MECP2 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "MECP2" in Japanese language version.

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cnn.com

Hunt, Katie (12 January 2016). “Chinese scientists create monkeys with autism gene”. CNN News 2016年1月27日閲覧。

cornell.edu

instruct1.cit.cornell.edu

Paul A. Wade (December 2001). “Methyl CpG-binding proteins and transcriptional repression”. BioEssays 23 (12): 1131–1137. doi:10.1002/bies.10008. PMID 11746232. オリジナルの2007-08-14時点におけるアーカイブ。.

doi.org

“Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2”. Nat. Genet. 23 (2): 185–8. (October 1999). doi:10.1038/13810. PMID 10508514.
“Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA”. Cell 69 (6): 905–14. (June 1992). doi:10.1016/0092-8674(92)90610-O. PMID 1606614.
“MECP2, a key contributor to neurological disease, activates and represses transcription”. Science 320 (5880): 1224–9. (2008). Bibcode: 2008Sci...320.1224C. doi:10.1126/science.1153252. PMC 2443785. PMID 18511691.
“Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases”. Scientific Reports 9 (1): 18577. (December 2019). Bibcode: 2019NatSR...918577S. doi:10.1038/s41598-019-54976-4. PMC 6901466. PMID 31819097.
“Medicine. Activating a repressor.”. Science 320 (5880): 1172–3. (May 2008). doi:10.1126/science.1159146. PMC 2857976. PMID 18511680.
“Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice”. Proc. Natl. Acad. Sci. U.S.A. 101 (16): 6033–8. (April 2004). Bibcode: 2004PNAS..101.6033L. doi:10.1073/pnas.0401626101. PMC 395918. PMID 15069197.
“Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes”. Proc. Natl. Acad. Sci. U.S.A. 104 (49): 19416–21. (December 2007). Bibcode: 2007PNAS..10419416Y. doi:10.1073/pnas.0707442104. PMC 2148304. PMID 18042715.
“MeCP2, a key contributor to neurological disease, activates and represses transcription”. Science 320 (5880): 1224–9. (May 2008). Bibcode: 2008Sci...320.1224C. doi:10.1126/science.1153252. PMC 2443785. PMID 18511691.
“Chromatin compaction by human MeCP2. Assembly of novel secondary chromatin structures in the absence of DNA methylation”. J. Biol. Chem. 278 (34): 32181–8. (August 2003). doi:10.1074/jbc.M305308200. PMID 12788925.
LaSalle JM (2007). “The odyssey of MeCP2 and parental imprinting”. Epigenetics 2 (1): 5–10. doi:10.4161/epi.2.1.3697. PMC 1866173. PMID 17486180.
“Neural stem cells from a mouse model of Rett syndrome are prone to senescence, show reduced capacity to cope with genotoxic stress, and are impaired in the differentiation process”. Exp. Mol. Med. 50 (3): 1. (March 2018). doi:10.1038/s12276-017-0005-x. PMC 6118406. PMID 29563495.
“The solution structure of the domain from MeCP2 that binds to methylated DNA”. J. Mol. Biol. 291 (5): 1055–65. (September 1999). doi:10.1006/jmbi.1999.3023. PMID 10518942.
Paul A. Wade (December 2001). “Methyl CpG-binding proteins and transcriptional repression”. BioEssays 23 (12): 1131–1137. doi:10.1002/bies.10008. PMID 11746232. オリジナルの2007-08-14時点におけるアーカイブ。.
“MeCP2 in neurons: closing in on the causes of Rett syndrome”. Hum. Mol. Genet. 14 Spec No 1: R19–26. (April 2005). doi:10.1093/hmg/ddi102. PMID 15809268.
“Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders”. Hum. Mol. Genet. 13 (6): 629–39. (March 2004). doi:10.1093/hmg/ddh063. PMID 14734626.
Trappe, R.; Laccone, F.; Cobilanschi, J.; Meins, M.; Huppke, P.; Hanefeld, F.; Engel, W. (2001-05). “MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin”. American Journal of Human Genetics 68 (5): 1093–1101. doi:10.1086/320109. ISSN 0002-9297. PMC 1226090. PMID 11309679.
Girard, M.; Couvert, P.; Carrié, A.; Tardieu, M.; Chelly, J.; Beldjord, C.; Bienvenu, T. (2001-03). “Parental origin of de novo MECP2 mutations in Rett syndrome”. European journal of human genetics: EJHG 9 (3): 231–236. doi:10.1038/sj.ejhg.5200618. ISSN 1018-4813. PMID 11313764.
Jin, Dong-Yan, ed (2008). “Common variants within MECP2 confer risk of systemic lupus erythematosus”. PLOS ONE 3 (3): e1727. Bibcode: 2008PLoSO...3.1727S. doi:10.1371/journal.pone.0001727. PMC 2253825. PMID 18320046.
“Pathophysiology of Locus Ceruleus Neurons in a Mouse Model of Rett Syndrome”. Journal of Neuroscience 29 (39): 12187–12195. (2009). doi:10.1523/JNEUROSCI.3156-09.2009. PMC 2846656. PMID 19793977.
“The Ski protein family is required for MeCP2-mediated transcriptional repression”. J. Biol. Chem. 276 (36): 34115–21. (September 2001). doi:10.1074/jbc.M105747200. PMID 11441023.
“Homeostatic regulation of MeCP2 expression by a CREB-induced microRNA”. Nat. Neurosci. 10 (12): 1513–4. (December 2007). doi:10.1038/nn2010. PMID 17994015.
“Sex difference in mecp2 expression during a critical period of rat brain development”. Epigenetics 2 (3): 173–8. (September 2007). doi:10.4161/epi.2.3.4841. PMID 17965589.
“Mecp2 organizes juvenile social behavior in a sex-specific manner”. J. Neurosci. 28 (28): 7137–42. (July 2008). doi:10.1523/JNEUROSCI.1345-08.2008. PMC 2569867. PMID 18614683.
“A role for central vasopressin in pair bonding in monogamous prairie voles”. Nature 365 (6446): 545–8. (October 1993). Bibcode: 1993Natur.365..545W. doi:10.1038/365545a0. PMID 8413608.
“Profound impairment in social recognition and reduction in anxiety-like behavior in vasopressin V1a receptor knockout mice”. Neuropsychopharmacology 29 (3): 483–93. (March 2004). doi:10.1038/sj.npp.1300360. PMID 14647484.
“Sexual differentiation of central vasopressin and vasotocin systems in vertebrates: different mechanisms, similar endpoints”. Neuroscience 138 (3): 947–55. (2006). doi:10.1016/j.neuroscience.2005.07.050. PMC 1457099. PMID 16310321.
“Neonatal MeCP2 is important for the organization of sex differences in vasopressin expression”. Epigenetics 7 (3): 230–8. (March 2012). doi:10.4161/epi.7.3.19265. PMC 3335947. PMID 22430799.
“Dynamic DNA methylation programs persistent adverse effects of early-life stress”. Nat. Neurosci. 12 (12): 1559–66. (December 2009). doi:10.1038/nn.2436. PMID 19898468.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000169057 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000031393 - Ensembl, May 2017

harvard.edu

ui.adsabs.harvard.edu

“MECP2, a key contributor to neurological disease, activates and represses transcription”. Science 320 (5880): 1224–9. (2008). Bibcode: 2008Sci...320.1224C. doi:10.1126/science.1153252. PMC 2443785. PMID 18511691.
“Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases”. Scientific Reports 9 (1): 18577. (December 2019). Bibcode: 2019NatSR...918577S. doi:10.1038/s41598-019-54976-4. PMC 6901466. PMID 31819097.
“Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice”. Proc. Natl. Acad. Sci. U.S.A. 101 (16): 6033–8. (April 2004). Bibcode: 2004PNAS..101.6033L. doi:10.1073/pnas.0401626101. PMC 395918. PMID 15069197.
“Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes”. Proc. Natl. Acad. Sci. U.S.A. 104 (49): 19416–21. (December 2007). Bibcode: 2007PNAS..10419416Y. doi:10.1073/pnas.0707442104. PMC 2148304. PMID 18042715.
“MeCP2, a key contributor to neurological disease, activates and represses transcription”. Science 320 (5880): 1224–9. (May 2008). Bibcode: 2008Sci...320.1224C. doi:10.1126/science.1153252. PMC 2443785. PMID 18511691.
Jin, Dong-Yan, ed (2008). “Common variants within MECP2 confer risk of systemic lupus erythematosus”. PLOS ONE 3 (3): e1727. Bibcode: 2008PLoSO...3.1727S. doi:10.1371/journal.pone.0001727. PMC 2253825. PMID 18320046.
“A role for central vasopressin in pair bonding in monogamous prairie voles”. Nature 365 (6446): 545–8. (October 1993). Bibcode: 1993Natur.365..545W. doi:10.1038/365545a0. PMID 8413608.

nih.gov

pubmed.ncbi.nlm.nih.gov

“Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2”. Nat. Genet. 23 (2): 185–8. (October 1999). doi:10.1038/13810. PMID 10508514.
“Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA”. Cell 69 (6): 905–14. (June 1992). doi:10.1016/0092-8674(92)90610-O. PMID 1606614.
“MECP2, a key contributor to neurological disease, activates and represses transcription”. Science 320 (5880): 1224–9. (2008). Bibcode: 2008Sci...320.1224C. doi:10.1126/science.1153252. PMC 2443785. PMID 18511691.
“Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases”. Scientific Reports 9 (1): 18577. (December 2019). Bibcode: 2019NatSR...918577S. doi:10.1038/s41598-019-54976-4. PMC 6901466. PMID 31819097.
“Medicine. Activating a repressor.”. Science 320 (5880): 1172–3. (May 2008). doi:10.1126/science.1159146. PMC 2857976. PMID 18511680.
“Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice”. Proc. Natl. Acad. Sci. U.S.A. 101 (16): 6033–8. (April 2004). Bibcode: 2004PNAS..101.6033L. doi:10.1073/pnas.0401626101. PMC 395918. PMID 15069197.
“Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes”. Proc. Natl. Acad. Sci. U.S.A. 104 (49): 19416–21. (December 2007). Bibcode: 2007PNAS..10419416Y. doi:10.1073/pnas.0707442104. PMC 2148304. PMID 18042715.
“MeCP2, a key contributor to neurological disease, activates and represses transcription”. Science 320 (5880): 1224–9. (May 2008). Bibcode: 2008Sci...320.1224C. doi:10.1126/science.1153252. PMC 2443785. PMID 18511691.
“Chromatin compaction by human MeCP2. Assembly of novel secondary chromatin structures in the absence of DNA methylation”. J. Biol. Chem. 278 (34): 32181–8. (August 2003). doi:10.1074/jbc.M305308200. PMID 12788925.
LaSalle JM (2007). “The odyssey of MeCP2 and parental imprinting”. Epigenetics 2 (1): 5–10. doi:10.4161/epi.2.1.3697. PMC 1866173. PMID 17486180.
“Neural stem cells from a mouse model of Rett syndrome are prone to senescence, show reduced capacity to cope with genotoxic stress, and are impaired in the differentiation process”. Exp. Mol. Med. 50 (3): 1. (March 2018). doi:10.1038/s12276-017-0005-x. PMC 6118406. PMID 29563495.
“The solution structure of the domain from MeCP2 that binds to methylated DNA”. J. Mol. Biol. 291 (5): 1055–65. (September 1999). doi:10.1006/jmbi.1999.3023. PMID 10518942.
Paul A. Wade (December 2001). “Methyl CpG-binding proteins and transcriptional repression”. BioEssays 23 (12): 1131–1137. doi:10.1002/bies.10008. PMID 11746232. オリジナルの2007-08-14時点におけるアーカイブ。.
“MeCP2 in neurons: closing in on the causes of Rett syndrome”. Hum. Mol. Genet. 14 Spec No 1: R19–26. (April 2005). doi:10.1093/hmg/ddi102. PMID 15809268.
“Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders”. Hum. Mol. Genet. 13 (6): 629–39. (March 2004). doi:10.1093/hmg/ddh063. PMID 14734626.
Trappe, R.; Laccone, F.; Cobilanschi, J.; Meins, M.; Huppke, P.; Hanefeld, F.; Engel, W. (2001-05). “MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin”. American Journal of Human Genetics 68 (5): 1093–1101. doi:10.1086/320109. ISSN 0002-9297. PMC 1226090. PMID 11309679.
Girard, M.; Couvert, P.; Carrié, A.; Tardieu, M.; Chelly, J.; Beldjord, C.; Bienvenu, T. (2001-03). “Parental origin of de novo MECP2 mutations in Rett syndrome”. European journal of human genetics: EJHG 9 (3): 231–236. doi:10.1038/sj.ejhg.5200618. ISSN 1018-4813. PMID 11313764.
Jin, Dong-Yan, ed (2008). “Common variants within MECP2 confer risk of systemic lupus erythematosus”. PLOS ONE 3 (3): e1727. Bibcode: 2008PLoSO...3.1727S. doi:10.1371/journal.pone.0001727. PMC 2253825. PMID 18320046.
“Pathophysiology of Locus Ceruleus Neurons in a Mouse Model of Rett Syndrome”. Journal of Neuroscience 29 (39): 12187–12195. (2009). doi:10.1523/JNEUROSCI.3156-09.2009. PMC 2846656. PMID 19793977.
“The Ski protein family is required for MeCP2-mediated transcriptional repression”. J. Biol. Chem. 276 (36): 34115–21. (September 2001). doi:10.1074/jbc.M105747200. PMID 11441023.
“Homeostatic regulation of MeCP2 expression by a CREB-induced microRNA”. Nat. Neurosci. 10 (12): 1513–4. (December 2007). doi:10.1038/nn2010. PMID 17994015.
“Sex difference in mecp2 expression during a critical period of rat brain development”. Epigenetics 2 (3): 173–8. (September 2007). doi:10.4161/epi.2.3.4841. PMID 17965589.
“Mecp2 organizes juvenile social behavior in a sex-specific manner”. J. Neurosci. 28 (28): 7137–42. (July 2008). doi:10.1523/JNEUROSCI.1345-08.2008. PMC 2569867. PMID 18614683.
“A role for central vasopressin in pair bonding in monogamous prairie voles”. Nature 365 (6446): 545–8. (October 1993). Bibcode: 1993Natur.365..545W. doi:10.1038/365545a0. PMID 8413608.
“Profound impairment in social recognition and reduction in anxiety-like behavior in vasopressin V1a receptor knockout mice”. Neuropsychopharmacology 29 (3): 483–93. (March 2004). doi:10.1038/sj.npp.1300360. PMID 14647484.
“Sexual differentiation of central vasopressin and vasotocin systems in vertebrates: different mechanisms, similar endpoints”. Neuroscience 138 (3): 947–55. (2006). doi:10.1016/j.neuroscience.2005.07.050. PMC 1457099. PMID 16310321.
“Neonatal MeCP2 is important for the organization of sex differences in vasopressin expression”. Epigenetics 7 (3): 230–8. (March 2012). doi:10.4161/epi.7.3.19265. PMC 3335947. PMID 22430799.
“Dynamic DNA methylation programs persistent adverse effects of early-life stress”. Nat. Neurosci. 12 (12): 1559–66. (December 2009). doi:10.1038/nn.2436. PMID 19898468.

ncbi.nlm.nih.gov

pmc.ncbi.nlm.nih.gov

web.archive.org

Paul A. Wade (December 2001). “Methyl CpG-binding proteins and transcriptional repression”. BioEssays 23 (12): 1131–1137. doi:10.1002/bies.10008. PMID 11746232. オリジナルの2007-08-14時点におけるアーカイブ。.

wikipedia.org

en.wikipedia.org

GRCh38: Ensembl release 89: ENSG00000169057 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000031393 - Ensembl, May 2017

worldcat.org

search.worldcat.org

Trappe, R.; Laccone, F.; Cobilanschi, J.; Meins, M.; Huppke, P.; Hanefeld, F.; Engel, W. (2001-05). “MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin”. American Journal of Human Genetics 68 (5): 1093–1101. doi:10.1086/320109. ISSN 0002-9297. PMC 1226090. PMID 11309679.
Girard, M.; Couvert, P.; Carrié, A.; Tardieu, M.; Chelly, J.; Beldjord, C.; Bienvenu, T. (2001-03). “Parental origin of de novo MECP2 mutations in Rett syndrome”. European journal of human genetics: EJHG 9 (3): 231–236. doi:10.1038/sj.ejhg.5200618. ISSN 1018-4813. PMID 11313764.