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  1. Article ; Online: Stress Resilience is Associated with Hippocampal Synaptoprotection in the Female Rat Learned Helplessness Paradigm.

    Huzian, Orsolya / Baka, Judith / Csakvari, Eszter / Dobos, Nikoletta / Leranth, Csaba / Siklos, Laszlo / Duman, Ronald S / Farkas, Tamas / Hajszan, Tibor

    Neuroscience

    2021  Volume 459, Page(s) 85–103

    Abstract: The synaptogenic hypothesis of major depressive disorder implies that preventing the onset of depressive-like behavior also prevents the loss of hippocampal spine synapses. By applying the psychoactive drugs, diazepam and fluoxetine, we investigated ... ...

    Abstract The synaptogenic hypothesis of major depressive disorder implies that preventing the onset of depressive-like behavior also prevents the loss of hippocampal spine synapses. By applying the psychoactive drugs, diazepam and fluoxetine, we investigated whether blocking the development of helpless behavior by promoting stress resilience in the rat learned helplessness paradigm is associated with a synaptoprotective action in the hippocampus. Adult ovariectomized and intact female Sprague-Dawley rats (n = 297) were treated with either diazepam, fluoxetine, or vehicle, exposed to inescapable footshocks or sham stress, and tested in an active escape task to assess helpless behavior. Escape-evoked corticosterone secretion, as well as remodeling of hippocampal spine synapses at a timepoint representing the onset of escape testing were also analyzed. In ovariectomized females, treatment with diazepam prior to stress exposure prevented helpless behavior, blocked the loss of hippocampal spine synapses, and muted the corticosterone surge evoked by escape testing. Although fluoxetine stimulated escape performance and hippocampal synaptogenesis under non-stressed conditions, almost all responses to fluoxetine were abolished following exposure to inescapable stress. Only a much higher dose of fluoxetine was capable of partly reproducing the strong protective actions of diazepam. Importantly, these protective actions were retained in the presence of ovarian hormones. Our findings indicate that stress resilience is associated with the preservation of spine synapses in the hippocampus, raising the possibility that, besides synaptogenesis, hippocampal synaptoprotection is also implicated in antidepressant therapy.
    MeSH term(s) Animals ; Depressive Disorder, Major ; Disease Models, Animal ; Female ; Fluoxetine/pharmacology ; Helplessness, Learned ; Hippocampus ; Rats ; Rats, Sprague-Dawley
    Chemical Substances Fluoxetine (01K63SUP8D)
    Language English
    Publishing date 2021-01-30
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 196739-3
    ISSN 1873-7544 ; 0306-4522
    ISSN (online) 1873-7544
    ISSN 0306-4522
    DOI 10.1016/j.neuroscience.2021.01.029
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The targeted LHRH analog AEZS-108 alters expression of genes related to angiogenesis and development of metastasis in uveal melanoma.

    Fodor, Klara / Dobos, Nikoletta / Schally, Andrew / Steiber, Zita / Olah, Gabor / Sipos, Eva / Szekvolgyi, Lorant / Halmos, Gabor

    Oncotarget

    2020  Volume 11, Issue 2, Page(s) 175–187

    Abstract: Uveal melanoma (UM) is the most common malignant tumor of the eye. Recently, we have established that 46% of UM specimens express LHRH receptors. This finding supports the idea of a LHRH receptor-targeted therapy of UM patients. Cytotoxic analog of LHRH, ...

    Abstract Uveal melanoma (UM) is the most common malignant tumor of the eye. Recently, we have established that 46% of UM specimens express LHRH receptors. This finding supports the idea of a LHRH receptor-targeted therapy of UM patients. Cytotoxic analog of LHRH, AEZS-108 exhibits effective anti-cancer activity in LHRH-receptor positive cancers. AEZS-108 is a hybrid molecule, composed of a synthetic peptide carrier and the cytotoxic doxorubicin (DOX). In the present study, we investigated AEZS-108 induced cytotoxicity and the altered mRNA expression profile of regulatory factors related to angiogenesis and metastasis in LHRH receptor positive OCM3 cells. Our results show that AEZS-108 upregulates the expression of
    Language English
    Publishing date 2020-01-14
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2560162-3
    ISSN 1949-2553 ; 1949-2553
    ISSN (online) 1949-2553
    ISSN 1949-2553
    DOI 10.18632/oncotarget.27431
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Expression of Luteinizing Hormone-Releasing Hormone (LHRH) and Type-I LHRH Receptor in Transitional Cell Carcinoma Type of Human Bladder Cancer.

    Szabó, Zsuzsanna / Dezső, Balázs / Fodor, Klára / Szegedi, Krisztián / Flaskó, Tibor / Szabó, Erzsébet / Oláh, Gábor / Sipos, Éva / Dobos, Nikoletta / Gardi, János / Schally, Andrew V / Halmos, Gábor

    Molecules (Basel, Switzerland)

    2021  Volume 26, Issue 5

    Abstract: Bladder cancer (BC) is the tenth most frequently detected cancer in both sexes. Type-I luteinizing hormone-releasing hormone (LHRH) receptor (LHRH-R-I) is expressed not only in the pituitary, but also in several types of cancer disease. There are few ... ...

    Abstract Bladder cancer (BC) is the tenth most frequently detected cancer in both sexes. Type-I luteinizing hormone-releasing hormone (LHRH) receptor (LHRH-R-I) is expressed not only in the pituitary, but also in several types of cancer disease. There are few data about LHRH-R-I expression in human BC. This study aimed to investigate the expression of LHRH and LHRH-R-I in the transitional cell carcinoma (TCC) type of human BC. RNA was extracted from 24 human bladder tumor specimens and three BC cell lines. RT-PCR was performed to detect mRNA for LHRH and LHRH-R-I. The protein of LHRH-R-I was further studied by immunohistochemistry (IHC), ligand competition assay, and Western Blot. PCR products of LHRH were found in 19 of 24 (79%) specimens and mRNA of LHRH-R-I was detected in 20 of 24 specimens (83%). Positive immunostaining for LHRH-R-I with different expression intensity was found in all samples examined, showing negative correlation with TCC grade. Radioligand binding studies also showed the presence of specific LHRH-R-I and high affinity binding of LHRH analogs. The high incidence of LHRH-R in BC suggests that it could serve as a molecular target for therapy of human BC with cytotoxic LHRH analogs or modern powerful antagonistic analogs of LHRH.
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Carcinoma, Transitional Cell/drug therapy ; Carcinoma, Transitional Cell/epidemiology ; Carcinoma, Transitional Cell/genetics ; Carcinoma, Transitional Cell/pathology ; Cell Line, Tumor ; Doxorubicin/administration & dosage ; Female ; Gene Expression Regulation, Neoplastic/drug effects ; Gonadotropin-Releasing Hormone/genetics ; Humans ; Male ; Middle Aged ; RNA, Messenger/genetics ; Receptors, LHRH/genetics ; Urinary Bladder Neoplasms/drug therapy ; Urinary Bladder Neoplasms/epidemiology ; Urinary Bladder Neoplasms/genetics ; Urinary Bladder Neoplasms/pathology
    Chemical Substances RNA, Messenger ; Receptors, LHRH ; Gonadotropin-Releasing Hormone (33515-09-2) ; Doxorubicin (80168379AG)
    Language English
    Publishing date 2021-02-26
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1413402-0
    ISSN 1420-3049 ; 1431-5165 ; 1420-3049
    ISSN (online) 1420-3049
    ISSN 1431-5165 ; 1420-3049
    DOI 10.3390/molecules26051253
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  4. Article ; Online: Drugging the R-loop interactome: RNA-DNA hybrid binding proteins as targets for cancer therapy.

    Boros-Oláh, Beáta / Dobos, Nikoletta / Hornyák, Lilla / Szabó, Zoltán / Karányi, Zsolt / Halmos, Gábor / Roszik, Jason / Székvölgyi, Lóránt

    DNA repair

    2019  Volume 84, Page(s) 102642

    Abstract: Unravelling the origin of genetic alterations from point mutations to chromosomal rearrangements was greatly enhanced by the discovery of RNA-DNA hybrids (R-loops) that behave as hotspots of genomic instability in a variety of organisms. Current models ... ...

    Abstract Unravelling the origin of genetic alterations from point mutations to chromosomal rearrangements was greatly enhanced by the discovery of RNA-DNA hybrids (R-loops) that behave as hotspots of genomic instability in a variety of organisms. Current models suggest that uncontrolled R-loops are a hazard to genome integrity, therefore, identifying proteins that are involved in recognising and signalling R-loop structures are of key importance. Herein we analysed key RNA-DNA hybrid binding proteins in humans taking advantage of large-scale gene expression, survival rate, and drug-sensitivity data from cancer genomics databases. We show that expression of RNA-DNA hybrid binding proteins in various cancer types is associated with survival and may have contrasting outcomes in responding to therapeutic treatments. Based on the revealed pharmacogenomic landscape of human RNA-DNA hybrid binding proteins, we propose that R-loops and R-loop binding proteins are potentially relevant new epigenetic markers and therapeutic targets in multiple cancers.
    MeSH term(s) Antineoplastic Agents/pharmacology ; Cell Line, Tumor ; DNA-Binding Proteins/metabolism ; Genomic Instability ; Humans ; Neoplasms/genetics ; Protein Binding/drug effects ; R-Loop Structures ; RNA-Binding Proteins/metabolism
    Chemical Substances Antineoplastic Agents ; DNA-Binding Proteins ; RNA-Binding Proteins
    Language English
    Publishing date 2019-07-06
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2071608-4
    ISSN 1568-7856 ; 1568-7864
    ISSN (online) 1568-7856
    ISSN 1568-7864
    DOI 10.1016/j.dnarep.2019.102642
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Characterization of luteinizing hormone-releasing hormone receptor type I (LH-RH-I) as a potential molecular target in OCM-1 and OCM-3 human uveal melanoma cell lines.

    Sipos, Eva / Dobos, Nikoletta / Rozsa, David / Fodor, Klara / Olah, Gabor / Szabo, Zsuzsanna / Szekvolgyi, Lorant / Schally, Andrew V / Halmos, Gabor

    OncoTargets and therapy

    2018  Volume 11, Page(s) 933–941

    Abstract: Introduction: Uveal melanoma (UM) is the most common primary intraocular malignancy with very poor prognosis. Conventional chemotherapy only rarely prolongs the survival, therefore patients require novel treatment modalities. The discovery of specific ... ...

    Abstract Introduction: Uveal melanoma (UM) is the most common primary intraocular malignancy with very poor prognosis. Conventional chemotherapy only rarely prolongs the survival, therefore patients require novel treatment modalities. The discovery of specific receptors for hypothalamic hormones on cancer cells has led to the development of radiolabeled and cytotoxic hormone analogs.
    Materials and methods: In the present study, our aim was to investigate the expression of mRNA for receptors of luteinizing hormone-releasing hormone type I (LH-RH-I) and LH-RH ligand in OCM-1 and OCM-3 human uveal melanoma cell lines. The presence and binding characteristics of LH-RH-I receptor protein was further studied by Western blot, immunocytochemistry and ligand competition assay. The expression of mRNA and protein for LH-RH-I receptors has been also studied using tumor samples originating from nude mice xenografted with OCM-1 or OCM-3 cells.
    Results: The mRNA for LH-RH-I receptor has been detected in OCM-1 and OCM-3 cell lines and was found markedly higher in OCM-3 cells. The mRNA for LH-RH-I receptors was also observed in both UM xenograft models in vivo with higher levels in OCM-3. The presence of LH-RH-I receptor protein was found in both cell lines in vitro by immunocytochemistry and Western blot, and also in tumor tissue samples grown in nude mice by Western blot. Both human uveal melanoma models investigated showed specific high affinity receptors for LH-RH-I using ligand competition assay. The mRNA for LH-RH ligand has also been detected in OCM-1 and OCM-3 cell lines and cancer tissues.
    Conclusion: The demonstration of the expression of LH-RH-I receptors in OCM-1 and OCM-3 human UM cell lines suggests that they could serve as potential molecular target for therapy. Our findings support the development of new therapeutic approaches based on cytotoxic LH-RH analogs or modern powerful antagonistic analogs of LH-RH targeting LH-RH-I receptors in UM.
    Language English
    Publishing date 2018-02-22
    Publishing country New Zealand
    Document type Journal Article
    ZDB-ID 2495130-4
    ISSN 1178-6930
    ISSN 1178-6930
    DOI 10.2147/OTT.S148174
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  6. Article ; Online: Experimental therapy of doxorubicin resistant human uveal melanoma with targeted cytotoxic luteinizing hormone-releasing hormone analog (AN-152).

    Oláh, Gábor / Dobos, Nikoletta / Vámosi, György / Szabó, Zsuzsanna / Sipos, Éva / Fodor, Klára / Harda, Kristóf / Schally, Andrew V / Halmos, Gábor

    European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences

    2018  Volume 123, Page(s) 371–376

    Abstract: Background: Cytotoxic analogs of LHRH (luteinizing hormone-releasing hormone) can be successfully used for the treatment of hormone-dependent cancers such as prostatic, ovarian, endometrial, but our knowledge about their effect on hormone-independent ... ...

    Abstract Background: Cytotoxic analogs of LHRH (luteinizing hormone-releasing hormone) can be successfully used for the treatment of hormone-dependent cancers such as prostatic, ovarian, endometrial, but our knowledge about their effect on hormone-independent cancers such as human uveal melanoma (UM) is limited. Previously, we have demonstrated that 46% of UM express full-length LHRH receptors. This finding has led us to further examine the mechanism of action of LHRH receptor based targeted therapies in this malignancy.
    Aims: In the present study we investigated the cellular uptake of doxorubicin (DOX) and cytotoxic LHRH analog AN-152 (AEZS-108, zoptarelin doxorubicin) on human UM cell lines (OCM3) and its DOX resistant form OCM3
    Results: We were able to establish a new, stable and DOX resistant human UM cell line OCM3
    Conclusions: Our results suggest that the antiproliferative effect of AN-152 can be detected even if only LHRH receptor isoforms are expressed. Our study also demonstrates the LHRH receptor-mediated uptake of AN-152 in DOX resistant OCM3
    MeSH term(s) Antineoplastic Agents/metabolism ; Antineoplastic Agents/pharmacology ; Biological Transport ; Cell Line, Tumor ; Cell Proliferation/drug effects ; Doxorubicin/analogs & derivatives ; Doxorubicin/metabolism ; Doxorubicin/pharmacology ; Drug Resistance, Neoplasm ; Gonadotropin-Releasing Hormone/agonists ; Gonadotropin-Releasing Hormone/analogs & derivatives ; Gonadotropin-Releasing Hormone/genetics ; Gonadotropin-Releasing Hormone/metabolism ; Gonadotropin-Releasing Hormone/pharmacology ; Humans ; Melanoma/drug therapy ; Melanoma/genetics ; Melanoma/metabolism ; Melanoma/pathology ; Protein Isoforms ; Signal Transduction/drug effects ; Uveal Neoplasms/drug therapy ; Uveal Neoplasms/genetics ; Uveal Neoplasms/metabolism ; Uveal Neoplasms/pathology
    Chemical Substances Antineoplastic Agents ; Protein Isoforms ; LHRH, lysine(6)-doxorubicin (27844X2J29) ; Gonadotropin-Releasing Hormone (33515-09-2) ; Doxorubicin (80168379AG)
    Language English
    Publishing date 2018-08-02
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 1154366-8
    ISSN 1879-0720 ; 0928-0987
    ISSN (online) 1879-0720
    ISSN 0928-0987
    DOI 10.1016/j.ejps.2018.08.002
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  7. Article: The Role of Indoleamine-2,3-Dioxygenase in Cancer Development, Diagnostics, and Therapy.

    Hornyák, Lilla / Dobos, Nikoletta / Koncz, Gábor / Karányi, Zsolt / Páll, Dénes / Szabó, Zoltán / Halmos, Gábor / Székvölgyi, Lóránt

    Frontiers in immunology

    2018  Volume 9, Page(s) 151

    Abstract: Tumors are composed of abnormally transformed cell types and tissues that differ from normal tissues in their genetic and epigenetic makeup, metabolism, and immunology. Molecular compounds that modulate the immune response against neoplasms offer ... ...

    Abstract Tumors are composed of abnormally transformed cell types and tissues that differ from normal tissues in their genetic and epigenetic makeup, metabolism, and immunology. Molecular compounds that modulate the immune response against neoplasms offer promising new strategies to combat cancer. Inhibitors targeting the indoleamine-2,3-dioxygenase 1 enzyme (IDO1) represent one of the most potent therapeutic opportunities to inhibit tumor growth. Herein, we assess the biochemical role of IDO1 in tumor metabolism and immune surveillance, and review current diagnostic and therapeutic approaches that are intended to increase the effectiveness of immunotherapies against highly aggressive and difficult-to-treat IDO-expressing cancers.
    MeSH term(s) Animals ; Humans ; Indoleamine-Pyrrole 2,3,-Dioxygenase/physiology ; Neoplasms/diagnosis ; Neoplasms/enzymology ; Neoplasms/therapy
    Chemical Substances Indoleamine-Pyrrole 2,3,-Dioxygenase
    Language English
    Publishing date 2018-01-31
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2606827-8
    ISSN 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2018.00151
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  8. Article: Correlation between the Expression of Angiogenic Factors and Stem Cell Markers in Human Uveal Melanoma.

    Fodor, Klára / Sipos, Éva / Dobos, Nikoletta / Nagy, János / Steiber, Zita / Méhes, Gábor / Dull, Kata / Székvölgyi, Lóránt / Schally, Andrew V / Halmos, Gábor

    Life (Basel, Switzerland)

    2020  Volume 10, Issue 12

    Abstract: Uveal melanoma (UM) is the most common malignant tumor of the eye with extremely high metastatic potential. UM tumor cells can disseminate only hematogenously, thus, angiogenic signals have a particular role in the prognosis of the disease. Although the ... ...

    Abstract Uveal melanoma (UM) is the most common malignant tumor of the eye with extremely high metastatic potential. UM tumor cells can disseminate only hematogenously, thus, angiogenic signals have a particular role in the prognosis of the disease. Although the presence of cancer stem cells (CSCs) in densely vascularized UMs has been reported previously, their role in the process of hematogenous spread of UM has not been studied. In this study, we investigated the regulation of angiogenesis in UM in correlation with the presence of CSCs. Seventy UM samples were collected to analyze the expression of CSC markers and angiogenic factors. The expression of CSC markers was studied by RT-PCR, Western blotting techniques and IHC-TMA technique. RT-PCR showed high expression of CSC markers, particularly nestin, FZD6 and SOX10 and somewhat lower expression of NGFR. The protein expression of FZD6, HIF-1α and VEGFA was further evaluated in 52 UM samples by the IHC-TMA technique. We report here for the first time a significant correlation between FZD6 and VEGFA expression in UM samples. The observed correlation between FZD6 and VEGFA suggests the presence of CSCs in UM that are associated with the vascularization process.
    Language English
    Publishing date 2020-11-25
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2662250-6
    ISSN 2075-1729
    ISSN 2075-1729
    DOI 10.3390/life10120310
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  9. Article ; Online: Stress induces equivalent remodeling of hippocampal spine synapses in a simulated postpartum environment and in a female rat model of major depression.

    Baka, Judith / Csakvari, Eszter / Huzian, Orsolya / Dobos, Nikoletta / Siklos, Laszlo / Leranth, Csaba / MacLusky, Neil J / Duman, Ronald S / Hajszan, Tibor

    Neuroscience

    2016  Volume 343, Page(s) 384–397

    Abstract: Stress and withdrawal of female reproductive hormones are known risk factors of postpartum depression. Although both of these factors are capable of powerfully modulating neuronal plasticity, there is no direct electron microscopic evidence of ... ...

    Abstract Stress and withdrawal of female reproductive hormones are known risk factors of postpartum depression. Although both of these factors are capable of powerfully modulating neuronal plasticity, there is no direct electron microscopic evidence of hippocampal spine synapse remodeling in postpartum depression. To address this issue, hormonal conditions of pregnancy and postpartum period were simulated in ovariectomized adult female Sprague-Dawley rats (n=76). The number of hippocampal spine synapses and the depressive behavior of rats in an active escape task were investigated in untreated control, hormone-withdrawn 'postpartum', simulated proestrus, and hormone-treated 'postpartum' animals. After 'postpartum' withdrawal of gonadal steroids, inescapable stress caused a loss of hippocampal spine synapses, which was related to poor escape performance in hormone-withdrawn 'postpartum' females. These responses were equivalent with the changes observed in untreated controls that is an established animal model of major depression. Maintaining proestrus levels of ovarian hormones during 'postpartum' stress exposure did not affect synaptic and behavioral responses to inescapable stress in simulated proestrus animals. By contrast, maintaining pregnancy levels of estradiol and progesterone during 'postpartum' stress exposure completely prevented the stress-induced loss of hippocampal spine synapses, which was associated with improved escape performance in hormone-treated 'postpartum' females. This protective effect appears to be mediated by a muted stress response as measured by serum corticosterone concentrations. In line with our emerging 'synaptogenic hypothesis' of depression, the loss of hippocampal spine synapses may be a novel perspective both in the pathomechanism and in the clinical management of postpartum affective illness.
    MeSH term(s) Animals ; Corticosterone/blood ; Depression, Postpartum/metabolism ; Depression, Postpartum/pathology ; Depressive Disorder, Major/metabolism ; Depressive Disorder, Major/pathology ; Disease Models, Animal ; Estradiol/administration & dosage ; Estradiol/metabolism ; Female ; Hippocampus/metabolism ; Hippocampus/pathology ; Neuronal Plasticity/physiology ; Ovariectomy ; Postpartum Period ; Proestrus/physiology ; Progesterone/administration & dosage ; Progesterone/metabolism ; Rats, Sprague-Dawley ; Synapses/metabolism ; Synapses/pathology
    Chemical Substances Progesterone (4G7DS2Q64Y) ; Estradiol (4TI98Z838E) ; Corticosterone (W980KJ009P)
    Language English
    Publishing date 2016-12-22
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 196739-3
    ISSN 1873-7544 ; 0306-4522
    ISSN (online) 1873-7544
    ISSN 0306-4522
    DOI 10.1016/j.neuroscience.2016.12.021
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  10. Article ; Online: Neuroinflammation in Alzheimer's disease and major depression.

    Dobos, Nikoletta / Korf, Jakob / Luiten, Paul G M / Eisel, Ulrich L M

    Biological psychiatry

    2010  Volume 67, Issue 6, Page(s) 503–504

    MeSH term(s) Alzheimer Disease/epidemiology ; Alzheimer Disease/etiology ; Depressive Disorder, Major/epidemiology ; Depressive Disorder, Major/etiology ; Encephalitis/complications ; Humans
    Language English
    Publishing date 2010-03-15
    Publishing country United States
    Document type Comment ; Journal Article
    ZDB-ID 209434-4
    ISSN 1873-2402 ; 0006-3223
    ISSN (online) 1873-2402
    ISSN 0006-3223
    DOI 10.1016/j.biopsych.2010.01.023
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