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Publications by Hirofumi Ohashi
Bi-Allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy With Brain Malformation
American Journal of Human Genetics
Genetics
Germline-Activating RRAS2 Mutations Cause Noonan Syndrome
American Journal of Human Genetics
Genetics
The Aryl Hydrocarbon Receptor-Cytochrome P450 1A1 Pathway Controls Lipid Accumulation and Enhances the Permissiveness for Hepatitis C Virus Assembly
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
A Founder Mutation of CANT1 Common in Korean and Japanese Desbuquois Dysplasia
Journal of Human Genetics
Genetics
HRAS Mutants Identified in Costello Syndrome Patients Can Induce Cellular Senescence: Possible Implications for the Pathogenesis of Costello Syndrome
Journal of Human Genetics
Genetics
Facultative Commensalism of a Free-Burrowing Urothoid Amphipod With a Deep Burrow-Dwelling Callianassid Shrimp in Intertidal Sand
Marine Biology
Evolution
Ecology
Systematics
Aquatic Science
Behavior
Multidrug Treatment With Nelfinavir and Cepharanthine Against COVID-19
Mutation of the Type X Collagen Gene (COL10A1) Causes Spondylometaphyseal Dysplasia
American Journal of Human Genetics
Genetics
Loss of CpG Methylation Is Strongly Correlated With Loss of Histone H3 Lysine 9 Methylation at DMR-LIT1 in Patients With Beckwith-Wiedemann Syndrome
American Journal of Human Genetics
Genetics
Preferential Paternal Origin of Microdeletions Caused by Prezygotic Chromosome or Chromatid Rearrangements in Sotos Syndrome
American Journal of Human Genetics
Genetics
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