%D9%83%D9%88%D8%AC%D9%8A_%D9%86%D8%A7%D9%83%D8%A7%D9%86%D9%8A%D8%B4%D9%8ACategory:Koji_NakanishiK%C5%8Dji_NakanishiKoji_Nakanishi%DA%A9%D9%88%D8%AC%DB%8C_%D9%86%D8%A7%DA%A9%D8%A7%D9%86%DB%8C%D8%B4%DB%8C%E4%B8%AD%E8%A5%BF%E9%A6%99%E7%88%BE%EB%82%98%EC%B9%B4%EB%8B%88%EC%8B%9C_%EA%B3%A0%EC%A7%80Q905369%E4%B8%AD%E8%A5%BF%E9%A6%99%E7%88%BE
about
P138
P185
A2E, a byproduct of the visual cycleRetinoylserine and retinoylalanine, natural products of the moth Trichoplusia niAbsolute configurational assignments of secondary amines by CD-sensitive dimeric zinc porphyrin host.Synthesis and characterization of water-soluble free-base, zinc and copper porphyrin-oligonucleotide conjugates.Immunochemical recognition of A2E, a pigment in the lipofuscin of retinal pigment epithelial cells.Absolute configuration of actinophyllic acid as determined through chiroptical data.Superoxidation of retinoic acid.Synthesis of antioxidants for prevention of age-related macular degenerationIsolation and characterization of a retinal pigment epithelial cell fluorophore: an all-trans-retinal dimer conjugate.A cleavable affinity biotinylating agent reveals a retinoid binding role for RPE65Anthocyanins protect against A2E photooxidation and membrane permeabilization in retinal pigment epithelial cellsA2E-epoxides damage DNA in retinal pigment epithelial cells. Vitamin E and other antioxidants inhibit A2E-epoxide formation.A2E, a fluorophore of RPE lipofuscin: can it cause RPE degeneration?Three challenges toward the assignment of absolute configuration of gymnocin-BCharacterization of dihydro-A2PE: an intermediate in the A2E biosynthetic pathway.Rpe65 Leu450Met variant is associated with reduced levels of the retinal pigment epithelium lipofuscin fluorophores A2E and iso-A2E.Structural analysis and dynamics of retinal chromophore in dark and meta I states of rhodopsin from 2H NMR of aligned membranes.A2E, a fluorophore of RPE lipofuscin, can destabilize membrane.Novel spectro-electrochemical cell for in situ/operando observation of common composite electrode with liquid electrolyte by X-ray absorption spectroscopy in the tender X-ray region.Biosynthetic studies of A2E, a major fluorophore of retinal pigment epithelial lipofuscin.Involvement of oxidative mechanisms in blue-light-induced damage to A2E-laden RPE.Synthesis of 11-cis-locked bicyclo[5.1.0]octanyl retinal and an enantioselective binding to bovine opsin.Solution and biologically relevant conformations of enantiomeric 11-cis-locked cyclopropyl retinals.Formation of a nonaoxirane from A2E, a lipofuscin fluorophore related to macular degeneration, and evidence of singlet oxygen involvement.A2-rhodopsin: a new fluorophore isolated from photoreceptor outer segments.Absolute stereochemistry of allylic alcohols, amines, and other ene moieties: a microscale cross metathesis/exciton chirality protocol.Absolute stereochemistry of dihydrofuroangelicins bearing C-8 substituted double bonds: a combined chemical/exciton chirality protocol.Photochemistry of A1E, a retinoid with a conjugated pyridinium moiety: competition between pericyclic photooxygenation and pericyclization.Primary events in dim light vision: a chemical and spectroscopic approach toward understanding protein/chromophore interactions in rhodopsin.Determination of the absolute configuration of Anisotome irregular diterpenes: application of CD and NMR methods.Absolute configurational determination of an all-trans-retinal dimer isolated from photoreceptor outer segments.Deuterium NMR structure of retinal in the ground state of rhodopsin.Chiral sulfinates studied by optical rotation, ECD and VCD: the absolute configuration of a cruciferous phytoalexin brassicanal C.Chiral recognition of cyclic alpha-hydroxyketones by CD-sensitive zinc tetraphenylporphyrin tweezer.Inherent chirality dominates the visible/near-ultraviolet CD spectrum of rhodopsin.Lactone-free ginkgolides via regioselective DIBAL-H reduction.Characterization of peroxy-A2E and furan-A2E photooxidation products and detection in human and mouse retinal pigment epithelial cell lipofuscin.Photooxidation of A2-PE, a photoreceptor outer segment fluorophore, and protection by lutein and zeaxanthin.Porphyrinmaleimides: towards thiol probes for cysteine residues in proteins.Circular dichroism of heterochromophoric and partially regenerated purple membrane: search for exciton coupling.
P50
Q28609934-69820A15-E349-45B4-B1EC-4F09B0A6E62AQ28757200-D1AD10DB-3971-4011-A9B8-AC942F6D1673Q29393859-72539B7A-2280-4C9E-8242-06F2AD051ABDQ30844295-2EB30CF6-72A4-4ABF-9AB4-7B51976F2ADBQ33297465-5F5564EE-23D6-4C67-9B58-B3ED241283B1Q33409597-AF60F778-5363-402F-9D44-C14C3B9D6180Q33435091-A973D983-6278-4BB2-8644-FA257A2DC356Q33801147-BA2E2E85-091A-4BE9-BD49-6DDD01DB9703Q33821589-47F80028-C59A-4BD4-899C-039A93978B04Q34198240-979551A8-0972-4268-83F3-DB571E8C9D50Q34314020-820576DA-5ABF-45D0-AEF1-27B4CEA36F23Q34532224-B3DCA9F1-EC26-4443-8610-2939CB6E74DBQ35793654-F84065AA-6033-4540-8554-0BEEB070305FQ36858345-46A37804-05C5-4A4F-A1A5-F4359D5BAA8FQ36917117-180228CA-A7A9-4CD6-8A83-C60495215F48Q37415751-8499F884-B8B2-4649-8D93-D193B72A30CCQ37584069-93D24603-66A7-4169-9CB9-A2CF6BDD2270Q40179703-979241B8-6061-4BC8-98B6-73F20712DFCEQ42812024-84201B98-3856-4EFF-B233-90936B3B9F1EQ43833680-F742D6FB-4F9A-4295-9064-0A67723599B9Q43940061-0FF8FAEB-E401-4450-B9A0-260707D6F9DFQ43968187-F6E72163-3AC3-4345-AA3D-CBF726FF3CDAQ44032916-A5FD53F7-825A-4D0D-A6D8-3F2D5EB92E1FQ44255419-B03AE09A-A1A6-45A9-B68B-F5216E1B81B9Q44554345-C0DB2FDC-27BE-43E8-9AC8-625D0FDDC1F2Q44571436-80C078BA-728D-4AB4-829B-9F0B07422F80Q44737905-EC9F9EB7-53F8-4E93-A058-73F833A6DBEBQ44834673-94C7BE7C-56B1-496C-988B-CE2BDA9172D4Q44837156-5C3B65E4-65A1-49EC-B674-A106AC313A8CQ45004700-FE4D1813-54DB-47D1-B561-D74375D64C33Q45070126-378076EC-CABF-43CB-A925-3A1B696F7A46Q45087964-3E66FB93-6F05-4F81-A8DD-1E5B391497E6Q46249888-38C143AB-D8BD-4850-8C00-38F1F7524C8BQ46455993-8F1E7A86-A058-4EEF-BD50-390EFB268751Q46639630-00512ACD-53DE-49AE-B0E1-00F8090CE4AEQ46711772-E0EFA561-65B0-49D2-96A6-6EEBE05194E1Q46722184-BBAC5ABD-EDCA-4E1E-B2E9-8FAD655AE3EDQ46858619-E3927848-B5AE-42AA-B3F1-FF8DDB92604EQ46860126-B8560F80-4895-4B13-BC63-0E39D2BA9294Q46873136-A32453EB-4D4F-4A70-9256-31F40C5E0C35
P50
description
Jaapani keemik
@et
Japanese chemist
@en
Japanese chemist
@en-ca
Japanese chemist
@en-gb
Japans scheikundige
@nl
ceimiceoir Seapánach
@ga
chimist japonez
@ro
chimiste japonais
@fr
japanischer Chemiker
@de
japansk kemiker
@da
name
Koji Nakanishi
@ast
Koji Nakanishi
@en
Koji Nakanishi
@es
Koji Nakanishi
@fr
Koji Nakanishi
@nl
Koji Nakanishi
@sl
Kōji Nakanishi
@de
Кодзи Наканиси
@ru
كوجي ناكانيشي
@ar
کوجی ناکانیشی
@fa
type
label
Koji Nakanishi
@ast
Koji Nakanishi
@en
Koji Nakanishi
@es
Koji Nakanishi
@fr
Koji Nakanishi
@nl
Koji Nakanishi
@sl
Kōji Nakanishi
@de
Кодзи Наканиси
@ru
كوجي ناكانيشي
@ar
کوجی ناکانیشی
@fa
altLabel
Koji Nakanishi
@de
Kouji Nakanishi
@de
Nakanishi Koji
@de
Nakanishi Kōji
@de
Наканиси, Кодзи
@ru
나카니시 코지
@ko
prefLabel
Koji Nakanishi
@ast
Koji Nakanishi
@en
Koji Nakanishi
@es
Koji Nakanishi
@fr
Koji Nakanishi
@nl
Koji Nakanishi
@sl
Kōji Nakanishi
@de
Кодзи Наканиси
@ru
كوجي ناكانيشي
@ar
کوجی ناکانیشی
@fa