Structural and Functional Mutations of the Perlecan Gene Cause Schwartz-Jampel Syndrome, with Myotonic Myopathy and ChondrodysplasiaEri Arikawa‐Hirasawa, Yoshihiko Yamada, Alexander H. Le et al.|The American Journal of Human Genetics|2002Cited by 195
Binding of laminin-1 to monosialoganglioside GM1 in lipid rafts is crucial for neurite outgrowthNaoki Ichikawa, Eri Arikawa‐Hirasawa, Kazuhisa Iwabuchi et al.|Journal of Cell Science|2008Cited by 113
Perlecan is required for FGF-2 signaling in the neural stem cell nicheAurélien Kerever, Eri Arikawa‐Hirasawa, F. Mercier et al.|Stem Cell Research|2014Cited by 89
Laminin α1 is essential for mouse cerebellar developmentNaoki Ichikawa‐Tomikawa, Eri Arikawa‐Hirasawa, Junko Ogawa et al.|Matrix Biology|2011Cited by 74
Perlecan, a heparan sulfate proteoglycan, regulates systemic metabolism with dynamic changes in adipose tissue and skeletal muscleYuri Yamashita, Eri Arikawa‐Hirasawa|Scientific Reports|2018Cited by 63