Yutaka Harita

Patients with Epstein–Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease

Takashi Sekine, Mutsuko Konno, Satoshi Sasaki et al. · Kidney International · 2010 · 111 citations · Full text

Medicine, Genetics, Molecular Genetics +9

Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5

Tomohiko Yamamura, Tomoko Horinouchi, Tomomi Adachi et al. · Nature Communications · 2020 · 91 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Neph1, a Component of the Kidney Slit Diaphragm, Is Tyrosine-phosphorylated by the Src Family Tyrosine Kinase and Modulates Intracellular Signaling by Binding to Grb2

Yutaka Harita, Hidetake Kurihara, Hidetaka Kosako et al. · Journal of Biological Chemistry · 2008 · 82 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17

ASPP2 Regulates Epithelial Cell Polarity through the PAR Complex

Wei-Li Cong, Tomonori Hirose, Yutaka Harita et al. · Current Biology · 2010 · 78 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +14

Tyrosine phosphorylation–dependent activation of TRPC6 regulated by PLC-γ1 and nephrin: effect of mutations associated with focal segmental glomerulosclerosis

Shoichiro Kanda, Yutaka Harita, Yoshio Shibagaki et al. · Molecular Biology of the Cell · 2011 · 76 citations

Life Sciences, Molecular Biology, Nephrology +17