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Qualitatively and quantitatively similar effects of active and passive maternal tobacco smoke exposure on in utero mutagenesis at the HPRT locusProspective screening study of 0.5 Tesla dedicated magnetic resonance imaging for the detection of breast cancer in young, high-risk women.Nucleotide excision repair deficiency is intrinsic in sporadic stage I breast cancerMelatonin and breast cancer: cellular mechanisms, clinical studies and future perspectives.Cell-type-specific level of DNA nucleotide excision repair in primary human mammary and ovarian epithelial cell cultures.Identification of Hydroxysteroid (17β) dehydrogenase type 12 (HSD17B12) as a CD8+ T-cell-defined human tumor antigen of human carcinomasRegulation and disregulation of mammalian nucleotide excision repair: a pathway to nongermline breast carcinogenesis.Permanently blocked stem cells derived from breast cancer cell lines.Association between biomarkers of environmental exposure and increased risk of breast cancerInduction of human breast cancer cell apoptosis from G2/M preceded by stimulation into the cell cycle by Z-1,1-dichloro-2,3-diphenylcyclopropane.Are Molecules Involved in Neuritogenesis and Axon Guidance Related to Autism Pathogenesis?(Z)-1,1-Dichloro-2-(4-methoxyphenyl)-3-phenylcyclopropane induces concentration-dependent growth inhibition, apoptosis, and coordinates regulation of apoptotic genes in TRAMP cells.In vivo somatic mutation and segregation at the human glycophorin A (GPA) locus: phenotypic variation encompassing both gene-specific and chromosomal mechanisms.Z-1,1-Dichloro-2,3-diphenylcyclopropanes block human prostate carcinoma cell proliferation, inhibit prostate-specific antigen expression, and initiate apoptosis.DNA double-strand break damage and repair assessed by pulsed-field gel electrophoresis.Molecular analysis of mutations in the human HPRT gene.Use of the glycophorin A somatic mutation assay for rapid, unambiguous identification of Fanconi anemia homozygotes regardless of GPA genotype.Efficient linkage of 10 loci in the proximal region of the mouse X chromosomeSomatic cell genotoxicity at the glycophorin A locus in humansLocalization of the rhodopsin gene to the distal half of mouse chromosome 6Sensitivity of somatic mutations in human umbilical cord blood to maternal environmentsUse of allele-specific glycophorin A antibodies to enumerate fetal erythroid cells in maternal circulationImpact of maternal lifestyle factors on newborn HPRT mutant frequencies and molecular spectrum--initial results from the Prenatal Exposures and Preeclampsia Prevention (PEPP) StudyGlycophorin A as a biological dosimeter for radiation dose to the bone marrow from iodine-131Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotesHuman in vivo somatic mutation measured at two loci: individuals with stably elevated background erythrocyte glycophorin A (gpa) variant frequencies exhibit normal T-lymphocyte hprt mutant frequenciesDiagnosis of ataxia telangiectasia with the glycophorin A somatic mutation assayThe GPA in vivo somatic mutation assayThe blood-based glycophorin A (GPA) human in vivo somatic mutation assay
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Stephen G Grant
@ast
Stephen G Grant
@en
Stephen G Grant
@es
Stephen G Grant
@nl
Stephen G Grant
@sl
type
label
Stephen G Grant
@ast
Stephen G Grant
@en
Stephen G Grant
@es
Stephen G Grant
@nl
Stephen G Grant
@sl
prefLabel
Stephen G Grant
@ast
Stephen G Grant
@en
Stephen G Grant
@es
Stephen G Grant
@nl
Stephen G Grant
@sl
P106
P21
P31
P496
0000-0002-9236-0913