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1.

001-es BibID:BIBFORM067884
Első szerző:Bácskai Tímea (biológus, neurobiológus)
Cím:Effect of fluorokinolone treatment on the peptidergic innervation of the salivary glands / Tímea Bácskai, Barna Kelentey, Ádám Deák, Tivadar Zelles, Boglárka Skopkó, Klara Matesz
Dátum:2010
Megjegyzések:Fluorokinolones (i.e. Peflacine, PEF) are used in the dental and medical therapy. It was demonstrated that chronic treatment on the rats resulted in disturbance in the secretory function of the salivary glands accompanied by the morphological sign of atrophy in the secretory units. The mechanism of this impairment is unknown. Because the peripheral neuropathy was previously described as the toxic side effect of the chronic PEF treatment we proposed that the morphological and functional disorder of salivary glands developed on the basis of a neuronal disorder. Earlier studies described, that the mast cells could release nerve growth factor (NGF), which is important in the surviving of neurons. The lack of NGF results degenerative processes in the peripheral neurons which can change the expression of neuropeptides (i.e. serotonine, SER). The aim of this study was to determine the number of mast cells and the qualitative and quantitative changes of SER immunoreactive (IR) nerve terminals in the salivary glands after PEF treatment. Adult rats were treated with PEF for 3 and 7 days. For the visualization of mast cell we have used Toluidine blue staining. Immunohistochemical methods were used to detect the SER containing fibers on the salivary glands. After the chronic treatment we could detect the increased number of mast cells which supports the protective role of the NGF. The number of SER IR fibers decreased compared to the control. The changes in the number of IR fibers support our previous results, that local denervation of salivary gland can cause the atrophy of the acini.
taa (hibás)
Tárgyszavak:Orvostudományok Elméleti orvostudományok idézhető absztrakt
saliva
Megjelenés:Frontiers in Neuroscience 2010 (2010), p. 1. -
További szerzők:Kelentey Barna (1959-) (fogszakorvos) Deák Ádám (1974-) (állatorvos) Zelles Tivadar Skopkó Boglárka Emese (1986-) (fogszakorvos) Matesz Klára (1949-) (anatómus, neurobiológus)
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2.

001-es BibID:BIBFORM095571
035-os BibID:(WoS)000627328400001 (Scopus)85102438552 (PubMed)33716672 (cikkazonosító)614947
Első szerző:Bayasgalan, Tsogbadrakh (Általános orvos)
Cím:Topographical Organization of M-Current on Dorsal and Median Raphe Serotonergic Neurons / Tsogbadrakh Bayasgalan, Andrea Csemer, Adrienn Kovacs, Krisztina Pocsai, Balazs Pal
Dátum:2021
ISSN:1662-5102
Megjegyzések:Dorsal and median raphe nuclei (DR and MR, respectively) are members of the reticular activating system and play important role in the regulation of the sleepwakefulness cycle, movement, and affective states. M-current is a voltage-gated potassium current under the control of neuromodulatory mechanisms setting neuronal excitability. Our goal was to determine the proportion of DR and MR serotonergic neurons possessing M-current and whether they are organized topographically. Electrophysiological parameters of raphe serotonergic neurons influenced by this current were also investigated. We performed slice electrophysiology on genetically identified serotonergic neurons. Neurons with M-current are located rostrally in the DR and dorsally in the MR. M-current determines firing rate, afterhyperpolarization amplitude, and adaptation index (AI) of these neurons, but does not affect input resistance, action potential width, and high threshold oscillations.These findings indicate that M-current has a strong impact on firing properties of certain serotonergic neuronal subpopulations and it might serve as an effective contributor to cholinergic and local serotonergic neuromodulatory actions.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Frontiers in Cellular Neuroscience. - 15 (2021), p. 614947. -
További szerzők:Csemer Andrea (1994-) (molekuláris biológus) Kovács Adrienn (1989-) (molekuláris biológus) Pocsai Krisztina (1978-) (élettanász) Pál Balázs (1975-) (élettanász)
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Intézményi repozitóriumban (DEA) tárolt változat
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3.

001-es BibID:BIBFORM095575
035-os BibID:(cikkazonosító)707789 (WoS)000683012200001 (Scopus)85112145519 (PubMed)34381336
Első szerző:Bayasgalan, Tsogbadrakh (Általános orvos)
Cím:Alteration of mesopontine cholinergic function by the lack of KCNQ4 subunit / Bayasgalan T., Stupniki S., Kovács A., Csemer A., Szentesi P., Pocsai K., Dionisio L., Spitzmaul G., Pál B.
Dátum:2021
ISSN:1662-5102
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Frontiers in Cellular Neuroscience. - 15 (2021), p. 707789. -
További szerzők:Stupniki, S. Kovács Adrienn (1989-) (molekuláris biológus) Csemer Andrea (1994-) (molekuláris biológus) Szentesi Péter (1967-) (élettanász) Pocsai Krisztina (1978-) (élettanász) Dionisio, L. Spitzmaul, G. Pál Balázs (1975-) (élettanász)
Internet cím:Intézményi repozitóriumban (DEA) tárolt változat
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4.

001-es BibID:BIBFORM060223
Első szerző:Bordás Csilla
Cím:The M-current contributes to high threshold membrane potential oscillations in a cell type-specific way in the pedunculopontine nucleus of mice / Bordas Csilla, Kovacs Adrienn, Pal Balazs
Dátum:2015
ISSN:1662-5102
Megjegyzések:The pedunculopontine nucleus is known as a cholinergic nucleus of the reticular activating system, participating in regulation of sleep and wakefulness. Besides cholinergic neurons, it consists of GABAergic and glutamatergic neurons as well. According to classical and recent studies, more subgroups of neurons were defined. Groups based on the neurotransmitter released by a neuron are not homogenous, but can be further subdivided. The PPN neurons do not only provide cholinergic and non-cholinergic inputs to several subcortical brain areas but they are also targets of cholinergic and other different neuromodulatory actions. Although cholinergic neuromodulation has been already investigated in the nucleus, one of its characteristic targets, the M-type potassium current has not been described yet. Using slice electrophysiology, we provide evidence in the present work that cholinergic neurons possess M-current, whereas GABAergic neurons lack it. The M-current contributes to certain functional differences of cholinergic and GABAergic neurons, as spike frequency adaptation, action potential firing frequency or the amplitude difference of medium afterhyperpolarizations (AHPs). Furthermore, we showed that high threshold membrane potential oscillation with high power, around 20 Hz frequency is a functional property of almost all cholinergic cells, whereas GABAergic neurons have only low amplitude oscillations. Blockade of the M-current abolished the oscillatory activity at 20 Hz, and largely diminished it at other frequencies. Taken together, the M-current seems to be characteristic for PPN cholinergic neurons. It provides a possibility for modulating gamma band activity of these cells, thus contributing to neuromodulatory regulation of the reticular activating system.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
M-current
Neuromodulation
oscillatory activity
pedunculopontine nucleus
spike frequency adaptation
Megjelenés:Frontiers in Cellular Neuroscience. - 9 (2015), Article ID 121. -
További szerzők:Kovács Adrienn (1989-) (molekuláris biológus) Pál Balázs (1975-) (élettanász)
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Intézményi repozitóriumban (DEA) tárolt változat
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5.

001-es BibID:BIBFORM067497
Első szerző:Dócs Klaudia (orvos)
Cím:The Ratio of 2-AG to Its Isomer 1-AG as an Intrinsic Fine Tuning Mechanism of CB1 Receptor Activation / Klaudia Dócs, Zoltán Mészár, Sándor Gonda, Attila Kiss-Szikszai, Krisztina Holló, Miklós Antal, Zoltán Hegyi
Dátum:2017
ISSN:1662-5102
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Frontiers in Cellular Neuroscience. - 11 (2017), p. 1-13. -
További szerzők:Mészár Zoltán Mihály (1977-) (agrármérnök) Gonda Sándor (1984-) (gyógyszerész) Kiss-Szikszai Attila (1975-) (vegyész) Holló Krisztina (1967-) (vegyész) Antal Miklós (1951-) (orvos, anatómus) Hegyi Zoltán (1983-) (molekuláris biológus)
Pályázati támogatás:MTA-TKI 242
MTA
KTIA_NAP_13-1-2013-001
Egyéb
PD 108467
OTKA
Internet cím:DOI
Intézményi repozitóriumban (DEA) tárolt változat
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6.

001-es BibID:BIBFORM109585
035-os BibID:(cikkazonosító)1115685 (Scopus)85150718609 (WoS)000951373400001
Első szerző:Ducza László (molekuláris biológus)
Cím:Neuronal P2X4 receptor may contribute to peripheral inflammatory pain in rat spinal dorsal horn / Ducza László, Gajtkó Andrea, Hegedűs Krisztina, Bakk Erzsébet, Kis Gréta, Gaál Botond, Takács Roland, Szücs Péter, Matesz Klára, Holló Krisztina
Dátum:2023
ISSN:1662-5099
Megjegyzések:Objective: Intense inflammation may result in pain, which manifests as spinal central sensitization. There is growing evidence that purinergic signaling plays a pivotal role in the orchestration of pain processing. Over the last decade the ionotropic P2X purino receptor 4 (P2X4) got into spotlight in neuropathic disorders, however its precise spinal expression was scantily characterized during inflammatory pain. Thus, we intended to analyze the receptor distribution within spinal dorsal horn and lumbar dorsal root ganglia (DRG) of rats suffering in inflammatory pain induced by complete Freund adjuvant (CFA). Methods: CFA-induced peripheral inflammation was validated by mechanical and thermal behavioral tests. In order to ensure about the putative alteration of spinal P2X4 receptor gene expression qPCR reactions were designed, followed by immunoperoxidase and Western blot experiments to assess changes at a protein level. Colocalization of P2X4 with neuronal and glial markers was investigated by double immunofluorescent labelings, which were subsequently analyzed with IMARIS software. Transmission electronmicroscopy was applied to study the ultrastructural localization of the receptor. Concurrently, in lumbar DRG cells similar methodology has been carried out to complete our observations. Results: The figures of mechanical and thermal behavioral tests proved the establishment of CFA-induced inflammatory pain. We observed significant enhancement of P2X4 transcript level within the spinal dorsal horn 3?days upon CFA administration. Elevation of P2X4 immunoreactivity within Rexed lamina I-II of the spinal gray matter was synchronous with mRNA expression, and confirmed by protein blotting. According to IMARIS analysis the robust protein increase was mainly detected on primary afferent axonterminals and GFAP-labelled astrocyte membrane compartments, but not on postsynaptic dendrites was also validated ultrastructurally within the spinal dorsal horn. Furthermore, lumbar DRG analysis demonstrated that peptidergic and non-peptidergic nociceptive subsets of ganglia cells were also abundantly positive for P2X4 receptor in CFA model. Conclusion: Here we provide novel evidence about involvement of neuronal and glial P2X4 receptor in the establishment of inflammatory pain.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
inflammatory pain
spinal dorsal horn
P2X4 receptor
central sensitization
primary afferents
glial cells
dorsal root ganglia
Megjelenés:Frontiers in Molecular Neuroscience. - 16 (2023), p. 1-16. -
További szerzők:Gajtkó Andrea (1989-) (molekuláris biológus) Hegedűs Krisztina Bakk Erzsébet Kis Gréta (1979-) (molekuláris biológus) Gaál Botond Ágoston (1982-) (anatómus, neurobiológus) Takács Roland Ádám (1985-) (molekuláris biológus, biokémikus) Szűcs Péter (1974-) (kutatóorvos) Matesz Klára (1949-) (anatómus, neurobiológus) Holló Krisztina (1967-) (vegyész)
Pályázati támogatás:KTIA_NAP_13-2-2014-0005
Egyéb
2017-1.2.1-NKP-2017-00002
Egyéb
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Intézményi repozitóriumban (DEA) tárolt változat
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7.

001-es BibID:BIBFORM099581
035-os BibID:(WoS)000748044100001 (Scopus)85123453367
Első szerző:Girgis, Michael Magdy Fahmy (Gyógyszerész)
Cím:Use of complementary and alternative medicine among patients with epilepsy and diabetes mellitus, focusing on the outcome of treatment / Michael Magdy Fahmy Girgis, Klára Fekete, Nóra Homoródi, Sándor Márton, István Fekete, László Horváth
Dátum:2022
ISSN:1662-453X
Megjegyzések:Introduction Millions all over the world live with epilepsy and they may require long-term drug treatment. The use and interest in complementary and alternative medicine (CAM) have grown over the previous years. Co-administration of herbal products with medicines may result in adverse drug reactions (ADR) and/or unfavourable interactions. The aims of this study were to determine the prevalence of CAM use among patients with epilepsy and, also, to compare the results to those of the patients with diabetes mellitus (DM); to reveal factors that may drive the use of CAM; and to measure outcomes and adherence. It was also our intent to have state-of-art information of CAM use in our region among patients with the two diseases above. Methods We conducted a non-interventional study using a self-developed questionnaire. It was distributed among adult patients with either epilepsy or diabetes mellitus who also suffered from cardiovascular consequences. A database was compiled from the anonymous questionnaires, filled in voluntarily by the patients. Basic statistics were used to analyse this database. Results A total of 227 questionnaires were filled in by 127 patients (55.9%) with epilepsy and 100 patients (44.1%) with diabetes mellitus. Mean age was 54.54?17.33 years. Of the patients, 50.2% were male. Average body weight was 80.3?17.3 kg. Of the patients, 22 (9.7%) used CAM because they believed in CAM. Two of them reported ADR. Among the patients with epilepsy, the ratio was only 7.9% compared to 12% among those with diabetes mellitus. While the number of CAM users was higher among younger patients with epilepsy, it was the elderly patients with diabetes mellitus who tended to use CAM. Conclusion Attention should be paid to reliance on CAM during the follow-up. Our finding that health-conscious patients tend to use CAM more often (than the general population) may indicate it is necessary to discuss CAM usage sincerely. CAMs modulating CYPs enzymes were the most common, leading to interactions with medication used and resulting in ADR. This shows the importance of educating patients and treating team including clinical pharmacist in this field is essential.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Frontiers in Neuroscience. - 15 (2022), p. 1-12. -
További szerzők:Fekete Klára (1978-) (neurológus) Homoródi Nóra (1974-) (kardiológus) Márton Sándor (1965-) (matematikus) Fekete István (1951-) (neurológus, pszichiáter) Horváth László (1973-) (gyógyszerész)
Internet cím:DOI
Intézményi repozitóriumban (DEA) tárolt változat
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8.

001-es BibID:BIBFORM082383
035-os BibID:(cikkazonosító)551
Első szerző:Kattuah, Wejdan
Cím:Heterogeneous Nuclear Ribonucleoprotein E2 (hnRNP E2) Is a Component of TDP-43 Aggregates Specifically in the A and C Pathological Subtypes of Frontotemporal Lobar Degeneration / Wejdan Kattuah, Boris Rogelj, Andrew King, Christopher E. Shaw, Tibor Hortobágyi, Claire Troakes
Dátum:2019
ISSN:1662-453X
Megjegyzések:TAR DNA-binding protein 43 (TDP-43) is the major component of the ubiquitin-positive protein aggregates seen in the majority of frontotemporal lobar degeneration and amyotrophic lateral sclerosis cases. TDP-43 belongs to the heterogeneous nuclear ribonucleoprotein (hnRNP) family that is involved in the regulation of RNA transcription, splicing, transport and translation. There are a great many hnRNPs, which often have overlapping functions and act cooperatively in RNA processing. Here we demonstrate that another hnRNP family member, hnRNP E2, shows a striking accumulation within dystrophic neurites and cytoplasmic inclusions in the frontal cortex and hippocampus of a subset of FTLD-TDP cases belonging to pathological subtypes A and C, where hnRNP E2 was found to co-localize with 87% of TDP-43 immunopositive inclusions. hnRNP E2-positive inclusions were not seen in FTLD-TDP cases with the C9orf72 expansion or in any other neurodegenerative disorders examined. This interaction with TDP-43 in specific FTLD subtypes suggests different underlying neurodegenerative pathways.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Frontiers in Neuroscience. - 13 (2019), p. 1-11. -
További szerzők:Rogelj, Boris King, Andrew Shaw, Christopher E. Hortobágyi Tibor (1965-) (patológus) Troakes, Claire
Pályázati támogatás:2017-1.2.1-NKP-2017-00002
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9.

001-es BibID:BIBFORM070540
Első szerző:Kovács Adrienn (molekuláris biológus)
Cím:Astrocyte-Dependent Slow Inward Currents (SICs) Participate in Neuromodulatory Mechanisms in the Pedunculopontine Nucleus (PPN) / Kovács Adrienn, Pál Balázs
Dátum:2017
Megjegyzések:Slow inward currents (SICs) are known as excitatory events of neurons caused by astrocytic glutamate release and consequential activation of neuronal extrasynaptic NMDA receptors. In the present article we investigate the role of these astrocyte-dependent excitatory events on a cholinergic nucleus of the reticular activating system (RAS), the pedunculopontine nucleus (PPN). It is well known about this and other elements of the RAS, that they do not only give rise to neuromodulatory innervation of several areas, but also targets neuromodulatory actions from other members of the RAS or factors providing the homeostatic drive for sleep. Using slice electrophysiology, optogenetics and morphological reconstruction, we revealed that SICs are present in a population of PPN neurons. The frequency of SICs recorded on PPN neurons was higher when the soma of the given neuron was close to an astrocytic soma. SICs do not appear simultaneously on neighboring neurons, thus it is unlikely that they synchronize neuronal activity in this structure. Occurrence of SICs is regulated by cannabinoid, muscarinic and serotonergic neuromodulatory mechanisms. In most cases, SICs occurred independently from tonic neuronal currents. SICs were affected by different neuromodulatory agents in a rather uniform way: if control SIC activity was low, the applied drugs increased it, but if SIC activity was increased in control, the same drugs lowered it. SICs of PPN neurons possibly represent a mechanism which elicits network-independent spikes on certain PPN neurons; forming an alternative, astrocyte-dependent pathway of neuromodulatory mechanisms.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
astrocyte
neuromodulation
optogenetics
pedunculopontine nucleus
slow inward current
Megjelenés:Frontiers in cellular neuroscience. - 11 : 16 (2017), p. 1-16. -
További szerzők:Pál Balázs (1975-) (élettanász)
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Intézményi repozitóriumban (DEA) tárolt változat
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10.

001-es BibID:BIBFORM062053
Első szerző:Pál Balázs (élettanász)
Cím:Astrocytic Actions on Extrasynaptic Neuronal Currents / Balázs Pál
Dátum:2015
ISSN:1662-5102
Megjegyzések:In the last few decades, knowledge about astrocytic functions has significantly increased. It was demonstrated that astrocytes are not passive elements of the central nervous system (CNS), but active partners of neurons. There is a growing body of knowledge about the calcium excitability of astrocytes, the actions of different gliotransmitters and their release mechanisms, as well as the participation of astrocytes in the regulation of synaptic functions and their contribution to synaptic plasticity. However, astrocytic functions are even more complex than being a partner of the "tripartite synapse," as they can influence extrasynaptic neuronal currents either by releasing substances or regulating ambient neurotransmitter levels. Several types of currents or changes of membrane potential with different kinetics and via different mechanisms can be elicited by astrocytic activity. Astrocyte-dependent phasic or tonic, inward or outward currents were described in several brain areas. Such currents, together with the synaptic actions of astrocytes, can contribute to neuromodulatory mechanisms, neurosensory and -secretory processes, cortical oscillatory activity, memory, and learning or overall neuronal excitability. This mini-review is an attempt to give a brief summary of astrocyte-dependent extrasynaptic neuronal currents and their possible functional significance.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
astrocyte-neuron interactions
gliotransmitters
slow inward current
slow outward current
tonic current
Megjelenés:Frontiers in Cellular Neuroscience. - 9 : 474(2015), p. 1-11. -
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Intézményi repozitóriumban (DEA) tárolt változat
Borító:

11.

001-es BibID:BIBFORM100951
035-os BibID:(Scopus)85127948706 (cikkazonosító)803356
Első szerző:Papp Tamás (orvos)
Cím:Ultrasound Used for Diagnostic Imaging Facilitates Dendritic Branching of Developing Neurons in the Mouse Cortex / Tamas Papp, Zsuzsanna Ferenczi, Bernadette Szilagyi, Matyas Petro, Angelika Varga, Eva Kókai, Ervin Berenyi, Gabor Olah, Gabor Halmos, Peter Szucs, Zoltan Meszar
Dátum:2022
ISSN:1662-453X
Tárgyszavak:Orvostudományok Gyógyszerészeti tudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Frontiers in Neuroscience. - 16 (2022), 803356. -
További szerzők:Ferenczi Zsuzsanna Szilágyi Bernadett (1993-) Petró Mátyás (1985-) (radiológus) Varga Angelika (1977-) (biológus) Kókai Éva (1989-) (molekuláris biológus) Berényi Ervin (1964-) (radiológus) Oláh Gábor (1987-) (gyógyszerész) Halmos Gábor (1962-) (gyógyszerész, receptorfarmakológus, experimentális onkológus) Szűcs Péter (1974-) (kutatóorvos) Mészár Zoltán Mihály (1977-) (agrármérnök)
Pályázati támogatás:TKP2021-EGA-20
Egyéb
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Intézményi repozitóriumban (DEA) tárolt változat
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12.

001-es BibID:BIBFORM091619
035-os BibID:(cikkazonosító)243
Első szerző:Perényi Helga
Cím:Physical Activity Protects the Pathological Alterations of Alzheimer's Disease Kidneys via the Activation of PACAP and BMP Signaling Pathways / Perényi Helga, Szegeczki Vince, Horváth Gabriella, Hinnah Barbara, Tamás Andrea, Radák Zsolt, Ábrahám Dóra, Zákány Róza, Reglodi Dora, Juhász Tamás
Dátum:2020
ISSN:1662-5102 1662-5102
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Frontiers in Cellular Neuroscience. - 14 (2020), p. 1-14. -
További szerzők:Szegeczki Vince (1992-) Horváth Gabriella Hinnah Barbara Tamás Andrea (Idegtudomány) (Pécs) Radák Zsolt Ábrahám Dóra Zákány Róza (1963-) (anatómus-, kötőszövetbiológus) Reglődi Dóra (Idegtudományok) Juhász Tamás (1976-) (biológus, orvosbiológus)
Pályázati támogatás:Bridging Fund
OTKA
NKFIK115874
OTKA
PD109644
OTKA
K119759
OTKA
NKFIHFK129190
NKFIH
GINOP2.3.2-15-2016-00050
GINOP
UNKP-16-4-IV
Egyéb
EFOP-3.6.2-16-2017-00008
EFOP
EFOP3.6.3-VEKOP-16-2017-00009
EFOP
EFOP-3.6.1.-16-2016-00004
EFOP
OTKA-NN 114458
OTKA
TÁMOP 4.2.4
TÁMOP
ÚNKP-19-3
Egyéb
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Intézményi repozitóriumban (DEA) tárolt változat
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