| Vol. 16.44 – 10 November, 2021 |
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| Researchers aimed to identify the causal pathogenic mutation in an early-onset osteoarthritis family, followed by functional studies in human iPSCs in an in vitro organoid cartilage model. [Science Advances] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| The authors showed that ARID1B-Brg1/Brm associated factor (BAF) regulated the exit from pluripotency and lineage commitment by attenuating thousands of enhancers and genes of the NANOG and SOX2 networks. In iPSCs, these enhancers were maintained active by ARID1A-containing BAF. [Nature Communications] |
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| Wdr5 deletion in p53-null mouse ESCs led to impaired self-renewal, defective retinal neuroectoderm differentiation, and de-repression of germ cell/meiosis-specific genes. [Stem Cell Reports] |
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| Proprotein convertase subtilisin kexin type 9 (PCSK9) inhibition in human iPSCs (hiPSCs) with the use of short hairpin RNA, CRISPR/cas9-mediated knockout, or endogenous PCSK9 loss-of-function mutation R104C/V114A unveiled its new role as a potential cell cycle regulator through the NODAL signaling pathway. [Stem Cell Reports] |
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| Scientists reported that the differentiation of robust proportions of epiblast-like and primitive endoderm-like cells in mouse ESC cultures emerged at the population level through cell-cell communication via a short-range fibroblast growth factor 4 (FGF4) signal. [Development] |
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| Investigators proposed thin films of functionalized carbon nanotubes as alternatives for the feeder-free in vitro culture of canine iPSCs, considered as the cellular model. [Nanomedicine-Nanotechnology Biology and Medicine] |
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| Researchers generated cerebral organoids derived from human iPSCs (hiPSCs) possessing the KCNJ11 mutation p.Val59Met (V59M) and from non-pathogenic/normal hiPSCs. [Scientific Reports] |
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| The authors differentiated iPSC from one donor into dendritic cells, macrophages, endothelial cells, and β-cells, and engineered T cell avatars from the same donor to provide an in vitro platform to study genetic influences on critical cellular interactions. [Frontiers in Endocrinology] |
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| iPSCs were virally transduced to express wild-type JAK2, JAK2p.V617F, or JAK2p.N542_E543del, differentiated into megakaryocytes in the presence versus absence of doxycycline, and compared to ensure that the differences were solely from mutated JAK2 expressions. [Platelets] |
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| Scientists used human iPSC-derived embryoid bodies as an in vitro model to investigate the embryotoxic effects of a carefully selected set of pharmacological compounds. [Toxicology and Applied Pharmacology] |
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| The authors review insights into mechanical control of early vertebrate development, including the role of forces in tissue patterning and embryonic axis formation. [Nature Reviews Molecular Cell Biology] |
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| EdiGene, Inc. has entered into a research collaboration with the University of Wisconsin–Madison as part of the company’s effort of translating proprietary LEAPER™ RNA editing technology into in vivo therapies. [EdiGene, Inc.] |
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| Dendreon Pharmaceuticals and Shoreline Biosciences, a biotechnology company developing allogeneic off-the-shelf, standardized, and targeted natural killer and macrophage cellular immunotherapies derived from iPSC for cancer, announced an alliance to advance the future of iPSC-derived cellular therapies. [Shoreline Biosciences] |
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| December 8 – 9, 2021 Virtual |
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| St. Jude Children’s Research Hospital – Memphis, Tennessee, United States |
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| KU Leuven – Leuven, Brussels |
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| The University of British Columbia – Vancouver, British Columbia, Canada |
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| Roche – Basel, Switzerland |
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| University of Southern California School of Dentistry – Los Angeles, California, United States |
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