Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP

ML Rahman, T Hyodo, MN Hasan, Y Mihara… - Bioscience …, 2021 - portlandpress.com
Targeted knock-in supported by the CRISPR/Cas systems enables the insertion, deletion,
and substitution of genome sequences exactly as designed. Although this technology is …
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[PDF] researchgate.net

[PDF][PDF] Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP

ML Rahman, T Hyodo, MN Hasan, Y Mihara, S Karnan… - 2021 - researchgate.net
Targeted knock-in supported by the CRISPR/Cas systems enables the insertion, deletion,
and substitution of genome sequences exactly as designed. Although this technology is …

Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP.

ML Rahman, T Hyodo, MN Hasan, Y Mihara… - Bioscience …, 2021 - europepmc.org
Targeted knock-in supported by the CRISPR/Cas systems enables the insertion, deletion,
and substitution of genome sequences exactly as designed. Although this technology is …
[HTML] nih.gov

[HTML][HTML] Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP

ML Rahman, T Hyodo, MN Hasan, Y Mihara… - Bioscience …, 2021 - ncbi.nlm.nih.gov
Targeted knock-in supported by the CRISPR/Cas systems enables the insertion, deletion,
and substitution of genome sequences exactly as designed. Although this technology is …

Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP.

ML Rahman, T Hyodo, MN Hasan… - Bioscience …, 2021 - search.ebscohost.com
Targeted knock-in supported by the CRISPR/Cas systems enables the insertion, deletion,
and substitution of genome sequences exactly as designed. Although this technology is …

Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP

ML Rahman, T Hyodo, MN Hasan, Y Mihara… - Bioscience …, 2021 - cir.nii.ac.jp
抄録< jats: title> Abstract</jats: title>< jats: p> Targeted knock-in supported by the
CRISPR/Cas systems enables the insertion, deletion, and substitution of genome …

Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP

ML Rahman, T Hyodo, MN Hasan… - Bioscience …, 2021 - pubmed.ncbi.nlm.nih.gov
Targeted knock-in supported by the CRISPR/Cas systems enables the insertion, deletion,
and substitution of genome sequences exactly as designed. Although this technology is …

Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP

ML Rahman, T Hyodo, MN Hasan, Y Mihara, S Karnan… - 2021 - portlandpress.com
Targeted knock-in supported by the CRISPR/Cas systems enables the insertion, deletion,
and substitution of genome sequences exactly as designed. Although this technology is …
[PDF] semanticscholar.org

[PDF][PDF] Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP

ML Rahman, T Hyodo, MN Hasan, Y Mihara, S Karnan… - 2021 - pdfs.semanticscholar.org
Targeted knock-in supported by the CRISPR/Cas systems enables the insertion, deletion,
and substitution of genome sequences exactly as designed. Although this technology is …

Flow cytometry-based quantification of targeted knock-in events in human cell lines using a GPI-anchor biosynthesis gene PIGP.

ML Rahman, T Hyodo, MN Hasan, Y Mihara… - Bioscience …, 2021 - europepmc.org
Targeted knock-in supported by the CRISPR/Cas systems enables the insertion, deletion,
and substitution of genome sequences exactly as designed. Although this technology is …