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Items: 1 to 20 of 35


Role of epigenetic mechanisms in transmitting the effects of neonatal sevoflurane exposure to the next generation of male, but not female, rats.

Ju LS, Yang JJ, Morey TE, Gravenstein N, Seubert CN, Resnick JL, Zhang JQ, Martynyuk AE.

Br J Anaesth. 2018 Aug;121(2):406-416. doi: 10.1016/j.bja.2018.04.034. Epub 2018 Jun 5.


Paradoxical leanness in the imprinting-centre deletion mouse model for Prader-Willi syndrome.

Golding DM, Rees DJ, Davies JR, Relkovic D, Furby HV, Guschina IA, Hopkins AL, Davies JS, Resnick JL, Isles AR, Wells T.

J Endocrinol. 2017 Jan;232(1):123-135. Epub 2016 Oct 31.


Correction for Lewis et al., Angelman syndrome imprinting center encodes a transcriptional promoter.

Lewis MW, Brant JO, Kramer JM, Moss JI, Yang TP, Hansen PJ, Williams RS, Resnick JL.

Proc Natl Acad Sci U S A. 2015 Jun 2;112(22):E2977. doi: 10.1073/pnas.1500034112. Epub 2015 Jan 14. No abstract available.


Influence of the Prader-Willi syndrome imprinting center on the DNA methylation landscape in the mouse brain.

Brant JO, Riva A, Resnick JL, Yang TP.

Epigenetics. 2014 Nov;9(11):1540-56. doi: 10.4161/15592294.2014.969667.


Angelman syndrome imprinting center encodes a transcriptional promoter.

Lewis MW, Brant JO, Kramer JM, Moss JI, Yang TP, Hansen PJ, Williams RS, Resnick JL.

Proc Natl Acad Sci U S A. 2015 Jun 2;112(22):6871-5. doi: 10.1073/pnas.1411261111. Epub 2014 Nov 5. Erratum in: Proc Natl Acad Sci U S A. 2015 Jun 2;112(22):E2977.


Adenine nucleotide translocase 4 is expressed within embryonic ovaries and dispensable during oogenesis.

Lim CH, Brower JV, Resnick JL, Oh SP, Terada N.

Reprod Sci. 2015 Feb;22(2):250-7. doi: 10.1177/1933719114542026. Epub 2014 Jul 16.


Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of Prader-Willi syndrome.

Yazdi PG, Su H, Ghimbovschi S, Fan W, Coskun PE, Nalbandian A, Knoblach S, Resnick JL, Hoffman E, Wallace DC, Kimonis VE.

Clin Transl Sci. 2013 Oct;6(5):347-55. doi: 10.1111/cts.12083. Epub 2013 Jul 29.


Recommendations for the investigation of animal models of Prader-Willi syndrome.

Resnick JL, Nicholls RD, Wevrick R; Prader-Willi Syndrome Animal Models Working Group.

Mamm Genome. 2013 Jun;24(5-6):165-78. doi: 10.1007/s00335-013-9454-2. Epub 2013 Apr 23.


Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain.

Rodriguez-Jato S, Shan J, Khadake J, Heggestad AD, Ma X, Johnstone KA, Resnick JL, Yang TP.

PLoS One. 2013;8(2):e52390. doi: 10.1371/journal.pone.0052390. Epub 2013 Feb 4.


Immunomagnetic purification of murine primordial germ cells.

Smith EY, Resnick JL.

Methods Mol Biol. 2012;925:61-6. doi: 10.1007/978-1-62703-011-3_4.


Temporal and developmental requirements for the Prader-Willi imprinting center.

DuBose AJ, Smith EY, Johnstone KA, Resnick JL.

Proc Natl Acad Sci U S A. 2012 Feb 28;109(9):3446-50. doi: 10.1073/pnas.1115057109. Epub 2012 Feb 13.


Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus.

Smith EY, Futtner CR, Chamberlain SJ, Johnstone KA, Resnick JL.

PLoS Genet. 2011 Dec;7(12):e1002422. doi: 10.1371/journal.pgen.1002422. Epub 2011 Dec 29.


A new deletion refines the boundaries of the murine Prader-Willi syndrome imprinting center.

Dubose AJ, Smith EY, Yang TP, Johnstone KA, Resnick JL.

Hum Mol Genet. 2011 Sep 1;20(17):3461-6. doi: 10.1093/hmg/ddr262. Epub 2011 Jun 9.


Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader-Willi syndrome.

Relkovic D, Doe CM, Humby T, Johnstone KA, Resnick JL, Holland AJ, Hagan JJ, Wilkinson LS, Isles AR.

Eur J Neurosci. 2010 Jan;31(1):156-64. doi: 10.1111/j.1460-9568.2009.07048.x. Epub 2009 Dec 23.


Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC.

DuBose AJ, Johnstone KA, Smith EY, Hallett RA, Resnick JL.

Neurogenetics. 2010 May;11(2):145-51. doi: 10.1007/s10048-009-0226-9. Epub 2009 Nov 6.


Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size.

Leung KN, Vallero RO, DuBose AJ, Resnick JL, LaSalle JM.

Hum Mol Genet. 2009 Nov 15;18(22):4227-38. doi: 10.1093/hmg/ddp373. Epub 2009 Aug 5.


A targeted deletion upstream of Snrpn does not result in an imprinting defect.

Peery EG, Elmore MD, Resnick JL, Brannan CI, Johnstone KA.

Mamm Genome. 2007 Apr;18(4):255-62. Epub 2007 May 19.


DNA methylation is a primary mechanism for silencing postmigratory primordial germ cell genes in both germ cell and somatic cell lineages.

Maatouk DM, Kellam LD, Mann MR, Lei H, Li E, Bartolomei MS, Resnick JL.

Development. 2006 Sep;133(17):3411-8. Epub 2006 Aug 3.


A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects.

Johnstone KA, DuBose AJ, Futtner CR, Elmore MD, Brannan CI, Resnick JL.

Hum Mol Genet. 2006 Feb 1;15(3):393-404. Epub 2005 Dec 20.


DNA methylation is required for silencing of ant4, an adenine nucleotide translocase selectively expressed in mouse embryonic stem cells and germ cells.

Rodić N, Oka M, Hamazaki T, Murawski MR, Jorgensen M, Maatouk DM, Resnick JL, Li E, Terada N.

Stem Cells. 2005 Oct;23(9):1314-23. Epub 2005 Jul 28.

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