article-title: Brain mechanisms of extinction of the classically conditioned eyeblink response publication-title: Learn Mem – volume: 295 start-page: 1311 year: 2012 end-page: 1320 article-title: A direct hippocampo‐cerebellar projection in chicken publication-title: Anat Rec (Hoboken) – volume: 13 start-page: 1977 year: 2015 end-page: 1988 article-title: Evolving models of Pavlovian conditioning: Cerebellar cortical dynamics in awake behaving mice publication-title: Cell Rep – volume: 17 start-page: 100 year: 2002 end-page: 115 article-title: Eyeblink‐related areas in human cerebellum as shown by fMRI publication-title: Hum Brain Mapp – volume: 10 start-page: 427 year: 2003 end-page: 455 article-title: Neural substrates of eyeblink conditioning: Acquisition and retention publication-title: Learn Mem – volume: 13 start-page: 1741 year: 2015 end-page: 1746 article-title: Activation of a temporal memory in Purkinje cells by the mGluR7 receptor publication-title: Cell Rep – volume: 18 start-page: 182 year: 1992 end-page: 192 article-title: Rapid reaquisition in conditioning of the rabbit's nictitating membrane response publication-title: J Exp Psychol Anim Behav Process – volume: 280 start-page: 77 year: 1998 end-page: 81 article-title: Classical conditioning and brain systems: The role of awareness publication-title: Science – volume: 70 start-page: 43 year: 2011 end-page: 50 article-title: Reevaluating the role of LTD in cerebellar motor learning publication-title: Neuron – start-page: 143 year: 1975 end-page: 179 – volume: 67 start-page: 1285 year: 2012 end-page: 1293 article-title: Quantitative assessment of the effects of high‐permittivity pads in 7 Tesla MRI of the brain publication-title: Magn Reson Med – volume: 4 start-page: 966 year: 1992 end-page: 980 article-title: The effect of kainic acid lesions of the cerebellar cortex on the conditioned nictitating membrane response in the rabbit publication-title: Eur J Neurosci – volume: 3 start-page: 74 year: 2010 end-page: 86 article-title: Cerebellar and extracerebellar involvement in mouse eyeblink conditioning: The ACDC model publication-title: Front Cell Neurosci – volume: 25 start-page: 3919 year: 2005 end-page: 3931 article-title: Timing of conditioned eyeblink responses is impaired in cerebellar patients publication-title: J Neurosci – volume: 46 start-page: 39 year: 2009 end-page: 46 article-title: A probabilistic MR atlas of the human cerebellum publication-title: Neuroimage – volume: 114 start-page: 1058 year: 2000 end-page: 1067 article-title: Cortical involvement in acquisition and extinction of trace eyeblink conditioning publication-title: Behav Neurosci – volume: 3 start-page: 649 year: 2000 end-page: 651 article-title: The potential effectiveness of simulations versus phenomenological models publication-title: Nat Neurosci – volume: 18 start-page: 666 year: 2011 end-page: 677 article-title: Neural circuitry and plasticity mechanisms underlying delay eyeblink conditioning publication-title: Learn Mem – volume: 9 start-page: 97 year: 1971 end-page: 113 article-title: The assessment and analysis of handedness: The Edinburgh inventory publication-title: Neuropsychologia – volume: 89 start-page: 645 year: 2016 end-page: 657 article-title: Excitatory cerebellar nucleocortical circuit provides internal amplification during associative conditioning publication-title: Neuron – volume: 107 start-page: 226 year: 2012 end-page: 238 article-title: Multiple sites of extinction for a single learned response publication-title: J Neurophysiol – ident: e_1_2_6_61_1 doi: 10.1101/lm.80004 – ident: e_1_2_6_11_1 doi: 10.1126/science.280.5360.77 – ident: e_1_2_6_27_1 doi: 10.1111/j.1460-9568.1992.tb00123.x – ident: e_1_2_6_34_1 doi: 10.1016/j.neuroimage.2010.11.028 – start-page: 64 volume-title: Classical Conditioning II: Current Research and Theory year: 1972 ident: e_1_2_6_60_1 – ident: e_1_2_6_53_1 doi: 10.1016/0028-3932(71)90067-4 – volume: 9 start-page: 1 year: 2015 ident: e_1_2_6_12_1 article-title: Editorial: The olivo‐cerebellar system publication-title: Front Neural Circuits – ident: e_1_2_6_71_1 doi: 10.1007/s00221-004-2181-x – ident: e_1_2_6_20_1 doi: 10.1101/lm.2023011 – ident: e_1_2_6_29_1 doi: 10.1016/j.nlm.2015.07.009 – ident: e_1_2_6_76_1 doi: 10.1016/j.acra.2011.10.004 – ident: e_1_2_6_4_1 doi: 10.1007/BF00232192 – ident: e_1_2_6_57_1 doi: 10.1523/JNEUROSCI.2061-08.2008 – ident: e_1_2_6_15_1 doi: 10.1016/j.neuroimage.2006.05.056 – ident: e_1_2_6_47_1 doi: 10.1038/nrn728 – ident: e_1_2_6_37_1 doi: 10.1016/0959-4388(93)90133-J – ident: e_1_2_6_56_1 doi: 10.3109/00016482709120085 – ident: e_1_2_6_77_1 doi: 10.1523/JNEUROSCI.0784-06.2006 – ident: e_1_2_6_69_1 doi: 10.1093/brain/awt107 – ident: e_1_2_6_38_1 doi: 10.1002/ar.22515 – ident: e_1_2_6_41_1 doi: 10.1038/76606 – ident: e_1_2_6_62_1 doi: 10.1006/nimg.1999.0459 – ident: e_1_2_6_43_1 doi: 10.1126/science.6701513 – ident: e_1_2_6_14_1 doi: 10.1101/cshperspect.a021683 – ident: e_1_2_6_52_1 doi: 10.1037/0097-7403.18.2.182 – ident: e_1_2_6_21_1 doi: 10.1016/j.neuron.2016.01.008 – ident: e_1_2_6_73_1 doi: 10.1037/0735-7044.114.6.1058 – ident: e_1_2_6_19_1 doi: 10.1016/j.neuropsychologia.2016.03.027 – ident: e_1_2_6_55_1 doi: 10.1007/s12311-012-0377-3 – ident: e_1_2_6_23_1 doi: 10.1016/j.bbr.2010.04.007 – ident: e_1_2_6_39_1 doi: 10.1073/pnas.92.16.7500 – ident: e_1_2_6_63_1 doi: 10.1016/j.neuron.2011.02.044 – ident: e_1_2_6_68_1 doi: 10.1016/j.celrep.2015.10.057 – ident: e_1_2_6_31_1 doi: 10.1016/j.celrep.2015.10.047 – ident: e_1_2_6_49_1 doi: 10.1523/JNEUROSCI.23-37-11753.2003 – ident: e_1_2_6_16_1 doi: 10.1016/j.neuroimage.2009.01.045 – ident: e_1_2_6_30_1 doi: 10.1523/JNEUROSCI.4202-06.2007 – ident: e_1_2_6_3_1 doi: 10.1097/WNR.0b013e3282e326e8 – ident: e_1_2_6_67_1 doi: 10.1002/mrm.23108 – ident: e_1_2_6_51_1 doi: 10.1073/pnas.91.17.8122 – ident: e_1_2_6_32_1 doi: 10.1152/jn.00381.2011 – ident: e_1_2_6_7_1 doi: 10.1523/JNEUROSCI.0511-13.2013 – ident: e_1_2_6_66_1 doi: 10.1146/annurev.neuro.31.060407.125606 – ident: e_1_2_6_9_1 doi: 10.1037/0097-7403.9.3.248 – ident: e_1_2_6_64_1 doi: 10.1152/jn.1997.77.4.2153 – ident: e_1_2_6_8_1 doi: 10.1016/j.ypmed.2014.06.010 – ident: e_1_2_6_26_1 doi: 10.1006/nlme.1996.0003 – ident: e_1_2_6_36_1 doi: 10.1016/j.neuroimage.2012.01.040 – ident: e_1_2_6_17_1 doi: 10.1016/j.neuroimage.2010.10.035 – ident: e_1_2_6_74_1 doi: 10.1016/j.neuroimage.2014.01.060 – start-page: 143 volume-title: Handbook of Learning and Cognitive Processes year: 1975 ident: e_1_2_6_25_1 – ident: e_1_2_6_65_1 doi: 10.1111/j.1601-183X.2008.00417.x – ident: e_1_2_6_24_1 doi: 10.1523/JNEUROSCI.0266-05.2005 – ident: e_1_2_6_13_1 doi: 10.1007/s12311-015-0711-7 – ident: e_1_2_6_22_1 doi: 10.1038/nrn3312 – ident: e_1_2_6_50_1 doi: 10.1016/S0006-8993(01)02111-4 – ident: e_1_2_6_59_1 doi: 10.1113/jphysiol.1996.sp021581 – ident: e_1_2_6_75_1 doi: 10.1016/S0074-7742(08)60359-1 – ident: e_1_2_6_18_1 doi: 10.1002/hbm.10056 – ident: e_1_2_6_48_1 doi: 10.1146/annurev.psych.121208.131631 – ident: e_1_2_6_33_1 doi: 10.1006/nimg.2002.1199 – ident: e_1_2_6_40_1 doi: 10.1016/B978-0-444-63356-9.00004-2 – ident: e_1_2_6_46_1 doi: 10.1038/416330a – ident: e_1_2_6_44_1 doi: 10.1523/JNEUROSCI.04-11-02811.1984 – ident: e_1_2_6_2_1 doi: 10.1523/JNEUROSCI.21-15-05715.2001 – ident: e_1_2_6_10_1 doi: 10.1101/lm.59603 – ident: e_1_2_6_35_1 doi: 10.1016/j.neubiorev.2015.09.019 – ident: e_1_2_6_58_1 doi: 10.1152/jn.2000.84.6.3026 – ident: e_1_2_6_45_1 doi: 10.1523/JNEUROSCI.21-11-04081.2001 – ident: e_1_2_6_5_1 doi: 10.1523/JNEUROSCI.16-12-04032.1996 – ident: e_1_2_6_28_1 doi: 10.1007/BF00241372 – ident: e_1_2_6_72_1 doi: 10.1016/j.nlm.2013.08.012 – ident: e_1_2_6_70_1 doi: 10.1523/JNEUROSCI.2492-14.2015 – ident: e_1_2_6_6_1 doi: 10.3389/neuro.03.019.2009 – ident: e_1_2_6_42_1 doi: 10.1016/B978-0-12-420247-4.00002-6 – ident: e_1_2_6_54_1 doi: 10.1016/j.neubiorev.2011.12.014 |
SSID | ssj0011501 |
Score | 2.3460588 |
Snippet | Classical delay eyeblink conditioning is likely the most commonly used paradigm to study cerebellar learning. As yet, few studies have focused on extinction... |
SourceID | pubmedcentral proquest pubmed crossref wiley |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 3957 |
SubjectTerms | Adolescent Adult Analysis of Variance associative learning Aversion learning Blinking - physiology Brain Brain Mapping Cerebellar Cortex - diagnostic imaging Cerebellar Cortex - physiology cerebellar imaging Cerebellar Nuclei - diagnostic imaging Cerebellar Nuclei - physiology Cerebellar plasticity Cerebellum Conditioning Conditioning, Eyelid - physiology deep cerebellar nuclei delay conditioning Extinction behavior Extinction, Psychological - physiology Eyelid conditioning Female Functional magnetic resonance imaging Hum human Humans Image processing Learning Magnetic resonance imaging Magnetic Resonance Imaging - instrumentation Male Memory Modulation Neuroimaging Neuropsychological Tests Nuclei Resonance Serial learning Unconditioned stimulus Young Adult |
Title | Modulation of 7 T fMRI Signal in the Cerebellar Cortex and Nuclei During Acquisition, Extinction, and Reacquisition of Conditioned Eyeblink Responses |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fhbm.23641 https://www.ncbi.nlm.nih.gov/pubmed/28474470 https://www.proquest.com/docview/1915749472 https://www.proquest.com/docview/1896036517 https://pubmed.ncbi.nlm.nih.gov/PMC6866767 |
Volume | 38 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
journalDatabaseRights | – providerCode: PRVAQN databaseName: PubMed Central customDbUrl: eissn: 1097-0193 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0011501 issn: 1065-9471 databaseCode: RPM dateStart: 19980101 isFulltext: true titleUrlDefault: https://www.ncbi.nlm.nih.gov/pmc/ providerName: National Library of Medicine – providerCode: PRVOVD databaseName: Journals@Ovid LWW All Open Access Journal Collection Rolling customDbUrl: eissn: 1097-0193 dateEnd: 99991231 omitProxy: true ssIdentifier: ssj0011501 issn: 1065-9471 databaseCode: OVEED dateStart: 19930101 isFulltext: true titleUrlDefault: http://ovidsp.ovid.com/ providerName: Ovid – providerCode: PRVWIB databaseName: Wiley Online Library - Core collection (SURFmarket) issn: 1065-9471 databaseCode: DR2 dateStart: 19960101 customDbUrl: isFulltext: true eissn: 1097-0193 dateEnd: 99991231 omitProxy: false ssIdentifier: ssj0011501 providerName: Wiley-Blackwell |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELaqHhAXHi2PpQUZhFAPZOskdrwWp2XZakFKD0sr9YAU2bFDo9Js2YfU8kM481v4Zcw4D1gKEuIWxZPYSWbG32TGnwl57pQLjYx1wIvYBHzAbKASCYGrgvmkEC4P_SKx9DCZHPN3J-Jkg7xq18LU_BDdDze0DO-v0cC1Wez_JA09Ned9ZD_H0CeMhU_RTjvqKAQ6PtiCKTZQ4IFbViEW7XdXrs9F1wDm9TrJX_Grn4AObpMP7dDrupOz_mpp-vmX31gd__PZ7pBbDTClw1qT7pINV22R7WEFQfn5FX1Bfamo_we_RW6kTUZ-m3xNZ7bZAYzOCiq_fzuiRTp9S9-XH_F-ZUUBYtKRmztMceg5HWF57yXVlaWHSKZc0jd-qSQd5p9XZV1C9pKOL5dlldfHKDoF1901Y0-jGSbbkWfJ0vEV1rpXZyDlK37d4h45PhgfjSZBs9dDkCMDWyASq4uIWScNLrY1oYxzLZVjccwFA5VJrFDC2VArZmNwU1EINsAdnDWcORXfJ5sVdPmQ0CJhkWOG5yrUvCgSZbTjkXGAjYQtHOuRvfarZ3lDhI77cXzKagrnKIPXn_nX3yPPOtGLmv3jT0K7repkjQNYZBAGC8lB8aIeedo1g-liPkZXbrYCmQGEj3EiQtkjD2pN63pB1MC5hMHKNR3sBJAWfL2lKk89PXgywLpluOeeV7G_DzybvE79waN_F90hNyMENr4EcpdsLucr9xhg2dI88fb3Ay9lNgw |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3db9MwELemIQEvfGx8FAYYhNAeSOckTlxLvJSuUwdLH0on7QVFduywaCyFrpU2_hCe-Vv4y7hzPqAMJMRbFF9iN707_853_pmQ51ZaX4tQeTwPtcd7zHgyFhC4SphP8shmvtsklozj0SF_cxQdrZFXzV6Yih-iXXBDy3D-Gg0cF6R3frKGHuvTLtKfQ-xzBfNzaJa7k5Y8CqGOC7dgkvUk-OCGV4gFO-2jq7PRJYh5uVLyVwTrpqC9m-R9M_iq8uSku1zobvblN17H__11t8iNGpvSfqVMt8maLTfIZr-EuPz0gr6grlrULcNvkKtJnZTfJF-TmakPAaOznIrv36Y0Tyb79F3xAd9XlBRQJh3YucUsh5rTAVb4nlNVGjpGPuWC7rrdkrSffV4WVRXZSzo8XxRlVl2j6AS8d9uMPQ1mmG9HqiVDhxdY7l6egJQr-rVnd8jh3nA6GHn1cQ9ehiRsXhQblQfMWKFxv632RZgpIS0LQx4x0JrYRDKyxleSmRA8VeCDGXALdzVnVoZ3yXoJXd4nNI9ZYJnmmfQVz_NYamV5oC3Ao8jklnXIdvO3p1nNhY5HcnxMKxbnIIXPn7rP3yHPWtFPFQHIn4S2Gt1Jax9wlkIkHAkOmhd0yNO2GawXUzKqtLMlyPQgggzjyBcdcq9StbYXBA6cCxisWFHCVgCZwVdbyuLYMYTHPSxdhnduOx37-8DT0evEXTz4d9En5NpomhykB_vjtw_J9QBxjquI3CLri_nSPgKUttCPnTH-AGODOig |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLamIU28cNm4lG1gEEJ7IF0uTlxrT6Vr1QGpUNmkPUyK4thm0bZ061pp44fsmd_CL-Mc5wJlICHeovo0dtNzjr8Tf_5MyGsttCd5kDrMBNJhHVc5IuJQuAqYT0yoM89uEotH0fCAvT8MD5fITr0XptSHaF64YWTYfI0Bfq7M9k_R0GN51kb1cyh97rAIqitERONGOwqRjq22YI51BKTgWlbI9bebry5ORrcQ5m2i5K8A1s5Ag_vkqB57STw5ac9nsp19_U3W8T9_3ANyr0KmtFu60kOypItVstYtoCo_u6ZvqOWK2pfwq2Qlrpbk18hNPFHVEWB0Yij__m2fmni8Rz_nX_B-eUEBY9Kenmpc40intIf83iuaFoqOUE05p7t2ryTtZhfzvOSQvaX9q1leZOU1mo4hdzfN2FNvgqvtKLSkaP8aye7FCVhZyq--fEQOBv393tCpDntwMpRgc8JIpcZ3leYSd9tKjwdZyoV2g4CFLvhMpEIRauWlwlUB5CnfgyBgGj6VzNUieEyWC-jyKaEGvEG7kmXCS5kxkZCpZr7UAI5CZbTbIlv1v55klRI6HshxmpQazn4Cjz-xj79FXjWm56X8x5-MNmrXSaoMcJlAHRxyBo7nt8jLphliFxdk0kJP5mDTgfoxiEKPt8iT0tOaXhA2MMZhsHzBBxsD1AVfbCnyY6sPHnWQuAz33LIu9veBJ8N3sb149u-mL8jKp91B8nFv9GGd3PUR5Fg65AZZnk3nehMg2kw-t6H4A5NSONc |
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=Modulation+of+7+T+fMRI+Signal+in+the+Cerebellar+Cortex+and+Nuclei+During+Acquisition%2C+Extinction%2C+and+Reacquisition+of+Conditioned+Eyeblink+Responses&rft.jtitle=Human+brain+mapping&rft.au=Ernst%2C+Thomas+M&rft.au=Th%C3%BCrling%2C+Markus&rft.au=M%C3%BCller%2C+Sarah&rft.au=Kahl%2C+Fabian&rft.date=2017-08-01&rft.pub=John+Wiley+%26+Sons%2C+Inc&rft.issn=1065-9471&rft.eissn=1097-0193&rft.volume=38&rft.issue=8&rft.spage=3957&rft.epage=3974&rft_id=info:doi/10.1002%2Fhbm.23641&rft.externalDBID=HAS_PDF_LINK |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1065-9471&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1065-9471&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1065-9471&client=summon |