M. Sato

Fetuin‐A negatively correlates with liver and vascular fibrosis in nonalcoholic fatty liver disease subjects

T. Takehara, E. Miyoshi, H. Hougaku, 2015, Liver international : official journal of the International Association for the Study of the Liver.

Mutations in the gene coding for guanylate cyclase-activating protein 2 (GUCA1B gene) in patients with autosomal dominant retinal dystrophies

N. Tanimoto, H. Abe, H. Ohguro, 2005, Graefe's Archive for Clinical and Experimental Ophthalmology.

Hepatic aberrant glycosylation by N-acetylglucosaminyltransferase V accelerates HDL assembly.

T. Takehara, A. Kimura, E. Miyoshi, 2016, American journal of physiology. Gastrointestinal and liver physiology.

N-acetylglucosaminyltransferase V exacerbates concanavalin A-induced hepatitis in mice.

T. Takehara, E. Miyoshi, S. Shinzaki, 2015, Molecular medicine reports.

Mutations in the gene coding for guanylate cyclase-activating protein 2 ( gene ) in patients with autosomal dominant retinal dystrophies GUCA 1 B

N. Tanimoto, H. Abe, H. Ohguro, 2004 .

Mutation c. 1142 del G in the PRPF31 Gene in a Family with Autosomal Dominant Retinitis Pigmentosa (RP11) and Its Implications

M. Nakazawa, M. Sato, Kurenai Taira, 2007, Japanese Journal of Ophthalmology.

Autosomal dominant central areolar choroidal dystrophy and a novel Arg195Leu mutation in the peripherin/RDS gene.

H. Ohguro, Y. Miyagawa, M. Nakazawa, 2003, Archives of ophthalmology.

Study of pharmacological effects of nilvadipine on RCS rat retinal degeneration by microarray analysis.

H. Ohguro, Ikuyo Ohguro, Y. Miyagawa, 2003, Biochemical and biophysical research communications.

Pharmacological Aspects of Nilvadipine-Induced Preservation of Retinal Degeneration in RCS Rat Analyzed by mRNA Profiling Assay

H. Ohguro, Y. Miyagawa, I. Maruyama, 2003 .

Serum Mac‐2 binding protein levels as a novel diagnostic biomarker for prediction of disease severity and nonalcoholic steatohepatitis

Y. Imai, N. Hiramatsu, N. Kawada, 2013, Proteomics. Clinical applications.