Search research articles
Contact Us
Filters
Showing results (61-70 of 108) with videos related to
Page
of 11
Sort By:
Bioorganic & Medicinal Chemistry Letters
|
May 22, 2012
Red fluorescent scaffold for highly sensitive protease activity probes
Yu Kushida, Kenjiro Hanaoka, Toru Komatsu, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
August 4, 2009
Molecular design strategies for near-infrared ratiometric fluorescent probes based on the unique spectral properties of aminocyanines
Kazuki Kiyose, Sakiko Aizawa, Eita Sasaki, et al.
Chemical Communications (Cambridge, England)
|
February 21, 2012
A reversible near-infrared fluorescence probe for reactive oxygen species based on Te-rhodamine
Yuichiro Koide, Mitsuyasu Kawaguchi, Yasuteru Urano, et al.
Nature Chemical Biology
|
September 22, 2022
Chemigenetic indicators based on synthetic chelators and green fluorescent protein
Wenchao Zhu, Shiori Takeuchi, Shosei Imai, et al.
Journal of the American Chemical Society
|
December 5, 2012
Rational design of highly sensitive fluorescence probes for protease and glycosidase based on precisely controlled spirocyclization
Masayo Sakabe, Daisuke Asanuma, Mako Kamiya, et al.
Nature Chemical Biology
|
April 21, 2023
Author Correction: Chemigenetic indicators based on synthetic chelators and green fluorescent protein
Wenchao Zhu, Shiori Takeuchi, Shosei Imai, et al.
Journal of the American Chemical Society
|
March 7, 2012
Development of NIR fluorescent dyes based on Si-rhodamine for in vivo imaging
Yuichiro Koide, Yasuteru Urano, Kenjiro Hanaoka, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 6, 2008
Development of a novel fluorescent probe for fluorescence correlation spectroscopic detection of kinase inhibitors
Mitsuyasu Kawaguchi, Takuya Terai, Rei Utata, et al.
Analytical Chemistry
|
April 10, 2012
Near-infrared fluorescence probes for enzymes based on binding affinity modulation of squarylium dye scaffold
Daihi Oushiki, Hirotatsu Kojima, Yuki Takahashi, et al.
ACS Chemical Biology
|
August 21, 2014
Boron dipyrromethene as a fluorescent caging group for single-photon uncaging with long-wavelength visible light
Nobuhiro Umeda, Hironori Takahashi, Mako Kamiya, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 108) with videos related to
Sort By:
Page
of 11
Bioorganic & Medicinal Chemistry Letters
|
May 22, 2012
Red fluorescent scaffold for highly sensitive protease activity probes
Yu Kushida, Kenjiro Hanaoka, Toru Komatsu, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
August 4, 2009
Molecular design strategies for near-infrared ratiometric fluorescent probes based on the unique spectral properties of aminocyanines
Kazuki Kiyose, Sakiko Aizawa, Eita Sasaki, et al.
Chemical Communications (Cambridge, England)
|
February 21, 2012
A reversible near-infrared fluorescence probe for reactive oxygen species based on Te-rhodamine
Yuichiro Koide, Mitsuyasu Kawaguchi, Yasuteru Urano, et al.
Nature Chemical Biology
|
September 22, 2022
Chemigenetic indicators based on synthetic chelators and green fluorescent protein
Wenchao Zhu, Shiori Takeuchi, Shosei Imai, et al.
Journal of the American Chemical Society
|
December 5, 2012
Rational design of highly sensitive fluorescence probes for protease and glycosidase based on precisely controlled spirocyclization
Masayo Sakabe, Daisuke Asanuma, Mako Kamiya, et al.
Nature Chemical Biology
|
April 21, 2023
Author Correction: Chemigenetic indicators based on synthetic chelators and green fluorescent protein
Wenchao Zhu, Shiori Takeuchi, Shosei Imai, et al.
Journal of the American Chemical Society
|
March 7, 2012
Development of NIR fluorescent dyes based on Si-rhodamine for in vivo imaging
Yuichiro Koide, Yasuteru Urano, Kenjiro Hanaoka, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 6, 2008
Development of a novel fluorescent probe for fluorescence correlation spectroscopic detection of kinase inhibitors
Mitsuyasu Kawaguchi, Takuya Terai, Rei Utata, et al.
Analytical Chemistry
|
April 10, 2012
Near-infrared fluorescence probes for enzymes based on binding affinity modulation of squarylium dye scaffold
Daihi Oushiki, Hirotatsu Kojima, Yuki Takahashi, et al.
ACS Chemical Biology
|
August 21, 2014
Boron dipyrromethene as a fluorescent caging group for single-photon uncaging with long-wavelength visible light
Nobuhiro Umeda, Hironori Takahashi, Mako Kamiya, et al.
Page
of 11