LaSalle JM - Search Results

1

Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome.

Peddada S, Yasui DH, LaSalle JM. Peddada S, et al. Among authors: lasalle jm. Hum Mol Genet. 2006 Jun 15;15(12):2003-14. doi: 10.1093/hmg/ddl124. Epub 2006 May 8. Hum Mol Genet. 2006. PMID: 16682435 Free PMC article.

2

Clonal maintenance of imprinted expression of SNRPN and IPW in normal lymphocytes: correlation with allele-specific methylation of SNRPN intron 1 but not intron 7.

Balmer D, LaSalle JM. Balmer D, et al. Among authors: lasalle jm. Hum Genet. 2001 Feb;108(2):116-22. doi: 10.1007/s004390000455. Hum Genet. 2001. PMID: 11281449

3

Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry.

LaSalle JM, Goldstine J, Balmer D, Greco CM. LaSalle JM, et al. Hum Mol Genet. 2001 Aug 15;10(17):1729-40. doi: 10.1093/hmg/10.17.1729. Hum Mol Genet. 2001. PMID: 11532982

4

MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.

Balmer D, Arredondo J, Samaco RC, LaSalle JM. Balmer D, et al. Among authors: lasalle jm. Hum Genet. 2002 Jun;110(6):545-52. doi: 10.1007/s00439-002-0724-4. Epub 2002 Apr 25. Hum Genet. 2002. PMID: 12107440

5

Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.

Balmer D, Goldstine J, Rao YM, LaSalle JM. Balmer D, et al. Among authors: lasalle jm. J Mol Med (Berl). 2003 Jan;81(1):61-8. doi: 10.1007/s00109-002-0396-5. Epub 2002 Dec 19. J Mol Med (Berl). 2003. PMID: 12545250

6

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders.

Samaco RC, Nagarajan RP, Braunschweig D, LaSalle JM. Samaco RC, et al. Among authors: lasalle jm. Hum Mol Genet. 2004 Mar 15;13(6):629-39. doi: 10.1093/hmg/ddh063. Epub 2004 Jan 20. Hum Mol Genet. 2004. PMID: 14734626

7

Paradoxical role of methyl-CpG-binding protein 2 in Rett syndrome.

LaSalle JM. LaSalle JM. Curr Top Dev Biol. 2004;59:61-86. doi: 10.1016/S0070-2153(04)59003-8. Curr Top Dev Biol. 2004. PMID: 14975247 Review. No abstract available.

8

X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.

Braunschweig D, Simcox T, Samaco RC, LaSalle JM. Braunschweig D, et al. Among authors: lasalle jm. Hum Mol Genet. 2004 Jun 15;13(12):1275-86. doi: 10.1093/hmg/ddh142. Epub 2004 Apr 28. Hum Mol Genet. 2004. PMID: 15115765

9

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

Samaco RC, Hogart A, LaSalle JM. Samaco RC, et al. Among authors: lasalle jm. Hum Mol Genet. 2005 Feb 15;14(4):483-92. doi: 10.1093/hmg/ddi045. Epub 2004 Dec 22. Hum Mol Genet. 2005. PMID: 15615769 Free PMC article.

10

Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples.

Thatcher KN, Peddada S, Yasui DH, Lasalle JM. Thatcher KN, et al. Among authors: lasalle jm. Hum Mol Genet. 2005 Mar 15;14(6):785-97. doi: 10.1093/hmg/ddi073. Epub 2005 Feb 2. Hum Mol Genet. 2005. PMID: 15689352

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