Chamberlain SJ - Search Results

1

Subtelomeric hotspots of aberrant 5-hydroxymethylcytosine-mediated epigenetic modifications during reprogramming to pluripotency.

Wang T, Wu H, Li Y, Szulwach KE, Lin L, Li X, Chen IP, Goldlust IS, Chamberlain SJ, Dodd A, Gong H, Ananiev G, Han JW, Yoon YS, Rudd MK, Yu M, Song CX, He C, Chang Q, Warren ST, Jin P. Wang T, et al. Among authors: chamberlain sj. Nat Cell Biol. 2013 Jun;15(6):700-11. doi: 10.1038/ncb2748. Epub 2013 May 19. Nat Cell Biol. 2013. PMID: 23685628 Free PMC article.

2

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.

3

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.

4

Polycomb repressive complex 2 is dispensable for maintenance of embryonic stem cell pluripotency.

Chamberlain SJ, Yee D, Magnuson T. Chamberlain SJ, et al. Stem Cells. 2008 Jun;26(6):1496-505. doi: 10.1634/stemcells.2008-0102. Epub 2008 Apr 10. Stem Cells. 2008. PMID: 18403752 Free PMC article.

5

Specific ZNF274 binding interference at SNORD116 activates the maternal transcripts in Prader-Willi syndrome neurons.

Langouët M, Gorka D, Orniacki C, Dupont-Thibert CM, Chung MS, Glatt-Deeley HR, Germain N, Crandall LJ, Cotney JL, Stoddard CE, Lalande M, Chamberlain SJ. Langouët M, et al. Among authors: chamberlain sj. Hum Mol Genet. 2020 Nov 25;29(19):3285-3295. doi: 10.1093/hmg/ddaa210. Hum Mol Genet. 2020. PMID: 32977341 Free PMC article.

6

Generation of isogenic models of Angelman syndrome and Prader-Willi syndrome in CRISPR/Cas9-engineered human embryonic stem cells.

Gilmore RB, Gorka D, Stoddard CE, Sonawane P, Cotney J, Chamberlain SJ. Gilmore RB, et al. Among authors: chamberlain sj. PLoS One. 2024 Nov 1;19(11):e0311565. doi: 10.1371/journal.pone.0311565. eCollection 2024. PLoS One. 2024. PMID: 39485792 Free PMC article.

7

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

8

Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype.

Lee S, Kozlov S, Hernandez L, Chamberlain SJ, Brannan CI, Stewart CL, Wevrick R. Lee S, et al. Among authors: chamberlain sj. Hum Mol Genet. 2000 Jul 22;9(12):1813-9. doi: 10.1093/hmg/9.12.1813. Hum Mol Genet. 2000. PMID: 10915770

9

Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice.

Chamberlain SJ, Johnstone KA, DuBose AJ, Simon TA, Bartolomei MS, Resnick JL, Brannan CI. Chamberlain SJ, et al. Hum Mol Genet. 2004 Dec 1;13(23):2971-7. doi: 10.1093/hmg/ddh314. Epub 2004 Sep 30. Hum Mol Genet. 2004. PMID: 15459179

10

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.

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