De Baere E - Search Results

1

Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation.

Beysen D, Moumné L, Veitia R, Peters H, Leroy BP, De Paepe A, De Baere E. Beysen D, et al. Among authors: de paepe a, de baere e. Hum Mol Genet. 2008 Jul 1;17(13):2030-8. doi: 10.1093/hmg/ddn100. Epub 2008 Mar 27. Hum Mol Genet. 2008. PMID: 18372316

2

Assignment of the cellular retinol-binding protein 1 gene (RBP1) and of the coatomer beta subunit gene (COPB2) to human chromosome band 3q23 by in situ hybridization.

De Baere E, Speleman F, Van Roy N, De Paepe A, Messiaen L. De Baere E, et al. Among authors: de paepe a. Cytogenet Cell Genet. 1998;82(3-4):226-7. doi: 10.1159/000015107. Cytogenet Cell Genet. 1998. PMID: 9858824 No abstract available.

3

Assignment of SHOX2 (alias OG12X and SHOT) to human chromosome bands 3q25-->q26.1 by in situ hybridization.

De Baere E, Speleman F, Van Roy N, De Paepe A, Messiaen L. De Baere E, et al. Among authors: de paepe a. Cytogenet Cell Genet. 1998;82(3-4):228-9. doi: 10.1159/000015108. Cytogenet Cell Genet. 1998. PMID: 9858825 No abstract available.

4

Assignment of the cellular retinol-binding protein 2 gene (RBP2) to human chromosome band 3q23 by in situ hybridization.

De Baere E, Speleman F, Van Roy N, Mortier K, De Paepe A, Messiaen L. De Baere E, et al. Among authors: de paepe a. Cytogenet Cell Genet. 1998;83(3-4):240-1. doi: 10.1159/000015191. Cytogenet Cell Genet. 1998. PMID: 10072590 No abstract available.

5

Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint.

De Baere E, Van Roy N, Speleman F, Fukushima Y, De Paepe A, Messiaen L. De Baere E, et al. Among authors: de paepe a. Genomics. 1999 Apr 1;57(1):70-8. doi: 10.1006/geno.1999.5747. Genomics. 1999. PMID: 10191085

6

Identification of BPESC1, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPES.

De Baere E, Fukushima Y, Small K, Udar N, Van Camp G, Verhoeven K, Palotie A, De Paepe A, Messiaen L. De Baere E, et al. Among authors: de paepe a. Genomics. 2000 Sep 15;68(3):296-304. doi: 10.1006/geno.2000.6304. Genomics. 2000. PMID: 10995571

7

Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation.

De Baere E, Dixon MJ, Small KW, Jabs EW, Leroy BP, Devriendt K, Gillerot Y, Mortier G, Meire F, Van Maldergem L, Courtens W, Hjalgrim H, Huang S, Liebaers I, Van Regemorter N, Touraine P, Praphanphoj V, Verloes A, Udar N, Yellore V, Chalukya M, Yelchits S, De Paepe A, Kuttenn F, Fellous M, Veitia R, Messiaen L. De Baere E, et al. Among authors: de paepe a. Hum Mol Genet. 2001 Jul 15;10(15):1591-600. doi: 10.1093/hmg/10.15.1591. Hum Mol Genet. 2001. PMID: 11468277

8

Evolution and expression of FOXL2.

Cocquet J, Pailhoux E, Jaubert F, Servel N, Xia X, Pannetier M, De Baere E, Messiaen L, Cotinot C, Fellous M, Veitia RA. Cocquet J, et al. Among authors: de baere e. J Med Genet. 2002 Dec;39(12):916-21. doi: 10.1136/jmg.39.12.916. J Med Genet. 2002. PMID: 12471206 Free PMC article. No abstract available.

9

FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation.

De Baere E, Beysen D, Oley C, Lorenz B, Cocquet J, De Sutter P, Devriendt K, Dixon M, Fellous M, Fryns JP, Garza A, Jonsrud C, Koivisto PA, Krause A, Leroy BP, Meire F, Plomp A, Van Maldergem L, De Paepe A, Veitia R, Messiaen L. De Baere E, et al. Among authors: de paepe a, de sutter p. Am J Hum Genet. 2003 Feb;72(2):478-87. doi: 10.1086/346118. Epub 2003 Jan 14. Am J Hum Genet. 2003. PMID: 12529855 Free PMC article.

10

Structure, evolution and expression of the FOXL2 transcription unit.

Cocquet J, De Baere E, Gareil M, Pannetier M, Xia X, Fellous M, Veitia RA. Cocquet J, et al. Among authors: de baere e. Cytogenet Genome Res. 2003;101(3-4):206-11. doi: 10.1159/000074338. Cytogenet Genome Res. 2003. PMID: 14684984 Review.

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