Cochran C - Search Results

1

Localization of the VHR phosphatase gene and its analysis as a candidate for BRCA1.

Kamb A, Futreal PA, Rosenthal J, Cochran C, Harshman KD, Liu Q, Phelps RS, Tavtigian SV, Tran T, Hussey C, et al. Kamb A, et al. Among authors: cochran c. Genomics. 1994 Sep 1;23(1):163-7. doi: 10.1006/geno.1994.1473. Genomics. 1994. PMID: 7829067

2

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.

Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K, Tavtigian S, Liu Q, Cochran C, Bennett LM, Ding W, et al. Miki Y, et al. Among authors: cochran c. Science. 1994 Oct 7;266(5182):66-71. doi: 10.1126/science.7545954. Science. 1994. PMID: 7545954

3

BRCA1 mutations in primary breast and ovarian carcinomas.

Futreal PA, Liu Q, Shattuck-Eidens D, Cochran C, Harshman K, Tavtigian S, Bennett LM, Haugen-Strano A, Swensen J, Miki Y, et al. Futreal PA, et al. Among authors: cochran c. Science. 1994 Oct 7;266(5182):120-2. doi: 10.1126/science.7939630. Science. 1994. PMID: 7939630

4

Isolation of a diverged homeobox gene, MOX1, from the BRCA1 region on 17q21 by solution hybrid capture.

Futreal PA, Cochran C, Rosenthal J, Miki Y, Swenson J, Hobbs M, Bennett LM, Haugen-Strano A, Marks J, Barrett JC, et al. Futreal PA, et al. Among authors: cochran c. Hum Mol Genet. 1994 Aug;3(8):1359-64. doi: 10.1093/hmg/3.8.1359. Hum Mol Genet. 1994. PMID: 7987315

5

Mutation analysis of the THRA1 gene in breast cancer: deletion/fusion of the gene to a novel sequence on 17q in the BT474 cell line.

Futreal PA, Cochran C, Marks JR, Iglehart JD, Zimmerman W, Barrett JC, Wiseman RW. Futreal PA, et al. Among authors: cochran c. Cancer Res. 1994 Apr 1;54(7):1791-4. Cancer Res. 1994. PMID: 7511052

6

Detection of BRCA1 mutations in women with early-onset ovarian cancer by use of the protein truncation test.

Lancaster JM, Cochran CJ, Brownlee HA, Evans AC, Berchuck A, Futreal PA, Wiseman RW. Lancaster JM, et al. Among authors: cochran cj. J Natl Cancer Inst. 1996 Apr 17;88(8):552-4. doi: 10.1093/jnci/88.8.552. J Natl Cancer Inst. 1996. PMID: 8606385 No abstract available.

7

Detection of frequent allelic loss on proximal chromosome 17q in sporadic breast carcinoma using microsatellite length polymorphisms.

Futreal PA, Söderkvist P, Marks JR, Iglehart JD, Cochran C, Barrett JC, Wiseman RW. Futreal PA, et al. Among authors: cochran c. Cancer Res. 1992 May 1;52(9):2624-7. Cancer Res. 1992. PMID: 1568230

8

Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families.

Phelan CM, Lancaster JM, Tonin P, Gumbs C, Cochran C, Carter R, Ghadirian P, Perret C, Moslehi R, Dion F, Faucher MC, Dole K, Karimi S, Foulkes W, Lounis H, Warner E, Goss P, Anderson D, Larsson C, Narod SA, Futreal PA. Phelan CM, et al. Among authors: cochran c. Nat Genet. 1996 May;13(1):120-2. doi: 10.1038/ng0596-120. Nat Genet. 1996. PMID: 8673090

9

Isolation of the mouse homologue of BRCA1 and genetic mapping to mouse chromosome 11.

Bennett LM, Haugen-Strano A, Cochran C, Brownlee HA, Fiedorek FT Jr, Wiseman RW. Bennett LM, et al. Among authors: cochran c. Genomics. 1995 Oct 10;29(3):576-81. doi: 10.1006/geno.1995.9963. Genomics. 1995. PMID: 8575748

10

BRCA2 mutations in primary breast and ovarian cancers.

Lancaster JM, Wooster R, Mangion J, Phelan CM, Cochran C, Gumbs C, Seal S, Barfoot R, Collins N, Bignell G, Patel S, Hamoudi R, Larsson C, Wiseman RW, Berchuck A, Iglehart JD, Marks JR, Ashworth A, Stratton MR, Futreal PA. Lancaster JM, et al. Among authors: cochran c. Nat Genet. 1996 Jun;13(2):238-40. doi: 10.1038/ng0696-238. Nat Genet. 1996. PMID: 8640235

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