about
2',6'-Dimethylazobenzene as an efficient and thermo-stable photo-regulator for the photoregulation of DNA hybridization.A cationic dye triplet as a unique "glue" that can connect fully matched termini of DNA duplexes.Bulge-like asymmetric heterodye clustering in DNA duplex results in efficient quenching of background emission based on the maximized excitonic interaction.p-Stilbazole moieties as artificial base pairs for photo-cross-linking of DNA duplex.Preparation of supramolecular chromophoric assemblies using a DNA duplex.Enhancement of RNA cleavage activity of 10-23 DNAzyme by covalently introduced intercalator.Faint electric treatment-induced rapid and efficient delivery of extraneous hydrophilic molecules into the cytoplasm.Orientation-dependent FRET system reveals differences in structures and flexibilities of nicked and gapped DNA duplexesA stem-less probe using spontaneous pairing between Cy3 and quencher for RNA detection.Unexpectedly stable artificial duplex from flexible acyclic threoninol.Coherent quenching of a fluorophore for the design of a highly sensitive in-stem molecular beacon.Accumulation of fluorophores into DNA duplexes to mimic the properties of quantum dots.An efficient fluorescence resonance energy transfer (FRET) between pyrene and perylene assembled in a DNA duplex and its potential for discriminating single-base changes.Analysis of coherent heteroclustering of different dyes by use of threoninol nucleotides for comparison with the molecular exciton theory.In-stem molecular beacon containing a pseudo base pair of threoninol nucleotides for the removal of background emission.Evaluation of intrinsic spectroscopic properties of chromophore assemblies by shielding with cyclohexyl base pairs within a DNA duplex.Modulation of pK(a) of Brooker's merocyanine by DNA hybridization.Covalent incorporation of methyl red dyes into double-stranded DNA for their ordered clustering.Highly sensitive and robust linear probe for detection of mRNA in cells.Chaperone-Polymer-Assisted, Photodriven DNA Strand Displacement.Ultrasensitive Molecular Beacon Designed with Totally Serinol Nucleic Acid (SNA) for Monitoring mRNA in Cells.Reversed assembly of dyes in an RNA duplex compared with those in DNA.Strand-invading linear probe combined with unmodified PNA.Visible-Light-Triggered Cross-Linking of DNA Duplexes by Reversible [2+2] Photocycloaddition of Styrylpyrene.Terminus-free siRNA prepared by photo-crosslinking activated via slicing by Ago2.Hetero-Selective DNA-Like Duplex Stabilized by Donor-Acceptor Interactions.Molecular design of Cy3 derivative for highly sensitive in-stem molecular beacon and its application to the wash-free FISH.Enhancement of stability and activity of siRNA by terminal substitution with serinol nucleic acid (SNA).De novo design of functional oligonucleotides with acyclic scaffolds.Efficiency of [2 + 2] photodimerization of various stilbene derivatives within the DNA duplex scaffold.A polycation-chaperoned in-stem molecular beacon systemAcyclic l-threoninol nucleic acid (l-aTNA) with suitable structural rigidity cross-pairs with DNA and RNADNA-dye conjugates for controllable H aggregation(1)Insertion of two pyrene moieties into oligodeoxyribonucleotides for the efficient detection of deletion polymorphismsAlternating hetero H aggregation of different dyes by interstrand stacking from two DNA-dye conjugatesCyclohexyl "base pairs" stabilize duplexes and intensify pyrene fluorescence by shielding it from natural base pairsDetection of three-base deletion by exciplex formation with perylene derivativesQuencher-free molecular beacon tethering 7-hydroxycoumarin detects targets through protonation/deprotonationHighly stable duplex formation by artificial nucleic acids acyclic threoninol nucleic acid (aTNA) and serinol nucleic acid (SNA) with acyclic scaffoldsBifacial Nucleobases for Hexaplex Formation in Aqueous Solution
P50
Q33303690-B7C79DAA-A26C-4A1A-B471-63F473CCCDFEQ33816128-85E173D5-C2E6-4CB3-B4DD-BF54F31D3B03Q34350639-BA7AB4AB-7602-49A7-B06B-9C855B2A5730Q34704951-CE982064-A348-434E-A380-D7EB3168D145Q38005343-F2A8DA55-E255-4171-BDA0-938E1411D72FQ38306990-11A4C05C-3956-40FF-B43C-FCD3450E1628Q38788820-8A72B685-2322-4823-9632-8C128D15125CQ40951341-D9D3129D-CC2F-43C1-83D1-BA5CA9320CF3Q42018330-16E19F92-1A56-4C7C-B942-3904A9CEF395Q42871894-7CA30C15-E1B6-480D-B1B0-6B4FD7DE191AQ42985808-E7C9FCD4-D84C-4546-8009-AC97B3B96CA7Q43104825-8E651E95-009B-4CB8-8677-409052718C03Q43196755-DF8DF6E8-FFFE-4672-BD6E-B646CDC24E83Q43282681-B5126346-E985-46B7-981F-32F0A0DCADE6Q43286537-379AB8BB-F775-4CF1-992F-C4D71FC36A18Q45823872-115A4F5D-2D14-4514-B86C-92B76A8D01A5Q46146594-51EFA460-F246-4A2B-9EF5-93F9047A094CQ46704134-BC110064-B6B5-498C-8015-723FA32D08E0Q50217388-B4DE736D-A14B-4501-A4BE-CFA520150087Q50249917-8416403B-7218-4197-8AE3-F8469DF617B8Q50437140-6172D4D4-A648-416E-92DC-0134C6747C5EQ50503205-5C9093F5-FA7B-4FEA-B802-D8AC25A11B1CQ51256597-8C8A1136-4CB7-49E3-8479-2BCC9CD60CB6Q51292707-2B6DD9FE-EEA0-41B1-B744-AA8700FDD3F7Q51661918-2207A088-A9D5-4C89-A73D-65EE77676E86Q51708621-4CA7B38D-E48D-437C-B296-184BFB275AB0Q53292367-17076453-4369-40F5-A095-8B5E6ACC3AEAQ53441592-1AEF8F5F-C4A6-427E-85FB-6E211D6E38BCQ53461396-E6B51422-97A1-4B41-AF0E-FA9973BF420BQ53605892-3FED6F60-7465-4766-B2B8-D02726685FB4Q57744038-7A6684D4-F852-4D7A-9150-DA7982C00241Q61987726-77804507-7153-4DA0-B864-7DADC2B9DDDEQ73011062-6B52570B-5688-4FFF-96ED-E24C11A7190CQ79158961-82F4814D-6B09-4AA3-AA64-23F1BBF71583Q81094811-62BC768F-9657-4703-BEBC-4DF8917A657EQ82431561-77AFD266-11EF-4487-B8B3-F14AB62B36A1Q84065889-3FCF732D-6C9B-41AD-8A04-393F1A1247A0Q84391584-D97157E2-B9AF-4EFB-9311-3B8A18F5F8EEQ85849055-6C006B14-262C-42E7-B8F8-D2F7C869EBEDQ89053472-383FCD45-A660-45B2-9206-1F62DDD0249D
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Hiromu Kashida
@ast
Hiromu Kashida
@en
Hiromu Kashida
@es
Hiromu Kashida
@nl
Hiromu Kashida
@sl
type
label
Hiromu Kashida
@ast
Hiromu Kashida
@en
Hiromu Kashida
@es
Hiromu Kashida
@nl
Hiromu Kashida
@sl
prefLabel
Hiromu Kashida
@ast
Hiromu Kashida
@en
Hiromu Kashida
@es
Hiromu Kashida
@nl
Hiromu Kashida
@sl
P1053
K-7486-2012
P106
P31
P3829
P496
0000-0002-0946-0113