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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 2
2005 21
2006 55
2007 45
2008 42
2009 57
2010 55
2011 56
2012 63
2013 54
2014 53
2015 52
2016 59
2017 53
2018 45
2019 32
2020 7
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Search Results

640 results
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Page 1
MeCP2 mutations: progress towards understanding and treating Rett syndrome.
Shah RR, Bird AP. Shah RR, et al. Genome Med. 2017 Feb 17;9(1):17. doi: 10.1186/s13073-017-0411-7. Genome Med. 2017. PMID: 28212680 Free PMC article. Review.
The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2.
Neul JL, Benke TA, Marsh ED, Skinner SA, Merritt J, Lieberman DN, Standridge S, Feyma T, Heydemann P, Peters S, Ryther R, Jones M, Suter B, Kaufmann WE, Glaze DG, Percy AK. Neul JL, et al. Am J Med Genet B Neuropsychiatr Genet. 2019 Jan;180(1):55-67. doi: 10.1002/ajmg.b.32707. Epub 2018 Dec 7. Am J Med Genet B Neuropsychiatr Genet. 2019. PMID: 30536762 Free PMC article.
[Interaction between abnormal expression of fragile histidine triad and methyl-CpG-binding protein 2 on cervical cancerization].
Yang Q, Li Y, Wang L, Song ZC, Feng MJ, Ding L, Wang JT. Yang Q, et al. Zhonghua Liu Xing Bing Xue Za Zhi. 2018 May 10;39(5):689-693. doi: 10.3760/cma.j.issn.0254-6450.2018.05.030. Zhonghua Liu Xing Bing Xue Za Zhi. 2018. PMID: 29860820 Chinese.
Autism-like behaviours and germline transmission in transgenic monkeys overexpressing MeCP2.
Liu Z, Li X, Zhang JT, Cai YJ, Cheng TL, Cheng C, Wang Y, Zhang CC, Nie YH, Chen ZF, Bian WJ, Zhang L, Xiao J, Lu B, Zhang YF, Zhang XD, Sang X, Wu JJ, Xu X, Xiong ZQ, Zhang F, Yu X, Gong N, Zhou WH, Sun Q, Qiu Z. Liu Z, et al. Nature. 2016 Feb 4;530(7588):98-102. doi: 10.1038/nature16533. Epub 2016 Jan 25. Nature. 2016. PMID: 26808898
Rett syndrome: insights into genetic, molecular and circuit mechanisms.
Ip JPK, Mellios N, Sur M. Ip JPK, et al. Nat Rev Neurosci. 2018 Jun;19(6):368-382. doi: 10.1038/s41583-018-0006-3. Nat Rev Neurosci. 2018. PMID: 29740174 Free PMC article. Review.
Methyl-CpG-Binding Protein 2 (MECP2) Polymorphism in Iranian Patients with Systemic Lupus Erythematosus.
Alesaeidi S, Karami J, Mahmoudi M, Akbarian M, Poursani S, Amirzadeh A, Haddadi NS, Saffari E, Jamshidi AR. Alesaeidi S, et al. Inflammation. 2015 Dec;38(6):2185-90. doi: 10.1007/s10753-015-0201-6. Inflammation. 2015. PMID: 26156810
Methyl-CpG-binding protein 2 mediates antifibrotic effects in scleroderma fibroblasts.
He Y, Tsou PS, Khanna D, Sawalha AH. He Y, et al. Ann Rheum Dis. 2018 Aug;77(8):1208-1218. doi: 10.1136/annrheumdis-2018-213022. Epub 2018 May 14. Ann Rheum Dis. 2018. PMID: 29760157 Free PMC article.
Rett syndrome: a neurological disorder with metabolic components.
Kyle SM, Vashi N, Justice MJ. Kyle SM, et al. Open Biol. 2018 Feb;8(2):170216. doi: 10.1098/rsob.170216. Open Biol. 2018. PMID: 29445033 Free PMC article. Review.
Disruption of DNA-methylation-dependent long gene repression in Rett syndrome.
Gabel HW, Kinde B, Stroud H, Gilbert CS, Harmin DA, Kastan NR, Hemberg M, Ebert DH, Greenberg ME. Gabel HW, et al. Nature. 2015 Jun 4;522(7554):89-93. doi: 10.1038/nature14319. Epub 2015 Mar 11. Nature. 2015. PMID: 25762136 Free PMC article.
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