Naphthalene, Phenanthrene, and Pyrene as DNA Base Analogues: Synthesis, Structure, and Fluorescence in DNA. - Wikidata - awgldk - TriplyDB

Naphthalene, Phenanthrene, and Pyrene as DNA Base Analogues: Synthesis, Structure, and Fluorescence in DNA.

Naphthalene, Phenanthrene, and Pyrene as DNA Base Analogues: Synthesis, Structure, and Fluorescence in DNA.

http://www.wikidata.org/entity/Q34143828

about

NMR structure of a DNA duplex containing nucleoside analog 1-(2'-deoxy-beta-D-ribofuranosyl)-3-nitropyrrole and the structure of the unmodified control Enzymatic capture of an extrahelical thymine in the search for uracil in DNA Ensemble hybridisation--a new method for exploring sequence dependent fluorescence of dye-nucleic acid conjugates.Polyfluorophores on a DNA backbone: a multicolor set of labels excited at one wavelength.Polyfluorophore labels on DNA: dramatic sequence dependence of quenching.C-Nucleosides Derived from Simple Aromatic Hydrocarbons Multispectral labeling of antibodies with polyfluorophores on a DNA backbone and application in cellular imaging Fluorescent analogs of biomolecular building blocks: design, properties, and applications.Difluorotoluene, a Nonpolar Isostere for Thymine, Codes Specifically and Efficiently for Adenine in DNA Replication.Selective and Stable DNA Base Pairing without Hydrogen Bonds.Factors Contributing to Aromatic Stacking in Water: Evaluation in the Context of DNA.Identification of critical residues for the tight binding of both correct and incorrect nucleotides to human DNA polymerase λ Effect of lesions on the dynamics of DNA on the picosecond and nanosecond timescales using a polarity sensitive probe.Quantifying the energetic contributions of desolvation and π-electron density during translesion DNA synthesis.Pyrene binary probes for unambiguous detection of mRNA using time-resolved fluorescence spectroscopy High-fidelity in vivo replication of DNA base shape mimics without Watson-Crick hydrogen bonds.Roles of Watson-Crick and minor groove hydrogen bonds in DNA replication.Effect of preorganization on the affinity of synthetic DNA binding motifs for nucleotide ligands.Pattern-Based Detection of Anion Pollutants in Water with DNA Polyfluorophores Mechanism of template-independent nucleotide incorporation catalyzed by a template-dependent DNA polymerase Furan Decorated Nucleoside Analogues as Fluorescent Probes: synthesis, photophysical evaluation and site-specific incorporation Development of a 'clickable' non-natural nucleotide to visualize the replication of non-instructional DNA lesions.Multisensing emissive pyrimidine.DNA-multichromophore systems Oligodeoxyfluorosides: Strong Sequence Dependence of Fluorescence Emission In Vitro Fluorogenic Real-Time Assay of the Repair of Oxidative DNA Damage.Templated chemistry for monitoring damage and repair directly in duplex DNA Protease probes built from DNA: multispectral fluorescent DNA-peptide conjugates as caspase chemosensors.Direct fluorescence monitoring of DNA base excision repair Exploring the limits of DNA size: naphtho-homologated DNA bases and pairs.Foldamers with hybrid biological and synthetic sequences as selective DNA fluorescent probes.Sensing metal ions with DNA building blocks: fluorescent pyridobenzimidazole nucleosides.Efficient synthesis of fluorescent alkynyl C-nucleosides via Sonogashira coupling for the preparation of DNA-based polyfluorophores A sequential indium-mediated aldehyde allylation/palladium-catalyzed cross-coupling reaction in the synthesis of 2-deoxy-beta-C-aryl glycosides.Novel Nucleoside Analogues with Fluorophores Replacing the DNA Base Polyfluorophore excimers and exciplexes as FRET donors in DNA.Fluorescent nucleic acid base analogues.Fluorescent DNA-based enzyme sensors.Probing the limits of electrostatic catalysis by uracil DNA glycosylase using transition state mimicry and mutagenesis.The Phe-X-Glu DNA binding motif of MutS. The role of hydrogen bonding in mismatch recognition.

P2860

Q27628081-B1E2232E-CA89-4B05-BBCE-08C01B44DC6A Q27647377-A48A420A-0D0D-4DDC-B71C-C885FF2DC548 Q33209385-C3AF2C1B-9B60-4554-A63C-40CD075D38BD Q33413958-748673D5-BAFB-4F0D-8D9A-BCEA5ECC0EE4 Q33724474-7C5C02E3-F80A-44E0-8D84-620FCF142007 Q33750525-28254ABF-DEF6-49C8-AE47-DEDE40570106 Q33820567-640FCFBF-7BEB-4625-9F77-149F5F561257 Q33846993-F5FC1081-B3B6-4580-BD7F-8D7556EEF43E Q34078211-8F8A537B-5F38-42F9-B5FB-1DCEE9E05840 Q34129256-6B24A1A5-463E-46A2-8252-5ABC56554DB7 Q34144275-82044710-5AF5-45C3-AFA5-DB010FB59B6C Q34213489-306683D6-E9D9-40D2-B12E-69DDCDAB10B1 Q34327013-10208CFC-1946-44E8-92AF-FA118B4CEE76 Q34609286-0E66F4BD-BE28-484E-982D-9D6F426DFE4E Q34674720-E8BA6268-D1DE-4389-BBCC-6EC31DA8EC32 Q34957121-73C43590-B2C5-45BA-A58E-96190F38F1BF Q35132478-7A0144EB-C0DC-4EAC-917D-FC36D68EAF8F Q35611700-1B038BC4-5CAB-492F-BB89-57ED7F5C47EB Q35683006-0A0EF304-3B6B-423B-A0E5-B6EB5D45D40B Q35785810-BCDE6610-D8C0-4172-99F4-B68544A6899B Q35793082-11223299-43C5-4AF4-A1B7-B890F9D9A814 Q35823753-A044E69E-DE65-49DF-A8E4-69FAEFDC2326 Q36002176-40BA72C3-9066-490F-AAE3-B85031D5B5C7 Q36069661-2C25F537-6887-4A9E-9D12-58AF0F23CCDF Q36076296-D9C94105-D9BA-4E05-9DD5-00D39A83ED32 Q36100762-C349B959-B905-454D-95D2-854E9F6AC4E3 Q36158008-B32219CF-7618-49D3-9E73-5147BDA54916 Q36452771-27572B8C-2E85-44D7-A6D0-3315F194BE14 Q36482186-2125A995-2A3E-48E6-87DE-004FF7C1AF4C Q36826609-84E64789-4736-4AB2-8C82-F875C067EAA7 Q36837712-8BE46A09-9329-4318-A084-DBAFC9E41B40 Q36871570-B9ABBE68-00C0-4613-B5A7-9FDEC17DAE18 Q37072028-314B7757-5608-4D91-86C9-454497468E33 Q37362482-68082E2D-B9A0-4CE9-B688-B98C3445C084 Q37459789-22A736A1-4C3B-433E-948B-93822C032DB9 Q37480911-DA22263B-0AAC-4281-8680-8DBED5CD4978 Q37755509-A7C7695C-FC04-470C-9E49-50179CD35E16 Q37835020-86EBA12A-B8D9-4A86-AACA-86F3F4C9A5E5 Q38291765-279A5FA9-19D1-4BD7-96DE-6BDCD76EA05D Q38295775-E6A5F518-26D1-496A-ADE4-109FFB9FAF97

P2860

Naphthalene, Phenanthrene, and Pyrene as DNA Base Analogues: Synthesis, Structure, and Fluorescence in DNA.

http://www.wikidata.org/entity/Q34143828

description

1996 nî lūn-bûn

@nan

1996 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1996 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

1996年の論文

@ja

1996年論文

@yue

1996年論文

@zh-hant

1996年論文

@zh-hk

1996年論文

@zh-mo

1996年論文

@zh-tw

1996年论文

@wuu

name

Naphthalene, Phenanthrene, and ...... ture, and Fluorescence in DNA.

@ast

Naphthalene, Phenanthrene, and ...... ture, and Fluorescence in DNA.

@en

Naphthalene, Phenanthrene, and ...... ture, and Fluorescence in DNA.

@nl

type

label

Naphthalene, Phenanthrene, and ...... ture, and Fluorescence in DNA.

@ast

Naphthalene, Phenanthrene, and ...... ture, and Fluorescence in DNA.

@en

Naphthalene, Phenanthrene, and ...... ture, and Fluorescence in DNA.

@nl

prefLabel

Naphthalene, Phenanthrene, and ...... ture, and Fluorescence in DNA.

@ast

Naphthalene, Phenanthrene, and ...... ture, and Fluorescence in DNA.

@en

Naphthalene, Phenanthrene, and ...... ture, and Fluorescence in DNA.

@nl

P1433

Q34143828-5914469A-44C7-404C-9337-B0E3C7A90803

P1476

Q34143828-8C1E59B7-B86E-4370-9824-696D0F6F6A54

P2093

Q34143828-5EE6B1A9-207D-41C2-91F9-45DB957915D6

Q34143828-6B3523CD-AED5-4388-B9F6-7723CC2A3286

Q34143828-AD058DE7-35D6-480A-8213-21550F375DC3

Q34143828-C4A83A89-F270-4ECD-98ED-1A0D1026AF43

Q34143828-E6D23F81-5D0D-4C31-9CD1-A696360902AC

P2860

Q34143828-000D0486-0DBC-44C3-8399-DF66BDAD1C0D

Q34143828-259E27D1-6355-47E4-8114-4C4AB1E49DB7

Q34143828-2F8D28B2-D04A-4051-B75C-2B910010C1DD

Q34143828-38B51F6F-CAAB-43F4-913F-7ECA63B258AA

Q34143828-6D7119CF-9B11-407F-8146-9D4D0A556D6D

Q34143828-7FAF5844-BA83-4E89-AD29-8B8A65196184

Q34143828-80EFC9E1-7DC7-4C0E-96D1-4F7B9626A939

Q34143828-8D9C6A16-30DF-4CF9-B7D5-DA3B8C641CD0

Q34143828-8F3FE3D0-91DF-484E-9297-EF7EDE3CA6D4

Q34143828-9C312CA8-0B8F-4DE3-BB8A-86E1FDD0A9CB

P304

Q34143828-7CBC5263-A18B-490D-BDFB-93E6AC70C749

P31

Q34143828-B9C7C63E-BE16-4BDD-B8A8-A847FFE75DEF

P356

Q34143828-EEB76D6A-BE31-4F29-A9BB-6CC9B416C603

P407

Q34143828-2BF15EE9-84EF-4568-A05C-243411EA172D

P433

Q34143828-DCA9E181-ACB7-4D4A-9C1A-31ED8E5F4784

P478

Q34143828-EA292EB6-ECDB-4075-9D35-2EF657FA77CB

P577

Q34143828-E46C9EB5-C5A6-41F6-B752-CCCD9968611F

P5875

Q34143828-1FEF006C-B90D-415A-AADB-B6580AAF861F

P698

Q34143828-08D7155A-B6BA-4641-8080-BE4E2388BFBD

P932

Q34143828-6F1721B3-50B8-40AF-8CE4-C42AFDC4B8A7

P356

P1433

Journal of the American Chemical Society

P1476

Naphthalene, Phenanthrene, and ...... ture, and Fluorescence in DNA.

@en

P2093

Eric T Kool

http://www.w3.org/2001/XMLSchema#string

Narayan C Chaudhuri

http://www.w3.org/2001/XMLSchema#string

Pamela L Paris

http://www.w3.org/2001/XMLSchema#string

Rex X-F Ren

http://www.w3.org/2001/XMLSchema#string

Squire Rumney

http://www.w3.org/2001/XMLSchema#string

P2860

Multiwavelength fluorescence detection for DNA sequencing using capillary electrophoresis.

Hydrophobic, Non-Hydrogen-Bonding Bases and Base Pairs in DNA.

Formation of Stable DNA Loops by Incorporation of Nonpolar, Non-Hydrogen-Bonding Nucleoside Isosteres.

Fluorescence studies of nucleotides and polynucleotides. I. Formycin, 2-aminopurine riboside, 2,6-diaminopurine riboside, and their derivatives.

A non-radioactive automated method for DNA sequence determination.

Fidelity mechanisms in DNA replication.

Sequence-specific cleavage of single-stranded DNA: oligodeoxynucleotide-EDTA X Fe(II).

Influence of 5'-nearest neighbors on the insertion kinetics of the fluorescent nucleotide analog 2-aminopurine by Klenow fragment.

The production of PCR products with 5' single-stranded tails using primers that incorporate novel phosphoramidite intermediates.

Synthesis and biophysical studies of short oligodeoxynucleotides with novel modifications: a possible approach to the problem of mixed base oligodeoxynucleotide synthesis.

P304

7671-7678

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1021/JA9612763

http://www.w3.org/2001/XMLSchema#string

P407

P433

33

http://www.w3.org/2001/XMLSchema#string

P478

118

http://www.w3.org/2001/XMLSchema#string

P577

1996-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

46414401

http://www.w3.org/2001/XMLSchema#string

P698

20865136

http://www.w3.org/2001/XMLSchema#string

P932

2943137

http://www.w3.org/2001/XMLSchema#string