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Advances in Experimental Medicine and Biology
|
January 1, 1991
Mutagens and carcinogens in cooked foods: concentration, potency, and risk
J 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 genes
E 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 leukemia
K 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 disease
I 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 homologs
K 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 experiments
H 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 XRCC3
J 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 mutation
J 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 gene
C 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 4
D B Busch, H van Vuuren, J de Wit, et al.
Page
of 18
Search research articles
Search
Showing results (161-170 of 173) with videos related to
Sort By:
Page
of 18
Advances in Experimental Medicine and Biology
|
January 1, 1991
Mutagens and carcinogens in cooked foods: concentration, potency, and risk
J 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 genes
E 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 leukemia
K 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 disease
I 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 homologs
K 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 experiments
H 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 XRCC3
J 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 mutation
J 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 gene
C 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 4
D B Busch, H van Vuuren, J de Wit, et al.
Page
of 18