Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 186 entries
Sorted by: Best Match Show Resources per page
Technique: Transcript tracking by CRISPR.

Nature reviews. Genetics

Burgess DJ.
PMID: 27040488
Nat Rev Genet. 2016 May;17(5):254-5. doi: 10.1038/nrg.2016.41. Epub 2016 Mar 30.

No abstract available.

Cite
Burgess DJ. Technique: Transcript tracking by CRISPR. Nat Rev Genet. 2016;17(5):254-5doi: 10.1038/nrg.2016.41.
Burgess, D. J. (2016). Technique: Transcript tracking by CRISPR. Nature reviews. Genetics, 17(5), 254-5. https://doi.org/10.1038/nrg.2016.41
Burgess, Darren J. "Technique: Transcript tracking by CRISPR." Nature reviews. Genetics vol. 17,5 (2016): 254-5. doi: https://doi.org/10.1038/nrg.2016.41
Burgess DJ. Technique: Transcript tracking by CRISPR. Nat Rev Genet. 2016 May;17(5):254-5. doi: 10.1038/nrg.2016.41. Epub 2016 Mar 30. PMID: 27040488.
Copy Download .nbib Format: NLM
CRISPR/Cas9 genome editing in human pluripotent stem cells: Harnessing human genetics in a dish.

Developmental dynamics : an official publication of the American Association of Anatomists

González F.
PMID: 27145095
Dev Dyn. 2016 Jul;245(7):788-806. doi: 10.1002/dvdy.24414. Epub 2016 Jun 09.

Because of their extraordinary differentiation potential, human pluripotent stem cells (hPSCs) can differentiate into virtually any cell type of the human body, providing a powerful platform not only for generating relevant cell types useful for cell replacement therapies, but...

Cite
González F. CRISPR/Cas9 genome editing in human pluripotent stem cells: Harnessing human genetics in a dish. Dev Dyn. 2016;245(7):788-806doi: 10.1002/dvdy.24414.
González, F. (2016). CRISPR/Cas9 genome editing in human pluripotent stem cells: Harnessing human genetics in a dish. Developmental dynamics : an official publication of the American Association of Anatomists, 245(7), 788-806. https://doi.org/10.1002/dvdy.24414
González, Federico. "CRISPR/Cas9 genome editing in human pluripotent stem cells: Harnessing human genetics in a dish." Developmental dynamics : an official publication of the American Association of Anatomists vol. 245,7 (2016): 788-806. doi: https://doi.org/10.1002/dvdy.24414
González F. CRISPR/Cas9 genome editing in human pluripotent stem cells: Harnessing human genetics in a dish. Dev Dyn. 2016 Jul;245(7):788-806. doi: 10.1002/dvdy.24414. Epub 2016 Jun 09. PMID: 27145095.
Copy Download .nbib Format: NLM
CRISPR-Cas Systems Reduced to a Minimum.

Molecular cell

Almendros C, Kieper SN, Brouns SJJ.
PMID: 30794791
Mol Cell. 2019 Feb 21;73(4):641-642. doi: 10.1016/j.molcel.2019.02.005.

In two recent studies in Molecular Cell, Wright et al. (2019) report complete spacer integration by a Cas1 mini-integrase and Edraki et al. (2019) describe accurate genome editing by a small Cas9 ortholog with less stringent PAM requirements.

Cite
Almendros C, Kieper SN, Brouns SJJ. CRISPR-Cas Systems Reduced to a Minimum. Mol Cell. 2019;73(4):641-642doi: 10.1016/j.molcel.2019.02.005.
Almendros, C., Kieper, S. N., & Brouns, S. J. J. (2019). CRISPR-Cas Systems Reduced to a Minimum. Molecular cell, 73(4), 641-642. https://doi.org/10.1016/j.molcel.2019.02.005
Almendros, Cristóbal, et al. "CRISPR-Cas Systems Reduced to a Minimum." Molecular cell vol. 73,4 (2019): 641-642. doi: https://doi.org/10.1016/j.molcel.2019.02.005
Almendros C, Kieper SN, Brouns SJJ. CRISPR-Cas Systems Reduced to a Minimum. Mol Cell. 2019 Feb 21;73(4):641-642. doi: 10.1016/j.molcel.2019.02.005. PMID: 30794791.
Copy Download .nbib Format: NLM
A RecET-assisted CRISPR-Cas9 genome editing in Corynebacterium glutamicum.

Microbial cell factories

Wang B, Hu Q, Zhang Y, Shi R, Chai X, Liu Z, Shang X, Zhang Y, Wen T.
PMID: 29685154
Microb Cell Fact. 2018 Apr 23;17(1):63. doi: 10.1186/s12934-018-0910-2.

BACKGROUND: Extensive modification of genome is an efficient manner to regulate the metabolic network for producing target metabolites or non-native products using Corynebacterium glutamicum as a cell factory. Genome editing approaches by means of homologous recombination and counter-selection markers...

Cite
Wang B, Hu Q, Zhang Y, et al. A RecET-assisted CRISPR-Cas9 genome editing in Corynebacterium glutamicum. Microb Cell Fact. 2018;17(1):63doi: 10.1186/s12934-018-0910-2.
Wang, B., Hu, Q., Zhang, Y., Shi, R., Chai, X., Liu, Z., Shang, X., Zhang, Y., & Wen, T. (2018). A RecET-assisted CRISPR-Cas9 genome editing in Corynebacterium glutamicum. Microbial cell factories, 17(1), 63. https://doi.org/10.1186/s12934-018-0910-2
Wang, Bo, et al. "A RecET-assisted CRISPR-Cas9 genome editing in Corynebacterium glutamicum." Microbial cell factories vol. 17,1 (2018): 63. doi: https://doi.org/10.1186/s12934-018-0910-2
Wang B, Hu Q, Zhang Y, Shi R, Chai X, Liu Z, Shang X, Zhang Y, Wen T. A RecET-assisted CRISPR-Cas9 genome editing in Corynebacterium glutamicum. Microb Cell Fact. 2018 Apr 23;17(1):63. doi: 10.1186/s12934-018-0910-2. PMID: 29685154; PMCID: PMC5913818.
Copy Download .nbib Format: NLM
CRISPR EnAbled Trackable genome Engineering for isopropanol production in Escherichia coli.

Metabolic engineering

Liang L, Liu R, Garst AD, Lee T, Nogué VSI, Beckham GT, Gill RT.
PMID: 28216108
Metab Eng. 2017 May;41:1-10. doi: 10.1016/j.ymben.2017.02.009. Epub 2017 Feb 16.

Isopropanol is an important target molecule for sustainable production of fuels and chemicals. Increases in DNA synthesis and synthetic biology capabilities have resulted in the development of a range of new strategies for the more rapid design, construction, and...

Cite
Liang L, Liu R, Garst AD, et al. CRISPR EnAbled Trackable genome Engineering for isopropanol production in Escherichia coli. Metab Eng. 2017;41:1-10doi: 10.1016/j.ymben.2017.02.009.
Liang, L., Liu, R., Garst, A. D., Lee, T., Nogué, V. S. I., Beckham, G. T., & Gill, R. T. (2017). CRISPR EnAbled Trackable genome Engineering for isopropanol production in Escherichia coli. Metabolic engineering, 411-10. https://doi.org/10.1016/j.ymben.2017.02.009
Liang, Liya, et al. "CRISPR EnAbled Trackable genome Engineering for isopropanol production in Escherichia coli." Metabolic engineering vol. 41 (2017): 1-10. doi: https://doi.org/10.1016/j.ymben.2017.02.009
Liang L, Liu R, Garst AD, Lee T, Nogué VSI, Beckham GT, Gill RT. CRISPR EnAbled Trackable genome Engineering for isopropanol production in Escherichia coli. Metab Eng. 2017 May;41:1-10. doi: 10.1016/j.ymben.2017.02.009. Epub 2017 Feb 16. PMID: 28216108.
Copy Download .nbib Format: NLM
Genome Editing in Human Neural Stem and Progenitor Cells.

Results and problems in cell differentiation

Bressan RB, Pollard SM.
PMID: 30209659
Results Probl Cell Differ. 2018;66:163-182. doi: 10.1007/978-3-319-93485-3_7.

Experimental tools for precise manipulation of mammalian genomes enable reverse genetic approaches to explore biology and disease. Powerful genome editing technologies built upon designer nucleases, such as CRISPR/Cas9, have recently emerged. Parallel progress has been made in methodologies for...

Cite
Bressan RB, Pollard SM. Genome Editing in Human Neural Stem and Progenitor Cells. Results Probl Cell Differ. 2018;66:163-182doi: 10.1007/978-3-319-93485-3_7.
Bressan, R. B., & Pollard, S. M. (2018). Genome Editing in Human Neural Stem and Progenitor Cells. Results and problems in cell differentiation, 66163-182. https://doi.org/10.1007/978-3-319-93485-3_7
Bressan, Raul Bardini, and Pollard, Steven M. "Genome Editing in Human Neural Stem and Progenitor Cells." Results and problems in cell differentiation vol. 66 (2018): 163-182. doi: https://doi.org/10.1007/978-3-319-93485-3_7
Bressan RB, Pollard SM. Genome Editing in Human Neural Stem and Progenitor Cells. Results Probl Cell Differ. 2018;66:163-182. doi: 10.1007/978-3-319-93485-3_7. PMID: 30209659.
Copy Download .nbib Format: NLM
High-throughput genetic screens using CRISPR-Cas9 system.

Archives of pharmacal research

Kweon J, Kim Y.
PMID: 29637495
Arch Pharm Res. 2018 Sep;41(9):875-884. doi: 10.1007/s12272-018-1029-z. Epub 2018 Apr 10.

The CRISPR-Cas9 system is a powerful tool for genome engineering, and its programmability and simplicity have enabled various types of gene manipulation such as gene disruption and transcriptional and epigenetic perturbation. Particularly, CRISPR-based pooled libraries facilitate high-throughput screening for...

Cite
Kweon J, Kim Y. High-throughput genetic screens using CRISPR-Cas9 system. Arch Pharm Res. 2018;41(9):875-884doi: 10.1007/s12272-018-1029-z.
Kweon, J., & Kim, Y. (2018). High-throughput genetic screens using CRISPR-Cas9 system. Archives of pharmacal research, 41(9), 875-884. https://doi.org/10.1007/s12272-018-1029-z
Kweon, Jiyeon, and Kim, Yongsub. "High-throughput genetic screens using CRISPR-Cas9 system." Archives of pharmacal research vol. 41,9 (2018): 875-884. doi: https://doi.org/10.1007/s12272-018-1029-z
Kweon J, Kim Y. High-throughput genetic screens using CRISPR-Cas9 system. Arch Pharm Res. 2018 Sep;41(9):875-884. doi: 10.1007/s12272-018-1029-z. Epub 2018 Apr 10. PMID: 29637495.
Copy Download .nbib Format: NLM
Systematic analysis of Type I-E Escherichia coli CRISPR-Cas PAM sequences ability to promote interference and primed adaptation.

Molecular microbiology

Musharova O, Sitnik V, Vlot M, Savitskaya E, Datsenko KA, Krivoy A, Fedorov I, Semenova E, Brouns SJJ, Severinov K.
PMID: 30875129
Mol Microbiol. 2019 Jun;111(6):1558-1570. doi: 10.1111/mmi.14237. Epub 2019 Apr 06.

CRISPR interference occurs when a protospacer recognized by the CRISPR RNA is destroyed by Cas effectors. In Type I CRISPR-Cas systems, protospacer recognition can lead to «primed adaptation» - acquisition of new spacers from in cis located sequences. Type...

Cite
Musharova O, Sitnik V, Vlot M, et al. Systematic analysis of Type I-E Escherichia coli CRISPR-Cas PAM sequences ability to promote interference and primed adaptation. Mol Microbiol. 2019;111(6):1558-1570doi: 10.1111/mmi.14237.
Musharova, O., Sitnik, V., Vlot, M., Savitskaya, E., Datsenko, K. A., Krivoy, A., Fedorov, I., Semenova, E., Brouns, S. J. J., & Severinov, K. (2019). Systematic analysis of Type I-E Escherichia coli CRISPR-Cas PAM sequences ability to promote interference and primed adaptation. Molecular microbiology, 111(6), 1558-1570. https://doi.org/10.1111/mmi.14237
Musharova, Olga, et al. "Systematic analysis of Type I-E Escherichia coli CRISPR-Cas PAM sequences ability to promote interference and primed adaptation." Molecular microbiology vol. 111,6 (2019): 1558-1570. doi: https://doi.org/10.1111/mmi.14237
Musharova O, Sitnik V, Vlot M, Savitskaya E, Datsenko KA, Krivoy A, Fedorov I, Semenova E, Brouns SJJ, Severinov K. Systematic analysis of Type I-E Escherichia coli CRISPR-Cas PAM sequences ability to promote interference and primed adaptation. Mol Microbiol. 2019 Jun;111(6):1558-1570. doi: 10.1111/mmi.14237. Epub 2019 Apr 06. PMID: 30875129; PMCID: PMC6568314.
Copy Download .nbib Format: NLM
Progress and Challenges for Live-cell Imaging of Genomic Loci Using CRISPR-based Platforms.

Genomics, proteomics & bioinformatics

Wu X, Mao S, Ying Y, Krueger CJ, Chen AK.
PMID: 30710789
Genomics Proteomics Bioinformatics. 2019 Apr;17(2):119-128. doi: 10.1016/j.gpb.2018.10.001. Epub 2019 Jan 30.

Chromatin conformation, localization, and dynamics are crucial regulators of cellular behaviors. Although fluorescence in situ hybridization-based techniques have been widely utilized for investigating chromatin architectures in healthy and diseased states, the requirement for cell fixation precludes the comprehensive dynamic...

Cite
Wu X, Mao S, Ying Y, et al. Progress and Challenges for Live-cell Imaging of Genomic Loci Using CRISPR-based Platforms. Genomics Proteomics Bioinformatics. 2019;17(2):119-128doi: 10.1016/j.gpb.2018.10.001.
Wu, X., Mao, S., Ying, Y., Krueger, C. J., & Chen, A. K. (2019). Progress and Challenges for Live-cell Imaging of Genomic Loci Using CRISPR-based Platforms. Genomics, proteomics & bioinformatics, 17(2), 119-128. https://doi.org/10.1016/j.gpb.2018.10.001
Wu, Xiaotian, et al. "Progress and Challenges for Live-cell Imaging of Genomic Loci Using CRISPR-based Platforms." Genomics, proteomics & bioinformatics vol. 17,2 (2019): 119-128. doi: https://doi.org/10.1016/j.gpb.2018.10.001
Wu X, Mao S, Ying Y, Krueger CJ, Chen AK. Progress and Challenges for Live-cell Imaging of Genomic Loci Using CRISPR-based Platforms. Genomics Proteomics Bioinformatics. 2019 Apr;17(2):119-128. doi: 10.1016/j.gpb.2018.10.001. Epub 2019 Jan 30. PMID: 30710789; PMCID: PMC6620262.
Copy Download .nbib Format: NLM
Off-target genome editing: A new discipline of gene science and a new class of medicine.

Cell biology and toxicology

Wang DC, Wang X.
PMID: 31030279
Cell Biol Toxicol. 2019 Jun;35(3):179-183. doi: 10.1007/s10565-019-09475-7. Epub 2019 Apr 27.

With an increasing growth of genome editing, off-target effects such as non-specific genetic modifications resulting from the designed process of genome editing become a new discipline of gene science and new class medicine. The degree of short-term and long-term...

Cite
Wang DC, Wang X. Off-target genome editing: A new discipline of gene science and a new class of medicine. Cell Biol Toxicol. 2019;35(3):179-183doi: 10.1007/s10565-019-09475-7.
Wang, D. C., & Wang, X. (2019). Off-target genome editing: A new discipline of gene science and a new class of medicine. Cell biology and toxicology, 35(3), 179-183. https://doi.org/10.1007/s10565-019-09475-7
Wang, Diane Catherine, and Wang, Xiangdong. "Off-target genome editing: A new discipline of gene science and a new class of medicine." Cell biology and toxicology vol. 35,3 (2019): 179-183. doi: https://doi.org/10.1007/s10565-019-09475-7
Wang DC, Wang X. Off-target genome editing: A new discipline of gene science and a new class of medicine. Cell Biol Toxicol. 2019 Jun;35(3):179-183. doi: 10.1007/s10565-019-09475-7. Epub 2019 Apr 27. PMID: 31030279.
Copy Download .nbib Format: NLM
Super-precise new CRISPR tool could tackle a plethora of genetic diseases.

Nature

Ledford H.
PMID: 31641267
Nature. 2019 Oct;574(7779):464-465. doi: 10.1038/d41586-019-03164-5.

No abstract available.

Cite
Ledford H. Super-precise new CRISPR tool could tackle a plethora of genetic diseases. Nature. 2019;574(7779):464-465doi: 10.1038/d41586-019-03164-5.
Ledford, H. (2019). Super-precise new CRISPR tool could tackle a plethora of genetic diseases. Nature, 574(7779), 464-465. https://doi.org/10.1038/d41586-019-03164-5
Ledford, Heidi. "Super-precise new CRISPR tool could tackle a plethora of genetic diseases." Nature vol. 574,7779 (2019): 464-465. doi: https://doi.org/10.1038/d41586-019-03164-5
Ledford H. Super-precise new CRISPR tool could tackle a plethora of genetic diseases. Nature. 2019 Oct;574(7779):464-465. doi: 10.1038/d41586-019-03164-5. PMID: 31641267.
Copy Download .nbib Format: NLM
Finding Her Niche: An Interview with Emmanuelle Charpentier.

The CRISPR journal

Davies K, Charpentier E.
PMID: 31021229
CRISPR J. 2019 Feb;2:17-22. doi: 10.1089/crispr.2019.29042.kda.

No abstract available.

Cite
Davies K, Charpentier E. Finding Her Niche: An Interview with Emmanuelle Charpentier. CRISPR J. 2019;2:17-22doi: 10.1089/crispr.2019.29042.kda.
Davies, K., & Charpentier, E. (2019). Finding Her Niche: An Interview with Emmanuelle Charpentier. The CRISPR journal, 217-22. https://doi.org/10.1089/crispr.2019.29042.kda
Davies, Kevin, and Charpentier, Emmanuelle. "Finding Her Niche: An Interview with Emmanuelle Charpentier." The CRISPR journal vol. 2 (2019): 17-22. doi: https://doi.org/10.1089/crispr.2019.29042.kda
Davies K, Charpentier E. Finding Her Niche: An Interview with Emmanuelle Charpentier. CRISPR J. 2019 Feb;2:17-22. doi: 10.1089/crispr.2019.29042.kda. PMID: 31021229.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 186 entries