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Items: 1 to 20 of 29

1.

Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.

Hogart A, Leung KN, Wang NJ, Wu DJ, Driscoll J, Vallero RO, Schanen NC, LaSalle JM.

J Med Genet. 2009 Feb;46(2):86-93. doi: 10.1136/jmg.2008.061580. Epub 2008 Oct 7.

2.

Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.

Kalsner L, Chamberlain SJ.

Pediatr Clin North Am. 2015 Jun;62(3):587-606. doi: 10.1016/j.pcl.2015.03.004. Epub 2015 Apr 22. Review.

3.

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.

PMID:
9237260
4.

Mechanisms of imprinting of the Prader-Willi/Angelman region.

Horsthemke B, Wagstaff J.

Am J Med Genet A. 2008 Aug 15;146A(16):2041-52. doi: 10.1002/ajmg.a.32364. Review.

PMID:
18627066
5.

Imprinting in Angelman and Prader-Willi syndromes.

Jiang Y, Tsai TF, Bressler J, Beaudet AL.

Curr Opin Genet Dev. 1998 Jun;8(3):334-42. Review.

PMID:
9691003
6.

Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.

Engelen JJ, Loots WJ, Albrechts JC, Schrander-Stumpel CT, Dirckx R, Smeets HJ, Hamers AJ, Geraedts JP.

Genet Couns. 1999;10(2):123-32. Review.

PMID:
10422004
7.

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.

Nicholls RD, Knepper JL.

Annu Rev Genomics Hum Genet. 2001;2:153-75. Review.

PMID:
11701647
8.

Prader-Willi and Angelman syndromes. Disorders of genomic imprinting.

Cassidy SB, Schwartz S.

Medicine (Baltimore). 1998 Mar;77(2):140-51. Review.

9.

Dosage-sensitivity of imprinted genes expressed in the brain: 15q11-q13 and neuropsychiatric illness.

McNamara GI, Isles AR.

Biochem Soc Trans. 2013 Jun;41(3):721-6. doi: 10.1042/BST20130008. Review.

PMID:
23697931
10.

Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models.

Nicholls RD, Ohta T, Gray TA.

Acta Paediatr Suppl. 1999 Dec;88(433):99-104. Review.

PMID:
10626556
11.

Parental imprinting and Angelman syndrome.

Lalande M, Minassian BA, DeLorey TM, Olsen RW.

Adv Neurol. 1999;79:421-9. Review.

PMID:
10514831
12.

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.

Hogart A, Wu D, LaSalle JM, Schanen NC.

Neurobiol Dis. 2010 May;38(2):181-91. doi: 10.1016/j.nbd.2008.08.011. Epub 2008 Sep 18. Review.

13.

Towards a molecular understanding of Prader-Willi and Angelman syndromes.

Mann MR, Bartolomei MS.

Hum Mol Genet. 1999;8(10):1867-73. Review.

PMID:
10469839
14.

Prader-Willi and Angelman syndromes: sister imprinted disorders.

Cassidy SB, Dykens E, Williams CA.

Am J Med Genet. 2000 Summer;97(2):136-46. Review.

PMID:
11180221
15.

Imprint switch mechanism indicated by mutations in Prader-Willi and Angelman syndromes.

Kelsey G, Reik W.

Bioessays. 1997 May;19(5):361-5. Review.

PMID:
9174400
16.

Genomic imprinting and candidate genes in the Prader-Willi and Angelman syndromes.

Nicholls RD.

Curr Opin Genet Dev. 1993 Jun;3(3):445-56. Review. Erratum in: Curr Opin Genet Dev 1993 Oct;3(5):802.

PMID:
8353420
17.

Molecular epigenetics of Angelman syndrome.

Lalande M, Calciano MA.

Cell Mol Life Sci. 2007 Apr;64(7-8):947-60. Review.

PMID:
17347796
18.

Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders.

LaSalle JM, Reiter LT, Chamberlain SJ.

Epigenomics. 2015 Oct;7(7):1213-28. doi: 10.2217/epi.15.70. Epub 2015 Nov 20. Review.

19.

15q Duplication Syndrome and Related Disorders.

Finucane BM, Lusk L, Arkilo D, Chamberlain S, Devinsky O, Dindot S, Jeste SS, LaSalle JM, Reiter LT, Schanen NC, Spence SJ, Thibert RL, Calvert G, Luchsinger K, Cook EH.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mefford HC, Stephens K, Amemiya A, Ledbetter N, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2016 Jun 16.

20.

[Angelman syndrome--the research model of epigenetic mechanisms expression genes regulation].

Szpecht-Potocka A, Gos M, Struniawski R, Bal J.

Med Wieku Rozwoj. 2009 Apr-Jun;13(2):123-30. Review. Polish.

PMID:
19837992

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