Segers K - Search Results

1

Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region.

Paulsen M, Takada S, Youngson NA, Benchaib M, Charlier C, Segers K, Georges M, Ferguson-Smith AC. Paulsen M, et al. Among authors: segers k. Genome Res. 2001 Dec;11(12):2085-94. doi: 10.1101/gr.206901. Genome Res. 2001. PMID: 11731499 Free PMC article.

2

Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8.

Charlier C, Segers K, Wagenaar D, Karim L, Berghmans S, Jaillon O, Shay T, Weissenbach J, Cockett N, Gyapay G, Georges M. Charlier C, et al. Among authors: segers k. Genome Res. 2001 May;11(5):850-62. doi: 10.1101/gr.172701. Genome Res. 2001. PMID: 11337479 Free PMC article.

3

Breakpoint mapping positions the callipyge gene within a 450-kilobase chromosome segment containing the DLK1 and GTL2 genes.

Berghmans S, Segers K, Shay T, Georges M, Cockett N, Charlier C. Berghmans S, et al. Among authors: segers k. Mamm Genome. 2001 Feb;12(2):183-5. doi: 10.1007/s003350010246. Mamm Genome. 2001. PMID: 11210193 Free article. No abstract available.

4

Fine-mapping and construction of a bovine contig spanning the ovine callipyge locus.

Shay TL, Berghmans S, Segers K, Meyers S, Beever JE, Womack JE, Georges M, Charlier C, Cockett NE. Shay TL, et al. Among authors: segers k. Mamm Genome. 2001 Feb;12(2):141-9. doi: 10.1007/s003350010248. Mamm Genome. 2001. PMID: 11210184

5

The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status.

Charlier C, Segers K, Karim L, Shay T, Gyapay G, Cockett N, Georges M. Charlier C, et al. Among authors: segers k. Nat Genet. 2001 Apr;27(4):367-9. doi: 10.1038/86856. Nat Genet. 2001. PMID: 11279514

6

Mosaicism of Solid Gold supports the causality of a noncoding A-to-G transition in the determinism of the callipyge phenotype.

Smit M, Segers K, Carrascosa LG, Shay T, Baraldi F, Gyapay G, Snowder G, Georges M, Cockett N, Charlier C. Smit M, et al. Among authors: segers k. Genetics. 2003 Jan;163(1):453-6. doi: 10.1093/genetics/163.1.453. Genetics. 2003. PMID: 12586730 Free PMC article.

7

Construction and characterization of an ovine BAC contig spanning the callipyge locus.

Segers K, Vaiman D, Berghmans S, Shay T, Meyers S, Beever J, Cockett N, Georges M, Charlier C. Segers K, et al. Anim Genet. 2000 Dec;31(6):352-9. doi: 10.1046/j.1365-2052.2000.00676.x. Anim Genet. 2000. PMID: 11167521

8

The callipyge mutation and other genes that affect muscle hypertrophy in sheep.

Cockett NE, Smit MA, Bidwell CA, Segers K, Hadfield TL, Snowder GD, Georges M, Charlier C. Cockett NE, et al. Among authors: segers k. Genet Sel Evol. 2005;37 Suppl 1(Suppl 1):S65-81. doi: 10.1186/1297-9686-37-S1-S65. Genet Sel Evol. 2005. PMID: 15601596 Free PMC article. Review.

9

Improved molecular diagnostics of idiopathic short stature and allied disorders: quantitative polymerase chain reaction-based copy number profiling of SHOX and pseudoautosomal region 1.

D'haene B, Hellemans J, Craen M, De Schepper J, Devriendt K, Fryns JP, Keymolen K, Debals E, de Klein A, de Jong EM, Segers K, De Paepe A, Mortier G, Vandesompele J, De Baere E. D'haene B, et al. Among authors: segers k. J Clin Endocrinol Metab. 2010 Jun;95(6):3010-8. doi: 10.1210/jc.2009-2218. Epub 2010 Apr 7. J Clin Endocrinol Metab. 2010. PMID: 20375215

10

Germline PTPN11 missense mutation in a case of Noonan syndrome associated with mediastinal and retroperitoneal neuroblastic tumors.

Mutesa L, Pierquin G, Janin N, Segers K, Thomée C, Provenzi M, Bours V. Mutesa L, et al. Among authors: segers k. Cancer Genet Cytogenet. 2008 Apr 1;182(1):40-2. doi: 10.1016/j.cancergencyto.2007.12.005. Cancer Genet Cytogenet. 2008. PMID: 18328949 Free article.

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