scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1017684725 |
P356 | DOI | 10.1038/NMETH915 |
P698 | PubMed publication ID | 16929319 |
P5875 | ResearchGate publication ID | 6859626 |
P50 | author | Shigeyuki Yokoyama | Q37376039 |
P2093 | author name string | Ichiro Hirao | |
Tsuneo Mitsui | |||
Tsuyoshi Fujiwara | |||
Akira Sato | |||
Michiko Kimoto | |||
Rie Kawai | |||
Yoko Harada | |||
P2860 | cites work | Synthesis of 6-(2-thienyl)purine nucleoside derivatives that form unnatural base pairs with pyridin-2-one nucleosides | Q43713833 |
An unnatural hydrophobic base pair with shape complementarity between pyrrole-2-carbaldehyde and 9-methylimidazo[(4,5)-b]pyridine | Q44422115 | ||
An unnatural hydrophobic base, 4-propynylpyrrole-2-carbaldehyde, as an efficient pairing partner of 9-methylimidazo[(4,5)-b]pyridine. | Q44672448 | ||
Site-specific incorporation of a photo-crosslinking component into RNA by T7 transcription mediated by unnatural base pairs | Q44867809 | ||
Evolution of a T7 RNA polymerase variant that transcribes 2'-O-methyl RNA. | Q45010727 | ||
A two-unnatural-base-pair system toward the expansion of the genetic code | Q45102708 | ||
A quantitative, non-radioactive single-nucleotide insertion assay for analysis of DNA replication fidelity by using an automated DNA sequencer. | Q51993186 | ||
A specific partner for abasic damage in DNA | Q59049012 | ||
Efficient replication between non-hydrogen-bonded nucleoside shape analogs | Q77530267 | ||
An unnatural base pair for incorporating amino acid analogs into proteins | Q22122123 | ||
PCR amplification of DNA containing non-standard base pairs by variants of reverse transcriptase from Human Immunodeficiency Virus-1 | Q24633837 | ||
Site-specific biotinylation of RNA molecules by transcription using unnatural base pairs | Q24814726 | ||
Nucleotide modification at the gamma-phosphate leads to the improved fidelity of HIV-1 reverse transcriptase. | Q24817042 | ||
The use of thymidine analogs to improve the replication of an extra DNA base pair: a synthetic biological system | Q24817153 | ||
Crystal structure of a bacteriophage T7 DNA replication complex at 2.2 Å resolution | Q27748814 | ||
Visualizing DNA replication in a catalytically active Bacillus DNA polymerase crystal | Q27748815 | ||
Enzymatic incorporation of a new base pair into DNA and RNA extends the genetic alphabet | Q28255626 | ||
Enzymic recognition of the base pair between isocytidine and isoguanosine | Q28298449 | ||
Comparison between DNA melting thermodynamics and DNA polymerase fidelity | Q33642760 | ||
A third base pair for the polymerase chain reaction: inserting isoC and isoG | Q33977027 | ||
Minor Groove Interactions between Polymerase and DNA: More Essential to Replication than Watson−Crick Hydrogen Bonds? | Q34129209 | ||
Beyond A, C, G and T: augmenting nature's alphabet | Q35595878 | ||
Polymerase evolution: efforts toward expansion of the genetic code | Q36882107 | ||
Site-specific fluorescent labeling of RNA molecules by specific transcription using unnatural base pairs | Q38318008 | ||
Enzymatic repair of an expanded genetic information system | Q39959019 | ||
Biochemical basis of DNA replication fidelity | Q40903454 | ||
P433 | issue | 9 | |
P921 | main subject | hydrophobicity | Q41854968 |
P304 | page(s) | 729-735 | |
P577 | publication date | 2006-09-01 | |
P1433 | published in | Nature Methods | Q680640 |
P1476 | title | An unnatural hydrophobic base pair system: site-specific incorporation of nucleotide analogs into DNA and RNA | |
P478 | volume | 3 |
Q38313026 | 6-Substituted purines containing thienyl or furyl substituents as artificial nucleobases for metal-mediated base pairing |
Q47647445 | A metallo-DNA nanowire with uninterrupted one-dimensional silver array. |
Q39557310 | A new usage of functionalized oligodeoxynucleotide probe for site-specific modification of a guanine base within RNA. |
Q21531652 | A semi-synthetic organism with an expanded genetic alphabet |
Q64983926 | Advances and Challenges in Cell-Free Incorporation of Unnatural Amino Acids Into Proteins. |
Q54508159 | Ag(I) ion mediated formation of a C-A mispair by DNA polymerases. |
Q37856759 | Alternative DNA base-pairs: from efforts to expand the genetic code to potential material applications. |
Q22162463 | Amplification, mutation, and sequencing of a six-letter synthetic genetic system |
Q80160112 | Amplify this! DNA and RNA get a third base pair |
Q30047870 | An unnatural base pair system for efficient PCR amplification and functionalization of DNA molecules |
Q58749805 | Aptamers as Diagnostic Tools in Cancer |
Q38290290 | Aptamers as targeted therapeutics: current potential and challenges |
Q43998579 | Are molecular alphabets universal enabling factors for the evolution of complex life? |
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Q38818821 | Cellular processing and destinies of artificial DNA nanostructures |
Q59004087 | Chemical fidelity of an RNA polymerase ribozyme |
Q35652657 | Chemistry of nucleic acids: impacts in multiple fields |
Q36874013 | Combined Approaches to Site-Specific Modification of RNA |
Q33620887 | DNA damage and interstrand cross-link formation upon irradiation of aryl iodide C-nucleotide analogues |
Q38246952 | Design and synthesis of triazolyl-donor/acceptor unnatural nucleosides and oligonucleotide probes containing triazolyl-phenanthrene nucleoside. |
Q33943425 | Discovery, characterization, and optimization of an unnatural base pair for expansion of the genetic alphabet |
Q22066267 | Efficient and sequence-independent replication of DNA containing a third base pair establishes a functional six-letter genetic alphabet |
Q27647030 | Efforts toward Expansion of the Genetic Alphabet: Structure and Replication of Unnatural Base Pairs |
Q38787655 | Enhancing aptamer function and stability via in vitro selection using modified nucleic acids |
Q42053767 | Enzymatic incorporation of emissive pyrimidine ribonucleotides |
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Q34296420 | Polymerase amplification, cloning, and gene expression of benzo-homologous "yDNA" base pairs |
Q39142811 | Posttranscriptional chemical labeling of RNA by using bioorthogonal chemistry |
Q38292382 | Proximal disruptor aided ligation (ProDAL) of kilobase-long RNAs |
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Q27674400 | Reversible bond formation enables the replication and amplification of a crosslinking salen complex as an orthogonal base pair |
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Q42949739 | Site-Specific Incorporation of Extra Components into RNA by Transcription Using Unnatural Base Pair Systems |
Q44477042 | Site-Specific Incorporation of Functional Components into RNA by an Unnatural Base Pair Transcription System |
Q37706361 | Site-Specific Labeling of DNA and RNA Using an Efficiently Replicated and Transcribed Class of Unnatural Base Pairs |
Q42993873 | Site-specific fluorescent probing of RNA molecules by unnatural base-pair transcription for local structural conformation analysis |
Q41624524 | Site-specific labeling of RNA by combining genetic alphabet expansion transcription and copper-free click chemistry |
Q27664633 | Solution Structure, Mechanism of Replication, and Optimization of an Unnatural Base Pair |
Q53887386 | Solution structure of S-DNA formed by covalent base pairing involving a disulfide bond |
Q36914336 | Steric and electrostatic effects in DNA synthesis by the SOS-induced DNA polymerases II and IV of Escherichia coli |
Q48307837 | Structural Basis for Expansion of the Genetic Alphabet with an Artificial Nucleobase Pair. |
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Q92152187 | Targeting microRNAs as a Therapeutic Strategy to Reduce Oxidative Stress in Diabetes |
Q37298585 | The effects of unnatural base pairs and mispairs on DNA duplex stability and solvation. |
Q36702404 | The expanded genetic alphabet |
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