---
_id: '14314'
abstract:
- lang: eng
  text: The execution of cognitive functions requires coordinated circuit activity
    across different brain areas that involves the associated firing of neuronal assemblies.
    Here, we tested the circuit mechanism behind assembly interactions between the
    hippocampus and the medial prefrontal cortex (mPFC) of adult rats by recording
    neuronal populations during a rule-switching task. We identified functionally
    coupled CA1-mPFC cells that synchronized their activity beyond that expected from
    common spatial coding or oscillatory firing. When such cell pairs fired together,
    the mPFC cell strongly phase locked to CA1 theta oscillations and maintained consistent
    theta firing phases, independent of the theta timing of their CA1 counterpart.
    These functionally connected CA1-mPFC cells formed interconnected assemblies.
    While firing together with their CA1 assembly partners, mPFC cells fired along
    specific theta sequences. Our results suggest that upregulated theta oscillatory
    firing of mPFC cells can signal transient interactions with specific CA1 assemblies,
    thus enabling distributed computations.
acknowledgement: We thank A. Cumpelik, H. Chiossi, and L. Bollman for comments on
  an earlier version of this manuscript. This work was funded by EU-FP7 MC-ITN IN-SENS
  (grant 607616).
article_number: '113015'
article_processing_charge: Yes
article_type: original
author:
- first_name: Michele
  full_name: Nardin, Michele
  id: 30BD0376-F248-11E8-B48F-1D18A9856A87
  last_name: Nardin
  orcid: 0000-0001-8849-6570
- first_name: Karola
  full_name: Käfer, Karola
  id: 2DAA49AA-F248-11E8-B48F-1D18A9856A87
  last_name: Käfer
- first_name: Federico
  full_name: Stella, Federico
  id: 39AF1E74-F248-11E8-B48F-1D18A9856A87
  last_name: Stella
  orcid: 0000-0001-9439-3148
- first_name: Jozsef L
  full_name: Csicsvari, Jozsef L
  id: 3FA14672-F248-11E8-B48F-1D18A9856A87
  last_name: Csicsvari
  orcid: 0000-0002-5193-4036
citation:
  ama: Nardin M, Käfer K, Stella F, Csicsvari JL. Theta oscillations as a substrate
    for medial prefrontal-hippocampal assembly interactions. <i>Cell Reports</i>.
    2023;42(9). doi:<a href="https://doi.org/10.1016/j.celrep.2023.113015">10.1016/j.celrep.2023.113015</a>
  apa: Nardin, M., Käfer, K., Stella, F., &#38; Csicsvari, J. L. (2023). Theta oscillations
    as a substrate for medial prefrontal-hippocampal assembly interactions. <i>Cell
    Reports</i>. Elsevier. <a href="https://doi.org/10.1016/j.celrep.2023.113015">https://doi.org/10.1016/j.celrep.2023.113015</a>
  chicago: Nardin, Michele, Karola Käfer, Federico Stella, and Jozsef L Csicsvari.
    “Theta Oscillations as a Substrate for Medial Prefrontal-Hippocampal Assembly
    Interactions.” <i>Cell Reports</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.celrep.2023.113015">https://doi.org/10.1016/j.celrep.2023.113015</a>.
  ieee: M. Nardin, K. Käfer, F. Stella, and J. L. Csicsvari, “Theta oscillations as
    a substrate for medial prefrontal-hippocampal assembly interactions,” <i>Cell
    Reports</i>, vol. 42, no. 9. Elsevier, 2023.
  ista: Nardin M, Käfer K, Stella F, Csicsvari JL. 2023. Theta oscillations as a substrate
    for medial prefrontal-hippocampal assembly interactions. Cell Reports. 42(9),
    113015.
  mla: Nardin, Michele, et al. “Theta Oscillations as a Substrate for Medial Prefrontal-Hippocampal
    Assembly Interactions.” <i>Cell Reports</i>, vol. 42, no. 9, 113015, Elsevier,
    2023, doi:<a href="https://doi.org/10.1016/j.celrep.2023.113015">10.1016/j.celrep.2023.113015</a>.
  short: M. Nardin, K. Käfer, F. Stella, J.L. Csicsvari, Cell Reports 42 (2023).
date_created: 2023-09-10T22:01:11Z
date_published: 2023-09-26T00:00:00Z
date_updated: 2023-09-15T07:14:12Z
day: '26'
ddc:
- '570'
department:
- _id: JoCs
doi: 10.1016/j.celrep.2023.113015
ec_funded: 1
external_id:
  pmid:
  - '37632747'
file:
- access_level: open_access
  checksum: ca77a304fb813c292550b8604b0fb41d
  content_type: application/pdf
  creator: dernst
  date_created: 2023-09-15T07:12:46Z
  date_updated: 2023-09-15T07:12:46Z
  file_id: '14337'
  file_name: 2023_CellPress_Nardin.pdf
  file_size: 4879455
  relation: main_file
  success: 1
file_date_updated: 2023-09-15T07:12:46Z
has_accepted_license: '1'
intvolume: '        42'
issue: '9'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 257BBB4C-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '607616'
  name: Inter-and intracellular signalling in schizophrenia
publication: Cell Reports
publication_identifier:
  eissn:
  - 2211-1247
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Theta oscillations as a substrate for medial prefrontal-hippocampal assembly
  interactions
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 42
year: '2023'
...
---
_id: '14402'
abstract:
- lang: eng
  text: Alpha oscillations are a distinctive feature of the awake resting state of
    the human brain. However, their functional role in resting-state neuronal dynamics
    remains poorly understood. Here we show that, during resting wakefulness, alpha
    oscillations drive an alternation of attenuation and amplification bouts in neural
    activity. Our analysis indicates that inhibition is activated in pulses that last
    for a single alpha cycle and gradually suppress neural activity, while excitation
    is successively enhanced over a few alpha cycles to amplify neural activity. Furthermore,
    we show that long-term alpha amplitude fluctuations—the “waxing and waning” phenomenon—are
    an attenuation-amplification mechanism described by a power-law decay of the activity
    rate in the “waning” phase. Importantly, we do not observe such dynamics during
    non-rapid eye movement (NREM) sleep with marginal alpha oscillations. The results
    suggest that alpha oscillations modulate neural activity not only through pulses
    of inhibition (pulsed inhibition hypothesis) but also by timely enhancement of
    excitation (or disinhibition).
acknowledgement: This research was funded in whole or in part by the Austrian Science
  Fund (FWF) (grant PT1013M03318 to F.L.). For the purpose of open access, the author
  has applied a CC BY public copyright license to any Author Accepted Manuscript version
  arising from this submission. The study was supported by the European Union Horizon
  2020 Research and Innovation Program under the Marie Sklodowska-Curie action (grant
  agreement 754411 to F.L.) and in part by the NextGenerationEU through the grant
  TAlent in ReSearch@University of Padua – STARS@UNIPD (to F.L.) (project BRAINCIP
  [brain criticality and information processing]). L.d.A. acknowledges support from
  the Italian MIUR project PRIN2017WZFTZP and partial support from NEXTGENERATIONEU
  (NGEU) funded by the Ministry of University and Research (MUR), National Recovery
  and Resilience Plan (NRRP), and project MNESYS (PE0000006)—a multiscale integrated
  approach to the study of the nervous system in health and disease (DN. 1553 11.10.2022).
  O.S. acknowledges support from the Israel Science Foundation, grant 504/17. The
  work was supported in part by DIRP ZIAMH02797 (to D.P.).
article_number: '113162'
article_processing_charge: Yes
article_type: original
author:
- first_name: Fabrizio
  full_name: Lombardi, Fabrizio
  id: A057D288-3E88-11E9-986D-0CF4E5697425
  last_name: Lombardi
  orcid: 0000-0003-2623-5249
- first_name: Hans J.
  full_name: Herrmann, Hans J.
  last_name: Herrmann
- first_name: Liborio
  full_name: Parrino, Liborio
  last_name: Parrino
- first_name: Dietmar
  full_name: Plenz, Dietmar
  last_name: Plenz
- first_name: Silvia
  full_name: Scarpetta, Silvia
  last_name: Scarpetta
- first_name: Anna Elisabetta
  full_name: Vaudano, Anna Elisabetta
  last_name: Vaudano
- first_name: Lucilla
  full_name: De Arcangelis, Lucilla
  last_name: De Arcangelis
- first_name: Oren
  full_name: Shriki, Oren
  last_name: Shriki
citation:
  ama: 'Lombardi F, Herrmann HJ, Parrino L, et al. Beyond pulsed inhibition: Alpha
    oscillations modulate attenuation and amplification of neural activity in the
    awake resting state. <i>Cell Reports</i>. 2023;42(10). doi:<a href="https://doi.org/10.1016/j.celrep.2023.113162">10.1016/j.celrep.2023.113162</a>'
  apa: 'Lombardi, F., Herrmann, H. J., Parrino, L., Plenz, D., Scarpetta, S., Vaudano,
    A. E., … Shriki, O. (2023). Beyond pulsed inhibition: Alpha oscillations modulate
    attenuation and amplification of neural activity in the awake resting state. <i>Cell
    Reports</i>. Elsevier. <a href="https://doi.org/10.1016/j.celrep.2023.113162">https://doi.org/10.1016/j.celrep.2023.113162</a>'
  chicago: 'Lombardi, Fabrizio, Hans J. Herrmann, Liborio Parrino, Dietmar Plenz,
    Silvia Scarpetta, Anna Elisabetta Vaudano, Lucilla De Arcangelis, and Oren Shriki.
    “Beyond Pulsed Inhibition: Alpha Oscillations Modulate Attenuation and Amplification
    of Neural Activity in the Awake Resting State.” <i>Cell Reports</i>. Elsevier,
    2023. <a href="https://doi.org/10.1016/j.celrep.2023.113162">https://doi.org/10.1016/j.celrep.2023.113162</a>.'
  ieee: 'F. Lombardi <i>et al.</i>, “Beyond pulsed inhibition: Alpha oscillations
    modulate attenuation and amplification of neural activity in the awake resting
    state,” <i>Cell Reports</i>, vol. 42, no. 10. Elsevier, 2023.'
  ista: 'Lombardi F, Herrmann HJ, Parrino L, Plenz D, Scarpetta S, Vaudano AE, De
    Arcangelis L, Shriki O. 2023. Beyond pulsed inhibition: Alpha oscillations modulate
    attenuation and amplification of neural activity in the awake resting state. Cell
    Reports. 42(10), 113162.'
  mla: 'Lombardi, Fabrizio, et al. “Beyond Pulsed Inhibition: Alpha Oscillations Modulate
    Attenuation and Amplification of Neural Activity in the Awake Resting State.”
    <i>Cell Reports</i>, vol. 42, no. 10, 113162, Elsevier, 2023, doi:<a href="https://doi.org/10.1016/j.celrep.2023.113162">10.1016/j.celrep.2023.113162</a>.'
  short: F. Lombardi, H.J. Herrmann, L. Parrino, D. Plenz, S. Scarpetta, A.E. Vaudano,
    L. De Arcangelis, O. Shriki, Cell Reports 42 (2023).
date_created: 2023-10-08T22:01:15Z
date_published: 2023-10-31T00:00:00Z
date_updated: 2024-01-30T14:07:40Z
day: '31'
ddc:
- '570'
department:
- _id: GaTk
doi: 10.1016/j.celrep.2023.113162
ec_funded: 1
external_id:
  isi:
  - '001086695500001'
  pmid:
  - '37777965'
file:
- access_level: open_access
  checksum: 9c71eb2a03aa160415f01ad95f49ceb5
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-30T14:07:08Z
  date_updated: 2024-01-30T14:07:08Z
  file_id: '14914'
  file_name: 2023_CellReports_Lombardi.pdf
  file_size: 5599007
  relation: main_file
  success: 1
file_date_updated: 2024-01-30T14:07:08Z
has_accepted_license: '1'
intvolume: '        42'
isi: 1
issue: '10'
language:
- iso: eng
month: '10'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: eb943429-77a9-11ec-83b8-9f471cdf5c67
  grant_number: M03318
  name: Functional Advantages of Critical Brain Dynamics
- _id: 260C2330-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '754411'
  name: ISTplus - Postdoctoral Fellowships
publication: Cell Reports
publication_identifier:
  eissn:
  - 2211-1247
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Beyond pulsed inhibition: Alpha oscillations modulate attenuation and amplification
  of neural activity in the awake resting state'
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 42
year: '2023'
...
---
_id: '12672'
abstract:
- lang: eng
  text: Cytosine methylation within CG dinucleotides (mCG) can be epigenetically inherited
    over many generations. Such inheritance is thought to be mediated by a semiconservative
    mechanism that produces binary present/absent methylation patterns. However, we
    show here that in Arabidopsis thaliana h1ddm1 mutants, intermediate heterochromatic
    mCG is stably inherited across many generations and is quantitatively associated
    with transposon expression. We develop a mathematical model that estimates the
    rates of semiconservative maintenance failure and de novo methylation at each
    transposon, demonstrating that mCG can be stably inherited at any level via a
    dynamic balance of these activities. We find that DRM2 – the core methyltransferase
    of the RNA-directed DNA methylation pathway – catalyzes most of the heterochromatic
    de novo mCG, with de novo rates orders of magnitude higher than previously thought,
    whereas chromomethylases make smaller contributions. Our results demonstrate that
    stable epigenetic inheritance of mCG in plant heterochromatin is enabled by extensive
    de novo methylation.
acknowledgement: The authors would like to thank Jasper Rine for advice and mentorship
  to D.B.L., Lesley Philips, Timothy Wells, Sophie Able, and Christina Wistrom for
  support with plant growth, and Bhagyshree Jamge and Frédéric Berger for help with
  analysis of ddm1 × WT RNA-sequencing data. This work was supported by BBSRC Institute
  Strategic Program GEN (BB/P013511/1) to X.F., M.H., and D.Z., a European Research
  Council grant MaintainMeth (725746) to D.Z., and a postdoctoral fellowship from
  the Helen Hay Whitney Foundation to D.B.L.
article_number: '112132'
article_processing_charge: Yes
article_type: original
author:
- first_name: David B.
  full_name: Lyons, David B.
  last_name: Lyons
- first_name: Amy
  full_name: Briffa, Amy
  last_name: Briffa
- first_name: Shengbo
  full_name: He, Shengbo
  last_name: He
- first_name: Jaemyung
  full_name: Choi, Jaemyung
  last_name: Choi
- first_name: Elizabeth
  full_name: Hollwey, Elizabeth
  id: b8c4f54b-e484-11eb-8fdc-a54df64ef6dd
  last_name: Hollwey
- first_name: Jack
  full_name: Colicchio, Jack
  last_name: Colicchio
- first_name: Ian
  full_name: Anderson, Ian
  last_name: Anderson
- first_name: Xiaoqi
  full_name: Feng, Xiaoqi
  id: e0164712-22ee-11ed-b12a-d80fcdf35958
  last_name: Feng
  orcid: 0000-0002-4008-1234
- first_name: Martin
  full_name: Howard, Martin
  last_name: Howard
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
citation:
  ama: Lyons DB, Briffa A, He S, et al. Extensive de novo activity stabilizes epigenetic
    inheritance of CG methylation in Arabidopsis transposons. <i>Cell Reports</i>.
    2023;42(3). doi:<a href="https://doi.org/10.1016/j.celrep.2023.112132">10.1016/j.celrep.2023.112132</a>
  apa: Lyons, D. B., Briffa, A., He, S., Choi, J., Hollwey, E., Colicchio, J., … Zilberman,
    D. (2023). Extensive de novo activity stabilizes epigenetic inheritance of CG
    methylation in Arabidopsis transposons. <i>Cell Reports</i>. Elsevier. <a href="https://doi.org/10.1016/j.celrep.2023.112132">https://doi.org/10.1016/j.celrep.2023.112132</a>
  chicago: Lyons, David B., Amy Briffa, Shengbo He, Jaemyung Choi, Elizabeth Hollwey,
    Jack Colicchio, Ian Anderson, Xiaoqi Feng, Martin Howard, and Daniel Zilberman.
    “Extensive de Novo Activity Stabilizes Epigenetic Inheritance of CG Methylation
    in Arabidopsis Transposons.” <i>Cell Reports</i>. Elsevier, 2023. <a href="https://doi.org/10.1016/j.celrep.2023.112132">https://doi.org/10.1016/j.celrep.2023.112132</a>.
  ieee: D. B. Lyons <i>et al.</i>, “Extensive de novo activity stabilizes epigenetic
    inheritance of CG methylation in Arabidopsis transposons,” <i>Cell Reports</i>,
    vol. 42, no. 3. Elsevier, 2023.
  ista: Lyons DB, Briffa A, He S, Choi J, Hollwey E, Colicchio J, Anderson I, Feng
    X, Howard M, Zilberman D. 2023. Extensive de novo activity stabilizes epigenetic
    inheritance of CG methylation in Arabidopsis transposons. Cell Reports. 42(3),
    112132.
  mla: Lyons, David B., et al. “Extensive de Novo Activity Stabilizes Epigenetic Inheritance
    of CG Methylation in Arabidopsis Transposons.” <i>Cell Reports</i>, vol. 42, no.
    3, 112132, Elsevier, 2023, doi:<a href="https://doi.org/10.1016/j.celrep.2023.112132">10.1016/j.celrep.2023.112132</a>.
  short: D.B. Lyons, A. Briffa, S. He, J. Choi, E. Hollwey, J. Colicchio, I. Anderson,
    X. Feng, M. Howard, D. Zilberman, Cell Reports 42 (2023).
date_created: 2023-02-23T09:17:44Z
date_published: 2023-03-28T00:00:00Z
date_updated: 2023-11-02T12:23:45Z
day: '28'
ddc:
- '580'
department:
- _id: DaZi
- _id: XiFe
doi: 10.1016/j.celrep.2023.112132
ec_funded: 1
external_id:
  isi:
  - '000944921600001'
file:
- access_level: open_access
  checksum: 6cbc44fdb18bf18834c9e2a5b9c67123
  content_type: application/pdf
  creator: kschuh
  date_created: 2023-05-11T10:41:42Z
  date_updated: 2023-05-11T10:41:42Z
  file_id: '12941'
  file_name: 2023_CellReports_Lyons.pdf
  file_size: 8401261
  relation: main_file
  success: 1
file_date_updated: 2023-05-11T10:41:42Z
has_accepted_license: '1'
intvolume: '        42'
isi: 1
issue: '3'
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
project:
- _id: 62935a00-2b32-11ec-9570-eff30fa39068
  call_identifier: H2020
  grant_number: '725746'
  name: Quantitative analysis of DNA methylation maintenance with chromatin
publication: Cell Reports
publication_identifier:
  eissn:
  - 2211-1247
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: Extensive de novo activity stabilizes epigenetic inheritance of CG methylation
  in Arabidopsis transposons
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 3E5EF7F0-F248-11E8-B48F-1D18A9856A87
volume: 42
year: '2023'
...
---
_id: '11143'
abstract:
- lang: eng
  text: 'Dravet syndrome is a neurodevelopmental disorder characterized by epilepsy,
    intellectual disability, and sudden death due to pathogenic variants in SCN1A
    with loss of function of the sodium channel subunit Nav1.1. Nav1.1-expressing
    parvalbumin GABAergic interneurons (PV-INs) from young Scn1a+/− mice show impaired
    action potential generation. An approach assessing PV-IN function in the same
    mice at two time points shows impaired spike generation in all Scn1a+/− mice at
    postnatal days (P) 16–21, whether deceased prior or surviving to P35, with normalization
    by P35 in surviving mice. However, PV-IN synaptic transmission is dysfunctional
    in young Scn1a+/− mice that did not survive and in Scn1a+/− mice ≥ P35. Modeling
    confirms that PV-IN axonal propagation is more sensitive to decreased sodium conductance
    than spike generation. These results demonstrate dynamic dysfunction in Dravet
    syndrome: combined abnormalities of PV-IN spike generation and propagation drives
    early disease severity, while ongoing dysfunction of synaptic transmission contributes
    to chronic pathology.'
acknowledgement: We would like to thank Bernardo Rudy, Joanna Mattis, and Laura Mcgarry
  for comments on a previous version of the manuscript; Xiaohong Zhang for expert
  technical support and mouse colony maintenance; Melody Cheng for assistance with
  generation of the graphical abstract; and Jennifer Kearney for the gift of Scn1a+/−
  mice. This work was supported by the National Institute of Neurological Disorders
  and Stroke of the National Institutes of Health under F31NS111803 (to K.M.G.) and
  K08NS097633 and R01NS110869 (to E.M.G.), the Dravet Syndrome Foundation (to A.S.),
  an ERC Consolidator Grant (SYNAPSEEK) (to T.P.V.), and the NOMIS Foundation through
  the NOMIS Fellowships program at IST Austria (to C.C.). The graphical abstract was
  prepared using BioRender software (BioRender.com).
article_number: '110580'
article_processing_charge: No
article_type: original
author:
- first_name: Keisuke
  full_name: Kaneko, Keisuke
  last_name: Kaneko
- first_name: Christopher
  full_name: Currin, Christopher
  id: e8321fc5-3091-11eb-8a53-83f309a11ac9
  last_name: Currin
  orcid: 0000-0002-4809-5059
- first_name: Kevin M.
  full_name: Goff, Kevin M.
  last_name: Goff
- first_name: Eric R.
  full_name: Wengert, Eric R.
  last_name: Wengert
- first_name: Ala
  full_name: Somarowthu, Ala
  last_name: Somarowthu
- first_name: Tim P
  full_name: Vogels, Tim P
  id: CB6FF8D2-008F-11EA-8E08-2637E6697425
  last_name: Vogels
  orcid: 0000-0003-3295-6181
- first_name: Ethan M.
  full_name: Goldberg, Ethan M.
  last_name: Goldberg
citation:
  ama: Kaneko K, Currin C, Goff KM, et al. Developmentally regulated impairment of
    parvalbumin interneuron synaptic transmission in an experimental model of Dravet
    syndrome. <i>Cell Reports</i>. 2022;38(13). doi:<a href="https://doi.org/10.1016/j.celrep.2022.110580">10.1016/j.celrep.2022.110580</a>
  apa: Kaneko, K., Currin, C., Goff, K. M., Wengert, E. R., Somarowthu, A., Vogels,
    T. P., &#38; Goldberg, E. M. (2022). Developmentally regulated impairment of parvalbumin
    interneuron synaptic transmission in an experimental model of Dravet syndrome.
    <i>Cell Reports</i>. Elsevier. <a href="https://doi.org/10.1016/j.celrep.2022.110580">https://doi.org/10.1016/j.celrep.2022.110580</a>
  chicago: Kaneko, Keisuke, Christopher Currin, Kevin M. Goff, Eric R. Wengert, Ala
    Somarowthu, Tim P Vogels, and Ethan M. Goldberg. “Developmentally Regulated Impairment
    of Parvalbumin Interneuron Synaptic Transmission in an Experimental Model of Dravet
    Syndrome.” <i>Cell Reports</i>. Elsevier, 2022. <a href="https://doi.org/10.1016/j.celrep.2022.110580">https://doi.org/10.1016/j.celrep.2022.110580</a>.
  ieee: K. Kaneko <i>et al.</i>, “Developmentally regulated impairment of parvalbumin
    interneuron synaptic transmission in an experimental model of Dravet syndrome,”
    <i>Cell Reports</i>, vol. 38, no. 13. Elsevier, 2022.
  ista: Kaneko K, Currin C, Goff KM, Wengert ER, Somarowthu A, Vogels TP, Goldberg
    EM. 2022. Developmentally regulated impairment of parvalbumin interneuron synaptic
    transmission in an experimental model of Dravet syndrome. Cell Reports. 38(13),
    110580.
  mla: Kaneko, Keisuke, et al. “Developmentally Regulated Impairment of Parvalbumin
    Interneuron Synaptic Transmission in an Experimental Model of Dravet Syndrome.”
    <i>Cell Reports</i>, vol. 38, no. 13, 110580, Elsevier, 2022, doi:<a href="https://doi.org/10.1016/j.celrep.2022.110580">10.1016/j.celrep.2022.110580</a>.
  short: K. Kaneko, C. Currin, K.M. Goff, E.R. Wengert, A. Somarowthu, T.P. Vogels,
    E.M. Goldberg, Cell Reports 38 (2022).
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