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Nucleic Acids Research
|
November 30, 2023
Self-delivering, chemically modified CRISPR RNAs for AAV co-delivery and genome editing in vivo
Han Zhang, Karen Kelly, Jonathan Lee, et al.
Biorxiv : the Preprint Server for Biology
|
October 31, 2023
Addressing the dNTP bottleneck restricting prime editing activity
Karthikeyan Ponnienselvan, Pengpeng Liu, Thomas Nyalile, et al.
Cell Stem Cell
|
April 23, 2020
Small-Molecule PAPD5 Inhibitors Restore Telomerase Activity in Patient Stem Cells
Neha Nagpal, Jianing Wang, Jing Zeng, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 29, 2017
CRISPR-Cas9-mediated saturated mutagenesis screen predicts clinical drug resistance with improved accuracy
Leyuan Ma, Jeffrey I Boucher, Janet Paulsen, et al.
Molecular Metabolism
|
July 23, 2023
Crosstalk between corepressor NRIP1 and cAMP signaling on adipocyte thermogenic programming
Emmanouela Tsagkaraki, Adilson Guilherme, Sarah M Nicoloro, et al.
Nature Communications
|
November 2, 2021
Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-directed repair in vivo
Raed Ibraheim, Phillip W L Tai, Aamir Mir, et al.
Cytotherapy
|
March 20, 2024
Ex vivo culture resting time impacts transplantation outcomes of genome-edited human hematopoietic stem and progenitor cells in xenograft mouse models
Selami Demirci, Muhammad B N Khan, Gabriela Hinojosa, et al.
Genome Biology
|
December 7, 2018
NmeCas9 is an intrinsically high-fidelity genome-editing platform
Nadia Amrani, Xin D Gao, Pengpeng Liu, et al.
Disease Models & Mechanisms
|
July 10, 2012
Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development
Jimann Shin, Arun Padmanabhan, Eric D de Groh, et al.
Nature Biotechnology
|
November 14, 2017
Structure-guided chemical modification of guide RNA enables potent non-viral in vivo genome editing
Hao Yin, Chun-Qing Song, Sneha Suresh, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 106) with videos related to
Sort By:
Page
of 11
Nucleic Acids Research
|
November 30, 2023
Self-delivering, chemically modified CRISPR RNAs for AAV co-delivery and genome editing in vivo
Han Zhang, Karen Kelly, Jonathan Lee, et al.
Biorxiv : the Preprint Server for Biology
|
October 31, 2023
Addressing the dNTP bottleneck restricting prime editing activity
Karthikeyan Ponnienselvan, Pengpeng Liu, Thomas Nyalile, et al.
Cell Stem Cell
|
April 23, 2020
Small-Molecule PAPD5 Inhibitors Restore Telomerase Activity in Patient Stem Cells
Neha Nagpal, Jianing Wang, Jing Zeng, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 29, 2017
CRISPR-Cas9-mediated saturated mutagenesis screen predicts clinical drug resistance with improved accuracy
Leyuan Ma, Jeffrey I Boucher, Janet Paulsen, et al.
Molecular Metabolism
|
July 23, 2023
Crosstalk between corepressor NRIP1 and cAMP signaling on adipocyte thermogenic programming
Emmanouela Tsagkaraki, Adilson Guilherme, Sarah M Nicoloro, et al.
Nature Communications
|
November 2, 2021
Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-directed repair in vivo
Raed Ibraheim, Phillip W L Tai, Aamir Mir, et al.
Cytotherapy
|
March 20, 2024
Ex vivo culture resting time impacts transplantation outcomes of genome-edited human hematopoietic stem and progenitor cells in xenograft mouse models
Selami Demirci, Muhammad B N Khan, Gabriela Hinojosa, et al.
Genome Biology
|
December 7, 2018
NmeCas9 is an intrinsically high-fidelity genome-editing platform
Nadia Amrani, Xin D Gao, Pengpeng Liu, et al.
Disease Models & Mechanisms
|
July 10, 2012
Zebrafish neurofibromatosis type 1 genes have redundant functions in tumorigenesis and embryonic development
Jimann Shin, Arun Padmanabhan, Eric D de Groh, et al.
Nature Biotechnology
|
November 14, 2017
Structure-guided chemical modification of guide RNA enables potent non-viral in vivo genome editing
Hao Yin, Chun-Qing Song, Sneha Suresh, et al.
Page
of 11