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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 11, 2012
G9a histone methyltransferase activity in retinal progenitors is essential for proper differentiation and survival of mouse retinal cellsKimiko Katoh, Ryoji Yamazaki, Akishi Onishi, et al.
Seminars in Cell & Developmental Biology|April 23, 2016
Random monoallelic expression of genes on autosomes: Parallels with X-chromosome inactivationAnne-Valerie Gendrel, Lucile Marion-Poll, Kimiko Katoh, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 14, 2010
Blimp1 suppresses Chx10 expression in differentiating retinal photoreceptor precursors to ensure proper photoreceptor developmentKimiko Katoh, Yoshihiro Omori, Akishi Onishi, et al.
Gene|February 26, 2018
Clinical and genetic characterization of a patient with SOX5 haploinsufficiency caused by a de novo balanced reciprocal translocationDaisuke Fukushi, Kenichiro Yamada, Kaoru Suzuki, et al.
Plos One|May 24, 2011
Analysis of transcriptional regulatory pathways of photoreceptor genes by expression profiling of the Otx2-deficient retinaYoshihiro Omori, Kimiko Katoh, Shigeru Sato, et al.
Applied Neuropsychology. Adult|January 29, 2019
Relation between cognitive and cerebello-thalamo-cortical functions in healthy elderly people: Evidence from the Yakumo StudyTakeshi Hatta, Hasegawa Yukiharu, Kimiko Katoh, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 18, 2011
An essential role for RAX homeoprotein and NOTCH-HES signaling in Otx2 expression in embryonic retinal photoreceptor cell fate determinationYuki Muranishi, Koji Terada, Tatsuya Inoue, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 2010
Negative regulation of ciliary length by ciliary male germ cell-associated kinase (Mak) is required for retinal photoreceptor survivalYoshihiro Omori, Taro Chaya, Kimiko Katoh, et al.
Human Mutation|June 3, 2020
Clinical and molecular genetic characterization of two female patients harboring the Xq27.3q28 deletion with different ratios of X chromosome inactivationKimiko Katoh, Kaori Aiba, Daisuke Fukushi, et al.
American Journal of Medical Genetics. Part A|March 22, 2021
R3HDM1 haploinsufficiency is associated with mild intellectual disabilityDaisuke Fukushi, Mie Inaba, Kimiko Katoh, et al.
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