Dagenais SL - Search Results

1

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.

2

The hepatocyte nuclear factor 3 alpha gene, HNF3alpha (FOXA1), on chromosome band 14q13 is amplified and overexpressed in esophageal and lung adenocarcinomas.

Lin L, Miller CT, Contreras JI, Prescott MS, Dagenais SL, Wu R, Yee J, Orringer MB, Misek DE, Hanash SM, Glover TW, Beer DG. Lin L, et al. Among authors: dagenais sl. Cancer Res. 2002 Sep 15;62(18):5273-9. Cancer Res. 2002. PMID: 12234996

3

Amplification and overexpression of the dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 2 (DYRK2) gene in esophageal and lung adenocarcinomas.

Miller CT, Aggarwal S, Lin TK, Dagenais SL, Contreras JI, Orringer MB, Glover TW, Beer DG, Lin L. Miller CT, et al. Among authors: dagenais sl. Cancer Res. 2003 Jul 15;63(14):4136-43. Cancer Res. 2003. PMID: 12874018

4

The murine Fhit gene is highly similar to its human orthologue and maps to a common fragile site region.

Glover TW, Hoge AW, Miller DE, Ascara-Wilke JE, Adam AN, Dagenais SL, Wilke CM, Dierick HA, Beer DG. Glover TW, et al. Among authors: dagenais sl. Cancer Res. 1998 Aug 1;58(15):3409-14. Cancer Res. 1998. PMID: 9699673

5

The canine copper toxicosis locus is not syntenic with ATP7B or ATX1 and maps to a region showing homology to human 2p21.

Dagenais SL, Guevara-Fujita M, Loechel R, Burgess AC, Miller DE, Yuzbasiyan-Gurkan V, Brewer GJ, Glover TW. Dagenais SL, et al. Mamm Genome. 1999 Jul;10(7):753-6. doi: 10.1007/s003359901085. Mamm Genome. 1999. PMID: 10384054 Free article. No abstract available.

6

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

7

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.

8

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.

9

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.

10

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

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