Výsledky vyhledávání - "Reinier C.A. van Ham"

Sturcture and expression of the humanXPBC/ERCC-3gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome

Autor: Jan H.J. Hoeijmakers, G. Weeda, Libin Ma, Alex J. van der Eb, Reinier C.A. van Ham

Publikováno v: Nucleic Acids Research. 19:6301-6308

The human XPBC/ERCC-3 was cloned by virtue of its ability to correct the excision repair defect of UV-sensitive rodent mutants of complementation group 3. The gene appeared to be in addition implicated in the human, cancer prone repair disorder xerod

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9b728be472a3b154944a479fe1480ea
https://doi.org/10.1093/nar/19.22.6301

Zobrazit plný text záznamu

A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome

Autor: Reinier C.A. van Ham, Dirk Bootsma, Wim Vermeulen, Geert Weeda, Alex J. van der Eb, Jan H.J. Hoeijmakers

Publikováno v: Cell. 62:777-791

The human gene ERCC-3 specifically corrects the defect in an early step of the DNA excision repair pathway of UV-sensitive rodent mutants of complementation group 3. The predicted 782 amino acid ERCC-3 protein harbors putative nucleotide, chromatin,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c31b9d6c9912781ad6737ffc8b32fea4
https://doi.org/10.1016/0092-8674(90)90122-u

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání