Rui Kamada

Prof. Rui Kamada

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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22 July 2016 in Peptide Science
Verified
Journal Article
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RKRui Kamada
Rui Kamada
YTYu Toguchi
Yu Toguchi
TNTakao Nomura
Takao Nomura
TIToshiaki Imagawa
Toshiaki Imagawa
KSKazuyasu Sakaguchi
Kazuyasu Sakaguchi

1 August 2010 in Bioorganic & Medicinal Chemistry Letters
Verified
Journal Article
Closed access
RKRui Kamada
Rui Kamada
WYWataru Yoshino
Wataru Yoshino
TNTakao Nomura
Takao Nomura
YCYoshiro Chuman
Yoshiro Chuman
TIToshiaki Imagawa
Toshiaki Imagawa
KSKazuyasu Sakaguchi
Kazuyasu Sakaguchi

1 October 2015 in Bioorganic & Medicinal Chemistry
Verified
Journal Article
Closed access
SOSari Ogasawara
Sari Ogasawara
YKYuhei Kiyota
Yuhei Kiyota
YCYoshiro Chuman
Yoshiro Chuman
AKAyano Kowata
Ayano Kowata
FYFumihiko Yoshimura
Fumihiko Yoshimura
KSKazuyasu Sakaguchi
Kazuyasu Sakaguchi

16 August 2013 in Chemistry – A European Journal
Verified
Journal Article
Closed access
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KMKazuya Matsuo
Kazuya Matsuo
RKRui Kamada
Rui Kamada
KMKeigo Mizusawa
Keigo Mizusawa
HIHirohiko Imai
Hirohiko Imai
YTYuki Takayama
Yuki Takayama
IHItaru Hamachi
Itaru Hamachi

4 August 2016 in PLOS ONE
Verified
Journal Article
Open access
PDF file
RKRui Kamada
Rui Kamada
FTFumi Tano
Fumi Tano
FKFuki Kudoh
Fuki Kudoh
NKNozomi Kimura
Nozomi Kimura
YCYoshiro Chuman
Yoshiro Chuman
KSKazuyasu Sakaguchi
Kazuyasu Sakaguchi
Nuclear and cytoplasmic morphological changes provide important information about cell differentiation processes, cell functions, and signal responses. There is a strong desire to develop a rapid and simple method for visualizing cytoplasmic and nuclear morphology. Here, we developed a novel and rapid method for probing cellular morphological changes of live cell differentiation process by a fluorescent probe, TAP-4PH, a 1,3a,6a-triazapentalene derivative. TAP-4PH showed high fluorescence in cytoplasmic area, and visualized cytoplasmic and nuclear morphological changes of live cells during differentiation. We demonstrated that TAP-4PH visualized dendritic axon and spine formation in neuronal differentiation, and nuclear structural changes during neutrophilic differentiation. We also showed that the utility of TAP-4PH for visualization of cytoplasmic and nuclear morphologies of various type of live cells. Our visualizing method has no toxicity and no influence on the cellular differentiation and function. The cell morphology can be rapidly observed after addition of TAP-4PH and can continue to be observed in the presence of TAP-4PH in cell culture medium. Moreover, TAP-4PH can be easily removed after observation by washing for subsequent biological assay. Taken together, these results demonstrate that our visualization method is a powerful tool to probe differentiation processes before subsequent biological assay in live cells.

1 April 2009 in Analytical Biochemistry
Verified
Journal Article
Closed access
TIToshiaki Imagawa
Toshiaki Imagawa
TTTomoko Terai
Tomoko Terai
YYYoshifumi Yamada
Yoshifumi Yamada
RKRui Kamada
Rui Kamada
KSKazuyasu Sakaguchi
Kazuyasu Sakaguchi