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Frontiers in Physiology|December 16, 2014
Specific and quantitative labeling of biomolecules using click chemistryKenichi HorisawaProceedings of the Japan Academy. Series B, Physical and Biological Sciences|April 14, 2020
Direct cell-fate conversion of somatic cells: Toward regenerative medicine and industriesKenichi Horisawa, Atsushi SuzukiRegenerative Therapy|July 3, 2023
The role of pioneer transcription factors in the induction of direct cellular reprogrammingKenichi Horisawa, Atsushi SuzukiJournal of Controlled Release : Official Journal of the Controlled Release Society|June 21, 2015
A fusogenic peptide from a sea urchin fertilization protein promotes intracellular delivery of biomacromolecules by facilitating endosomal escapeKeisuke Niikura, Kenichi Horisawa, Nobuhide DoiJournal of Biochemistry|September 5, 2015
Endosomal escape efficiency of fusogenic B18 and B55 peptides fused with anti-EGFR single chain Fv as estimated by nuclear translocationKeisuke Niikura, Kenichi Horisawa, Nobuhide DoiPlos One|February 21, 2008
Use of cDNA tiling arrays for identifying protein interactions selected by in vitro display technologiesKenichi Horisawa, Nobuhide Doi, Hiroshi YanagawaBiomolecular Concepts|May 12, 2015
The Musashi family RNA-binding proteins in stem cellsKenichi Horisawa, Takao Imai, Hideyuki Okano, et al.Journal of Biochemistry|March 8, 2005
Application of quantitative real-time PCR for monitoring the process of enrichment of clones on in vitro protein selectionKenichi Horisawa, Nobuhide Doi, Hideaki Takashima, et al.FEBS Letters|July 4, 2009
3'-Untranslated region of doublecortin mRNA is a binding target of the Musashi1 RNA-binding proteinKenichi Horisawa, Takao Imai, Hideyuki Okano, et al.Journal of Biochemistry|December 30, 2015
PURE mRNA display for in vitro selection of single-chain antibodiesYu Nagumo, Kei Fujiwara, Kenichi Horisawa, et al.Pageof 4