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Biochemical and Biophysical Research Communications|September 25, 2007
Wnt/Lrp/beta-catenin signaling suppresses adipogenesis by inhibiting mutual activation of PPARgamma and C/EBPalphaMasanobu Kawai, Sotaro Mushiake, Kazuhiko Bessho, et al.
Scientific Reports|March 16, 2019
Differential transactivation of the upstream aggrecan enhancer regulated by PAX1/9 depends on SOX9-driven transactivationAki Takimoto, Chikara Kokubu, Hitomi Watanabe, et al.
BMC Genomics|November 25, 2014
Simulation and estimation of gene number in a biological pathway using almost complete saturation mutagenesis screening of haploid mouse cellsMasahiro Tokunaga, Chikara Kokubu, Yusuke Maeda, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 29, 2008
Lrp6 hypomorphic mutation affects bone mass through bone resorption in mice and impairs interaction with MesdTakuo Kubota, Toshimi Michigami, Naoko Sakaguchi, et al.
Nucleic Acids Research|March 20, 2018
Collection of homozygous mutant mouse embryonic stem cells arising from autodiploidization during haploid gene trap mutagenesisAyako Yamanishi, Atsushi Matsuba, Ryohei Kondo, et al.
Nature Methods|October 25, 2011
A homozygous mutant embryonic stem cell bank applicable for phenotype-driven genetic screeningKyoji Horie, Chikara Kokubu, Junko Yoshida, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|October 2, 2009
Delayed dopaminergic neuron differentiation in Lrp6 mutant miceGonçalo Castelo-Branco, Emma R Andersson, Eleonora Minina, et al.
Development (Cambridge, England)|October 8, 2004
Skeletal defects in ringelschwanz mutant mice reveal that Lrp6 is required for proper somitogenesis and osteogenesisChikara Kokubu, Ulrich Heinzmann, Tomoko Kokubu, et al.
Nature Genetics|July 28, 2009
A transposon-based chromosomal engineering method to survey a large cis-regulatory landscape in miceChikara Kokubu, Kyoji Horie, Koichiro Abe, et al.
Genetics|September 25, 2003
Undulated short-tail deletion mutation in the mouse ablates Pax1 and leads to ectopic activation of neighboring Nkx2-2 in domains that normally express Pax1Chikara Kokubu, Bettina Wilm, Tomoko Kokubu, et al.
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