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Results: 11

1.

Genome-wide DNA methylation profiles in hematopoietic stem and progenitor cells reveal overrepresentation of ETS transcription factor binding sites.

Hogart A, Lichtenberg J, Ajay SS, Anderson S; NIH Intramural Sequencing Center, Margulies EH, Bodine DM.

Genome Res. 2012 Aug;22(8):1407-18. doi: 10.1101/gr.132878.111. Epub 2012 Jun 8.

PMID:
22684279
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Associated symptoms in the ten days before diagnosis of Kawasaki disease.

Baker AL, Lu M, Minich LL, Atz AM, Klein GL, Korsin R, Lambert L, Li JS, Mason W, Radojewski E, Vetter VL, Newburger JW; Pediatric Heart Network Investigators.

J Pediatr. 2009 Apr;154(4):592-595.e2. doi: 10.1016/j.jpeds.2008.10.006. Epub 2008 Nov 28.

PMID:
19038400
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

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.

PMID:
18840528
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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.

PMID:
18835857
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Gender influences monoallelic expression of ATP10A in human brain.

Hogart A, Patzel KA, LaSalle JM.

Hum Genet. 2008 Oct;124(3):235-42. doi: 10.1007/s00439-008-0546-0. Epub 2008 Aug 23.

PMID:
18726118
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes.

Yasui DH, Peddada S, Bieda MC, Vallero RO, Hogart A, Nagarajan RP, Thatcher KN, Farnham PJ, Lasalle JM.

Proc Natl Acad Sci U S A. 2007 Dec 4;104(49):19416-21. Epub 2007 Nov 27.

PMID:
18042715
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation.

Nagarajan RP, Hogart AR, Gwye Y, Martin MR, LaSalle JM.

Epigenetics. 2006 Oct-Dec;1(4):e1-11.

PMID:
17486179
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders.

Hogart A, Nagarajan RP, Patzel KA, Yasui DH, Lasalle JM.

Hum Mol Genet. 2007 Mar 15;16(6):691-703. Epub 2007 Mar 5.

PMID:
17339270
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism.

LaSalle JM, Hogart A, Thatcher KN.

Int Rev Neurobiol. 2005;71:131-65. Review. No abstract available.

PMID:
16512349
[PubMed - indexed for MEDLINE]
10.

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

Samaco RC, Hogart A, LaSalle JM.

Hum Mol Genet. 2005 Feb 15;14(4):483-92. Epub 2004 Dec 22.

PMID:
15615769
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Analysis of novel and recurrent mutations responsible for the tricho-rhino-phalangeal syndromes.

Hilton MJ, Sawyer JM, GutiƩrrez L, Hogart A, Kung TC, Wells DE.

J Hum Genet. 2002;47(3):103-6.

PMID:
11950061
[PubMed - indexed for MEDLINE]
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