---
_id: '14783'
abstract:
- lang: eng
  text: Connexin 43, an astroglial gap junction protein, is enriched in perisynaptic
    astroglial processes and plays major roles in synaptic transmission. We have previously
    found that astroglial Cx43 controls synaptic glutamate levels and allows for activity-dependent
    glutamine release to sustain physiological synaptic transmissions and cognitiogns.
    However, whether Cx43 is important for the release of synaptic vesicles, which
    is a critical component of synaptic efficacy, remains unanswered. Here, using
    transgenic mice with a glial conditional knockout of Cx43 (Cx43−/−), we investigate
    whether and how astrocytes regulate the release of synaptic vesicles from hippocampal
    synapses. We report that CA1 pyramidal neurons and their synapses develop normally
    in the absence of astroglial Cx43. However, a significant impairment in synaptic
    vesicle distribution and release dynamics were observed. In particular, the FM1-43
    assays performed using two-photon live imaging and combined with multi-electrode
    array stimulation in acute hippocampal slices, revealed a slower rate of synaptic
    vesicle release in Cx43−/− mice. Furthermore, paired-pulse recordings showed that
    synaptic vesicle release probability was also reduced and is dependent on glutamine
    supply via Cx43 hemichannel (HC). Taken together, we have uncovered a role for
    Cx43 in regulating presynaptic functions by controlling the rate and probability
    of synaptic vesicle release. Our findings further highlight the significance of
    astroglial Cx43 in synaptic transmission and efficacy.
acknowledgement: 'This research was funded by grants from the European Research Council
  (Consolidator grant #683154) and European Union’s Horizon 2020 research and innovation
  program (Marie Sklodowska-Curie Innovative Training Networks, grant #722053, EU-GliaPhD)
  to N.R., as well as from FP7-PEOPLE Marie Curie Intra-European Fellowship for career
  development (grant #622289) to G.C. We thank Elena Dossi, Grégory Ghézali, and Jérémie
  Teillon for support with setting up the MEA system for the two-photon microscope.
  We would also like to thank Tayfun Palaz for their technical assistance with the
  EM preparations.'
article_number: '1133'
article_processing_charge: Yes
article_type: original
author:
- first_name: Giselle T
  full_name: Cheung, Giselle T
  id: 471195F6-F248-11E8-B48F-1D18A9856A87
  last_name: Cheung
  orcid: 0000-0001-8457-2572
- first_name: Oana
  full_name: Chever, Oana
  last_name: Chever
- first_name: Astrid
  full_name: Rollenhagen, Astrid
  last_name: Rollenhagen
- first_name: Nicole
  full_name: Quenech’du, Nicole
  last_name: Quenech’du
- first_name: Pascal
  full_name: Ezan, Pascal
  last_name: Ezan
- first_name: Joachim H. R.
  full_name: Lübke, Joachim H. R.
  last_name: Lübke
- first_name: Nathalie
  full_name: Rouach, Nathalie
  last_name: Rouach
citation:
  ama: Cheung GT, Chever O, Rollenhagen A, et al. Astroglial connexin 43 regulates
    synaptic vesicle release at hippocampal synapses. <i>Cells</i>. 2023;12(8). doi:<a
    href="https://doi.org/10.3390/cells12081133">10.3390/cells12081133</a>
  apa: Cheung, G. T., Chever, O., Rollenhagen, A., Quenech’du, N., Ezan, P., Lübke,
    J. H. R., &#38; Rouach, N. (2023). Astroglial connexin 43 regulates synaptic vesicle
    release at hippocampal synapses. <i>Cells</i>. MDPI. <a href="https://doi.org/10.3390/cells12081133">https://doi.org/10.3390/cells12081133</a>
  chicago: Cheung, Giselle T, Oana Chever, Astrid Rollenhagen, Nicole Quenech’du,
    Pascal Ezan, Joachim H. R. Lübke, and Nathalie Rouach. “Astroglial Connexin 43
    Regulates Synaptic Vesicle Release at Hippocampal Synapses.” <i>Cells</i>. MDPI,
    2023. <a href="https://doi.org/10.3390/cells12081133">https://doi.org/10.3390/cells12081133</a>.
  ieee: G. T. Cheung <i>et al.</i>, “Astroglial connexin 43 regulates synaptic vesicle
    release at hippocampal synapses,” <i>Cells</i>, vol. 12, no. 8. MDPI, 2023.
  ista: Cheung GT, Chever O, Rollenhagen A, Quenech’du N, Ezan P, Lübke JHR, Rouach
    N. 2023. Astroglial connexin 43 regulates synaptic vesicle release at hippocampal
    synapses. Cells. 12(8), 1133.
  mla: Cheung, Giselle T., et al. “Astroglial Connexin 43 Regulates Synaptic Vesicle
    Release at Hippocampal Synapses.” <i>Cells</i>, vol. 12, no. 8, 1133, MDPI, 2023,
    doi:<a href="https://doi.org/10.3390/cells12081133">10.3390/cells12081133</a>.
  short: G.T. Cheung, O. Chever, A. Rollenhagen, N. Quenech’du, P. Ezan, J.H.R. Lübke,
    N. Rouach, Cells 12 (2023).
date_created: 2024-01-10T09:46:35Z
date_published: 2023-04-11T00:00:00Z
date_updated: 2024-01-16T09:29:35Z
day: '11'
ddc:
- '570'
department:
- _id: SiHi
doi: 10.3390/cells12081133
external_id:
  isi:
  - '000977445700001'
  pmid:
  - '37190042'
file:
- access_level: open_access
  checksum: 6798cd75d8857976fbc58a43fd173d68
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-16T09:26:52Z
  date_updated: 2024-01-16T09:26:52Z
  file_id: '14808'
  file_name: 2023_Cells_Cheung.pdf
  file_size: 7931643
  relation: main_file
  success: 1
file_date_updated: 2024-01-16T09:26:52Z
has_accepted_license: '1'
intvolume: '        12'
isi: 1
issue: '8'
keyword:
- General Medicine
language:
- iso: eng
month: '04'
oa: 1
oa_version: Published Version
pmid: 1
publication: Cells
publication_identifier:
  issn:
  - 2073-4409
publication_status: published
publisher: MDPI
quality_controlled: '1'
status: public
title: Astroglial connexin 43 regulates synaptic vesicle release at hippocampal synapses
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: 12
year: '2023'
...
---
_id: '13214'
abstract:
- lang: eng
  text: Nitrogen is an important macronutrient required for plant growth and development,
    thus directly impacting agricultural productivity. In recent years, numerous studies
    have shown that nitrogen-driven growth depends on pathways that control nitrate/nitrogen
    homeostasis and hormonal networks that act both locally and systemically to coordinate
    growth and development of plant organs. In this review, we will focus on recent
    advances in understanding the role of the plant hormones auxin and cytokinin and
    their crosstalk in nitrate-regulated growth and discuss the significance of novel
    findings and possible missing links.
acknowledgement: 'This work was supported by the Austrian Academy of Sciences ÖAW:
  Doc fellowship (26130) to Stefan Riegler.'
article_number: '1613'
article_processing_charge: Yes
article_type: review
author:
- first_name: R
  full_name: Abualia, R
  last_name: Abualia
- first_name: Stefan
  full_name: Riegler, Stefan
  id: FF6018E0-D806-11E9-8E43-0B14E6697425
  last_name: Riegler
  orcid: 0000-0003-3413-1343
- first_name: Eva
  full_name: Benková, Eva
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
citation:
  ama: Abualia R, Riegler S, Benková E. Nitrate, auxin and cytokinin - a trio to tango.
    <i>Cells</i>. 2023;12(12). doi:<a href="https://doi.org/10.3390/cells12121613">10.3390/cells12121613</a>
  apa: Abualia, R., Riegler, S., &#38; Benková, E. (2023). Nitrate, auxin and cytokinin
    - a trio to tango. <i>Cells</i>. MDPI. <a href="https://doi.org/10.3390/cells12121613">https://doi.org/10.3390/cells12121613</a>
  chicago: Abualia, R, Stefan Riegler, and Eva Benková. “Nitrate, Auxin and Cytokinin
    - a Trio to Tango.” <i>Cells</i>. MDPI, 2023. <a href="https://doi.org/10.3390/cells12121613">https://doi.org/10.3390/cells12121613</a>.
  ieee: R. Abualia, S. Riegler, and E. Benková, “Nitrate, auxin and cytokinin - a
    trio to tango,” <i>Cells</i>, vol. 12, no. 12. MDPI, 2023.
  ista: Abualia R, Riegler S, Benková E. 2023. Nitrate, auxin and cytokinin - a trio
    to tango. Cells. 12(12), 1613.
  mla: Abualia, R., et al. “Nitrate, Auxin and Cytokinin - a Trio to Tango.” <i>Cells</i>,
    vol. 12, no. 12, 1613, MDPI, 2023, doi:<a href="https://doi.org/10.3390/cells12121613">10.3390/cells12121613</a>.
  short: R. Abualia, S. Riegler, E. Benková, Cells 12 (2023).
date_created: 2023-07-12T07:41:25Z
date_published: 2023-06-13T00:00:00Z
date_updated: 2024-03-06T14:00:33Z
day: '13'
ddc:
- '570'
department:
- _id: EvBe
doi: 10.3390/cells12121613
external_id:
  isi:
  - '001017033600001'
  pmid:
  - '37371083'
file:
- access_level: open_access
  checksum: 6dc9df5f4f59fc27c509c275060354a5
  content_type: application/pdf
  creator: alisjak
  date_created: 2023-07-12T10:01:54Z
  date_updated: 2023-07-12T10:01:54Z
  file_id: '13218'
  file_name: 2023_cells_Abualia.pdf
  file_size: 1066802
  relation: main_file
  success: 1
file_date_updated: 2023-07-12T10:01:54Z
has_accepted_license: '1'
intvolume: '        12'
isi: 1
issue: '12'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 62883ed7-2b32-11ec-9570-93580204e56b
  grant_number: '26130'
  name: Functional asymmetry of medial habenula outputs in mice
publication: Cells
publication_identifier:
  issn:
  - 2073-4409
publication_status: published
publisher: MDPI
quality_controlled: '1'
status: public
title: Nitrate, auxin and cytokinin - a trio to tango
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: 12
year: '2023'
...
---
_id: '10015'
abstract:
- lang: eng
  text: "Auxin plays a dual role in growth regulation and, depending on the tissue
    and concentration of the hormone, it can either promote or inhibit division and
    expansion processes in plants. Recent studies have revealed that, beyond transcriptional
    reprogramming, alternative auxincontrolled mechanisms regulate root growth. Here,
    we explored the impact of different concentrations of the synthetic auxin NAA
    that establish growth-promoting and -repressing conditions on the root tip proteome
    and phosphoproteome, generating a unique resource. From the phosphoproteome data,
    we pinpointed (novel) growth regulators, such as the RALF34-THE1 module. Our results,
    together with previously published studies, suggest that auxin, H+-ATPases, cell
    wall modifications and cell wall sensing receptor-like kinases are tightly embedded
    in a pathway regulating cell elongation. Furthermore, our study assigned a novel
    role to MKK2 as a regulator of primary root growth and a (potential) regulator
    of auxin biosynthesis and signalling, and suggests the importance of the MKK2\r\nThr31
    phosphorylation site for growth regulation in the Arabidopsis root tip."
acknowledgement: We thank the Nottingham Stock Centre for seeds, Frank Van Breusegem
  for the phb3 mutant, and Herman Höfte for the the1 mutant. Open Access Funding by
  the Austrian Science Fund (FWF).
alternative_title:
- Protein Phosphorylation and Cell Signaling in Plants
article_number: '1665 '
article_processing_charge: Yes
article_type: original
author:
- first_name: N
  full_name: Nikonorova, N
  last_name: Nikonorova
- first_name: E
  full_name: Murphy, E
  last_name: Murphy
- first_name: CF
  full_name: Fonseca de Lima, CF
  last_name: Fonseca de Lima
- first_name: S
  full_name: Zhu, S
  last_name: Zhu
- first_name: B
  full_name: van de Cotte, B
  last_name: van de Cotte
- first_name: LD
  full_name: Vu, LD
  last_name: Vu
- first_name: D
  full_name: Balcerowicz, D
  last_name: Balcerowicz
- first_name: Lanxin
  full_name: Li, Lanxin
  id: 367EF8FA-F248-11E8-B48F-1D18A9856A87
  last_name: Li
  orcid: 0000-0002-5607-272X
- first_name: X
  full_name: Kong, X
  last_name: Kong
- first_name: G
  full_name: De Rop, G
  last_name: De Rop
- first_name: T
  full_name: Beeckman, T
  last_name: Beeckman
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: K
  full_name: Vissenberg, K
  last_name: Vissenberg
- first_name: PC
  full_name: Morris, PC
  last_name: Morris
- first_name: Z
  full_name: Ding, Z
  last_name: Ding
- first_name: I
  full_name: De Smet, I
  last_name: De Smet
citation:
  ama: Nikonorova N, Murphy E, Fonseca de Lima C, et al. The Arabidopsis root tip
    (phospho)proteomes at growth-promoting versus growth-repressing conditions reveal
    novel root growth regulators. <i>Cells</i>. 2021;10. doi:<a href="https://doi.org/10.3390/cells10071665">10.3390/cells10071665</a>
  apa: Nikonorova, N., Murphy, E., Fonseca de Lima, C., Zhu, S., van de Cotte, B.,
    Vu, L., … De Smet, I. (2021). The Arabidopsis root tip (phospho)proteomes at growth-promoting
    versus growth-repressing conditions reveal novel root growth regulators. <i>Cells</i>.
    MDPI. <a href="https://doi.org/10.3390/cells10071665">https://doi.org/10.3390/cells10071665</a>
  chicago: Nikonorova, N, E Murphy, CF Fonseca de Lima, S Zhu, B van de Cotte, LD
    Vu, D Balcerowicz, et al. “The Arabidopsis Root Tip (Phospho)Proteomes at Growth-Promoting
    versus Growth-Repressing Conditions Reveal Novel Root Growth Regulators.” <i>Cells</i>.
    MDPI, 2021. <a href="https://doi.org/10.3390/cells10071665">https://doi.org/10.3390/cells10071665</a>.
  ieee: N. Nikonorova <i>et al.</i>, “The Arabidopsis root tip (phospho)proteomes
    at growth-promoting versus growth-repressing conditions reveal novel root growth
    regulators,” <i>Cells</i>, vol. 10. MDPI, 2021.
  ista: Nikonorova N, Murphy E, Fonseca de Lima C, Zhu S, van de Cotte B, Vu L, Balcerowicz
    D, Li L, Kong X, De Rop G, Beeckman T, Friml J, Vissenberg K, Morris P, Ding Z,
    De Smet I. 2021. The Arabidopsis root tip (phospho)proteomes at growth-promoting
    versus growth-repressing conditions reveal novel root growth regulators. Cells.
    10, 1665.
  mla: Nikonorova, N., et al. “The Arabidopsis Root Tip (Phospho)Proteomes at Growth-Promoting
    versus Growth-Repressing Conditions Reveal Novel Root Growth Regulators.” <i>Cells</i>,
    vol. 10, 1665, MDPI, 2021, doi:<a href="https://doi.org/10.3390/cells10071665">10.3390/cells10071665</a>.
  short: N. Nikonorova, E. Murphy, C. Fonseca de Lima, S. Zhu, B. van de Cotte, L.
    Vu, D. Balcerowicz, L. Li, X. Kong, G. De Rop, T. Beeckman, J. Friml, K. Vissenberg,
    P. Morris, Z. Ding, I. De Smet, Cells 10 (2021).
date_created: 2021-09-14T11:36:20Z
date_published: 2021-07-02T00:00:00Z
date_updated: 2024-10-29T10:22:44Z
day: '02'
ddc:
- '575'
department:
- _id: JiFr
doi: 10.3390/cells10071665
ec_funded: 1
external_id:
  isi:
  - '000676604700001'
  pmid:
  - '34359847'
file:
- access_level: open_access
  checksum: 2a9f534b9c2200e72e2cde95afaf4eed
  content_type: application/pdf
  creator: cchlebak
  date_created: 2021-09-16T09:07:06Z
  date_updated: 2021-09-16T09:07:06Z
  file_id: '10021'
  file_name: 2021_Cells_Nikonorova.pdf
  file_size: 2667848
  relation: main_file
  success: 1
file_date_updated: 2021-09-16T09:07:06Z
has_accepted_license: '1'
intvolume: '        10'
isi: 1
keyword:
- primary root
- (phospho)proteomics
- auxin
- (receptor) kinase
language:
- iso: eng
month: '07'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
- _id: 3AC91DDA-15DF-11EA-824D-93A3E7B544D1
  call_identifier: FWF
  name: FWF Open Access Fund
publication: Cells
publication_identifier:
  issn:
  - 2073-4409
publication_status: published
publisher: MDPI
quality_controlled: '1'
related_material:
  record:
  - id: '10083'
    relation: dissertation_contains
    status: public
status: public
title: The Arabidopsis root tip (phospho)proteomes at growth-promoting versus growth-repressing
  conditions reveal novel root growth regulators
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: 10
year: '2021'
...
---
_id: '8949'
abstract:
- lang: eng
  text: <jats:p>Development of the nervous system undergoes important transitions,
    including one from neurogenesis to gliogenesis which occurs late during embryonic
    gestation. Here we report on clonal analysis of gliogenesis in mice using Mosaic
    Analysis with Double Markers (MADM) with quantitative and computational methods.
    Results reveal that developmental gliogenesis in the cerebral cortex occurs in
    a fraction of earlier neurogenic clones, accelerating around E16.5, and giving
    rise to both astrocytes and oligodendrocytes. Moreover, MADM-based genetic deletion
    of the epidermal growth factor receptor (Egfr) in gliogenic clones revealed that
    Egfr is cell autonomously required for gliogenesis in the mouse dorsolateral cortices.
    A broad range in the proliferation capacity, symmetry of clones, and competitive
    advantage of MADM cells was evident in clones that contained one cellular lineage
    with double dosage of Egfr relative to their environment, while their sibling
    Egfr-null cells failed to generate glia. Remarkably, the total numbers of glia
    in MADM clones balance out regardless of significant alterations in clonal symmetries.
    The variability in glial clones shows stochastic patterns that we define mathematically,
    which are different from the deterministic patterns in neuronal clones. This study
    sets a foundation for studying the biological significance of stochastic and deterministic
    clonal principles underlying tissue development, and identifying mechanisms that
    differentiate between neurogenesis and gliogenesis.</jats:p>
acknowledgement: This research was funded by grants from the National Institutes of
  Health to H.T.G. (R01NS098370 and R01NS089795). C.V.M. was supported by a National
  Science Foundation Graduate Research Fellowship (DGE-1746939). R.B. was supported
  by the FWF Lise-Meitner program (M 2416), and S.H. was supported by the European
  Research Council (ERC) under the European Union’s Horizon 2020 research and innovation
  programme (grant agreement No 725780 LinPro).The authors thank members of the Ghashghaei
  lab for discussions, technical support, and help with preparation of the manuscript.
article_number: '2662'
article_processing_charge: No
article_type: original
author:
- first_name: Xuying
  full_name: Zhang, Xuying
  last_name: Zhang
- first_name: Christine V.
  full_name: Mennicke, Christine V.
  last_name: Mennicke
- first_name: Guanxi
  full_name: Xiao, Guanxi
  last_name: Xiao
- first_name: Robert J
  full_name: Beattie, Robert J
  id: 2E26DF60-F248-11E8-B48F-1D18A9856A87
  last_name: Beattie
  orcid: 0000-0002-8483-8753
- first_name: Mansoor
  full_name: Haider, Mansoor
  last_name: Haider
- first_name: Simon
  full_name: Hippenmeyer, Simon
  id: 37B36620-F248-11E8-B48F-1D18A9856A87
  last_name: Hippenmeyer
  orcid: 0000-0003-2279-1061
- first_name: H. Troy
  full_name: Ghashghaei, H. Troy
  last_name: Ghashghaei
citation:
  ama: Zhang X, Mennicke CV, Xiao G, et al. Clonal analysis of gliogenesis in the
    cerebral cortex reveals stochastic expansion of glia and cell autonomous responses
    to Egfr dosage. <i>Cells</i>. 2020;9(12). doi:<a href="https://doi.org/10.3390/cells9122662">10.3390/cells9122662</a>
  apa: Zhang, X., Mennicke, C. V., Xiao, G., Beattie, R. J., Haider, M., Hippenmeyer,
    S., &#38; Ghashghaei, H. T. (2020). Clonal analysis of gliogenesis in the cerebral
    cortex reveals stochastic expansion of glia and cell autonomous responses to Egfr
    dosage. <i>Cells</i>. MDPI. <a href="https://doi.org/10.3390/cells9122662">https://doi.org/10.3390/cells9122662</a>
  chicago: Zhang, Xuying, Christine V. Mennicke, Guanxi Xiao, Robert J Beattie, Mansoor
    Haider, Simon Hippenmeyer, and H. Troy Ghashghaei. “Clonal Analysis of Gliogenesis
    in the Cerebral Cortex Reveals Stochastic Expansion of Glia and Cell Autonomous
    Responses to Egfr Dosage.” <i>Cells</i>. MDPI, 2020. <a href="https://doi.org/10.3390/cells9122662">https://doi.org/10.3390/cells9122662</a>.
  ieee: X. Zhang <i>et al.</i>, “Clonal analysis of gliogenesis in the cerebral cortex
    reveals stochastic expansion of glia and cell autonomous responses to Egfr dosage,”
    <i>Cells</i>, vol. 9, no. 12. MDPI, 2020.
  ista: Zhang X, Mennicke CV, Xiao G, Beattie RJ, Haider M, Hippenmeyer S, Ghashghaei
    HT. 2020. Clonal analysis of gliogenesis in the cerebral cortex reveals stochastic
    expansion of glia and cell autonomous responses to Egfr dosage. Cells. 9(12),
    2662.
  mla: Zhang, Xuying, et al. “Clonal Analysis of Gliogenesis in the Cerebral Cortex
    Reveals Stochastic Expansion of Glia and Cell Autonomous Responses to Egfr Dosage.”
    <i>Cells</i>, vol. 9, no. 12, 2662, MDPI, 2020, doi:<a href="https://doi.org/10.3390/cells9122662">10.3390/cells9122662</a>.
  short: X. Zhang, C.V. Mennicke, G. Xiao, R.J. Beattie, M. Haider, S. Hippenmeyer,
    H.T. Ghashghaei, Cells 9 (2020).
date_created: 2020-12-14T08:04:03Z
date_published: 2020-12-11T00:00:00Z
date_updated: 2023-08-24T10:57:48Z
day: '11'
ddc:
- '570'
department:
- _id: SiHi
doi: 10.3390/cells9122662
ec_funded: 1
external_id:
  isi:
  - '000601787300001'
file:
- access_level: open_access
  checksum: 5095cbdc728c9a510c5761cf60a8861c
  content_type: application/pdf
  creator: dernst
  date_created: 2020-12-14T08:09:43Z
  date_updated: 2020-12-14T08:09:43Z
  file_id: '8950'
  file_name: 2020_Cells_Zhang.pdf
  file_size: 3504525
  relation: main_file
  success: 1
file_date_updated: 2020-12-14T08:09:43Z
has_accepted_license: '1'
intvolume: '         9'
isi: 1
issue: '12'
language:
- iso: eng
month: '12'
oa: 1
oa_version: Published Version
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  call_identifier: FWF
  grant_number: M02416
  name: Molecular Mechanisms Regulating Gliogenesis in the Cerebral Cortex
- _id: 260018B0-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '725780'
  name: Principles of Neural Stem Cell Lineage Progression in Cerebral Cortex Development
publication: Cells
publication_identifier:
  issn:
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publication_status: published
publisher: MDPI
quality_controlled: '1'
status: public
title: Clonal analysis of gliogenesis in the cerebral cortex reveals stochastic expansion
  of glia and cell autonomous responses to Egfr dosage
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: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 9
year: '2020'
...
