Showing results (1741-1750 of 1,877) with videos related to
Sort By:
Pageof 188
Genes & Cancer|October 3, 2017
Correlation between c-Met and ALDH1 contributes to the survival and tumor-sphere formation of ALDH1 positive breast cancer stem cells and predicts poor clinical outcome in breast cancerYuka Nozaki, Shoma Tamori, Masahiro Inada, et al.Scientific Reports|October 10, 2018
Visualising peripheral arterioles and venules through high-resolution and large-area photoacoustic imagingYoshiaki Matsumoto, Yasufumi Asao, Hiroyuki Sekiguchi, et al.Plos Genetics|October 17, 2009
A novel system of polymorphic and diverse NK cell receptors in primatesAnne Averdam, Beatrix Petersen, Cornelia Rosner, et al.Bioorganic & Medicinal Chemistry Letters|January 14, 2014
Identification of the 5,5-dioxo-7,8-dihydro-6H-thiopyrano[3,2-d]pyrimidine derivatives as highly selective PDE4B inhibitorsTaiji Goto, Akiko Shiina, Takeshi Murata, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 24, 2006
Epigenetic inactivation of Wnt inhibitory factor-1 plays an important role in bladder cancer through aberrant canonical Wnt/beta-catenin signaling pathwayShinji Urakami, Hiroaki Shiina, Hideki Enokida, et al.Annals of Neurology|March 14, 2018
De novo hotspot variants in CYFIP2 cause early-onset epileptic encephalopathyMitsuko Nakashima, Mitsuhiro Kato, Kazushi Aoto, et al.Nature Biomedical Engineering|December 12, 2022
Optimization of the proliferation and persistency of CAR T cells derived from human induced pluripotent stem cellsTatsuki Ueda, Sara Shiina, Shoichi Iriguchi, et al.Nature Communications|June 3, 2014
De novo SOX11 mutations cause Coffin-Siris syndromeYoshinori Tsurusaki, Eriko Koshimizu, Hirofumi Ohashi, et al.Scientific Reports|February 8, 2017
Visualization of tumor-related blood vessels in human breast by photoacoustic imaging system with a hemispherical detector arrayM Toi, Y Asao, Y Matsumoto, et al.Annals of Clinical and Translational Neurology|March 22, 2018
De novo variants in CAMK2A and CAMK2B cause neurodevelopmental disordersTenpei Akita, Kazushi Aoto, Mitsuhiro Kato, et al.Pageof 188