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Items: 1 to 20 of 131

1.

Comparison of Genomic and Epigenomic Expression in Monozygotic Twins Discordant for Rett Syndrome.

Miyake K, Yang C, Minakuchi Y, Ohori K, Soutome M, Hirasawa T, Kazuki Y, Adachi N, Suzuki S, Itoh M, Goto Y, Andoh T, Kurosawa H, Oshimura M, Sasaki M, Toyoda A, Kubota T.

PLoS One. 2013 Jun 21;8(6):e66729. doi: 10.1371/journal.pone.0066729. Print 2013. Erratum in: PLoS One. 2014;9(4):e94737.

2.

Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis.

Baranzini SE, Mudge J, van Velkinburgh JC, Khankhanian P, Khrebtukova I, Miller NA, Zhang L, Farmer AD, Bell CJ, Kim RW, May GD, Woodward JE, Caillier SJ, McElroy JP, Gomez R, Pando MJ, Clendenen LE, Ganusova EE, Schilkey FD, Ramaraj T, Khan OA, Huntley JJ, Luo S, Kwok PY, Wu TD, Schroth GP, Oksenberg JR, Hauser SL, Kingsmore SF.

Nature. 2010 Apr 29;464(7293):1351-6. doi: 10.1038/nature08990.

3.

De novo deletion in MECP2 in a monozygotic twin pair: a case report.

Mittal K, Kabra M, Juyal R, BK T.

BMC Med Genet. 2011 Aug 27;12:113. doi: 10.1186/1471-2350-12-113.

4.
5.

Genome, epigenome and transcriptome analyses of a pair of monozygotic twins discordant for systemic lupus erythematosus.

Furukawa H, Oka S, Matsui T, Hashimoto A, Arinuma Y, Komiya A, Fukui N, Tsuchiya N, Tohma S.

Hum Immunol. 2013 Feb;74(2):170-5. doi: 10.1016/j.humimm.2012.11.007. Epub 2012 Nov 29.

PMID:
23200755
6.

Genomic and epigenomic analyses of monozygotic twins discordant for congenital renal agenesis.

Jin M, Zhu S, Hu P, Liu D, Li Q, Li Z, Zhang X, Xie Y, Chen X.

Am J Kidney Dis. 2014 Jul;64(1):119-22. doi: 10.1053/j.ajkd.2014.01.423. Epub 2014 Feb 28.

PMID:
24583054
7.

DNA methylation differences in monozygotic twin pairs discordant for schizophrenia identifies psychosis related genes and networks.

Castellani CA, Laufer BI, Melka MG, Diehl EJ, O'Reilly RL, Singh SM.

BMC Med Genomics. 2015 May 6;8:17. doi: 10.1186/s12920-015-0093-1.

8.

MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning.

Zahorakova D, Lelkova P, Gregor V, Magner M, Zeman J, Martasek P.

J Hum Genet. 2016 Jul;61(7):617-25. doi: 10.1038/jhg.2016.19. Epub 2016 Mar 17.

PMID:
26984561
9.

The role of different X-inactivation pattern on the variable clinical phenotype with Rett syndrome.

Ishii T, Makita Y, Ogawa A, Amamiya S, Yamamoto M, Miyamoto A, Oki J.

Brain Dev. 2001 Dec;23 Suppl 1:S161-4.

PMID:
11738865
10.

Epigenetic investigation of variably X chromosome inactivated genes in monozygotic female twins discordant for primary biliary cirrhosis.

Mitchell MM, Lleo A, Zammataro L, Mayo MJ, Invernizzi P, Bach N, Shimoda S, Gordon S, Podda M, Gershwin ME, Selmi C, LaSalle JM.

Epigenetics. 2011 Jan;6(1):95-102. doi: 10.4161/epi.6.1.13405. Epub 2011 Jan 1.

11.

[X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome].

Jiang SL, Bao XH, Song FY, Pan H, Li MR, Wu XR.

Zhonghua Er Ke Za Zhi. 2006 Sep;44(9):648-52. Chinese.

PMID:
17217653
12.

X chromosome inactivation in Rett Syndrome and its correlations with MECP2 mutations and phenotype.

Xinhua Bao, Shengling Jiang, Fuying Song, Hong Pan, Meirong Li, Wu XR.

J Child Neurol. 2008 Jan;23(1):22-5. doi: 10.1177/0883073807307077.

PMID:
18184939
13.

[Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in fifteen sporadic cases with Rett syndrome].

Zhu XW, Pan H, Li MR, Bao XH, Zhang JJ, Wu XR.

Zhonghua Er Ke Za Zhi. 2009 Aug;47(8):565-9. Chinese.

PMID:
19951486
14.

Intra-Monozygotic Twin Pair Discordance and Longitudinal Variation of Whole-Genome Scale DNA Methylation in Adults.

Zhang N, Zhao S, Zhang SH, Chen J, Lu D, Shen M, Li C.

PLoS One. 2015 Aug 6;10(8):e0135022. doi: 10.1371/journal.pone.0135022. eCollection 2015.

15.

Evolving role of MeCP2 in Rett syndrome and autism.

LaSalle JM, Yasui DH.

Epigenomics. 2009 Oct;1(1):119-30. doi: 10.2217/epi.09.13. Review.

16.

Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence.

Gordon L, Joo JE, Powell JE, Ollikainen M, Novakovic B, Li X, Andronikos R, Cruickshank MN, Conneely KN, Smith AK, Alisch RS, Morley R, Visscher PM, Craig JM, Saffery R.

Genome Res. 2012 Aug;22(8):1395-406. doi: 10.1101/gr.136598.111. Epub 2012 Jul 16.

17.

Differential methylation of the X-chromosome is a possible source of discordance for bipolar disorder female monozygotic twins.

Rosa A, Picchioni MM, Kalidindi S, Loat CS, Knight J, Toulopoulou T, Vonk R, van der Schot AC, Nolen W, Kahn RS, McGuffin P, Murray RM, Craig IW.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):459-62.

PMID:
17955481
18.

Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations.

Ravn K, Roende G, Duno M, Fuglsang K, Eiklid KL, Tümer Z, Nielsen JB, Skjeldal OH.

Orphanet J Rare Dis. 2011 Aug 30;6:58. doi: 10.1186/1750-1172-6-58. Review.

19.

Differentiation of multipotent neural stem cells derived from Rett syndrome patients is biased toward the astrocytic lineage.

Andoh-Noda T, Akamatsu W, Miyake K, Matsumoto T, Yamaguchi R, Sanosaka T, Okada Y, Kobayashi T, Ohyama M, Nakashima K, Kurosawa H, Kubota T, Okano H.

Mol Brain. 2015 May 27;8:31. doi: 10.1186/s13041-015-0121-2.

20.

Uneven X inactivation in a female monozygotic twin pair with Fabry disease and discordant expression of a novel mutation in the alpha-galactosidase A gene.

Redonnet-Vernhet I, Ploos van Amstel JK, Jansen RP, Wevers RA, Salvayre R, Levade T.

J Med Genet. 1996 Aug;33(8):682-8.

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