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L H Thompson

Showing results (161-170 of 173) with videos related to

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Advances in Experimental Medicine and Biology|January 1, 1991
Mutagens and carcinogens in cooked foods: concentration, potency, and riskJ S Felton, M K Knize, K W Turteltaub, et al.
Genomics|November 1, 1990
Myogenin is in an evolutionarily conserved linkage group on human chromosome 1q31-q41 and unlinked to other mapped muscle regulatory factor genesE Olson, D Edmondson, W E Wright, et al.
Leukemia|May 1, 1987
The localization of the human myeloperoxidase gene is in close proximity to the translocation breakpoint in acute promyelocytic leukemiaK S Chang, W Schroeder, M J Siciliano, et al.
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.
Pageof 18

Showing results (161-170 of 173) with videos related to

Sort By:
Pageof 18
Advances in Experimental Medicine and Biology|January 1, 1991
Mutagens and carcinogens in cooked foods: concentration, potency, and riskJ S Felton, M K Knize, K W Turteltaub, et al.
Genomics|November 1, 1990
Myogenin is in an evolutionarily conserved linkage group on human chromosome 1q31-q41 and unlinked to other mapped muscle regulatory factor genesE Olson, D Edmondson, W E Wright, et al.
Leukemia|May 1, 1987
The localization of the human myeloperoxidase gene is in close proximity to the translocation breakpoint in acute promyelocytic leukemiaK S Chang, W Schroeder, M J Siciliano, et al.
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.
Pageof 18