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sequence repair /ercc protein region group complementation xpbc /ercc gene ercc -3 cdna analysis excision figure helicase promoter genomic probe xpllbe clone mutation fragment nucleotide ercc -3 ercc -3 gene blot analysis expression domain defect xp complementation groups nature patient xpbc /ercc promoter experiment level position fibroblast transfection binding splice disorder xpbc /ercc cdna result mutant filter rodent yeast hoeijmaker 4 bp insertion acid sequence function xpbciercc number hela cells acids research motif plasmid hybridized wild-type xeroderma nucleotide sequence signal restriction transcription hybridization oligonucleotide pigmentosum hela tk pcd 1 allele transformant westerveld insertion primers lymphoblastoid cell line procedure acids res cos 8 xpbciercc -3 gene representative cell lines xpbc /ercc mrna ercc -3 protein
3 Most Recent Publications
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Characterization of the mouse homolog of the XPBC/ERCC-3 gene implicated in xeroderma pigmentosum and Cockayne's Syndrome.
(Article)
Weeda, G. Ma, L. Ham, R.C.A. van Bootsma, D. Eb, A.J. van der Hoeijmakers, J.H.J. |
1991-01-01
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Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's Syndrome.
(Article)
Weeda, G. Ma, L. Ham, R.C.A. van Eb, A.J. van der Hoeijmakers, J.H.J. |
1991-01-01
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A presumed DNA helicase, encoded by the excision repair gene ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome.
(Article)
Weeda, G. Ham, R.C.A. van Vermeulen, W. Bootsma, D. Eb, A.J. van der Hoeijmakers, J.H.J. |
1990-09-17
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