Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 149

1.

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.

2.

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.

3.

Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains.

Rabinovitz S, Kaufman Y, Ludwig G, Razin A, Shemer R.

Proc Natl Acad Sci U S A. 2012 May 8;109(19):7403-8. doi: 10.1073/pnas.1116661109. Epub 2012 Apr 23.

4.

An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in mice.

Wu MY, Jiang M, Zhai X, Beaudet AL, Wu RC.

PLoS One. 2012;7(4):e34348. doi: 10.1371/journal.pone.0034348. Epub 2012 Apr 4.

5.

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.

6.

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.

7.

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.

8.

Control elements within the PWS/AS imprinting box and their function in the imprinting process.

Kantor B, Makedonski K, Green-Finberg Y, Shemer R, Razin A.

Hum Mol Genet. 2004 Apr 1;13(7):751-62. Epub 2004 Feb 12.

9.

Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.

Glenn CC, Driscoll DJ, Yang TP, Nicholls RD.

Mol Hum Reprod. 1997 Apr;3(4):321-32. Review.

10.

Establishing the epigenetic status of the Prader-Willi/Angelman imprinting center in the gametes and embryo.

Kantor B, Kaufman Y, Makedonski K, Razin A, Shemer R.

Hum Mol Genet. 2004 Nov 15;13(22):2767-79. Epub 2004 Sep 14.

11.

Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domain.

Kaufman Y, Heled M, Perk J, Razin A, Shemer R.

Proc Natl Acad Sci U S A. 2009 Jun 23;106(25):10242-7. doi: 10.1073/pnas.0902087106. Epub 2009 Jun 8.

12.

The imprinting box of the Prader-Willi/Angelman syndrome domain.

Shemer R, Hershko AY, Perk J, Mostoslavsky R, Tsuberi B, Cedar H, Buiting K, Razin A.

Nat Genet. 2000 Dec;26(4):440-3.

PMID:
11101841
13.

Structure and function correlations at the imprinted mouse Snrpn locus.

Gabriel JM, Gray TA, Stubbs L, Saitoh S, Ohta T, Nicholls RD.

Mamm Genome. 1998 Oct;9(10):788-93.

PMID:
9745031
14.

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.

15.

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.

17.

Disruption of the bipartite imprinting center in a family with Angelman syndrome.

Buiting K, Barnicoat A, Lich C, Pembrey M, Malcolm S, Horsthemke B.

Am J Hum Genet. 2001 May;68(5):1290-4. Epub 2001 Mar 23.

18.

Mouse imprinting defect mutations that model Angelman syndrome.

Wu MY, Chen KS, Bressler J, Hou A, Tsai TF, Beaudet AL.

Genesis. 2006 Jan;44(1):12-22.

PMID:
16397868
19.
20.
Items per page

Supplemental Content

Write to the Help Desk