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Results: 1 to 20 of 110

Similar articles for PubMed (Select 2762303)

1.

Mutator phenotype of Werner syndrome is characterized by extensive deletions.

Fukuchi K, Martin GM, Monnat RJ Jr.

Proc Natl Acad Sci U S A. 1989 Aug;86(15):5893-7. Erratum in: Proc Natl Acad Sci U S A 1989 Oct;86(20):7994.

2.

Failure to complement abnormal phenotypes of simian virus 40-transformed Werner syndrome cells by introduction of a normal human chromosome 8.

Kodama S, Kashino G, Suzuki K, Takatsuji T, Okumura Y, Oshimura M, Watanabe M, Barrett JC.

Cancer Res. 1998 Nov 15;58(22):5188-95.

3.

Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (HPRT) gene deletions.

Monnat RJ Jr, Hackmann AF, Chiaverotti TA.

Genomics. 1992 Jul;13(3):777-87.

PMID:
1639404
4.
5.

Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients.

Fukuchi K, Tanaka K, Kumahara Y, Marumo K, Pride MB, Martin GM, Monnat RJ Jr.

Hum Genet. 1990 Feb;84(3):249-52.

PMID:
2303247
6.

High frequency of large spontaneous deletions of DNA in tumor-derived CHEF cells.

Kaden DA, Bardwell L, Newmark P, Anisowicz A, Skopek TR, Sager R.

Proc Natl Acad Sci U S A. 1989 Apr;86(7):2306-10.

9.

Telomere dysfunction as a cause of genomic instability in Werner syndrome.

Crabbe L, Jauch A, Naeger CM, Holtgreve-Grez H, Karlseder J.

Proc Natl Acad Sci U S A. 2007 Feb 13;104(7):2205-10. Epub 2007 Feb 6.

11.

Hypermutable ligation of plasmid DNA ends in cells from patients with Werner syndrome.

Rünger TM, Bauer C, Dekant B, Möller K, Sobotta P, Czerny C, Poot M, Martin GM.

J Invest Dermatol. 1994 Jan;102(1):45-8.

PMID:
8288910
12.

Molecular analysis of hypoxanthine phosphoribosyltransferase gene deletions induced by alpha- and X-radiation in human lymphoblastoid cells.

Bao CY, Ma AH, Evans HH, Horng MF, Mencl J, Hui TE, Sedwick WD.

Mutat Res. 1995 Jan;326(1):1-15.

PMID:
7528877
13.

Elevated spontaneous mutation rate in SV40-transformed Werner syndrome fibroblast cell lines.

Fukuchi K, Tanaka K, Nakura J, Kumahara Y, Uchida T, Okada Y.

Somat Cell Mol Genet. 1985 Jul;11(4):303-8.

PMID:
2992100
14.

Accelerated loss of telomeric repeats may not explain accelerated replicative decline of Werner syndrome cells.

Schulz VP, Zakian VA, Ogburn CE, McKay J, Jarzebowicz AA, Edland SD, Martin GM.

Hum Genet. 1996 Jun;97(6):750-4.

PMID:
8641691
15.

Mismatch repair in extracts of Werner syndrome cell lines.

Bennett SE, Umar A, Oshima J, Monnat RJ Jr, Kunkel TA.

Cancer Res. 1997 Jul 15;57(14):2956-60.

16.

Molecular changes in UV-induced and gamma-ray-induced mutations in human lymphoblastoid cells.

Tachibana A, Ohbayashi T, Takebe H, Tatsumi K.

Mutat Res. 1990 Jun;230(2):159-66.

PMID:
1973821
17.

Werner syndrome and biological ageing: a molecular genetic hypothesis.

Thweatt R, Goldstein S.

Bioessays. 1993 Jun;15(6):421-6. Review.

PMID:
8357345
18.

Comparisons of the frequencies and molecular spectra of HPRT mutants when human cancer cells were X-irradiated during G1 or S phase.

Leonhardt EA, Trinh M, Forrester HB, Johnson RT, Dewey WC.

Radiat Res. 1997 Dec;148(6):548-60.

PMID:
9399700
19.
20.

Human in vivo somatic mutation measured at two loci: individuals with stably elevated background erythrocyte glycophorin A (gpa) variant frequencies exhibit normal T-lymphocyte hprt mutant frequencies.

Bigbee WL, Fuscoe JC, Grant SG, Jones IM, Gorvad AE, Harrington-Brock K, Strout CL, Thomas CB, Moore MM.

Mutat Res. 1998 Feb 2;397(2):119-36.

PMID:
9541637
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