Search Results - "Hackmann, Alden F.M."
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Generation of Highly Site-Specific DNA Double-Strand Breaks in Human Cells by the Homing Endonucleases I-PpoI and I-CreI
Published in Biochemical and biophysical research communications (05-02-1999)“…We have determined the ability of two well-characterized eukaryotic homing endonucleases, I-PpoI from the myxomycetePhysarum polycephalumand I-CreI from the…”
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Erratum: Different somatic and germline HPRT1 mutations promote use of a common, cryptic intron 1 splice site
Published in Human mutation (1999)“…Aberrant hypoxanthine phosphoribosyltransferase (HUGO‐approved gene symbol HPRT1; MIM# 308000) RNA splicing promoted by splice site mutation or loss is a…”
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Different somatic and germline HPRT1 mutations promote use of a common, cryptic intron 1 splice site
Published in Human mutation (1999)“…Aberrant hypoxanthine phosphoribosyltransferase (HUGO‐approved gene symbol HPRT1; MIM# 308000) mRNA splicing, promoted by splice site mutation or loss, is a…”
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Molecular structure and genetic stability of human hypoxanthine phosphoribosyltransferase (HPRT) gene duplications
Published in Genomics (San Diego, Calif.) (01-07-1992)“…We have determined the genetic stability of three independent intragenic human HPRT gene duplications and the structure of each duplication at the nucleotide…”
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The Unexpected Landscape of in vivo Somatic Mutation in a Human Epithelial Cell Lineage
Published in Proceedings of the National Academy of Sciences - PNAS (05-02-2002)“…Few data exist on somatic mutation in the epithelial cell lineages that play a central role in human biology and disease. To delineate the "landscape" of…”
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Different somatic and germlineHPRT1 mutations promote use of a common, cryptic intron 1 splice site
Published in Human mutation (1999)Get full text
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Nucleotide sequence analysis of human hypoxanthine phosphoribosyltransferase (HPRT) gene deletions
Published in Genomics (San Diego, Calif.) (01-07-1992)“…We have determined the nucleotide sequences of 10 intragenic human HPRT gene deletion junctions isolated from thioguanine-resistant PSV811 Werner syndrome…”
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