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Masakazu Hashimoto
Osaka University
19Publications
7H-index
427Citations
Publications 19
Newest
#1Masakazu Hashimoto (Osaka University)H-Index: 7
#2Hiroshi Sasaki (Osaka University)H-Index: 51
Summary The epiblast is a pluripotent cell population first formed in preimplantation embryos, and its quality is important for proper development. Here, we examined the mechanisms of epiblast formation and found that the Hippo pathway transcription factor TEAD and its coactivator YAP regulate expression of pluripotency factors. After specification of the inner cell mass, YAP accumulates in the nuclei and activates TEAD. TEAD activity is required for strong expression of pluripotency factors and...
2 CitationsSource
#1Masakazu HashimotoH-Index: 7
Last.Hiroshi SasakiH-Index: 51
view all 4 authors...
#1Katsura Minegishi (Osaka University)H-Index: 3
#2Masakazu Hashimoto (Osaka University)H-Index: 7
Last.Hiroshi Hamada (Osaka University)H-Index: 59
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Summary Polarization of node cells along the anterior-posterior axis of mouse embryos is responsible for left-right symmetry breaking. How node cells become polarized has remained unknown, however. Wnt5a and Wnt5b are expressed posteriorly relative to the node, whereas genes for Sfrp inhibitors of Wnt signaling are expressed anteriorly. Here we show that polarization of node cells is impaired in Wnt5a –/– Wnt5b –/– and Sfrp mutant embryos, and also in the presence of a uniform distribution of Wn...
24 CitationsSource
#1Masakazu Hashimoto (Osaka University)H-Index: 7
#2Yusuke Takenoshita (Osaka University)
Last.Hiroshi Sasaki (Osaka University)H-Index: 51
view all 4 authors...
#1Kenta YashiroH-Index: 20
#2Hidekazu IshidaH-Index: 9
Last.Ken SuzukiH-Index: 32
view all 15 authors...
#1Masakazu Hashimoto (Osaka University)H-Index: 7
#2Yukiko Yamashita (University of Tokushima)H-Index: 2
Last.Tatsuya Takemoto (University of Tokushima)H-Index: 13
view all 3 authors...
The CRISPR/Cas9 system is a powerful tool for elucidating the roles of genes in a wide variety of organisms including mice. To obtain genetically modified embryos or mice by this method, Cas9 mRNA and sgRNA are usually introduced into zygotes by microinjection or electroporation. However, most mutants generated with this method are genetically mosaic, composed of several types of cells carrying different mutations, which complicates phenotype analysis in founder embryos or mice. To simplify the ...
65 CitationsSource
#1Fuminori Tanihara (University of Tokushima)H-Index: 9
#2Tatsuya Takemoto (University of Tokushima)H-Index: 13
Last.Takeshige Otoi (University of Tokushima)H-Index: 30
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Genetically modified pigs for biomedical applications have been mainly generated using the somatic cell nuclear transfer technique; however, this approach requires complex micromanipulation techniques and sometimes increases the risks of both prenatal and postnatal death by faulty epigenetic reprogramming of a donor somatic cell nucleus. As a result, the production of genetically modified pigs has not been widely applied. We provide a simple method for CRISPR (clustered regularly interspaced sho...
28 CitationsSource
#1Hidekazu Ishida (Osaka University)H-Index: 9
#2Rie Saba (QMUL: Queen Mary University of London)H-Index: 5
Last.Kenta Yashiro (QMUL: Queen Mary University of London)H-Index: 20
view all 21 authors...
A surface marker that distinctly identifies cardiac progenitors (CPs) is essential for the robust isolation of these cells, circumventing the necessity of genetic modification. Here, we demonstrate that a Glycosylphosphatidylinositol-anchor containing neurotrophic factor receptor, Glial cell line-derived neurotrophic factor receptor alpha 2 (Gfra2), specifically marks CPs. GFRA2 expression facilitates the isolation of CPs by fluorescence activated cell sorting from differentiating mouse and huma...
10 CitationsSource
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