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Publications by Kazuhiro Ogata
Biallelic Mutations in MYPN , Encoding Myopalladin, Are Associated With Childhood-Onset, Slowly Progressive Nemaline Myopathy
American Journal of Human Genetics
Genetics
De Novo Mutations in GNAO1, Encoding a Gαo Subunit of Heterotrimeric G Proteins, Cause Epileptic Encephalopathy
American Journal of Human Genetics
Genetics
Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy
American Journal of Human Genetics
Genetics
A Novel GFI1B Mutation at the First Zinc Finger Domain Causes Congenital Macrothrombocytopenia
British Journal of Haematology
Hematology
Graphical Animations of the Suzuki-Kasami Distributed Mutual Exclusion Protocol
Foxo1 Links Insulin Signaling to C/EBPα and Regulates Gluconeogenesis During Liver Development
EMBO Journal
Immunology
Molecular Biology
Biochemistry
Microbiology
Neuroscience
Medicine
Genetics
Formal Analysis of Suzuki&Kasami Distributed Mutual Exclusion Algorithm
