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scopus: 7005450602

Eb, A.J. van der

( A.J. van der Eb)


/ercc sequence repair xpbc /ercc gene region promoter xpbc /ercc promoter protein fragment analysis transcription probe group element excision plasmid complementation ercc -3 cdna position nucleotide expression binding figure cap site helicase defect genomic xpllbe clone mutation ercc -3 oligonucleotide ercc -3 gene activity blot analysis acids research domain transfection hela tk result xpbc /ercc xp complementation groups nature factor patient experiment level fibroblast splice disorder transcription initiation site xpbc /ercc cdna mutant transcript filter rodent yeast hoeijmaker 4 bp insertion function initiation xpbciercc number hela cells cat activity research acid sequence assay deletion extension primer motif wild-type xeroderma nucleotide sequence signal hybridized restriction van der eb cre /tre element




6 Most Recent Publications

Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2/TFIIH. (Article)
Vuuren, A.J. van Vermeulen, W. Egly, J-M. Ma, L. Weeda, G. Appeldoorn, E. Jaspers, N.G.J. Eb, A.J. van der Hoeijmakers, J.H.J. Humbert, S. Schaeffer, L.
1994-01-01
Molecular and functional analysis of the XPBC/ERCC-3 promoter: Transcription activity is dependent on the integrity of an Sp1 binding element. (Article)
Ma, L. Weeda, G. Jochemsen, A.G. Bootsma, D. Hoeijmakers, J.H.J. Eb, A.J. van der
1992-01-01
Localization of the xeroderma pigmentosum group B-correcting gene ERCC-3 to human chromosome 2q21. (Article)
Weeda, G. Wiegant, J. Ploeg, M. van der Geurts van Kessel, A.H.M. Eb, A.J. van der Hoeijmakers, J.H.J.
1991-01-01
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
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
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