Search Results - "Magis, Wendy"
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Selection-free genome editing of the sickle mutation in human adult hematopoietic stem/progenitor cells
Published in Science translational medicine (12-10-2016)“…Genetic diseases of blood cells are prime candidates for treatment through ex vivo gene editing of CD34 hematopoietic stem/progenitor cells (HSPCs), and a…”
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CRISPR-Cas9 interrogation of a putative fetal globin repressor in human erythroid cells
Published in PloS one (15-01-2019)“…Sickle Cell Disease and ß-thalassemia, which are caused by defective or deficient adult ß-globin (HBB) respectively, are the most common serious genetic blood…”
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Deep sequencing reveals novel microRNAs and regulation of microRNA expression during cell senescence
Published in PloS one (26-05-2011)“…In cell senescence, cultured cells cease proliferating and acquire aberrant gene expression patterns. MicroRNAs (miRNAs) modulate gene expression through…”
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Nuclear Relocation of a Transactivator Subunit Precedes Target Gene Activation
Published in Proceedings of the National Academy of Sciences - PNAS (09-10-2001)“…Murine erythroleukemia (MEL) cells are a model system to study reorganization of the eukaryotic nucleus during terminal differentiation. Upon chemical…”
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The Chicken β-Globin 5′HS4 Boundary Element Blocks Enhancer-Mediated Suppression of Silencing
Published in Molecular and Cellular Biology (01-05-1999)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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An Upstream Activator of Transcription Coordinately Increases the Level and Epigenetic Stability of Gene Expression
Published in Proceedings of the National Academy of Sciences - PNAS (26-11-1996)“…The mouse metallothionein-I (mMT-I) promoter is activated by the metal response element-binding transcription factor (MTF), which binds metal response elements…”
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High-level correction of the sickle mutation is amplified in vivo during erythroid differentiation
Published in iScience (17-06-2022)“…A point mutation in sickle cell disease (SCD) alters one amino acid in the β-globin subunit of hemoglobin, with resultant anemia and multiorgan damage that…”
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Enhancers Increase the Probability But not the Level of Gene Expression
Published in Proceedings of the National Academy of Sciences - PNAS (18-07-1995)“…We have studied enhancer function in transient and stable expression assays in mammalian cells by using systems that distinguish expressing from nonexpressing…”
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Transcriptional enhancers act in cis to suppress position-effect variegation
Published in Genes & development (15-01-1996)“…We have examined the basis of enhancer effects on gene expression by altering the action of enhancers on expression of a stably integrated reporter gene. We…”
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The chicken beta-globin 5'HS4 boundary element blocks enhancer-mediated suppression of silencing
Published in Molecular and cellular biology (01-05-1999)“…A constitutive DNase I-hypersensitive site 5' of the chicken beta-globin locus, termed 5'HS4 or cHS4, has been shown to insulate a promoter from the effect of…”
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HMG-I Binds to GATA Motifs: Implications for an HPFH Syndrome
Published in Biochemical and biophysical research communications (25-09-1995)“…We have examined binding of the nuclear protein HMG-I to the human γ-globin promoter. We find that HMG-I binds preferentially to the more 3′ of a pair of GATA…”
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γ Gene Promoter and Enhancer Structure in Seattle Variant of Hereditary Persistence of Fetal Hemoglobin
Published in Blood (01-04-1988)“…A variant of hereditary persistence of fetal hemoglobin (HPFH), first described in a patient from Seattle, was studied by structural analysis of the γ-globin…”
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