Jennifer Anne Doudna
Doudna, Jennifer A.
Doudna, Jennifer A., 1964-....
Doudna, Jennifer
VIAF ID: 43652981 (Personal)
Permalink: http://viaf.org/viaf/43652981
Preferred Forms
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100 1 _ ‡a Doudna, Jennifer
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100 1 _ ‡a Doudna, Jennifer A.
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100 1 _ ‡a Doudna, Jennifer A. ‡d 1964-
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100 1 _ ‡a Doudna, Jennifer A. ‡d 1964-
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100 1 _ ‡a Doudna, Jennifer A., ‡d 1964-
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100 1 _ ‡a Doudna, Jennifer A., ‡d 1964-....
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100 0 _ ‡a Jennifer Anne Doudna
4xx's: Alternate Name Forms (53)
5xx's: Related Names (1)
Works
Title | Sources |
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Un coup de ciseaux dans la création : CRISPR-Cas9 : le redoutable pouvoir de contrôler l'évolution |
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Crack in creation |
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CRISPR-Cas : a laboratory manual |
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Edycja genów : władza nad ewolucją |
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Edytorzy genów |
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Eingriff in die Evolution die Macht der CRISPR-Technologie und die Frage, wie wir sie nutzen wollen |
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Hijacking the ribosome, 2001: |
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Mass spectrometric analysis of the human 40S ribosomal subunit: native and HCV IRES-bound complexes |
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Mass spectrometry reveals modularity and a complete subunit interaction map of the eukaryotic translation factor eIF3 |
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Mechanism of ribosome recruitment by hepatitis C IRES RNA |
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Mechanism of substrate selection by a highly specific CRISPR endoribonuclease. |
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Mechanisms of internal ribosome entry in translation initiation. |
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Methods to crystallize RNA. |
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Molecular biology : principles and practice |
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A molecular contortionist |
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Molecular mechanisms of RNA interference |
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Multiplexed RNA structure characterization with selective 2'-hydroxyl acylation analyzed by primer extension sequencing (SHAPE-Seq) |
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Mutational analysis of conserved nucleotides in a self-splicing group I intron |
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n2001128894 |
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Nucleosome breathing and remodeling constrain CRISPR-Cas9 function. |
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Optimized high-throughput screen for hepatitis C virus translation inhibitors. |
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Paul Sigler (1934-2000). |
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Perspective: Embryo editing needs scrutiny. |
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Phage-assisted evolution of an adenine base editor with improved Cas domain compatibility and activity |
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A phosphoramidate substrate analog is a competitive inhibitor of the Tetrahymena group I ribozyme. |
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Potent CRISPR-Cas9 inhibitors from Staphylococcus genomes |
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Precise and heritable genome editing in evolutionarily diverse nematodes using TALENs and CRISPR/Cas9 to engineer insertions and deletions |
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Preliminary X-ray diffraction studies of an RNA pseudoknot that inhibits HIV-1 reverse transcriptase |
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Preparation of homogeneous ribozyme RNA for crystallization |
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Profiling of engineering hotspots identifies an allosteric CRISPR-Cas9 switch |
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Programmable RNA recognition using a CRISPR-associated Argonaute. |
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Programmable RNA Tracking in Live Cells with CRISPR/Cas9. |
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Programmed DNA destruction by miniature CRISPR-Cas14 enzymes |
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Protecting genome integrity during CRISPR immune adaptation. |
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Quantitative studies of ribosome conformational dynamics. |
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Rapid detection of SARS-CoV-2 with Cas13 |
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Rational design of a split-Cas9 enzyme complex |
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Real-time observation of DNA recognition and rejection by the RNA-guided endonuclease Cas9. |
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Reassortment and mutation of the avian influenza virus polymerase PA subunit overcome species barriers |
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Receptor-Mediated Delivery of CRISPR-Cas9 Endonuclease for Cell Type Specific Gene Editing. |
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Reconsidering movement of eukaryotic mRNAs between polysomes and P bodies. |
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Reconstitution of selective HIV-1 RNA packaging in vitro by membrane-bound Gag assemblies. |
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Reply to Nathamgari et al.: Nanopore electroporation for intracellular delivery of biological macromolecules |
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Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression |
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Ribonuclease revisited: structural insights into ribonuclease III family enzymes |
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Ribozyme catalysis: not different, just worse. |
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Ribozyme-catalyzed primer extension by trinucleotides: a model for the RNA-catalyzed replication of RNA. |
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Ribozyme structures and mechanisms. |
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Ribozymes: the hammerhead swings into action |
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RNA-based recognition and targeting: sowing the seeds of specificity. |
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RNA binding and HEPN nuclease activation are decoupled in CRISPR-Cas13a |
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RNA-catalysed synthesis of complementary-strand RNA |
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RNA-dependent RNA targeting by CRISPR-Cas9. |
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RNA folds: insights from recent crystal structures |
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RNA-guided assembly of Rev-RRE nuclear export complexes |
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RNA-guided complex from a bacterial immune system enhances target recognition through seed sequence interactions. |
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RNA-guided genetic silencing systems in bacteria and archaea |
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RNA-mediated interaction between the peptide-binding and GTPase domains of the signal recognition particle. |
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RNA: primed for packing? |
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RNA processing enables predictable programming of gene expression. |
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RNA-programmed genome editing in human cells |
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RNA-protein analysis using a conditional CRISPR nuclease |
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RNA Scanning of a Molecular Machine with a Built-in Ruler. |
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RNA seeing double: close-packing of helices in RNA tertiary structure. |
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RNA structure, not sequence, determines the 5' splice-site specificity of a group I intron. |
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RNA tertiary structure mediation by adenosine platforms. |
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RNAs regulate biology. |
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Ro's role in RNA reconnaissance. |
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Selection of an RNA molecule that mimics a major autoantigenic epitope of human insulin receptor. |
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Selective stalling of human translation through small-molecule engagement of the ribosome nascent chain. |
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Self-assembly of a group I intron active site from its component tertiary structural domains. |
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Sequence- and Structure-Specific RNA Processing by a CRISPR Endonuclease |
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Single-Stranded DNA Cleavage by Divergent CRISPR-Cas9 Enzymes |
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siRNA repositioning for guide strand selection by human Dicer complexes. |
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Site-Specific Generation of Protein-Protein Conjugates Using Native Amino Acids |
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Solving large RNA structures by X-ray crystallography |
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Spacer Acquisition Rates Determine the Immunological Diversity of the Type II CRISPR-Cas Immune Response |
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A sparse matrix approach to crystallizing ribozymes and RNA motifs |
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A thermostable Cas9 with increased lifetime in human plasma |
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A Unified Resource for Tracking Anti-CRISPR Names |
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A universal mode of helix packing in RNA. |
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An unusual case of pseudo-merohedral twinning in orthorhombic crystals of Dicer |
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The use of CRISPR/Cas9, ZFNs and TALENs in generating site-specific genome alterations |
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(콕스) 분자생물학 |
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크리스퍼가 온다 진화를 지배하는 놀라운 힘, 크리스퍼 유전자가위 |
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