about
Small-molecule control of protein function through Staudinger reduction.Synthesis and Characterization of Benzylidene Acetal-Type Bridged Nucleic Acids (BA-BNA).Systematic Evaluation of Biophysical and Functional Characteristics of Selenomethylene-Locked Nucleic Acid-Mediated Inhibition of miR-21.Synthesis and Properties of 7-Deazapurine- and 8-Aza-7-deazapurine-Locked Nucleic Acid Analogues: Effect of the Glycosidic Torsion Angle.Biological applications of xeno nucleic acids.Small Molecule Release and Activation through DNA Computing.Photoinduced changes in hydrogen bonding patterns of 8-thiopurine nucleobase analogues in a DNA strand.Hydrogen peroxide-triggered gene silencing in mammalian cells through boronated antisense oligonucleotides.Polymerase incorporation of a 2'-deoxynucleoside-5'-triphosphate bearing a 4-hydroxy-2-mercaptobenzimidazole nucleobase analogue.Synthesis of selenomethylene-locked nucleic acid (SeLNA)-modified oligonucleotides by polymerases.Consecutive incorporation of functionalized nucleotides with amphiphilic side chains by novel KOD polymerase mutant.Aryl Azides as Phosphine-Activated Switches for Small Molecule FunctionSynthesis of light-responsive bridged nucleic acid and changes in affinity with complementary ssRNASelenomethylene locked nucleic acid enables reversible hybridization in response to redox changesWavelength-selective light-triggered strand exchange reactionC5-azobenzene-functionalized locked nucleic acid uridine: isomerization properties, hybridization ability, and enzymatic stabilityC5-azobenzene-substituted 2'-deoxyuridine-containing oligodeoxynucleotides for photo-switching hybridizationA highly constrained nucleic acid analog based on α-l-threosamineSynthesis and Evaluation of Artificial Nucleic Acid Bearing an Oxanorbornane Scaffold
P50
Q37429201-DADCA172-24EA-4AA0-8B3D-23881B681999Q38246951-9599787F-6EBC-4C35-8A07-E985518DD357Q38289706-980ED048-39C7-417F-BFF5-E78FD89B2148Q38289808-BBBD3EE6-4BAE-4969-AAD4-A5FD67547EE6Q39003630-8F724F73-F15E-40F9-9ABD-0129CE61BC4EQ48295495-26CC9E36-0724-4D11-8597-C518BEC40370Q51749914-7343B909-3781-43CB-818B-7697959C6F67Q52599519-DEB62BBD-A229-44A7-9DD1-2363F37145B8Q54267474-5AE9A1DB-6417-4842-BBC3-96C4465B048FQ54288888-6E6674CE-331A-4E58-A05C-855868376043Q55035539-7C48D86B-F043-42E4-8431-E93A128F317FQ61799028-C20F7237-31A2-42BA-A57F-E7A4F97F5D32Q84165012-A6F729B3-1AAF-4CE3-8868-B2B339EA2FA2Q86583188-F8ED16E2-7CE6-439D-B049-5C61517A761CQ87030818-01094BD7-F5BB-4299-8D97-29313F7C2715Q87076938-C93C6499-07F9-4FF3-ACA2-C2968B18F976Q87738870-7CA49BFC-7618-4A66-9B44-7083722845D8Q90145418-C66B785F-AF67-4CC0-A5CF-0D555B9A7005Q91869014-29AFEE60-95B8-44DA-AB96-3363F008062A
P50
description
investigador
@es
researcher
@en
name
Kunihiko Morihiro
@en
type
label
Kunihiko Morihiro
@en
prefLabel
Kunihiko Morihiro
@en
P31
P496
0000-0002-9642-1031