Suchergebnisse - "CRISPR-Associated Proteins metabolism"

Classically Derived Nanobot Architecture: Viral-Scale Medibots via CRISPR and Nanoscale Robotic Engineering

Autoren: Daniels, Justin

Schlagwörter: Nanobots, Nano-materials, Nano-processes, CRISPR-Associated Proteins, CRISPR-Cas Systems, CRISPR-Cas Systems/genetics, CRISPR-Cas Systems/physiology, CRISPR-Associated Proteins/economics, CRISPR-Associated Proteins/physiology, CRISPR-Associated Proteins/poisoning, CRISPR-Associated Protein 9, CRISPR-Cas Systems/immunology, CRISPR-Associated Proteins/analysis, CRISPR-Associated Proteins/blood, CRISPR-Associated Proteins/classification, CRISPR-Associated Proteins/chemistry, CRISPR-Associated Proteins/metabolism, CRISPR-Associated Proteins/immunology, CRISPR-Associated Proteins/standards, CRISPR-Associated Proteins/ultrastructure, CRISPR-Associated Proteins/toxicity, CRISPR-Associated Proteins/biosynthesis, CRISPR-Associated Proteins/history, Genetic engineering, Medibots, Nano medicine

Relation: https://zenodo.org/records/16279260; oai:zenodo.org:16279260; https://doi.org/10.5281/zenodo.16279260

Verfügbarkeit: https://doi.org/10.5281/zenodo.16279260
https://zenodo.org/records/16279260

Molecular basis of cyclic tetra-oligoadenylate processing by small standalone CRISPR-Cas ring nucleases

Autoren: Rafael Molina Ricardo Garcia-Martin Blanca López-Méndez et al.

Weitere Verfasser: Rafael Molina Ricardo Garcia-Martin Blanca López-Méndez et al.

Quelle: Nucleic Acids Res
Digital.CSIC. Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Molina, R, Garcia-Martin, R, López-Méndez, B, Jensen, A L G, Ciges-Tomas, J R, Marchena-Hurtado, J, Stella, S & Montoya, G 2022, ' Molecular basis of cyclic tetra-oligoadenylate processing by small standalone CRISPR-Cas ring nucleases ', Nucleic Acids Research, vol. 50, no. 19, pp. 11199-11213 . https://doi.org/10.1093/nar/gkac923

Schlagwörter: 0301 basic medicine, 0303 health sciences, Oligoribonucleotides, Adenine Nucleotides/metabolism, Nucleic Acid Enzymes, Adenine Nucleotides, CRISPR-Associated Proteins, Endonucleases/metabolism, Endonucleases, 03 medical and health sciences, Oligoribonucleotides/chemistry, CRISPR-Associated Proteins/metabolism, CRISPR-Cas Systems

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/36271789
http://hdl.handle.net/10261/288333
https://api.elsevier.com/content/abstract/scopus_id/85144569290
https://curis.ku.dk/ws/files/325025812/gkac923.pdf

Allosteric control of type I-A CRISPR-Cas3 complexes and establishment as effective nucleic acid detection and human genome editing tools.

Autoren: Hu, C. Ni, D. Nam, K.H. et al.

Schlagwörter: CRISPR-Associated Proteins/genetics, CRISPR-Associated Proteins/metabolism, CRISPR-Cas Systems, Cryoelectron Microscopy, DNA/genetics, DNA/metabolism, Endonucleases/genetics, Gene Editing, Humans, RNA, CRISPR, Cas3, deletion, genome editing, nucleic acid detection, type I CRISPR-Cas

Relation: Molecular Cell; https://iris.unil.ch/handle/iris/172487; serval:BIB_BC6F62E8C518; 000841899600006

Verfügbarkeit: https://iris.unil.ch/handle/iris/172487
https://doi.org/10.1016/j.molcel.2022.06.007

New vectors for simple and streamlined CRISPR-Cas9 genome editing inSaccharomyces cerevisiae: Vectors for simple CRISPR-Cas9 genome editing in yeast

Autoren: Laughery, Marian F Hunter, Tierra Brown, Alexander et al.

Quelle: Yeast. 32:711-720

Schlagwörter: Genetic Markers, 0301 basic medicine, CRISPR-Associated Proteins - genetics, CRISPR-Associated Proteins, Genetic Vectors, Endonucleases - genetics, Gene Expression, DNA - metabolism, Saccharomyces cerevisiae, RNA, Guide, CRISPR-Cas Systems, Polymerase Chain Reaction, Transformation, Double-Stranded, 03 medical and health sciences, Transformation, Genetic, Genetic, Genetic Markers - genetics, Clustered Regularly Interspaced Short Palindromic Repeats, DNA Breaks, Double-Stranded, CRISPR-Associated Proteins - metabolism, Guide - genetics, 0303 health sciences, Saccharomyces cerevisiae - genetics, Base Sequence, DNA Breaks, Computational Biology, DNA, Endonucleases, RNA Editing - genetics, 13. Climate action, Gene Targeting, Computational Biology - methods, RNA, RNA Editing, CRISPR-Cas Systems

Zugangs-URL: https://europepmc.org/articles/pmc4715497?pdf=render
https://pubmed.ncbi.nlm.nih.gov/26305040
https://europepmc.org/article/MED/26305040
https://onlinelibrary.wiley.com/doi/10.1002/yea.3098
http://onlinelibrary.wiley.com/doi/10.1002/yea.3098/full?scrollTo=references
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715497/
https://pubmed.ncbi.nlm.nih.gov/26305040/
http://onlinelibrary.wiley.com/doi/10.1002/yea.3098/full

DNA binding specificities of Escherichia coli Cas1–Cas2 integrase drive its recruitment at the CRISPR locus

Autoren: Moch, Clara Fromant, Michel Blanquet, Sylvain et al.

Weitere Verfasser: Moch, Clara Fromant, Michel Blanquet, Sylvain et al.

Quelle: ISSN: 0305-1048.

Schlagwörter: MESH: Binding, Competitive, MESH: CRISPR-Associated Proteins/metabolism, MESH: Integrases/metabolism, MESH: Inverted Repeat Sequences, MESH: Plasmids/metabolism, MESH: Protein Binding, MESH: Clustered Regularly Interspaced Short Palindromic Repeats, MESH: DNA, Bacterial/metabolism, MESH: Endodeoxyribonucleases/metabolism, MESH: Endonucleases/metabolism, MESH: Escherichia coli/genetics, MESH: Escherichia coli Proteins/metabolism, [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, [SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM], [SDV.CAN]Life Sciences [q-bio]/Cancer

Relation: info:eu-repo/semantics/altIdentifier/pmid/28034956; PUBMED: 28034956; PUBMEDCENTRAL: PMC5389526

Verfügbarkeit: https://polytechnique.hal.science/hal-01961608
https://polytechnique.hal.science/hal-01961608v1/document
https://polytechnique.hal.science/hal-01961608v1/file/gkw1309.pdf
https://doi.org/10.1093/nar/gkw1309

Molecular basis of cyclic tetra-oligoadenylate processing by small standalone CRISPR-Cas ring nucleases

Autoren: Molina, Rafael Garcia-Martin, Ricardo López-Méndez, Blanca et al.

Quelle: Molina , R , Garcia-Martin , R , López-Méndez , B , Jensen , A L G , Ciges-Tomas , J R , Marchena-Hurtado , J , Stella , S & Montoya , G 2022 , ' Molecular basis of cyclic tetra-oligoadenylate processing by small standalone CRISPR-Cas ring nucleases ' , Nucleic Acids Research , vol. 50 , no. 19 , pp. 11199-11213 .

Index Begriffe: CRISPR-Associated Proteins/metabolism, CRISPR-Cas Systems, Oligoribonucleotides/chemistry, Adenine Nucleotides/metabolism, Endonucleases/metabolism, article

URL: https://researchprofiles.ku.dk/da/publications/molecular-basis-of-cyclic-tetraoligoadenylate-processing-by-small-standalone-crisprcas-ring-nucleases(0cd26589-97dd-46b0-b961-fbc36899ba9f).html
https://doi.org/10.1093/nar/gkac923
https://curis.ku.dk/ws/files/325025812/gkac923.pdf