Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores. - Wikidata - wikimedia - TriplyDB

Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

http://www.wikidata.org/entity/Q34708605

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Real-time near-infrared fluorescence imaging using cRGD-ZW800-1 for intraoperative visualization of multiple cancer types.Renal Clearable Organic Nanocarriers for Bioimaging and Drug Delivery PSMA-targeted contrast agents for intraoperative imaging of prostate cancer.Synthesis of N,N-Dialkylamino-nor-Dihydroxanthene-Hemicyanine Fused Near-Infrared Fluorophores and Their First Water-Soluble and/or Bioconjugatable Analogues.

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Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

http://www.wikidata.org/entity/Q34708605

description

2014 nî lūn-bûn

@nan

2014 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հունվարին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

@ast

Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

@en

Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

@nl

type

label

Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

@ast

Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

@en

Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

@nl

prefLabel

Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

@ast

Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

@en

Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

@nl

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Central C-C Bonding Increases Optical and Chemical Stability of NIR Fluorophores.

@en

P2093

Eric A Owens

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

Hak Soo Choi

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

Hideyuki Wada

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

Hoon Hyun

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

Julien Gravier

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

Kai Bao

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

Lakshminarayana Narayana

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

Maged Henary

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

P2860

Near IR heptamethine cyanine dye-mediated cancer imaging

Nanoparticles for biomedical imaging: fundamentals of clinical translation

cGMP-Compatible preparative scale synthesis of near-infrared fluorophores

Rapid translocation of nanoparticles from the lung airspaces to the body.

Synthesis and in vivo fate of zwitterionic near-infrared fluorophores

Handling and detection of 0.8 amol of a near-infrared cyanine dye by capillary electrophoresis with laser-induced fluorescence detection.

Simultaneous mapping of pan and sentinel lymph nodes for real-time image-guided surgery.

IR-780 dye loaded tumor targeting theranostic nanoparticles for NIR imaging and photothermal therapy.

Targeted zwitterionic near-infrared fluorophores for improved optical imaging

A dual-site simultaneous binding mode in the interaction between parallel-stranded G-quadruplex [d(TGGGGT)]4 and cyanine dye 2,2'-diethyl-9-methyl-selenacarbocyanine bromide

P304

58762-58768

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

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scholarly article

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10.1039/C4RA11225C

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102

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

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4

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John V Frangioni

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2014-01-01T00:00:00Z

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25530846

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4267294

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