Lefebvre L - Search Results

1

Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes.

Yuen RK, Avila L, Peñaherrera MS, von Dadelszen P, Lefebvre L, Kobor MS, Robinson WP. Yuen RK, et al. Among authors: lefebvre l. PLoS One. 2009 Oct 19;4(10):e7389. doi: 10.1371/journal.pone.0007389. PLoS One. 2009. PMID: 19838307 Free PMC article.

2

Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia.

Kaiser-Rogers KA, McFadden DE, Livasy CA, Dansereau J, Jiang R, Knops JF, Lefebvre L, Rao KW, Robinson WP. Kaiser-Rogers KA, et al. Among authors: lefebvre l. J Med Genet. 2006 Feb;43(2):187-92. doi: 10.1136/jmg.2005.033571. Epub 2005 May 20. J Med Genet. 2006. PMID: 15908568 Free PMC article.

3

Epigenetic and phenotypic consequences of a truncation disrupting the imprinted domain on distal mouse chromosome 7.

Oh R, Ho R, Mar L, Gertsenstein M, Paderova J, Hsien J, Squire JA, Higgins MJ, Nagy A, Lefebvre L. Oh R, et al. Among authors: lefebvre l. Mol Cell Biol. 2008 Feb;28(3):1092-103. doi: 10.1128/MCB.01019-07. Epub 2007 Nov 26. Mol Cell Biol. 2008. PMID: 18039841 Free PMC article.

4

Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth.

Jacob KJ, Robinson WP, Lefebvre L. Jacob KJ, et al. Among authors: lefebvre l. Clin Genet. 2013 Oct;84(4):326-34. doi: 10.1111/cge.12143. Epub 2013 Apr 9. Clin Genet. 2013. PMID: 23495910 Review.

5

An imprinted GFP insertion reveals long-range epigenetic regulation in embryonic lineages.

Jones MJ, Lefebvre L. Jones MJ, et al. Among authors: lefebvre l. Dev Biol. 2009 Dec 1;336(1):42-52. doi: 10.1016/j.ydbio.2009.09.023. Epub 2009 Sep 22. Dev Biol. 2009. PMID: 19778534 Free PMC article.

6

Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome.

Oh-McGinnis R, Bogutz AB, Lee KY, Higgins MJ, Lefebvre L. Oh-McGinnis R, et al. Among authors: lefebvre l. BMC Dev Biol. 2010 May 11;10:50. doi: 10.1186/1471-213X-10-50. BMC Dev Biol. 2010. PMID: 20459838 Free PMC article.

7

Applications of the site-specific recombinase Cre to the study of genomic imprinting.

Oh-McGinnis R, Jones MJ, Lefebvre L. Oh-McGinnis R, et al. Among authors: lefebvre l. Brief Funct Genomics. 2010 Jul;9(4):281-93. doi: 10.1093/bfgp/elq017. Epub 2010 Jul 2. Brief Funct Genomics. 2010. PMID: 20601421 Free PMC article. Review.

8

Partial loss of Ascl2 function affects all three layers of the mature placenta and causes intrauterine growth restriction.

Oh-McGinnis R, Bogutz AB, Lefebvre L. Oh-McGinnis R, et al. Among authors: lefebvre l. Dev Biol. 2011 Mar 15;351(2):277-86. doi: 10.1016/j.ydbio.2011.01.008. Epub 2011 Jan 14. Dev Biol. 2011. PMID: 21238448 Free PMC article.

9

An extended domain of Kcnq1ot1 silencing revealed by an imprinted fluorescent reporter.

Jones MJ, Bogutz AB, Lefebvre L. Jones MJ, et al. Among authors: lefebvre l. Mol Cell Biol. 2011 Jul;31(14):2827-37. doi: 10.1128/MCB.01435-10. Epub 2011 May 16. Mol Cell Biol. 2011. PMID: 21576366 Free PMC article.

10

Tissue-specific alternative polyadenylation at the imprinted gene Mest regulates allelic usage at Copg2.

MacIsaac JL, Bogutz AB, Morrissy AS, Lefebvre L. MacIsaac JL, et al. Among authors: lefebvre l. Nucleic Acids Res. 2012 Feb;40(4):1523-35. doi: 10.1093/nar/gkr871. Epub 2011 Nov 3. Nucleic Acids Res. 2012. PMID: 22053079 Free PMC article.

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