Dagenais SL - Search Results

1

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.

Fang J, Dagenais SL, Erickson RP, Arlt MF, Glynn MW, Gorski JL, Seaver LH, Glover TW. Fang J, et al. Among authors: dagenais sl. Am J Hum Genet. 2000 Dec;67(6):1382-8. doi: 10.1086/316915. Epub 2000 Nov 8. Am J Hum Genet. 2000. PMID: 11078474 Free PMC article.

2

Mutation of the FOXC2 gene in familial distichiasis.

Brooks BP, Dagenais SL, Nelson CC, Glynn MW, Caulder MS, Downs CA, Glover TW. Brooks BP, et al. Among authors: dagenais sl. J AAPOS. 2003 Oct;7(5):354-7. doi: 10.1016/s1091-8531(03)00144-7. J AAPOS. 2003. PMID: 14566319

3

Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome.

Dagenais SL, Hartsough RL, Erickson RP, Witte MH, Butler MG, Glover TW. Dagenais SL, et al. Gene Expr Patterns. 2004 Oct;4(6):611-9. doi: 10.1016/j.modgep.2004.07.004. Gene Expr Patterns. 2004. PMID: 15465483

4

A novel VEGFR3 mutation causes Milroy disease.

Butler MG, Dagenais SL, Rockson SG, Glover TW. Butler MG, et al. Among authors: dagenais sl. Am J Med Genet A. 2007 Jun 1;143A(11):1212-7. doi: 10.1002/ajmg.a.31703. Am J Med Genet A. 2007. PMID: 17458866 Free article.

5

FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.

Kriederman BM, Myloyde TL, Witte MH, Dagenais SL, Witte CL, Rennels M, Bernas MJ, Lynch MT, Erickson RP, Caulder MS, Miura N, Jackson D, Brooks BP, Glover TW. Kriederman BM, et al. Among authors: dagenais sl. Hum Mol Genet. 2003 May 15;12(10):1179-85. doi: 10.1093/hmg/ddg123. Hum Mol Genet. 2003. PMID: 12719382

6

A novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes disease.

Dagenais SL, Adam AN, Innis JW, Glover TW. Dagenais SL, et al. Am J Hum Genet. 2001 Aug;69(2):420-7. doi: 10.1086/321290. Epub 2001 Jun 26. Am J Hum Genet. 2001. PMID: 11431706 Free PMC article.

7

Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations.

Erickson RP, Dagenais SL, Caulder MS, Downs CA, Herman G, Jones MC, Kerstjens-Frederikse WS, Lidral AC, McDonald M, Nelson CC, Witte M, Glover TW. Erickson RP, et al. Among authors: dagenais sl. J Med Genet. 2001 Nov;38(11):761-6. doi: 10.1136/jmg.38.11.761. J Med Genet. 2001. PMID: 11694548 Free PMC article.

8

Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.

Butler MG, Dagenais SL, Garcia-Perez JL, Brouillard P, Vikkula M, Strouse P, Innis JW, Glover TW. Butler MG, et al. Among authors: dagenais sl. Am J Med Genet A. 2012 Apr;158A(4):839-49. doi: 10.1002/ajmg.a.35229. Epub 2012 Mar 9. Am J Med Genet A. 2012. PMID: 22407726 Free PMC article.

9

Isolation of a murine copper transporter gene, tissue specific expression and functional complementation of a yeast copper transport mutant.

Lee J, Prohaska JR, Dagenais SL, Glover TW, Thiele DJ. Lee J, et al. Among authors: dagenais sl. Gene. 2000 Aug 22;254(1-2):87-96. doi: 10.1016/s0378-1119(00)00287-0. Gene. 2000. PMID: 10974539

10

Translocation breakpoints in FHIT and FRA3B in both homologs of chromosome 3 in an esophageal adenocarcinoma.

Fang JM, Arlt MF, Burgess AC, Dagenais SL, Beer DG, Glover TW. Fang JM, et al. Among authors: dagenais sl. Genes Chromosomes Cancer. 2001 Mar;30(3):292-8. doi: 10.1002/1098-2264(2000)9999:9999<::aid-gcc1095>3.0.co;2-f. Genes Chromosomes Cancer. 2001. PMID: 11170287 Free article.

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