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Items: 1 to 20 of 129

1.

Correction of a nucleotide-excision-repair mutation by human chromosome 19 in hamster-human hybrid cells.

Thompson LH, Mooney CL, Burkhart-Schultz K, Carrano AV, Siciliano MJ.

Somat Cell Mol Genet. 1985 Jan;11(1):87-92.

PMID:
3919454
2.

Genetic complementation between UV-sensitive CHO mutants and xeroderma pigmentosum fibroblasts.

Thompson LH, Mooney CL, Brookman KW.

Mutat Res. 1985 Jun-Jul;150(1-2):423-9.

PMID:
4000167
3.

Identification of nucleotide-excision-repair genes on human chromosomes 2 and 13 by functional complementation in hamster-human hybrids.

Thompson LH, Carrano AV, Sato K, Salazar EP, White BF, Stewart SA, Minkler JL, Siciliano MJ.

Somat Cell Mol Genet. 1987 Sep;13(5):539-51.

PMID:
3477874
4.

Regional mapping of human DNA excision repair gene ERCC4 to chromosome 16p13.13-p13.2.

Liu P, Siciliano J, White B, Legerski R, Callen D, Reeders S, Siciliano MJ, Thompson LH.

Mutagenesis. 1993 May;8(3):199-205.

PMID:
8332082
5.

DNA repair genes of mammalian cells.

Thompson LH, Brookman KW, Salazar EP, Fuscoe JC, Weber CA.

Basic Life Sci. 1986;39:349-58.

PMID:
3767840
6.
8.
9.

Interspecies complementation analysis of xeroderma pigmentosum and UV-sensitive Chinese hamster cells.

Stefanini M, Keijzer W, Westerveld A, Bootsma D.

Exp Cell Res. 1985 Dec;161(2):373-80.

PMID:
4065224
10.

Assignment of the XRCC2 human DNA repair gene to chromosome 7q36 by complementation analysis.

Jones NJ, Zhao Y, Siciliano MJ, Thompson LH.

Genomics. 1995 Apr 10;26(3):619-22.

PMID:
7607692
11.

Mutation and expression of the XPA gene in revertants and hybrids of a xeroderma pigmentosum cell line.

Cleaver JE, McDowell M, Jones C, Wood R, Karentz D.

Somat Cell Mol Genet. 1994 Jul;20(4):327-37.

PMID:
7974007
12.

A screening method for isolating DNA repair-deficient mutants of CHO cells.

Thompson LH, Rubin JS, Cleaver JE, Whitmore GF, Brookman K.

Somatic Cell Genet. 1980 May;6(3):391-405.

PMID:
7404270
13.

Localization of the xeroderma pigmentosum group B-correcting gene ERCC3 to human chromosome 2q21.

Weeda G, Wiegant J, van der Ploeg M, Geurts van Kessel AH, van der Eb AJ, Hoeijmakers JH.

Genomics. 1991 Aug;10(4):1035-40.

PMID:
1916809
14.

Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1.

Keijzer W, Stefanini M, Bootsma D, Verkerk A, Geurts van Kessel AH, Jongkind JF, Westerveld A.

Exp Cell Res. 1987 Apr;169(2):490-501.

PMID:
3556430
15.

Localization of the nucleotide excision repair gene ERCC6 to human chromosome 10q11-q21.

Troelstra C, Landsvater RM, Wiegant J, van der Ploeg M, Viel G, Buys CH, Hoeijmakers JH.

Genomics. 1992 Apr;12(4):745-9.

PMID:
1349298
16.
18.

Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19.

Thompson LH, Bachinski LL, Stallings RL, Dolf G, Weber CA, Westerveld A, Siciliano MJ.

Genomics. 1989 Nov;5(4):670-9.

PMID:
2591959
19.
20.

Large-scale isolation of UV-sensitive clones of CHO cells.

Busch DB, Cleaver JE, Glaser DA.

Somatic Cell Genet. 1980 May;6(3):407-18.

PMID:
7404271

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