S
Shang Cai
Researcher at Stanford University
Publications - 38
Citations - 1955
Shang Cai is an academic researcher from Stanford University. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 14, co-authored 23 publications receiving 1306 citations. Previous affiliations of Shang Cai include Peking University & Indiana University.
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Journal ArticleDOI
Single-cell transcriptional diversity is a hallmark of developmental potential.
Gunsagar S. Gulati,Shaheen S. Sikandar,Daniel J. Wesche,Anoop Manjunath,Anjan Bharadwaj,Mark J. Berger,Francisco Ilagan,Angera H. Kuo,Robert W. Hsieh,Shang Cai,Maider Zabala,Ferenc A. Scheeren,Neethan A. Lobo,Dalong Qian,Feiqiao Brian Yu,Frederick M. Dirbas,Michael F. Clarke,Aaron M. Newman +17 more
TL;DR: A simple, yet robust, determinant of developmental potential—the number of expressed genes per cell—is demonstrated and leverage this measure of transcriptional diversity to develop a computational framework (CytoTRACE) for predicting differentiation states from scRNA-seq data.
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Mechanisms of chromosome behaviour during mitosis.
TL;DR: Recent discoveries, enabled by high-resolution imaging combined with the various genetic, molecular, cell biological and chemical tools, support the idea that establishing and controlling the dynamic interaction between chromosomes and microtubules is a major factor in genomic fidelity.
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Kinesin-14 Family Proteins HSET/XCTK2 Control Spindle Length by Cross-Linking and Sliding Microtubules
TL;DR: This work shows that mutation of the nuclear localization signal (NLS) of human Kinesin-14 HSET caused an accumulation of HSET in the cytoplasm, which resulted in strong microtubule bundling and changes in spindle length, consistent with a model in which Ran regulates the association of Kines in-14s with importin alpha/beta to prevent aberrant cross-linking and bundling of microtubules by sequestering KinesIn-14
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Tumor-resident intracellular microbiota promotes metastatic colonization in breast cancer
Aikun Fu,Bing-Qing Yao,Tingting Dong,Yongyi Chen,J.L. Yao,Yu Liu,Hang Li,Hui-ru Bai,Xiaoqin Liu,Yue Zhang,Chunhui Wang,Yajing Guo,Na Li,Shang Cai +13 more
TL;DR: In this article , the authors explored the functional significance of these intratumor bacteria, primarily using a murine spontaneous breast-tumor model MMTV-PyMT, and found that depletion of intratumors significantly reduced lung metastasis without affecting primary tumor growth.
Journal ArticleDOI
miR-142 regulates the tumorigenicity of human breast cancer stem cells through the canonical WNT signaling pathway
Taichi Isobe,Shigeo Hisamori,Daniel J. Hogan,Maider Zabala,David G. Hendrickson,Piero Dalerba,Shang Cai,Ferenc A. Scheeren,Angera H. Kuo,Shaheen S. Sikandar,Jessica Lam,Dalong Qian,Frederick M. Dirbas,George Somlo,Kaiqin Lao,Patrick O. Brown,Michael F. Clarke,Yohei Shimono +17 more
TL;DR: This study reports that miR-142 efficiently recruits the APC mRNA to an RNA-induced silencing complex, activates the canonical WNT signaling pathway in an APC-suppression dependent manner, and activates the expression ofmiR-150.