M. Biggerstaff

Publication List Details

Period

1995 - 1996

Number

6

Co-Authors

Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease. (1996)

Sijbers, A.M., Laat, W.L. De, Ariza, R.A., Biggerstaff, M., Wei, Y.-F., Moggs, J.G., ...

Nucleotide excision repair, which is defective in xeroderma pigmentosum (XP), involves incision of a DNA strand on each side of a lesion. We isolated a human gene homologous to yeast Rad1 and found...

Co-correction of the ERCC1, ERCC4 and xeroderma pigmentosum group F DNA repair defects in vitro.

Biggerstaff, M, Szymkowski, D E, Wood, R D

The mammalian ERCC1-encoded polypeptide is required for nucleotide excision repair of damaged DNA and is homologous to Saccharomyces cerevisiae RAD10, which functions in repair and mitotic...

Complementation of DNA repair in xeroderma pigmentosum group A cell extracts by a protein with affinity for damaged DNA.

Robins, P, Jones, C J, Biggerstaff, M, Lindahl, T, Wood, R D

Complementation group A of xeroderma pigmentosum (XP) represents one of the most prevalent and serious forms of this cancer-prone disorder. Because of a marked defect in DNA excision repair, cells...

Co-correction of the ERCC1, ERCC4 and xeroderma pigmentosum group F DNA repair defects in vitro.

Biggerstaff, M, Szymkowski, D E, Wood, R D

The mammalian ERCC1-encoded polypeptide is required for nucleotide excision repair of damaged DNA and is homologous to Saccharomyces cerevisiae RAD10, which functions in repair and mitotic...

Complementation of DNA repair in xeroderma pigmentosum group A cell extracts by a protein with affinity for damaged DNA.

Robins, P, Jones, C J, Biggerstaff, M, Lindahl, T, Wood, R D

Complementation group A of xeroderma pigmentosum (XP) represents one of the most prevalent and serious forms of this cancer-prone disorder. Because of a marked defect in DNA excision repair, cells...