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Karen Dyer Montgomery

Researcher at WiCell

Publications -  8
Citations -  1638

Karen Dyer Montgomery is an academic researcher from WiCell. The author has contributed to research in topics: Induced pluripotent stem cell & Embryonic stem cell. The author has an hindex of 7, co-authored 8 publications receiving 1500 citations.

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Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage

Katherine Amps, +124 more
- 27 Nov 2011 - 
TL;DR: Of these genes, BCL2L1 is a strong candidate for driving culture adaptation of ES cells, and single-nucleotide polymorphism analysis revealed that they included representatives of most major ethnic groups.
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Karotypic abnormalities in human induced pluripotent stem cells and embryonic stem cells.

TL;DR: The data show that the recurrent chromosome abnormalities in human ESC and iPSC cultures are similar to each other and distinct from those reported in embryos, both in frequency and in type.
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Efficient generation of transgene-free induced pluripotent stem cells from normal and neoplastic bone marrow and cord blood mononuclear cells

TL;DR: It is demonstrated that iPSCs free of transgene and vector sequences could be generated from human BM and CB mononuclear cells using non-integrating episomal vectors and showed a unique complex chromosomal translocation identified in marrow sample while displaying typical embryonic stem cell phenotype and pluripotent differentiation potential.
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Recurrent copy number variations in human induced pluripotent stem cells.

TL;DR: The American public has five distinct attitudes toward (i) cloning animals, (ii) cloning humans, (iii) curing serious diseases by therapeutic cloning or by using stem cells from an IVF embryo, (iv) curingserious diseases using adult stem cells and (v) using any of these for cosmetic purposes.
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Genetic correction and analysis of induced pluripotent stem cells from a patient with gyrate atrophy

TL;DR: It is confirmed that iPS cells themselves may carry a significant mutational load at initial isolation, but that the clonal events and prolonged cultured required for correction of a genetic defect can be accomplished without a substantial increase in mutational burden.