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Items: 1 to 50 of 51

1.

MLH1 mediates PARP-dependent cell death in response to the methylating agent N-methyl-N-nitrosourea.

McDaid JR, Loughery J, Dunne P, Boyer JC, Downes CS, Farber RA, Walsh CP.

Br J Cancer. 2009 Aug 4;101(3):441-51. doi: 10.1038/sj.bjc.6605186. Epub 2009 Jul 21. Erratum in: Br J Cancer. 2010 Mar 16;102(6):1080.

2.

Sequence-dependent effect of interruptions on microsatellite mutation rate in mismatch repair-deficient human cells.

Boyer JC, Hawk JD, Stefanovic L, Farber RA.

Mutat Res. 2008 Apr 2;640(1-2):89-96. doi: 10.1016/j.mrfmmm.2007.12.005. Epub 2007 Dec 23.

PMID:
18242644
5.

Mosaicism for an FMR1 gene deletion in a fragile X female.

Fan H, Booker JK, McCandless SE, Shashi V, Fleming A, Farber RA.

Am J Med Genet A. 2005 Jul 15;136(2):214-7.

PMID:
15940701
6.

Variation in efficiency of DNA mismatch repair at different sites in the yeast genome.

Hawk JD, Stefanovic L, Boyer JC, Petes TD, Farber RA.

Proc Natl Acad Sci U S A. 2005 Jun 14;102(24):8639-43. Epub 2005 Jun 2.

7.

Microsatellite instability testing in colorectal carcinoma: choice of markers affects sensitivity of detection of mismatch repair-deficient tumors.

Hatch SB, Lightfoot HM Jr, Garwacki CP, Moore DT, Calvo BF, Woosley JT, Sciarrotta J, Funkhouser WK, Farber RA.

Clin Cancer Res. 2005 Mar 15;11(6):2180-7.

8.
9.

Mutation frequency analysis of mononucleotide and dinucleotide repeats after oxidative stress.

Yamada NA, Parker JM, Farber RA.

Environ Mol Mutagen. 2003;42(2):75-84.

PMID:
12929119
10.
11.
12.

Sequence dependent instability of mononucleotide microsatellites in cultured mismatch repair proficient and deficient mammalian cells.

Boyer JC, Yamada NA, Roques CN, Hatch SB, Riess K, Farber RA.

Hum Mol Genet. 2002 Mar 15;11(6):707-13.

PMID:
11912186
13.
14.
15.

Incorrect use of the term synteny.

Passarge E, Horsthemke B, Farber RA.

Nat Genet. 1999 Dec;23(4):387. No abstract available.

PMID:
10581019
16.

Relative stabilities of dinucleotide and tetranucleotide repeats in cultured mammalian cells.

Lee JS, Hanford MG, Genova JL, Farber RA.

Hum Mol Genet. 1999 Dec;8(13):2567-72.

PMID:
10556306
17.

Relative rates of insertion and deletion mutations in a microsatellite sequence in cultured cells.

Twerdi CD, Boyer JC, Farber RA.

Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):2875-9.

18.

Stability of microsatellites in myeloid neoplasias.

Boyer JC, Risinger JI, Farber RA.

Cancer Genet Cytogenet. 1998 Oct 1;106(1):54-61.

PMID:
9772910
19.

Mutation rate of a microsatellite sequence in normal human fibroblasts.

Boyer JC, Farber RA.

Cancer Res. 1998 Sep 1;58(17):3946-9.

20.

Microsatellite mutation rates in cancer cell lines deficient or proficient in mismatch repair.

Hanford MG, Rushton BC, Gowen LC, Farber RA.

Oncogene. 1998 May 7;16(18):2389-93.

21.

Prenatal exposure to disulfiram implicated in the cause of malformations in discordant monozygotic twins.

Reitnauer PJ, Callanan NP, Farber RA, Aylsworth AS.

Teratology. 1997 Dec;56(6):358-62. Review.

PMID:
9485545
22.
23.

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.

Hum Mol Genet. 1995 Jun;4(6):975-81.

PMID:
7655472
24.

Xeroderma pigmentosum variant: generation and characterization of fibroblastic cell lines transformed with SV40 large T antigen.

King SA, Wilson SJ, Farber RA, Kaufmann WK, Cordeiro-Stone M.

Exp Cell Res. 1995 Mar;217(1):100-8.

PMID:
7867708
25.

Screening for truncated NF1 proteins.

Heim RA, Silverman LM, Farber RA, Kam-Morgan LN, Luce MC.

Nat Genet. 1994 Nov;8(3):218-9. No abstract available.

PMID:
7874161
26.

Instability of simple sequence repeats in a mammalian cell line.

Farber RA, Petes TD, Dominska M, Hudgens SS, Liskay RM.

Hum Mol Genet. 1994 Feb;3(2):253-6.

PMID:
8004091
27.

HRAS protooncogene polymorphism and breast cancer.

Garrett PA, Hulka BS, Kim YL, Farber RA.

Cancer Epidemiol Biomarkers Prev. 1993 Mar-Apr;2(2):131-8.

28.

Longitudinal follow-up of malignant osteopetrosis by skeletal radiographs and restriction fragment length polymorphism analysis after bone marrow transplantation.

Schroeder RF, Johnson FL, Silberstein MJ, Neuman WL, Hoag JM, Farber RA, Noguchi A.

Pediatrics. 1992 Dec;90(6):986-9. No abstract available.

PMID:
1359502
29.

Detection of alpha 1-antitrypsin Z and S mutations by polymerase chain reaction-mediated site-directed mutagenesis.

Tazelaar JP, Friedman KJ, Kline RS, Guthrie ML, Farber RA.

Clin Chem. 1992 Aug;38(8 Pt 1):1486-8.

PMID:
1643720
30.

Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosomes 5 and 7 in malignant myeloid disorders.

Neuman WL, Rubin CM, Rios RB, Larson RA, Le Beau MM, Rowley JD, Vardiman JW, Schwartz JL, Farber RA.

Blood. 1992 Mar 15;79(6):1501-10.

PMID:
1347709
31.

Somatic cell hybrid mapping of human chromosome band 5q31: a region important to hematopoiesis.

Neuman WL, Le Beau MM, Farber RA, Lindgren V, Westbrook CA.

Cytogenet Cell Genet. 1992;61(2):103-6.

PMID:
1395713
32.

Sexual discordance in monozygotic twins.

Perlman EJ, Stetten G, Tuck-Müller CM, Farber RA, Neuman WL, Blakemore KJ, Hutchins GM.

Am J Med Genet. 1990 Dec;37(4):551-7. Review.

PMID:
1979713
33.

DNA analysis of unilateral twin ectopic gestation.

Neuman WL, Ponto K, Farber RA, Shangold GA.

Obstet Gynecol. 1990 Mar;75(3 Pt 2):479-83.

PMID:
1968246
34.

The HuT series of 'carcinogen-transformed' human fibroblast cell lines are derived from the human fibrosarcoma cell line 8387.

McCormick JJ, Yang DJ, Maher VM, Farber RA, Neuman W, Peterson WD Jr, Pollack MS.

Carcinogenesis. 1988 Nov;9(11):2073-9.

PMID:
2902939
35.

An anonymous DNA segment pTP5E (D5S70) maps to the long arm of chromosome 5 and identifies a Taq I polymorphism.

Farber RA, Phalen T, Neuman WL, Le Beau MM, Wasmuth JJ, Dobbs M.

Nucleic Acids Res. 1988 Mar 25;16(5):2360. No abstract available.

36.

Assignment of a processed mouse Aprt pseudogene to the same chromosome as the functional gene.

Farber RA, Zielinski D.

Cytogenet Cell Genet. 1986;42(4):198-201.

PMID:
2875850
37.
38.
39.

Chromosome replication in normal and transformed human lymphocytes.

Lindgren V, Farber RA.

Cancer Genet Cytogenet. 1983 May;9(1):71-9.

PMID:
6601510
40.

Relationships among DNA sequences of the 1.3 kb EcoRI family of mouse DNA.

Dubnick M, Chou J, Petes TD, Farber RA.

J Mol Evol. 1983;19(2):115-21.

PMID:
6100837
41.

Chromosome replication in aging human diploid fibroblasts.

Lindgren V, Farber RA.

Exp Cell Res. 1982 Dec;142(2):301-7. No abstract available.

PMID:
7173326
42.
43.
44.

Maintenance of replication patterns in human-mouse hybrids retaining only one human chromosome.

Farber RA, Davidson RL.

Somatic Cell Genet. 1979 Jul;5(4):519-28.

PMID:
227124
45.

Altered pattern of replication of human chromosomes in a human fibroblast-mouse cell hybrid.

Farber RA, Davidson RL.

Proc Natl Acad Sci U S A. 1978 Mar;75(3):1470-4.

47.

Induction and isolation of cold-sensitive lines of Chinese hamster cells.

Farber RA, Unrau P.

Methods Cell Biol. 1976;14:265-71. No abstract available.

PMID:
1004229
48.

Isolation of cold-sensitive Chinese hamster cells.

Farber RA, Unrau P.

Mol Gen Genet. 1975 Jun 19;138(3):233-42.

PMID:
1237784
49.

Altered rate of DNA replication in ageing human fibroblast cultures.

Petes TD, Farber RA, Tarrant GM, Holliday R.

Nature. 1974 Oct 4;251(5474):434-6. No abstract available.

PMID:
4423711
50.

Karyotypic analysis of a near-diploid established mouse cell line.

Farber RA, Liskay RM.

Cytogenet Cell Genet. 1974;13(4):384-96. No abstract available.

PMID:
4138999

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