Chamberlain SJ - Search Results

1

Modeling Genomic Imprinting Disorders Using Induced Pluripotent Stem Cells.

Chamberlain SJ, Germain ND, Chen PF, Hsiao JS, Glatt-Deeley H. Chamberlain SJ, et al. Methods Mol Biol. 2016;1353:45-64. doi: 10.1007/7651_2014_169. Methods Mol Biol. 2016. PMID: 25520291

2

Induced pluripotent stem (iPS) cells as in vitro models of human neurogenetic disorders.

Chamberlain SJ, Li XJ, Lalande M. Chamberlain SJ, et al. Neurogenetics. 2008 Oct;9(4):227-35. doi: 10.1007/s10048-008-0147-z. Epub 2008 Sep 13. Neurogenetics. 2008. PMID: 18791750 Review.

3

Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13.

Chamberlain SJ, Lalande M. Chamberlain SJ, et al. Neurobiol Dis. 2010 Jul;39(1):13-20. doi: 10.1016/j.nbd.2010.03.011. Epub 2010 Mar 18. Neurobiol Dis. 2010. PMID: 20304067 Review.

4

Angelman syndrome, a genomic imprinting disorder of the brain.

Chamberlain SJ, Lalande M. Chamberlain SJ, et al. J Neurosci. 2010 Jul 28;30(30):9958-63. doi: 10.1523/JNEUROSCI.1728-10.2010. J Neurosci. 2010. PMID: 20668179 Free PMC article. No abstract available.

5

Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes.

Chamberlain SJ, Chen PF, Ng KY, Bourgois-Rocha F, Lemtiri-Chlieh F, Levine ES, Lalande M. Chamberlain SJ, et al. Proc Natl Acad Sci U S A. 2010 Oct 12;107(41):17668-73. doi: 10.1073/pnas.1004487107. Epub 2010 Sep 27. Proc Natl Acad Sci U S A. 2010. PMID: 20876107 Free PMC article.

6

Comment on "Do repeated arrays of box C/D small nucleolar RNA and microRNA genes elicit genomic imprinting?" DOI 10.1002/bies201100032.

Chamberlain SJ. Chamberlain SJ. Bioessays. 2011 Aug;33(8):563-4. doi: 10.1002/bies.201100081. Bioessays. 2011. PMID: 21769903 No abstract available.

7

RNAs of the human chromosome 15q11-q13 imprinted region.

Chamberlain SJ. Chamberlain SJ. Wiley Interdiscip Rev RNA. 2013 Mar-Apr;4(2):155-66. doi: 10.1002/wrna.1150. Epub 2012 Dec 3. Wiley Interdiscip Rev RNA. 2013. PMID: 23208756 Free PMC article. Review.

8

Topoisomerases facilitate transcription of long genes linked to autism.

King IF, Yandava CN, Mabb AM, Hsiao JS, Huang HS, Pearson BL, Calabrese JM, Starmer J, Parker JS, Magnuson T, Chamberlain SJ, Philpot BD, Zylka MJ. King IF, et al. Among authors: chamberlain sj. Nature. 2013 Sep 5;501(7465):58-62. doi: 10.1038/nature12504. Epub 2013 Aug 28. Nature. 2013. PMID: 23995680 Free PMC article.

9

Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion.

Martins-Taylor K, Hsiao JS, Chen PF, Glatt-Deeley H, De Smith AJ, Blakemore AI, Lalande M, Chamberlain SJ. Martins-Taylor K, et al. Among authors: chamberlain sj. Hum Mol Genet. 2014 May 1;23(9):2364-73. doi: 10.1093/hmg/ddt628. Epub 2013 Dec 20. Hum Mol Genet. 2014. PMID: 24363065 Free PMC article.

10

Reactivation of maternal SNORD116 cluster via SETDB1 knockdown in Prader-Willi syndrome iPSCs.

Cruvinel E, Budinetz T, Germain N, Chamberlain S, Lalande M, Martins-Taylor K. Cruvinel E, et al. Hum Mol Genet. 2014 Sep 1;23(17):4674-85. doi: 10.1093/hmg/ddu187. Epub 2014 Apr 23. Hum Mol Genet. 2014. PMID: 24760766 Free PMC article.

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