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Neuroscience Letters|December 3, 2011
Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorderEriko Fujita, Yuko Tanabe, Mariko Y Momoi, et al.
Brain Research. Developmental Brain Research|February 15, 2005
Distribution of RA175/TSLC1/SynCAM, a member of the immunoglobulin superfamily, in the developing nervous systemEriko Fujita, Koko Urase, Akiko Soyama, et al.
Journal of Neurochemistry|May 16, 2015
CASPR2 forms a complex with GPR37 via MUPP1 but not with GPR37(R558Q), an autism spectrum disorder-related mutationYuko Tanabe, Eriko Fujita-Jimbo, Mariko Y Momoi, et al.
Journal of Neurochemistry|September 22, 2012
A complex of synaptic adhesion molecule CADM1, a molecule related to autism spectrum disorder, with MUPP1 in the cerebellumEriko Fujita, Yuko Tanabe, Beat A Imhof, et al.
Plos One|January 25, 2012
Cadm1-expressing synapses on Purkinje cell dendrites are involved in mouse ultrasonic vocalization activityEriko Fujita, Yuko Tanabe, Beat A Imhof, et al.
Cerebral Cortex (New York, N.Y. : 1991)|July 8, 2016
Foxp2 Regulates Identities and Projection Patterns of Thalamic Nuclei During DevelopmentHaruka Ebisu, Lena Iwai-Takekoshi, Eriko Fujita-Jimbo, et al.
Biochemical and Biophysical Research Communications|October 30, 2008
Mutations in the gene encoding CADM1 are associated with autism spectrum disorderYu Zhiling, Eriko Fujita, Yuko Tanabe, et al.
Biochemical and Biophysical Research Communications|January 2, 2007
Intracellular distribution of a speech/language disorder associated FOXP2 mutantAkifumi Mizutani, Ayumi Matsuzaki, Mariko Y Momoi, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|November 21, 2022
Functional analysis of PAX8 variants identified in patients with congenital hypothyroidism in situKhishigjargal Batjargal, Toshihiro Tajima, Eriko Fujita-Jimbo, et al.
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