Hiromi Hirata
Affiliations: | Aoyama Gakuin University - Japan, Shibuya-ku, Tōkyō-to, Japan |
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Publications
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Watai K, Sadamitsu K, Wada S, et al. (2024) Zebrafish trpm7 mutants show reduced motility in free movement. Development, Growth & Differentiation |
Sadamitsu K, Yanagi K, Hasegawa Y, et al. (2024) A novel homozygous variant of the PIGK gene caused by paternal disomy in a patient with neurodevelopmental disorder, cerebellar atrophy, and seizures. Journal of Human Genetics |
Uehara T, Sanuki R, Ogura Y, et al. (2021) Recurrent NFIA K125E substitution represents a loss-of-function allele: Sensitive in vitro and in vivo assays for nontruncating alleles. American Journal of Medical Genetics. Part A |
Ito D, Kawazoe Y, Sato A, et al. (2020) Identification of the hypertension drug niflumic acid as a glycine receptor inhibitor. Scientific Reports. 10: 13999 |
Maeta M, Kataoka M, Nishiya Y, et al. (2020) RNA polymerase II subunit D is essential for zebrafish development. Scientific Reports. 10: 13213 |
Ogino K, Yamada K, Nishioka T, et al. (2019) Phosphorylation of gephyrin in zebrafish Mauthner cells governs glycine receptor clustering and behavioral desensitization to sound. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
Sugihara M, Morito D, Ainuki S, et al. (2019) The AAA+ ATPase/ubiquitin ligase mysterin stabilizes cytoplasmic lipid droplets. The Journal of Cell Biology |
Low SE, Ito D, Hirata H. (2018) Characterization of the Zebrafish Glycine Receptor Family Reveals Insights Into Glycine Receptor Structure Function and Stoichiometry. Frontiers in Molecular Neuroscience. 11: 286 |
Schaefer N, Zheng F, van Brederode J, et al. (2018) Functional Consequences of the Postnatal Switch From Neonatal to Mutant Adult Glycine Receptor α1 Subunits in the Mouse Model of Startle Disease. Frontiers in Molecular Neuroscience. 11: 167 |
Boubakri M, Chaya T, Hirata H, et al. (2016) Loss of ift122, a Retrograde Intraflagellar Transport (IFT) Complex Component, Leads to Slow, Progressive Photoreceptor Degeneration Due to Inefficient Opsin Transport. The Journal of Biological Chemistry. 291: 24465-24474 |