Kazuhiro Ogata

De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy

Hirotomo Saitsu, Mitsuhiro Kato, Takeshi Mizuguchi et al. · Nature Genetics · 2008 · 539 citations

Neurological Disorder, Genetic Disorder, Genetics +8

Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome

Yoshinori Tsurusaki, Nobuhiko Okamoto, Hirofumi Ohashi et al. · Nature Genetics · 2012 · 515 citations

Mendelian Disorder, Translational Biology, Disease Mechanism +6

Solution structure of a specific DNA complex of the Myb DNA-binding domain with cooperative recognition helices

Kazuhiro Ogata, Souichi Morikawa, Haruki Nakamura et al. · Cell · 1994 · 487 citations

Myb Dna-binding Domain, Protein Assembly, Specific Dna Complex +7

The cavity in the hydrophobic core of Myb DNA-binding domain is reserved for DNA recognition and trans-activation

Kazuhiro Ogata, Chie Kanei‐Ishii, Motoko Sasaki et al. · Nature Structural Biology · 1996 · 318 citations

Chromatin, Hydrophobic Core, Myb Dna-binding Domain +10

Solution structure of a DNA-binding unit of Myb: a helix-turn-helix-related motif with conserved tryptophans forming a hydrophobic core.

Kazuhiro Ogata, Hironobu Hojo, Saburo Aimoto et al. · Proceedings of the National Academy of Sciences · 1992 · 286 citations · Full text

Structural Bioinformatics, Protein Assembly, Biomolecular Structure Prediction +18