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Cancer Science|January 20, 2007
MutationView/KMcancerDB: a database for cancer gene mutationsNobuyoshi Shimizu, Masafumi Ohtsubo, Shinsei Minoshima
Human Mutation|April 25, 2015
The KM-parkin-DB: A Sub-set MutationView Database Specialized for PARK2 (PARKIN) VariantsSusumu Mitsuyama, Masafumi Ohtsubo, Shinsei Minoshima, et al.
Plos One|July 2, 2014
Oligomerization of optineurin and its oxidative stress- or E50K mutation-driven covalent cross-linking: possible relationship with glaucoma pathologyJie Gao, Masafumi Ohtsubo, Yoshihiro Hotta, et al.
Human Mutation|March 17, 2010
KMeyeDB: a graphical database of mutations in genes that cause eye diseasesTakashi Kawamura, Masafumi Ohtsubo, Susumu Mitsuyama, et al.
Journal of Human Genetics|July 3, 2010
Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genesHiroshi Nakanishi, Masafumi Ohtsubo, Satoshi Iwasaki, et al.
Genomics|June 29, 2010
YPEL5 protein of the YPEL gene family is involved in the cell cycle progression by interacting with two distinct proteins RanBPM and RanBP10Katsuhiro Hosono, Setsuko Noda, Atsushi Shimizu, et al.
Experimental Cell Research|May 22, 2007
Parkin interacts with LIM Kinase 1 and reduces its cofilin-phosphorylation activity via ubiquitinationMeng K Lim, Takeshi Kawamura, Yosuke Ohsawa, et al.
Carcinogenesis|March 29, 2003
Increased nuclear factor-kappa B activation is related to the tumor development of renal cell carcinomaMototsugu Oya, Atsushi Takayanagi, Akio Horiguchi, et al.
Journal of Human Genetics|May 20, 2011
Novel USH2A mutations in Japanese Usher syndrome type 2 patients: marked differences in the mutation spectrum between the Japanese and other populationsHiroshi Nakanishi, Masafumi Ohtsubo, Satoshi Iwasaki, et al.
Human Genome Variation|April 18, 2019
A Japanese family with cone-rod dystrophy of delayed onset caused by a compound heterozygous combination of novel <i>CDHR1</i> frameshift and known missense variantsMuhammad Nazmul Haque, Kentaro Kurata, Katsuhiro Hosono, et al.
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