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Expression patterns of AEG-1 in the normal brain.
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- Author(s): Kim H;Kim H; Choi M; Choi M; Choi M; Han S; Han S; Park SY; Park SY; Jeong M; Jeong M; Kim SR; Kim SR; Hwang EM; Hwang EM; Lee SG; Lee SG
- Source:
Brain structure & function [Brain Struct Funct] 2023 Sep; Vol. 228 (7), pp. 1629-1641. Date of Electronic Publication: 2023 Jul 08.- Publication Type:
Journal Article- Language:
English - Source:
- Additional Information
- Source: Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 101282001 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1863-2661 (Electronic) Linking ISSN: 18632653 NLM ISO Abbreviation: Brain Struct Funct Subsets: MEDLINE
- Publication Information: Original Publication: Berlin : Springer-Verlag, c2007-
- Subject Terms:
- Abstract: Astrocyte elevated gene-1 (AEG-1) is a well-known oncogene implicated in various types of human cancers, including brain tumors. Recently, AEG-1 has also been reported to play pivotal roles in glioma-associated neurodegeneration and neurodegenerative diseases like Parkinson's disease and amyotrophic lateral sclerosis. However, the normal physiological functions and expression patterns of AEG-1 in the brain are not well understood. In this study, we investigated the expression patterns of AEG-1 in the normal mouse brain and found that AEG-1 is widely expressed in neurons and neuronal precursor cells, but little in glial cells. We observed differential expression levels of AEG-1 in various brain regions, and its expression was mainly localized in the cell body of neurons rather than the nucleus. Additionally, AEG-1 was expressed in the cytoplasm of Purkinje cells in both the mouse and human cerebellum, suggesting its potential role in this brain region. These findings suggest that AEG-1 may have important functions in normal brain physiology and warrant further investigation. Our results may also shed light on the differential expression patterns of AEG-1 in normal and pathological brains, providing insights into its roles in various neurological disorders.
(© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.) - References: Anttila V, Wessman M, Kallela M, Palotie A (2011) Towards an understanding of genetic predisposition to migraine. Genome Med 3(3):17. https://doi.org/10.1186/gm231. (PMID: 10.1186/gm231214575143092102)
Benes FM, Berretta S (2001) GABAergic interneurons: implications for understanding schizophrenia and bipolar disorder. Neuropsychopharmacology 25(1):1–27. https://doi.org/10.1016/S0893-133X(01)00225-1. (PMID: 10.1016/S0893-133X(01)00225-111377916)
Britt DE, Yang DF, Yang DQ, Flanagan D, Callanan H, Lim YP, Lin SH, Hixson DC (2004) Identification of a novel protein, LYRIC, localized to tight junctions of polarized epithelial cells. Exp Cell Res 300(1):134–148. https://doi.org/10.1016/j.yexcr.2004.06.026. (PMID: 10.1016/j.yexcr.2004.06.02615383321)
Carnemolla A, Fossale E, Agostoni E, Michelazzi S, Calligaris R, De Maso L, Del Sal G, MacDonald ME, Persichetti F (2009) Rrs1 is involved in endoplasmic reticulum stress response in Huntington disease. J Biol Chem 284(27):18167–18173. https://doi.org/10.1074/jbc.M109.018325. (PMID: 10.1074/jbc.M109.018325194338662709382)
Chen X, Li XY, Long M, Wang X, Gao ZW, Cui Y, Ren J, Zhang Z, Liu C, Dong K, Zhang H (2018) The FBXW7 tumor suppressor inhibits breast cancer proliferation and promotes apoptosis by targeting MTDH for degradation. Neoplasma 65(2):201–209. https://doi.org/10.4149/neo_2018_170228N149. (PMID: 10.4149/neo_2018_170228N14929534580)
Choi M, Lee Y, Cho SH (2018) Angelica tenuissima nakai ameliorates cognitive impairment and promotes neurogenesis in mouse model of Alzheimer’s disease. Chin J Integr Med 24(5):378–384. https://doi.org/10.1007/s11655-017-2812-2. (PMID: 10.1007/s11655-017-2812-228578486)
Crews L, Adame A, Patrick C, Delaney A, Pham E, Rockenstein E, Hansen L, Masliah E (2010) Increased BMP6 levels in the brains of Alzheimer’s disease patients and APP transgenic mice are accompanied by impaired neurogenesis. J Neurosci 30(37):12252–12262. https://doi.org/10.1523/JNEUROSCI.1305-10.2010. (PMID: 10.1523/JNEUROSCI.1305-10.2010208441212978735)
Dudek SM, Alexander GM, Farris S (2016) Rediscovering area CA2: unique properties and functions. Nat Rev Neurosci 17(2):89–102. https://doi.org/10.1038/nrn.2015.22. (PMID: 10.1038/nrn.2015.22268066284856153)
Emdad L, Das SK, Dasgupta S, Hu B, Sarkar D, Fisher PB (2013) AEG-1/MTDH/LYRIC: signaling pathways, downstream genes, interacting proteins, and regulation of tumor angiogenesis. Adv Cancer Res 120:75–111. https://doi.org/10.1016/B978-0-12-401676-7.00003-6. (PMID: 10.1016/B978-0-12-401676-7.00003-6238899883928810)
Emdad L, Das SK, Hu B, Kegelman T, Kang DC, Lee SG, Sarkar D, Fisher PB (2016) AEG-1/MTDH/LYRIC: a promiscuous protein partner critical in cancer, obesity, and CNS diseases. Adv Cancer Res 131:97–132. https://doi.org/10.1016/bs.acr.2016.05.002. (PMID: 10.1016/bs.acr.2016.05.00227451125)
Emdad L, Hu B, Das SK, Sarkar D, Fisher PB (2015) AEG-1-AKT2: a novel complex controlling the aggressiveness of glioblastoma. Molecular Cell Oncol 2(3):e995008. https://doi.org/10.4161/23723556.2014.995008. (PMID: 10.4161/23723556.2014.995008)
Habib N, Li Y, Heidenreich M, Swiech L, Avraham-Davidi I, Trombetta JJ, Hession C, Zhang F, Regev A (2016) Div-Seq: single-nucleus RNA-Seq reveals dynamics of rare adult newborn neurons. Science 353(6302):925–928. https://doi.org/10.1126/science.aad7038. (PMID: 10.1126/science.aad7038274712525480621)
Handel AE, Disanto G, Ramagopalan SV (2013) Next-generation sequencing in understanding complex neurological disease. Expert Rev Neurother 13(2):215–227. https://doi.org/10.1586/ern.12.165. (PMID: 10.1586/ern.12.16523368808)
Hendrickson ML, Rao AJ, Demerdash ON, Kalil RE (2011) Expression of nestin by neural cells in the adult rat and human brain. PLoS ONE 6(4):e18535. https://doi.org/10.1371/journal.pone.0018535. (PMID: 10.1371/journal.pone.0018535214909213072400)
Jeon HY, Choi M, Howlett EL, Vozhilla N, Yoo BK, Lloyd JA, Sarkar D, Lee SG, Fisher PB (2010) Expression patterns of astrocyte elevated gene-1 (AEG-1) during development of the mouse embryo. Gene Expr Patterns 10(7–8):361–367. https://doi.org/10.1016/j.gep.2010.08.004. (PMID: 10.1016/j.gep.2010.08.004207360863165053)
Kang DC, Su ZZ, Sarkar D, Emdad L, Volsky DJ, Fisher PB (2005) Cloning and characterization of HIV-1-inducible astrocyte elevated gene-1, AEG-1. Gene 353(1):8–15. https://doi.org/10.1016/j.gene.2005.04.006. (PMID: 10.1016/j.gene.2005.04.00615927426)
Kann O, Papageorgiou IE, Draguhn A (2014) Highly energized inhibitory interneurons are a central element for information processing in cortical networks. J Cereb Blood Flow Metab 34(8):1270–1282. https://doi.org/10.1038/jcbfm.2014.104. (PMID: 10.1038/jcbfm.2014.104248965674126088)
Kelsom C, Lu W (2013) Development and specification of GABAergic cortical interneurons. Cell Biosci 3(1):19. https://doi.org/10.1186/2045-3701-3-19. (PMID: 10.1186/2045-3701-3-19236184633668182)
Khan UA, Liu L, Provenzano FA, Berman DE, Profaci CP, Sloan R, Mayeux R, Duff KE, Small SA (2014) Molecular drivers and cortical spread of lateral entorhinal cortex dysfunction in preclinical Alzheimer’s disease. Nat Neurosci 17(2):304–311. https://doi.org/10.1038/nn.3606. (PMID: 10.1038/nn.360624362760)
Khuda II, Koide N, Noman AS, Dagvadorj J, Tumurkhuu G, Naiki Y, Komatsu T, Yoshida T, Yokochi T (2009) Astrocyte elevated gene-1 (AEG-1) is induced by lipopolysaccharide as toll-like receptor 4 (TLR4) ligand and regulates TLR4 signalling. Immunology 128(1 Suppl):e700-706. https://doi.org/10.1111/j.1365-2567.2009.03063.x. (PMID: 10.1111/j.1365-2567.2009.03063.x197403312753960)
Kim A, Jung HG, Kim SC, Choi M, Park JY, Lee SG, Hwang EM (2019) Astrocytic AEG-1 regulates expression of TREK-1 under acute hypoxia. Cell Biochem Funct. https://doi.org/10.1002/cbf.3469. (PMID: 10.1002/cbf.346931782179)
Krishnan RK, Nolte H, Sun TL, Kaur H, Sreenivasan K, Looso M, Offermanns S, Kruger M, Swiercz JM (2015) Quantitative analysis of the TNF-alpha-induced phosphoproteome reveals AEG-1/MTDH/LYRIC as an IKK beta substrate. Nat Commun. https://doi.org/10.1038/Ncomms7658. (PMID: 10.1038/Ncomms765825923988)
Lazarov O, Hollands C (2016) Hippocampal neurogenesis: learning to remember. Prog Neurobiol 138–140:1–18. https://doi.org/10.1016/j.pneurobio.2015.12.006. (PMID: 10.1016/j.pneurobio.2015.12.006268553694828289)
Lee SG, Kang DC, DeSalle R, Sarkar D, Fisher PB (2013) AEG-1/MTDH/LYRIC, the beginning: initial cloning, structure, expression profile, and regulation of expression. Adv Cancer Res 120:1–38. https://doi.org/10.1016/B978-0-12-401676-7.00001-2. (PMID: 10.1016/B978-0-12-401676-7.00001-2238899863930353)
Lee SG, Kim K, Kegelman TP, Dash R, Das SK, Choi JK, Emdad L, Howlett EL, Jeon HY, Su ZZ, Yoo BK, Sarkar D, Kim SH, Kang DC, Fisher PB (2011) Oncogene AEG-1 promotes glioma-induced neurodegeneration by increasing glutamate excitotoxicity. Can Res 71(20):6514–6523. https://doi.org/10.1158/0008-5472.CAN-11-0782. (PMID: 10.1158/0008-5472.CAN-11-0782)
Lee SG, Su ZZ, Emdad L, Sarkar D, Fisher PB (2006) Astrocyte elevated gene-1 (AEG-1) is a target gene of oncogenic Ha-ras requiring phosphatidylinositol 3-kinase and c-Myc. Proc Natl Acad Sci USA 103(46):17390–17395. https://doi.org/10.1073/pnas.0608386103. (PMID: 10.1073/pnas.0608386103170885301859939)
Lee SG, Su ZZ, Emdad L, Sarkar D, Franke TF, Fisher PB (2008) Astrocyte elevated gene-1 activates cell survival pathways through PI3K-Akt signaling. Oncogene 27(8):1114–1121. https://doi.org/10.1038/sj.onc.1210713. (PMID: 10.1038/sj.onc.121071317704808)
Leem E, Kim HJ, Choi M, Kim S, Oh YS, Lee KJ, Choe YS, Um JY, Shin WH, Jeong JY, Jin BK, Kim DW, McLean C, Fisher PB, Kholodilov N, Ahn KS, Lee JM, Jung UJ, Lee SG, Kim SR (2018) Upregulation of neuronal astrocyte elevated gene-1 protects nigral dopaminergic neurons in vivo. Cell Death Dis 9(5):449. https://doi.org/10.1038/s41419-018-0491-3. (PMID: 10.1038/s41419-018-0491-3296700795906475)
Lein ES, Hawrylycz MJ, Ao N, Ayres M, Bensinger A, Bernard A, Boe AF, Boguski MS, Brockway KS, Byrnes EJ, Chen L, Chen L, Chen TM, Chin MC, Chong J, Crook BE, Czaplinska A, Dang CN, Datta S, Dee NR, Desaki AL, Desta T, Diep E, Dolbeare TA, Donelan MJ, Dong HW, Dougherty JG, Duncan BJ, Ebbert AJ, Eichele G, Estin LK, Faber C, Facer BA, Fields R, Fischer SR, Fliss TP, Frensley C, Gates SN, Glattfelder KJ, Halverson KR, Hart MR, Hohmann JG, Howell MP, Jeung DP, Johnson RA, Karr PT, Kawal R, Kidney JM, Knapik RH, Kuan CL, Lake JH, Laramee AR, Larsen KD, Lau C, Lemon TA, Liang AJ, Liu Y, Luong LT, Michaels J, Morgan JJ, Morgan RJ, Mortrud MT, Mosqueda NF, Ng LL, Ng R, Orta GJ, Overly CC, Pak TH, Parry SE, Pathak SD, Pearson OC, Puchalski RB, Riley ZL, Rockett HR, Rowland SA, Royall JJ, Ruiz MJ, Sarno NR, Schaffnit K, Shapovalova NV, Sivisay T, Slaughterbeck CR, Smith SC, Smith KA, Smith BI, Sodt AJ, Stewart NN, Stumpf KR, Sunkin SM, Sutram M, Tam A, Teemer CD, Thaller C, Thompson CL, Varnam LR, Visel A, Whitlock RM, Wohnoutka PE, Wolkey CK, Wong VY, Wood M, Yaylaoglu MB, Young RC, Youngstrom BL, Yuan XF, Zhang B, Zwingman TA, Jones AR (2007) Genome-wide atlas of gene expression in the adult mouse brain. Nature 445(7124):168–176. https://doi.org/10.1038/nature05453. (PMID: 10.1038/nature0545317151600)
Li B, Yamamori H, Tatebayashi Y, Shafit-Zagardo B, Tanimukai H, Chen S, Iqbal K, Grundke-Iqbal I (2008) Failure of neuronal maturation in Alzheimer disease dentate gyrus. J Neuropathol Exp Neurol 67(1):78–84. https://doi.org/10.1097/nen.0b013e318160c5db. (PMID: 10.1097/nen.0b013e318160c5db18091557)
Li Q, Wang M, Wang N, Wang J, Qi L, Mao P (2018) Downregulation of microRNA-216b contributes to glioma cell growth and migration by promoting AEG-1-mediated signaling. Biomed Pharmacother = Biomedecine Pharmacotherapie 104:420–426. https://doi.org/10.1016/j.biopha.2018.05.048. (PMID: 10.1016/j.biopha.2018.05.04829787989)
Ligthart L, de Vries B, Smith AV, Ikram MA, Amin N, Hottenga JJ, Koelewijn SC, Kattenberg VM, de Moor MH, Janssens AC, Aulchenko YS, Oostra BA, de Geus EJ, Smit JH, Zitman FG, Uitterlinden AG, Hofman A, Willemsen G, Nyholt DR, Montgomery GW, Terwindt GM, Gudnason V, Penninx BW, Breteler M, Ferrari MD, Launer LJ, van Duijn CM, van den Maagdenberg AM, Boomsma DI (2011) Meta-analysis of genome-wide association for migraine in six population-based European cohorts. Eur J Hum Genet 19(8):901–907. https://doi.org/10.1038/ejhg.2011.48. (PMID: 10.1038/ejhg.2011.48214482383172930)
Lv S, Zhang J, He Y, Liu Q, Wang Z, Liu B, Shi L, Wu Y (2020) MicroRNA-520e targets AEG-1 to suppress the proliferation and invasion of colorectal cancer cells through Wnt/GSK-3beta/beta-catenin signalling. Clin Exp Pharmacol Physiol 47(1):158–167. https://doi.org/10.1111/1440-1681.13185. (PMID: 10.1111/1440-1681.1318531574178)
Moran LV, Hong LE (2011) High vs low frequency neural oscillations in schizophrenia. Schizophr Bull 37(4):659–663. https://doi.org/10.1093/schbul/sbr056. (PMID: 10.1093/schbul/sbr056216532783122299)
Reddy-Thootkur M, Kraguljac NV, Lahti AC (2020) The role of glutamate and GABA in cognitive dysfunction in schizophrenia and mood disorders—a systematic review of magnetic resonance spectroscopy studies. Schizophr Res. https://doi.org/10.1016/j.schres.2020.02.001. (PMID: 10.1016/j.schres.2020.02.001321071027874516)
Sarkar D, Park ES, Emdad L, Lee SG, Su ZZ, Fisher PB (2008) Molecular basis of nuclear factor-kappaB activation by astrocyte elevated gene-1. Can Res 68(5):1478–1484. https://doi.org/10.1158/0008-5472.CAN-07-6164. (PMID: 10.1158/0008-5472.CAN-07-6164)
SEER Training Modules (2021) Introduction to the nervous system. US National Institutes of Health, National Cancer Institute. https://training.seer.cancer.gov/anatomy/nervous/ . Accessed 14 Jan 2021.
Solomon BL (1980) The hypothalamus and the pituitary gland: an overview. Nurs Clin North Am 15(3):435–451. (PMID: 10.1016/S0029-6465(22)00560-66905073)
Srivastava J, Robertson CL, Gredler R, Siddiq A, Rajasekaran D, Akiel MA, Emdad L, Mas V, Mukhopadhyay ND, Fisher PB, Sarkar D (2015) Astrocyte elevated gene-1 (AEG-1) contributes to non-thyroidal illness syndrome (NTIS) associated with hepatocellular carcinoma (HCC). J Biol Chem 290(25):15549–15558. https://doi.org/10.1074/jbc.M115.649707. (PMID: 10.1074/jbc.M115.649707259449094505468)
Stan AD, Schirda CV, Bertocci MA, Bebko GM, Kronhaus DM, Aslam HA, LaBarbara EJ, Tanase C, Lockovich JC, Pollock MH, Stiffler RS, Phillips ML (2014) Glutamate and GABA contributions to medial prefrontal cortical activity to emotion: implications for mood disorders. Psychiatry Res 223(3):253–260. https://doi.org/10.1016/j.pscychresns.2014.05.016. (PMID: 10.1016/j.pscychresns.2014.05.01624973815)
Sutherland HG, Lam YW, Briers S, Lamond AI, Bickmore WA (2004) 3D3/lyric: a novel transmembrane protein of the endoplasmic reticulum and nuclear envelope, which is also present in the nucleolus. Exp Cell Res 294(1):94–105. https://doi.org/10.1016/j.yexcr.2003.11.020. (PMID: 10.1016/j.yexcr.2003.11.02014980505)
Terranova JI, Ogawa SK, Kitamura T (2019) Adult hippocampal neurogenesis for systems consolidation of memory. Behav Brain Res 372:112035. https://doi.org/10.1016/j.bbr.2019.112035. (PMID: 10.1016/j.bbr.2019.11203531201874)
Thirkettle HJ, Girling J, Warren AY, Mills IG, Sahadevan K, Leung H, Hamdy F, Whitaker HC, Neal DE (2009) LYRIC/AEG-1 is targeted to different subcellular compartments by ubiquitinylation and intrinsic nuclear localization signals. Clin Cancer Res 15(9):3003–3013. https://doi.org/10.1158/1078-0432.CCR-08-2046. (PMID: 10.1158/1078-0432.CCR-08-204619383828)
Toda T, Parylak SL, Linker SB, Gage FH (2019) The role of adult hippocampal neurogenesis in brain health and disease. Mol Psychiatry 24(1):67–87. https://doi.org/10.1038/s41380-018-0036-2. (PMID: 10.1038/s41380-018-0036-229679070)
Tydlacka S, Wang CE, Wang X, Li S, Li XJ (2008) Differential activities of the ubiquitin-proteasome system in neurons versus glia may account for the preferential accumulation of misfolded proteins in neurons. J Neurosci 28(49):13285–13295. https://doi.org/10.1523/JNEUROSCI.4393-08.2008. (PMID: 10.1523/JNEUROSCI.4393-08.2008190522202662777)
Vartak-Sharma N, Gelman BB, Joshi C, Borgamann K, Ghorpade A (2014) Astrocyte elevated gene-1 is a novel modulator of HIV-1-associated neuroinflammation via regulation of nuclear factor-κB signaling and excitatory amino acid transporter-2 repression. J Biol Chem 289(28):19599–19612. https://doi.org/10.1074/jbc.M114.567644. (PMID: 10.1074/jbc.M114.567644248556484094071)
Vartak-Sharma N, Ghorpade A (2012) Astrocyte elevated gene-1 regulates astrocyte responses to neural injury: implications for reactive astrogliosis and neurodegeneration. J Neuroinflammation 9:195. https://doi.org/10.1186/1742-2094-9-195. (PMID: 10.1186/1742-2094-9-195228840853488579)
Vartak-Sharma N, Nooka S, Ghorpade A (2017) Astrocyte elevated gene-1 (AEG-1) and the A(E)Ging HIV/AIDS-HAND. Prog Neurobiol 157:133–157. https://doi.org/10.1016/j.pneurobio.2016.03.006. (PMID: 10.1016/j.pneurobio.2016.03.00627090750)
Wang Z, He S, Guo P, Guo X, Zheng J (2017) MicroRNA-1297 inhibits metastasis and epithelial-mesenchymal transition by targeting AEG-1 in cervical cancer. Oncol Rep 38(5):3121–3129. https://doi.org/10.3892/or.2017.5979. (PMID: 10.3892/or.2017.597929048632)
Yin X, Ren M, Jiang H, Cui S, Wang S, Jiang H, Qi Y, Wang J, Wang X, Dong G, Leeds P, Chuang DM, Feng H (2015) Downregulated AEG-1 together with inhibited PI3K/Akt pathway is associated with reduced viability of motor neurons in an ALS model. Mol Cell Neurosci 68:303–313. https://doi.org/10.1016/j.mcn.2015.08.009. (PMID: 10.1016/j.mcn.2015.08.00926320681)
Yin X, Wang S, Qi Y, Wang X, Jiang H, Wang T, Yang Y, Wang Y, Zhang C, Feng H (2018) Astrocyte elevated gene-1 is a novel regulator of astrogliosis and excitatory amino acid transporter-2 via interplaying with nuclear factor-κB signaling in astrocytes from amyotrophic lateral sclerosis mouse model with hSOD1(G93A) mutation. Mol Cell Neurosci 90:1–11. https://doi.org/10.1016/j.mcn.2018.05.004. (PMID: 10.1016/j.mcn.2018.05.00429777762)
Yip J, Soghomonian JJ, Blatt GJ (2007) Decreased GAD67 mRNA levels in cerebellar Purkinje cells in autism: pathophysiological implications. Acta Neuropathol 113(5):559–568. https://doi.org/10.1007/s00401-006-0176-3. (PMID: 10.1007/s00401-006-0176-317235515)
Yoo BK, Emdad L, Lee SG, Su ZZ, Santhekadur P, Chen D, Gredler R, Fisher PB, Sarkar D (2011a) Astrocyte elevated gene-1 (AEG-1): a multifunctional regulator of normal and abnormal physiology. Pharmacol Ther 130(1):1–8. https://doi.org/10.1016/j.pharmthera.2011.01.008. (PMID: 10.1016/j.pharmthera.2011.01.008212561563043119)
Yoo BK, Santhekadur PK, Gredler R, Chen D, Emdad L, Bhutia S, Pannell L, Fisher PB, Sarkar D (2011b) Increased RNA-induced silencing complex (RISC) activity contributes to hepatocellular carcinoma. Hepatology 53(5):1538–1548. https://doi.org/10.1002/hep.24216. (PMID: 10.1002/hep.2421621520169)
Zhang S, Liu L, Lv Z, Li Q, Gong W, Wu H (2017) MicroRNA-342-3p inhibits the proliferation, migration, and invasion of osteosarcoma cells by targeting astrocyte-elevated gene-1 (AEG-1). Oncol Res 25(9):1505–1515. https://doi.org/10.3727/096504017X14886485417426. (PMID: 10.3727/096504017X14886485417426282763157841055) - Grant Information: NRF-2020R1F1A1071525 National Research Foundation of Korea; NRF-2017R1D1A1B03032218 National Research Foundation of Korea
- Contributed Indexing: Keywords: AEG-1; Glial cells; Neurons; Normal brain
- Accession Number: 0 (Cell Adhesion Molecules)
0 (Membrane Proteins)
0 (MTDH protein, human)
0 (Mtdh protein, mouse) - Publication Date: Date Created: 20230708 Date Completed: 20230901 Latest Revision: 20230901
- Publication Date: 20230902
- Accession Number: 10.1007/s00429-023-02676-1
- Accession Number: 37421418
- Source:
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