Luce M - Search Results

1

BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.

Shattuck-Eidens D, Oliphant A, McClure M, McBride C, Gupte J, Rubano T, Pruss D, Tavtigian SV, Teng DH, Adey N, Staebell M, Gumpper K, Lundstrom R, Hulick M, Kelly M, Holmen J, Lingenfelter B, Manley S, Fujimura F, Luce M, Ward B, Cannon-Albright L, Steele L, Offit K, Thomas A, et al. Shattuck-Eidens D, et al. Among authors: luce m. JAMA. 1997 Oct 15;278(15):1242-50. JAMA. 1997. PMID: 9333265

2

Low proportion of BRCA1 and BRCA2 mutations in Finnish breast cancer families: evidence for additional susceptibility genes.

Vehmanen P, Friedman LS, Eerola H, McClure M, Ward B, Sarantaus L, Kainu T, Syrjäkoski K, Pyrhönen S, Kallioniemi OP, Muhonen T, Luce M, Frank TS, Nevanlinna H. Vehmanen P, et al. Among authors: luce m. Hum Mol Genet. 1997 Dec;6(13):2309-15. doi: 10.1093/hmg/6.13.2309. Hum Mol Genet. 1997. PMID: 9361038

3

In vitro transcription/translation analysis for the identification of translation-terminating mutations.

Luce MC, Binnie CG, Kam-Morgan LN, Cayouette MC. Luce MC, et al. Methods Mol Biol. 1998;92:127-44. doi: 10.1385/0-89603-497-6:127. Methods Mol Biol. 1998. PMID: 9664509 No abstract available.

4

Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.

Laken SJ, Petersen GM, Gruber SB, Oddoux C, Ostrer H, Giardiello FM, Hamilton SR, Hampel H, Markowitz A, Klimstra D, Jhanwar S, Winawer S, Offit K, Luce MC, Kinzler KW, Vogelstein B. Laken SJ, et al. Among authors: luce mc. Nat Genet. 1997 Sep;17(1):79-83. doi: 10.1038/ng0997-79. Nat Genet. 1997. PMID: 9288102

5

Recurrent germ-line BRCA1 mutations in extended African American families with early-onset breast cancer.

Gao Q, Neuhausen S, Cummings S, Luce M, Olopade OI. Gao Q, et al. Among authors: luce m. Am J Hum Genet. 1997 May;60(5):1233-6. Am J Hum Genet. 1997. PMID: 9150171 Free PMC article. No abstract available.

6

Rapid identification of RT-PCR clones containing translation-terminating mutations.

Binnie CG, Kam-Morgan LN, Cayouette MC, Marra G, Boland CR, Luce M. Binnie CG, et al. Among authors: luce m. Mutat Res. 1997 Jan 15;388(1):21-6. doi: 10.1016/s1383-5718(96)00104-0. Mutat Res. 1997. PMID: 9025788

7

In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer.

Luce MC, Marra G, Chauhan DP, Laghi L, Carethers JM, Cherian SP, Hawn M, Binnie CG, Kam-Morgan LN, Cayouette MC, et al. Luce MC, et al. Gastroenterology. 1995 Oct;109(4):1368-74. doi: 10.1016/0016-5085(95)90600-2. Gastroenterology. 1995. PMID: 7557107

8

Identification of DNA mismatch repair gene mutations in hereditary nonpolyposis colon cancer patients.

Luce MC, Binnie CG, Cayouette MC, Kam-Morgan LN. Luce MC, et al. Int J Cancer. 1996 Feb 20;69(1):50-2. doi: 10.1002/(SICI)1097-0215(19960220)69:1<50::AID-IJC12>3.0.CO;2-O. Int J Cancer. 1996. PMID: 8600061 Review.

9

Distribution of 13 truncating mutations in the neurofibromatosis 1 gene.

Heim RA, Kam-Morgan LN, Binnie CG, Corns DD, Cayouette MC, Farber RA, Aylsworth AS, Silverman LM, Luce MC. Heim RA, et al. Among authors: luce mc. Hum Mol Genet. 1995 Jun;4(6):975-81. doi: 10.1093/hmg/4.6.975. Hum Mol Genet. 1995. PMID: 7655472

10

Attenuated familial adenomatous polyposis (AFAP). A phenotypically and genotypically distinctive variant of FAP.

Lynch HT, Smyrk T, McGinn T, Lanspa S, Cavalieri J, Lynch J, Slominski-Castor S, Cayouette MC, Priluck I, Luce MC. Lynch HT, et al. Among authors: luce mc. Cancer. 1995 Dec 15;76(12):2427-33. doi: 10.1002/1097-0142(19951215)76:12<2427::aid-cncr2820761205>3.0.co;2-b. Cancer. 1995. PMID: 8625067

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