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Experimental Neurology|September 2, 2022
Identifying the optimal developmental age of human pluripotent stem cell-derived midbrain dopaminergic progenitors for transplantation in a rodent model of Parkinson's diseaseI R de Luzy, C Pavan, N Moriarty, et al.
Molecular and Cellular Biology|November 1, 1996
ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologsK W Brookman, J E Lamerdin, M P Thelen, et al.
Journal of Toxicology and Environmental Health|May 1, 1982
Mutagenic and toxic activity of environmental effluents from underground coal gasification experimentsH Timourian, J S Felton, D H Stuermer, et al.
Oncogene|January 24, 2008
FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3J B Wilson, K Yamamoto, A S Marriott, et al.
Molecular and Cellular Biology|October 5, 2001
Restoration of nucleotide excision repair in a helicase-deficient XPD mutant from intragenic suppression by a trichothiodystrophy mutationJ W George, E P Salazar, M P Vreeswijk, et al.
Stem Cell Research|October 27, 2023
Generation of the iPSC line FINi002-A from a male Parkinson's disease patient carrying compound heterozygous mutations in the PRKN geneC Pavan, J Jin, S Jong, et al.
Mutation Research|March 12, 1997
Phenotypic heterogeneity in nucleotide excision repair mutants of rodent complementation groups 1 and 4D B Busch, H van Vuuren, J de Wit, et al.
Mutation Research|August 8, 1996
A CHO mutant, UV40, that is sensitive to diverse mutagens and represents a new complementation group of mitomycin C sensitivityD B Busch, M Z Zdzienicka, A T Natarajan, et al.
Nature Communications|January 28, 2023
Hydrogel oxygen reservoirs increase functional integration of neural stem cell grafts by meeting metabolic demandsY Wang, E R Zoneff, J W Thomas, et al.
Molecular Cell|July 14, 1998
XRCC2 and XRCC3, new human Rad51-family members, promote chromosome stability and protect against DNA cross-links and other damagesN Liu, J E Lamerdin, R S Tebbs, et al.
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