References analysis of the Wikipedia article "Epigenetics of neurodegenerative diseases" in the English version

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Sghirlanzoni A, Pareyson D, Lauria G (June 2005). "Sensory neuron diseases". review. The Lancet. Neurology. 4 (6): 349–61. doi:10.1016/S1474-4422(05)70096-X. PMID 15907739. S2CID 35053543.

Goll MG, Bestor TH (2005). "Eukaryotic cytosine methyltransferases". Annual Review of Biochemistry. 74: 481–514. doi:10.1146/annurev.biochem.74.010904.153721. PMID 15952895.

Bernstein BE, Meissner A, Lander ES (February 2007). "The mammalian epigenome". review. Cell. 128 (4): 669–81. doi:10.1016/j.cell.2007.01.033. PMID 17320505. S2CID 2722988.

Faghihi MA, Modarresi F, Khalil AM, Wood DE, Sahagan BG, Morgan TE, Finch CE, St Laurent G, Kenny PJ, Wahlestedt C (July 2008). "Expression of a noncoding RNA is elevated in Alzheimer's disease and drives rapid feed-forward regulation of beta-secretase". primary. Nature Medicine. 14 (7): 723–30. doi:10.1038/nm1784. PMC 2826895. PMID 18587408.

Urdinguio RG, Sanchez-Mut JV, Esteller M (November 2009). "Epigenetic mechanisms in neurological diseases: genes, syndromes, and therapies". The Lancet. Neurology. 8 (11): 1056–72. doi:10.1016/S1474-4422(09)70262-5. PMID 19833297. S2CID 25946604.

Peedicayil J (April 2013). "Epigenetic drugs for Alzheimer's disease". British Journal of Clinical Pharmacology. 75 (4): 1152–3. doi:10.1111/j.1365-2125.2012.04444.x. PMC 3612735. PMID 22905989.

Del Signore SJ, Amante DJ, Kim J, Stack EC, Goodrich S, Cormier K, Smith K, Cudkowicz ME, Ferrante RJ (April 2009). "Combined riluzole and sodium phenylbutyrate therapy in transgenic amyotrophic lateral sclerosis mice". primary. Amyotrophic Lateral Sclerosis. 10 (2): 85–94. doi:10.1080/17482960802226148. PMID 18618304. S2CID 24124109.

Petri S, Kiaei M, Kipiani K, Chen J, Calingasan NY, Crow JP, Beal MF (April 2006). "Additive neuroprotective effects of a histone deacetylase inhibitor and a catalytic antioxidant in a transgenic mouse model of amyotrophic lateral sclerosis". Neurobiology of Disease. 22 (1): 40–9. doi:10.1016/j.nbd.2005.09.013. PMID 16289867. S2CID 22794616.

Cudkowicz ME, Andres PL, Macdonald SA, Bedlack RS, Choudry R, Brown RH, Zhang H, Schoenfeld DA, Shefner J, Matson S, Matson WR, Ferrante RJ (April 2009). "Phase 2 study of sodium phenylbutyrate in ALS". primary. Amyotrophic Lateral Sclerosis. 10 (2): 99–106. doi:10.1080/17482960802320487. PMID 18688762. S2CID 12390136.

Piepers S, Veldink JH, de Jong SW, van der Tweel I, van der Pol WL, Uijtendaal EV, Schelhaas HJ, Scheffer H, de Visser M, de Jong JM, Wokke JH, Groeneveld GJ, van den Berg LH (August 2009). "Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis". primary. Annals of Neurology. 66 (2): 227–34. doi:10.1002/ana.21620. PMID 19743466. S2CID 44949619.

Yoo YE, Ko CP (September 2011). "Treatment with trichostatin A initiated after disease onset delays disease progression and increases survival in a mouse model of amyotrophic lateral sclerosis". primary. Experimental Neurology. 231 (1): 147–59. doi:10.1016/j.expneurol.2011.06.003. PMID 21712032. S2CID 42608157.

Fischer A, Sananbenesi F, Wang X, Dobbin M, Tsai LH (May 2007). "Recovery of learning and memory is associated with chromatin remodelling". primary. Nature. 447 (7141): 178–82. Bibcode:2007Natur.447..178F. doi:10.1038/nature05772. PMID 17468743. S2CID 36395789.

Ricobaraza A, Cuadrado-Tejedor M, Marco S, Pérez-Otaño I, García-Osta A (May 2012). "Phenylbutyrate rescues dendritic spine loss associated with memory deficits in a mouse model of Alzheimer disease". primary. Hippocampus. 22 (5): 1040–50. doi:10.1002/hipo.20883. PMID 21069780. S2CID 20052391.

Govindarajan N, Agis-Balboa RC, Walter J, Sananbenesi F, Fischer A (2011). "Sodium butyrate improves memory function in an Alzheimer's disease mouse model when administered at an advanced stage of disease progression". primary. Journal of Alzheimer's Disease. 26 (1): 187–97. doi:10.3233/JAD-2011-110080. PMID 21593570.

Kilgore M, Miller CA, Fass DM, Hennig KM, Haggarty SJ, Sweatt JD, Rumbaugh G (March 2010). "Inhibitors of class 1 histone deacetylases reverse contextual memory deficits in a mouse model of Alzheimer's disease". primary. Neuropsychopharmacology. 35 (4): 870–80. doi:10.1038/npp.2009.197. PMC 3055373. PMID 20010553.

Francis YI, Fà M, Ashraf H, Zhang H, Staniszewski A, Latchman DS, Arancio O (2009). "Dysregulation of histone acetylation in the APP/PS1 mouse model of Alzheimer's disease". Journal of Alzheimer's Disease. 18 (1): 131–9. doi:10.3233/JAD-2009-1134. PMC 8962655. PMID 19625751.

Steffan JS, Bodai L, Pallos J, Poelman M, McCampbell A, Apostol BL, Kazantsev A, Schmidt E, Zhu YZ, Greenwald M, Kurokawa R, Housman DE, Jackson GR, Marsh JL, Thompson LM (October 2001). "Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila". primary. Nature. 413 (6857): 739–43. Bibcode:2001Natur.413..739S. doi:10.1038/35099568. PMID 11607033. S2CID 4419980.

Gardian G, Browne SE, Choi DK, Klivenyi P, Gregorio J, Kubilus JK, Ryu H, Langley B, Ratan RR, Ferrante RJ, Beal MF (January 2005). "Neuroprotective effects of phenylbutyrate in the N171-82Q transgenic mouse model of Huntington's disease". primary. The Journal of Biological Chemistry. 280 (1): 556–63. doi:10.1074/jbc.M410210200. PMID 15494404.

Dompierre JP, Godin JD, Charrin BC, Cordelières FP, King SJ, Humbert S, Saudou F (March 2007). "Histone deacetylase 6 inhibition compensates for the transport deficit in Huntington's disease by increasing tubulin acetylation". primary. The Journal of Neuroscience. 27 (13): 3571–83. doi:10.1523/JNEUROSCI.0037-07.2007. PMC 6672116. PMID 17392473.

Zhou W, Bercury K, Cummiskey J, Luong N, Lebin J, Freed CR (April 2011). "Phenylbutyrate up-regulates the DJ-1 protein and protects neurons in cell culture and in animal models of Parkinson disease". primary. The Journal of Biological Chemistry. 286 (17): 14941–51. doi:10.1074/jbc.M110.211029. PMC 3083206. PMID 21372141.

Rane P, Shields J, Heffernan M, Guo Y, Akbarian S, King JA (June 2012). "The histone deacetylase inhibitor, sodium butyrate, alleviates cognitive deficits in pre-motor stage PD". primary. Neuropharmacology. 62 (7): 2409–12. doi:10.1016/j.neuropharm.2012.01.026. PMID 22353286. S2CID 23078279.

St Laurent R, O'Brien LM, Ahmad ST (August 2013). "Sodium butyrate improves locomotor impairment and early mortality in a rotenone-induced Drosophila model of Parkinson's disease". primary. Neuroscience. 246: 382–90. doi:10.1016/j.neuroscience.2013.04.037. PMC 3721507. PMID 23623990.

Monti B, Gatta V, Piretti F, Raffaelli SS, Virgili M, Contestabile A (February 2010). "Valproic acid is neuroprotective in the rotenone rat model of Parkinson's disease: involvement of alpha-synuclein". primary. Neurotoxicity Research. 17 (2): 130–41. doi:10.1007/s12640-009-9090-5. PMID 19626387. S2CID 40159513.

Kontopoulos E, Parvin JD, Feany MB (October 2006). "Alpha-synuclein acts in the nucleus to inhibit histone acetylation and promote neurotoxicity". primary. Human Molecular Genetics. 15 (20): 3012–23. doi:10.1093/hmg/ddl243. PMID 16959795.

Riessland M, Brichta L, Hahnen E, Wirth B (August 2006). "The benzamide M344, a novel histone deacetylase inhibitor, significantly increases SMN2 RNA/protein levels in spinal muscular atrophy cells". primary. Human Genetics. 120 (1): 101–10. doi:10.1007/s00439-006-0186-1. PMID 16724231. S2CID 24804136.

Andreassi C, Angelozzi C, Tiziano FD, Vitali T, De Vincenzi E, Boninsegna A, Villanova M, Bertini E, Pini A, Neri G, Brahe C (January 2004). "Phenylbutyrate increases SMN expression in vitro: relevance for treatment of spinal muscular atrophy". European Journal of Human Genetics. 12 (1): 59–65. doi:10.1038/sj.ejhg.5201102. PMID 14560316.

Mercuri E, Bertini E, Messina S, Solari A, D'Amico A, Angelozzi C, Battini R, Berardinelli A, Boffi P, Bruno C, Cini C, Colitto F, Kinali M, Minetti C, Mongini T, Morandi L, Neri G, Orcesi S, Pane M, Pelliccioni M, Pini A, Tiziano FD, Villanova M, Vita G, Brahe C (January 2007). "Randomized, double-blind, placebo-controlled trial of phenylbutyrate in spinal muscular atrophy". primary. Neurology. 68 (1): 51–5. doi:10.1212/01.wnl.0000249142.82285.d6. PMID 17082463. S2CID 30429093.

Brahe C, Vitali T, Tiziano FD, Angelozzi C, Pinto AM, Borgo F, Moscato U, Bertini E, Mercuri E, Neri G (February 2005). "Phenylbutyrate increases SMN gene expression in spinal muscular atrophy patients". primary. European Journal of Human Genetics. 13 (2): 256–9. doi:10.1038/sj.ejhg.5201320. PMID 15523494.

Sumner CJ, Huynh TN, Markowitz JA, Perhac JS, Hill B, Coovert DD, Schussler K, Chen X, Jarecki J, Burghes AH, Taylor JP, Fischbeck KH (November 2003). "Valproic acid increases SMN levels in spinal muscular atrophy patient cells". primary. Annals of Neurology. 54 (5): 647–54. doi:10.1002/ana.10743. PMID 14595654. S2CID 7983521.

Brichta L, Hofmann Y, Hahnen E, Siebzehnrubl FA, Raschke H, Blumcke I, Eyupoglu IY, Wirth B (October 2003). "Valproic acid increases the SMN2 protein level: a well-known drug as a potential therapy for spinal muscular atrophy". primary. Human Molecular Genetics. 12 (19): 2481–9. doi:10.1093/hmg/ddg256. PMID 12915451.

Tsai LK, Tsai MS, Lin TB, Hwu WL, Li H (November 2006). "Establishing a standardized therapeutic testing protocol for spinal muscular atrophy". primary. Neurobiology of Disease. 24 (2): 286–95. doi:10.1016/j.nbd.2006.07.004. PMID 16952456. S2CID 31974628.

Weihl CC, Connolly AM, Pestronk A (August 2006). "Valproate may improve strength and function in patients with type III/IV spinal muscle atrophy". primary. Neurology. 67 (3): 500–1. doi:10.1212/01.wnl.0000231139.26253.d0. PMID 16775228. S2CID 13138072.

Piepers S, Cobben JM, Sodaar P, Jansen MD, Wadman RI, Meester-Delver A, Poll-The BT, Lemmink HH, Wokke JH, van der Pol WL, van den Berg LH (August 2011). "Quantification of SMN protein in leucocytes from spinal muscular atrophy patients: effects of treatment with valproic acid". primary. Journal of Neurology, Neurosurgery, and Psychiatry. 82 (8): 850–2. doi:10.1136/jnnp.2009.200253. PMID 20551479. S2CID 27844635.

Swoboda KJ, Scott CB, Crawford TO, Simard LR, Reyna SP, Krosschell KJ, Acsadi G, Elsheik B, Schroth MK, D'Anjou G, LaSalle B, Prior TW, Sorenson SL, Maczulski JA, Bromberg MB, Chan GM, Kissel JT (August 2010). "SMA CARNI-VAL trial part I: double-blind, randomized, placebo-controlled trial of L-carnitine and valproic acid in spinal muscular atrophy". primary. PLOS ONE. 5 (8): e12140. Bibcode:2010PLoSO...512140S. doi:10.1371/journal.pone.0012140. PMC 2924376. PMID 20808854.

Darbar IA, Plaggert PG, Resende MB, Zanoteli E, Reed UC (March 2011). "Evaluation of muscle strength and motor abilities in children with type II and III spinal muscle atrophy treated with valproic acid". primary. BMC Neurology. 11: 36. doi:10.1186/1471-2377-11-36. PMC 3078847. PMID 21435220.

Narver HL, Kong L, Burnett BG, Choe DW, Bosch-Marcé M, Taye AA, Eckhaus MA, Sumner CJ (October 2008). "Sustained improvement of spinal muscular atrophy mice treated with trichostatin A plus nutrition". primary. Annals of Neurology. 64 (4): 465–70. doi:10.1002/ana.21449. PMC 10103738. PMID 18661558. S2CID 5595968.

Avila AM, Burnett BG, Taye AA, Gabanella F, Knight MA, Hartenstein P, Cizman Z, Di Prospero NA, Pellizzoni L, Fischbeck KH, Sumner CJ (March 2007). "Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy". primary. The Journal of Clinical Investigation. 117 (3): 659–71. doi:10.1172/JCI29562. PMC 1797603. PMID 17318264.

Hahnen E, Eyüpoglu IY, Brichta L, Haastert K, Tränkle C, Siebzehnrübl FA, Riessland M, Hölker I, Claus P, Romstöck J, Buslei R, Wirth B, Blümcke I (July 2006). "In vitro and ex vivo evaluation of second-generation histone deacetylase inhibitors for the treatment of spinal muscular atrophy". primary. Journal of Neurochemistry. 98 (1): 193–202. doi:10.1111/j.1471-4159.2006.03868.x. PMID 16805808.

Kernochan LE, Russo ML, Woodling NS, Huynh TN, Avila AM, Fischbeck KH, Sumner CJ (May 2005). "The role of histone acetylation in SMN gene expression". primary. Human Molecular Genetics. 14 (9): 1171–82. doi:10.1093/hmg/ddi130. PMID 15772088.

Riessland M, Ackermann B, Förster A, Jakubik M, Hauke J, Garbes L, Fritzsche I, Mende Y, Blumcke I, Hahnen E, Wirth B (April 2010). "SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy". primary. Human Molecular Genetics. 19 (8): 1492–506. doi:10.1093/hmg/ddq023. PMID 20097677.

Dewey CM, Cenik B, Sephton CF, Johnson BA, Herz J, Yu G (June 2012). "TDP-43 aggregation in neurodegeneration: are stress granules the key?". review. Brain Research. 1462: 16–25. doi:10.1016/j.brainres.2012.02.032. PMC 3372581. PMID 22405725.

Polymenidou M, Lagier-Tourenne C, Hutt KR, Bennett CF, Cleveland DW, Yeo GW (June 2012). "Misregulated RNA processing in amyotrophic lateral sclerosis". review. Brain Research. 1462: 3–15. doi:10.1016/j.brainres.2012.02.059. PMC 3707312. PMID 22444279.

Rouaux C, Jokic N, Mbebi C, Boutillier S, Loeffler JP, Boutillier AL (December 2003). "Critical loss of CBP/p300 histone acetylase activity by caspase-6 during neurodegeneration". primary. The EMBO Journal. 22 (24): 6537–49. doi:10.1093/emboj/cdg615. PMC 291810. PMID 14657026.

Battistini S, Ricci C, Lotti EM, Benigni M, Gagliardi S, Zucco R, Bondavalli M, Marcello N, Ceroni M, Cereda C (June 2010). "Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene". primary. Journal of the Neurological Sciences. 293 (1–2): 112–5. doi:10.1016/j.jns.2010.03.009. PMID 20385392. S2CID 24895265.

Bruijn LI, Houseweart MK, Kato S, Anderson KL, Anderson SD, Ohama E, Reaume AG, Scott RW, Cleveland DW (September 1998). "Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1". primary. Science. 281 (5384): 1851–4. Bibcode:1998Sci...281.1851B. doi:10.1126/science.281.5384.1851. PMID 9743498.

Furukawa Y, Fu R, Deng HX, Siddique T, O'Halloran TV (May 2006). "Disulfide cross-linked protein represents a significant fraction of ALS-associated Cu, Zn-superoxide dismutase aggregates in spinal cords of model mice". primary. Proceedings of the National Academy of Sciences of the United States of America. 103 (18): 7148–53. Bibcode:2006PNAS..103.7148F. doi:10.1073/pnas.0602048103. PMC 1447524. PMID 16636274.

Boillée S, Vande Velde C, Cleveland DW (October 2006). "ALS: a disease of motor neurons and their nonneuronal neighbors". review. Neuron. 52 (1): 39–59. doi:10.1016/j.neuron.2006.09.018. PMID 17015226. S2CID 12968143.

Cudkowicz ME, McKenna-Yasek D, Sapp PE, Chin W, Geller B, Hayden DL, Schoenfeld DA, Hosler BA, Horvitz HR, Brown RH (February 1997). "Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis". primary. Annals of Neurology. 41 (2): 210–21. doi:10.1002/ana.410410212. PMID 9029070. S2CID 25595595.

Todd TW, Petrucelli L (August 2016). "Insights into the pathogenic mechanisms of Chromosome 9 open reading frame 72 (C9orf72) repeat expansions". review. Journal of Neurochemistry. 138 (Suppl 1): 145–62. doi:10.1111/jnc.13623. PMID 27016280.

Yoshimura S, Gerondopoulos A, Linford A, Rigden DJ, Barr FA (October 2010). "Family-wide characterization of the DENN domain Rab GDP-GTP exchange factors". primary. The Journal of Cell Biology. 191 (2): 367–81. doi:10.1083/jcb.201008051. PMC 2958468. PMID 20937701.

Deng HX, Chen W, Hong ST, Boycott KM, Gorrie GH, Siddique N, et al. (August 2011). "Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia". primary. Nature. 477 (7363): 211–5. Bibcode:2011Natur.477..211D. doi:10.1038/nature10353. PMC 3169705. PMID 21857683.

Rouaux C, Loeffler JP, Boutillier AL (September 2004). "Targeting CREB-binding protein (CBP) loss of function as a therapeutic strategy in neurological disorders". review. Biochemical Pharmacology. 68 (6): 1157–64. doi:10.1016/j.bcp.2004.05.035. PMID 15313413.

Ryu H, Smith K, Camelo SI, Carreras I, Lee J, Iglesias AH, Dangond F, Cormier KA, Cudkowicz ME, Brown RH, Ferrante RJ (June 2005). "Sodium phenylbutyrate prolongs survival and regulates expression of anti-apoptotic genes in transgenic amyotrophic lateral sclerosis mice". primary. Journal of Neurochemistry. 93 (5): 1087–98. doi:10.1111/j.1471-4159.2005.03077.x. PMID 15934930.

Corcoran LJ, Mitchison TJ, Liu Q (March 2004). "A novel action of histone deacetylase inhibitors in a protein aggresome disease model". primary. Current Biology. 14 (6): 488–92. Bibcode:2004CBio...14..488C. doi:10.1016/j.cub.2004.03.003. PMID 15043813. S2CID 6465499.

Crochemore C, Virgili M, Bonamassa B, Canistro D, Pena-Altamira E, Paolini M, Contestabile A (April 2009). "Long-term dietary administration of valproic acid does not affect, while retinoic acid decreases, the lifespan of G93A mice, a model for amyotrophic lateral sclerosis". primary. Muscle & Nerve. 39 (4): 548–52. doi:10.1002/mus.21260. PMID 19296491. S2CID 26101773.

Rouaux C, Panteleeva I, René F, Gonzalez de Aguilar JL, Echaniz-Laguna A, Dupuis L, Menger Y, Boutillier AL, Loeffler JP (May 2007). "Sodium valproate exerts neuroprotective effects in vivo through CREB-binding protein-dependent mechanisms but does not improve survival in an amyotrophic lateral sclerosis mouse model". primary. The Journal of Neuroscience. 27 (21): 5535–45. doi:10.1523/JNEUROSCI.1139-07.2007. PMC 6672753. PMID 17522299.

Brzustowicz LM, Lehner T, Castilla LH, Penchaszadeh GK, Wilhelmsen KC, Daniels R, Davies KE, Leppert M, Ziter F, Wood D (April 1990). "Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2–13.3". primary. Nature. 344 (6266): 540–1. Bibcode:1990Natur.344..540B. doi:10.1038/344540a0. PMID 2320125. S2CID 4259327.

Prior TW, Krainer AR, Hua Y, Swoboda KJ, Snyder PC, Bridgeman SJ, Burghes AH, Kissel JT (September 2009). "A positive modifier of spinal muscular atrophy in the SMN2 gene". primary. American Journal of Human Genetics. 85 (3): 408–13. doi:10.1016/j.ajhg.2009.08.002. PMC 2771537. PMID 19716110.

Schreml J, Riessland M, Paterno M, Garbes L, Roßbach K, Ackermann B, Krämer J, Somers E, Parson SH, Heller R, Berkessel A, Sterner-Kock A, Wirth B (June 2013). "Severe SMA mice show organ impairment that cannot be rescued by therapy with the HDACi JNJ-26481585". primary. European Journal of Human Genetics. 21 (6): 643–52. doi:10.1038/ejhg.2012.222. PMC 3658191. PMID 23073311.

Lazaridis K, Tzartos SJ (2020). "Autoantibody Specificities in Myasthenia Gravis; Implications for Improved Diagnostics and Therapeutics". Frontiers in Immunology. 11: 212. doi:10.3389/fimmu.2020.00212. ISSN 1664-3224. PMC 7033452. PMID 32117321.

Avidan N, Le Panse R, Berrih-Aknin S, Miller A (2014-08-01). "Genetic basis of myasthenia gravis – A comprehensive review". Journal of Autoimmunity. Myasthenia Gravis: A Comprehensive Review. 52: 146–153. doi:10.1016/j.jaut.2013.12.001. ISSN 0896-8411. PMID 24361103.

Golfinopoulou R, Papageorgiou L, Efthimiadou A, Bacopoulou F, Chrousos GP, Eliopoulos E, Vlachakis D (2021-07-01). "Clinical Genomic, phenotype and epigenetic insights into the pathology, autoimmunity and weight management of patients with Myasthenia Gravis (Review)". Molecular Medicine Reports. 24 (1): 1–9. doi:10.3892/mmr.2021.12151. ISSN 1791-2997. PMID 34225443. S2CID 235744938.

Wang L, Zhang L (2020). "Emerging Roles of Dysregulated MicroRNAs in Myasthenia Gravis". Frontiers in Neuroscience. 14: 507. doi:10.3389/fnins.2020.00507. ISSN 1662-453X. PMC 7253668. PMID 32508584.

Ströbel P, Rosenwald A, Beyersdorf N, Kerkau T, Elert O, Murumägi A, Sillanpää N, Peterson P, Hummel V, Rieckmann P, Burek C (2004). "Selective loss of regulatory T cells in thymomas". Annals of Neurology. 56 (6): 901–904. doi:10.1002/ana.20340. ISSN 0364-5134. PMID 15562414. S2CID 43398892.

Cron MA, Maillard S, Delisle F, Samson N, Truffault F, Foti M, Fadel E, Guihaire J, Berrih-Aknin S, Le Panse R (2018). "Analysis of microRNA expression in the thymus of Myasthenia Gravis patients opens new research avenues". Autoimmunity Reviews. 17 (6): 588–600. doi:10.1016/j.autrev.2018.01.008. ISSN 1873-0183. PMID 29655674. S2CID 4882702.

Liu XF, Wang RQ, Hu B, Luo MC, Zeng QM, Zhou H, Huang K, Dong XH, Luo YB, Luo ZH, Yang H (2016-03-01). "MiR-15a contributes abnormal immune response in myasthenia gravis by targeting CXCL10". Clinical Immunology. 164: 106–113. doi:10.1016/j.clim.2015.12.009. ISSN 1521-6616. PMID 26845678.

Lu J, Yan M, Wang Y, Zhang J, Yang H, Tian Ff, Zhou W, Zhang N, Li J (2013-10-25). "Altered expression of miR-146a in myasthenia gravis". Neuroscience Letters. 555: 85–90. doi:10.1016/j.neulet.2013.09.014. ISSN 0304-3940. PMID 24036458. S2CID 5317928.

Vanyushin BF (2004). "Enzymatic DNA Methylation Is an Epigenetic Control for Genetic Functions of the Cell". Biochemistry (Moscow). 70 (5): 488–499. doi:10.1007/s10541-005-0143-y. PMID 15948703. S2CID 25973184.

Fang TK, Yan CJ, Du J (2018). "CTLA-4 methylation regulates the pathogenesis of myasthenia gravis and the expression of related cytokines". Medicine. 97 (18): e0620. doi:10.1097/MD.0000000000010620. ISSN 0025-7974. PMC 6393147. PMID 29718870.

Cron MA, Guillochon É, Kusner L, Le Panse R (2020-06-10). "Role of miRNAs in Normal and Myasthenia Gravis Thymus". Frontiers in Immunology. 11: 1074. doi:10.3389/fimmu.2020.01074. ISSN 1664-3224. PMC 7297979. PMID 32587589.

Xu S, Wang T, Lu X, Zhang H, Liu L, Kong X, Li S, Wang X, Gao H, Wang J, Wang L (2021). "Identification of LINC00173 in Myasthenia Gravis by Integration Analysis of Aberrantly Methylated- Differentially Expressed Genes and ceRNA Networks". Frontiers in Genetics. 12: 726751. doi:10.3389/fgene.2021.726751. ISSN 1664-8021. PMC 8481885. PMID 34603387.

De Waal Malefyt R, Abrams J, Bennett B, Figdor CG, De Vries JE (1991-11-01). "Interleukin 10(IL-10) inhibits cytokine synthesis by human monocytes: an autoregulatory role of IL-10 produced by monocytes". The Journal of Experimental Medicine. 174 (5): 1209–1220. doi:10.1084/jem.174.5.1209. ISSN 0022-1007. PMC 2119001. PMID 1940799.

Fujii Si, Shimizu K, Shimizu T, Lotze MT (2001-10-01). "Interleukin-10 promotes the maintenance of antitumor CD8+ T-cell effector function in situ". Blood. 98 (7): 2143–2151. doi:10.1182/blood.V98.7.2143. ISSN 0006-4971. PMID 11568001.

Punga AR, Andersson M, Alimohammadi M, Punga T (2015-09-15). "Disease specific signature of circulating miR-150-5p and miR-21-5p in myasthenia gravis patients". Journal of the Neurological Sciences. 356 (1): 90–96. doi:10.1016/j.jns.2015.06.019. ISSN 0022-510X. PMID 26095457. S2CID 9099858.

Bennett DA, Yu L, Yang J, Srivastava GP, Aubin C, De Jager PL (January 2015). "Epigenomics of Alzheimer's disease". review. Translational Research. 165 (1): 200–20. doi:10.1016/j.trsl.2014.05.006. PMC 4233194. PMID 24905038.

Mastroeni D, McKee A, Grover A, Rogers J, Coleman PD (August 2009). "Epigenetic differences in cortical neurons from a pair of monozygotic twins discordant for Alzheimer's disease". primary. PLOS ONE. 4 (8): e6617. Bibcode:2009PLoSO...4.6617M. doi:10.1371/journal.pone.0006617. PMC 2719870. PMID 19672297.

Chouliaras L, Mastroeni D, Delvaux E, Grover A, Kenis G, Hof PR, Steinbusch HW, Coleman PD, Rutten BP, van den Hove DL (September 2013). "Consistent decrease in global DNA methylation and hydroxymethylation in the hippocampus of Alzheimer's disease patients". primary. Neurobiology of Aging. 34 (9): 2091–9. doi:10.1016/j.neurobiolaging.2013.02.021. PMC 3955118. PMID 23582657.

Mastroeni D, Grover A, Delvaux E, Whiteside C, Coleman PD, Rogers J (December 2010). "Epigenetic changes in Alzheimer's disease: decrements in DNA methylation". primary. Neurobiology of Aging. 31 (12): 2025–37. doi:10.1016/j.neurobiolaging.2008.12.005. PMC 2962691. PMID 19117641.

Bakulski KM, Dolinoy DC, Sartor MA, Paulson HL, Konen JR, Lieberman AP, Albin RL, Hu H, Rozek LS (2012). "Genome-wide DNA methylation differences between late-onset Alzheimer's disease and cognitively normal controls in human frontal cortex". Journal of Alzheimer's Disease. 29 (3): 571–88. doi:10.3233/JAD-2012-111223. PMC 3652332. PMID 22451312.

Rao JS, Keleshian VL, Klein S, Rapoport SI (July 2012). "Epigenetic modifications in frontal cortex from Alzheimer's disease and bipolar disorder patients". primary. Translational Psychiatry. 2 (7): e132. doi:10.1038/tp.2012.55. PMC 3410632. PMID 22760556.

Wang Y, Zhang JX, Du XX, Zhao L, Tian Q, Zhu LQ, Wang SH, Wang JZ (September 2008). "Temporal correlation of the memory deficit with Alzheimer-like lesions induced by activation of glycogen synthase kinase-3". Journal of Neurochemistry. 106 (6): 2364–74. doi:10.1111/j.1471-4159.2008.05578.x. PMID 18643871.

Nicolia V, Fuso A, Cavallaro RA, Di Luzio A, Scarpa S (2010). "B vitamin deficiency promotes tau phosphorylation through regulation of GSK3beta and PP2A". primary. Journal of Alzheimer's Disease. 19 (3): 895–907. doi:10.3233/JAD-2010-1284. PMID 20157245.

Byun CJ, Seo J, Jo SA, Park YJ, Klug M, Rehli M, Park MH, Jo I (January 2012). "DNA methylation of the 5'-untranslated region at +298 and +351 represses BACE1 expression in mouse BV-2 microglial cells". primary. Biochemical and Biophysical Research Communications. 417 (1): 387–92. doi:10.1016/j.bbrc.2011.11.123. PMID 22166205.

Chen KL, Wang SS, Yang YY, Yuan RY, Chen RM, Hu CJ (January 2009). "The epigenetic effects of amyloid-beta(1–40) on global DNA and neprilysin genes in murine cerebral endothelial cells". primary. Biochemical and Biophysical Research Communications. 378 (1): 57–61. doi:10.1016/j.bbrc.2008.10.173. PMID 19007750.

Tohgi H, Abe T, Yamazaki K, Murata T, Ishizaki E, Isobe C (July 1999). "Alterations of 3-nitrotyrosine concentration in the cerebrospinal fluid during aging and in patients with Alzheimer's disease". primary. Neuroscience Letters. 269 (1): 52–4. doi:10.1016/S0304-3940(99)00406-1. PMID 10821643. S2CID 20536297.

Zhang K, Schrag M, Crofton A, Trivedi R, Vinters H, Kirsch W (April 2012). "Targeted proteomics for quantification of histone acetylation in Alzheimer's disease". primary. Proteomics. 12 (8): 1261–8. doi:10.1002/pmic.201200010. PMC 6812507. PMID 22577027.

Gräff J, Rei D, Guan JS, Wang WY, Seo J, Hennig KM, Nieland TJ, Fass DM, Kao PF, Kahn M, Su SC, Samiei A, Joseph N, Haggarty SJ, Delalle I, Tsai LH (February 2012). "An epigenetic blockade of cognitive functions in the neurodegenerating brain". primary. Nature. 483 (7388): 222–6. Bibcode:2012Natur.483..222G. doi:10.1038/nature10849. PMC 3498952. PMID 22388814.

Peleg S, Sananbenesi F, Zovoilis A, Burkhardt S, Bahari-Javan S, Agis-Balboa RC, Cota P, Wittnam JL, Gogol-Doering A, Opitz L, Salinas-Riester G, Dettenhofer M, Kang H, Farinelli L, Chen W, Fischer A (May 2010). "Altered histone acetylation is associated with age-dependent memory impairment in mice". primary. Science. 328 (5979): 753–6. Bibcode:2010Sci...328..753P. doi:10.1126/science.1186088. PMID 20448184. S2CID 7370920.

Fuso A (March 2013). "The 'golden age' of DNA methylation in neurodegenerative diseases". review. Clinical Chemistry and Laboratory Medicine. 51 (3): 523–34. doi:10.1515/cclm-2012-0618. PMID 23183753. S2CID 36486849.

Khan AA, Mao XO, Banwait S, Jin K, Greenberg DA (November 2007). "Neuroglobin attenuates beta-amyloid neurotoxicity in vitro and transgenic Alzheimer phenotype in vivo". primary. Proceedings of the National Academy of Sciences of the United States of America. 104 (48): 19114–9. Bibcode:2007PNAS..10419114K. doi:10.1073/pnas.0706167104. PMC 2141917. PMID 18025470.

Zhang W, Tian Z, Sha S, Cheng LY, Philipsen S, Tan-Un KC (2011). "Functional and sequence analysis of human neuroglobin gene promoter region". primary. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1809 (4–6): 236–44. doi:10.1016/j.bbagrm.2011.02.003. PMID 21362510.

Guan JS, Haggarty SJ, Giacometti E, Dannenberg JH, Joseph N, Gao J, Nieland TJ, Zhou Y, Wang X, Mazitschek R, Bradner JE, DePinho RA, Jaenisch R, Tsai LH (May 2009). "HDAC2 negatively regulates memory formation and synaptic plasticity". primary. Nature. 459 (7243): 55–60. Bibcode:2009Natur.459...55G. doi:10.1038/nature07925. PMC 3498958. PMID 19424149.

Nasir J, Floresco SB, O'Kusky JR, Diewert VM, Richman JM, Zeisler J, Borowski A, Marth JD, Phillips AG, Hayden MR (June 1995). "Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes". primary. Cell. 81 (5): 811–23. doi:10.1016/0092-8674(95)90542-1. PMID 7774020. S2CID 16835259.

Chen S, Ferrone FA, Wetzel R (September 2002). "Huntington's disease age-of-onset linked to polyglutamine aggregation nucleation". primary. Proceedings of the National Academy of Sciences of the United States of America. 99 (18): 11884–9. Bibcode:2002PNAS...9911884C. doi:10.1073/pnas.182276099. PMC 129363. PMID 12186976.

Ryu H, Lee J, Hagerty SW, Soh BY, McAlpin SE, Cormier KA, Smith KM, Ferrante RJ (December 2006). "ESET/SETDB1 gene expression and histone H3 (K9) trimethylation in Huntington's disease". primary. Proceedings of the National Academy of Sciences of the United States of America. 103 (50): 19176–81. Bibcode:2006PNAS..10319176R. doi:10.1073/pnas.0606373103. PMC 1748195. PMID 17142323.

Hazeki N, Tsukamoto T, Yazawa I, Koyama M, Hattori S, Someki I, Iwatsubo T, Nakamura K, Goto J, Kanazawa I (June 2002). "Ultrastructure of nuclear aggregates formed by expressing an expanded polyglutamine". primary. Biochemical and Biophysical Research Communications. 294 (2): 429–40. doi:10.1016/S0006-291X(02)00498-9. PMID 12051730.

Sadri-Vakili G, Bouzou B, Benn CL, Kim MO, Chawla P, Overland RP, Glajch KE, Xia E, Qiu Z, Hersch SM, Clark TW, Yohrling GJ, Cha JH (June 2007). "Histones associated with downregulated genes are hypo-acetylated in Huntington's disease models". primary. Human Molecular Genetics. 16 (11): 1293–306. doi:10.1093/hmg/ddm078. PMID 17409194.

Hogarth P, Lovrecic L, Krainc D (October 2007). "Sodium phenylbutyrate in Huntington's disease: a dose-finding study". primary. Movement Disorders. 22 (13): 1962–4. doi:10.1002/mds.21632. PMID 17702032. S2CID 10846780.

Kim J, Inoue K, Ishii J, Vanti WB, Voronov SV, Murchison E, Hannon G, Abeliovich A (August 2007). "A MicroRNA feedback circuit in midbrain dopamine neurons". primary. Science. 317 (5842): 1220–4. Bibcode:2007Sci...317.1220K. doi:10.1126/science.1140481. PMC 2782470. PMID 17761882.

Jankovic J, Chen S, Le WD (2005). "The role of Nurr1 in the development of dopaminergic neurons and Parkinson's disease". review. Progress in Neurobiology. 77 (1–2): 128–38. doi:10.1016/j.pneurobio.2005.09.001. PMID 16243425. S2CID 22764367.

Doxakis E (April 2010). "Post-transcriptional regulation of alpha-synuclein expression by mir-7 and mir-153". primary. The Journal of Biological Chemistry. 285 (17): 12726–34. doi:10.1074/jbc.M109.086827. PMC 2857101. PMID 20106983.

Pieper HC, Evert BO, Kaut O, Riederer PF, Waha A, Wüllner U (December 2008). "Different methylation of the TNF-alpha promoter in cortex and substantia nigra: Implications for selective neuronal vulnerability". primary. Neurobiology of Disease. 32 (3): 521–7. doi:10.1016/j.nbd.2008.09.010. PMID 18930140. S2CID 8673158.

Mogi M, Harada M, Narabayashi H, Inagaki H, Minami M, Nagatsu T (June 1996). "Interleukin (IL)-1 beta, IL-2, IL-4, IL-6 and transforming growth factor-alpha levels are elevated in ventricular cerebrospinal fluid in juvenile parkinsonism and Parkinson's disease". primary. Neuroscience Letters. 211 (1): 13–6. doi:10.1016/0304-3940(96)12706-3. PMID 8809836. S2CID 54279479.

Bönsch D, Lenz B, Kornhuber J, Bleich S (February 2005). "DNA hypermethylation of the alpha synuclein promoter in patients with alcoholism". primary. NeuroReport. 16 (2): 167–70. doi:10.1097/00001756-200502080-00020. PMID 15671870. S2CID 43289612.

Jowaed A, Schmitt I, Kaut O, Wüllner U (May 2010). "Methylation regulates alpha-synuclein expression and is decreased in Parkinson's disease patients' brains". primary. The Journal of Neuroscience. 30 (18): 6355–9. doi:10.1523/JNEUROSCI.6119-09.2010. PMC 6632710. PMID 20445061.

Desplats P, Spencer B, Coffee E, Patel P, Michael S, Patrick C, Adame A, Rockenstein E, Masliah E (March 2011). "Alpha-synuclein sequesters Dnmt1 from the nucleus: a novel mechanism for epigenetic alterations in Lewy body diseases". primary. The Journal of Biological Chemistry. 286 (11): 9031–7. doi:10.1074/jbc.C110.212589. PMC 3059002. PMID 21296890.

Outeiro TF, Kontopoulos E, Altmann SM, Kufareva I, Strathearn KE, Amore AM, Volk CB, Maxwell MM, Rochet JC, McLean PJ, Young AB, Abagyan R, Feany MB, Hyman BT, Kazantsev AG (July 2007). "Sirtuin 2 inhibitors rescue alpha-synuclein-mediated toxicity in models of Parkinson's disease". primary. Science. 317 (5837): 516–9. Bibcode:2007Sci...317..516O. doi:10.1126/science.1143780. PMID 17588900. S2CID 84493360.

Song C, Kanthasamy A, Jin H, Anantharam V, Kanthasamy AG (October 2011). "Paraquat induces epigenetic changes by promoting histone acetylation in cell culture models of dopaminergic degeneration". primary. Neurotoxicology. 32 (5): 586–95. doi:10.1016/j.neuro.2011.05.018. PMC 3407036. PMID 21777615.

Harrison IF, Dexter DT (October 2013). "Epigenetic targeting of histone deacetylase: therapeutic potential in Parkinson's disease?". review. Pharmacology & Therapeutics. 140 (1): 34–52. doi:10.1016/j.pharmthera.2013.05.010. PMID 23711791.

Graves MC, Benton M, Lea RA, Boyle M, Tajouri L, Macartney-Coxson D, Scott RJ, Lechner-Scott J (2013-12-12). "Methylation differences at the HLA-DRB1 locus in CD4+ T-Cells are associated with multiple sclerosis". Multiple Sclerosis Journal. 20 (8): 1033–1041. doi:10.1177/1352458513516529. ISSN 1352-4585. PMID 24336351. S2CID 45718656.

Kular L, Liu Y, Ruhrmann S, Zheleznyakova G, Marabita F, Gomez-Cabrero D, James T, Ewing E, Lindén M, Górnikiewicz B, Aeinehband S (2018-06-19). "DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis". Nature Communications. 9 (1): 2397. Bibcode:2018NatCo...9.2397K. doi:10.1038/s41467-018-04732-5. ISSN 2041-1723. PMC 6008330. PMID 29921915.

Küçükali Cİ, Kürtüncü M, Çoban A, Çebi M, Tüzün E (2015). "Epigenetics of multiple sclerosis: an updated review". Neuromolecular Medicine. 17 (2): 83–96. doi:10.1007/s12017-014-8298-6. ISSN 1559-1174. PMID 24652042. S2CID 9147572.

Peedicayil J (2016). "Epigenetic Drugs for Multiple Sclerosis". Current Neuropharmacology. 14 (1): 3–9. doi:10.2174/1570159X13666150211001600. ISSN 1570-159X. PMC 4787283. PMID 26813117.

harvard.edu

ui.adsabs.harvard.edu

nih.gov

pubmed.ncbi.nlm.nih.gov

Sghirlanzoni A, Pareyson D, Lauria G (June 2005). "Sensory neuron diseases". review. The Lancet. Neurology. 4 (6): 349–61. doi:10.1016/S1474-4422(05)70096-X. PMID 15907739. S2CID 35053543.

Goll MG, Bestor TH (2005). "Eukaryotic cytosine methyltransferases". Annual Review of Biochemistry. 74: 481–514. doi:10.1146/annurev.biochem.74.010904.153721. PMID 15952895.

Bernstein BE, Meissner A, Lander ES (February 2007). "The mammalian epigenome". review. Cell. 128 (4): 669–81. doi:10.1016/j.cell.2007.01.033. PMID 17320505. S2CID 2722988.

Peedicayil J (April 2013). "Epigenetic drugs for Alzheimer's disease". British Journal of Clinical Pharmacology. 75 (4): 1152–3. doi:10.1111/j.1365-2125.2012.04444.x. PMC 3612735. PMID 22905989.

Peedicayil J (2016). "Epigenetic Drugs for Multiple Sclerosis". Current Neuropharmacology. 14 (1): 3–9. doi:10.2174/1570159X13666150211001600. ISSN 1570-159X. PMC 4787283. PMID 26813117.

ncbi.nlm.nih.gov

ninds.nih.gov

ghr.nlm.nih.gov

Entrez Gene. "BDNF". United States National Center for Biotechnology Information.

semanticscholar.org

api.semanticscholar.org

Sghirlanzoni A, Pareyson D, Lauria G (June 2005). "Sensory neuron diseases". review. The Lancet. Neurology. 4 (6): 349–61. doi:10.1016/S1474-4422(05)70096-X. PMID 15907739. S2CID 35053543.

Bernstein BE, Meissner A, Lander ES (February 2007). "The mammalian epigenome". review. Cell. 128 (4): 669–81. doi:10.1016/j.cell.2007.01.033. PMID 17320505. S2CID 2722988.

web.archive.org

Epigenetics of neurodegenerative diseases (English Wikipedia)

doi.org

escholarship.org

harvard.edu

ui.adsabs.harvard.edu

hopkinsmedicine.org

jns-journal.com

lww.com

journals.lww.com

mayoclinic.org

medlineplus.gov

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

ninds.nih.gov

ghr.nlm.nih.gov

ntu.edu.tw

ntur.lib.ntu.edu.tw

omim.org

researchgate.net

sagepub.com

journals.sagepub.com

sciencedirect.com

semanticscholar.org

api.semanticscholar.org

uva.nl

dare.uva.nl

web.archive.org

worldcat.org

search.worldcat.org