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Atsuo Fukuda

Showing results (121-130 of 125) with videos related to

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Annals of Clinical and Translational Neurology|March 22, 2018
<i>De novo</i> variants in <i>CAMK2A</i> and <i>CAMK2B</i> cause neurodevelopmental disordersTenpei Akita, Kazushi Aoto, Mitsuhiro Kato, et al.
Biomolecules|May 27, 2023
Tubulin Polyglutamylation by TTLL1 and TTLL7 Regulate Glutamate Concentration in the Mice BrainYashuang Ping, Kenji Ohata, Kenji Kikushima, et al.
Nature Communications|April 9, 2021
ATP6V0A1 encoding the a1-subunit of the V0 domain of vacuolar H<sup>+</sup>-ATPases is essential for brain development in humans and miceKazushi Aoto, Mitsuhiro Kato, Tenpei Akita, et al.
American Journal of Human Genetics|September 3, 2013
De Novo mutations in GNAO1, encoding a Gαo subunit of heterotrimeric G proteins, cause epileptic encephalopathyKazuyuki Nakamura, Hirofumi Kodera, Tenpei Akita, et al.
American Journal of Human Genetics|May 25, 2010
Dominant-negative mutations in alpha-II spectrin cause West syndrome with severe cerebral hypomyelination, spastic quadriplegia, and developmental delayHirotomo Saitsu, Jun Tohyama, Tatsuro Kumada, et al.
Pageof 13

Showing results (121-130 of 125) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 125 results.
Annals of Clinical and Translational Neurology|March 22, 2018
<i>De novo</i> variants in <i>CAMK2A</i> and <i>CAMK2B</i> cause neurodevelopmental disordersTenpei Akita, Kazushi Aoto, Mitsuhiro Kato, et al.
Biomolecules|May 27, 2023
Tubulin Polyglutamylation by TTLL1 and TTLL7 Regulate Glutamate Concentration in the Mice BrainYashuang Ping, Kenji Ohata, Kenji Kikushima, et al.
Nature Communications|April 9, 2021
ATP6V0A1 encoding the a1-subunit of the V0 domain of vacuolar H<sup>+</sup>-ATPases is essential for brain development in humans and miceKazushi Aoto, Mitsuhiro Kato, Tenpei Akita, et al.
American Journal of Human Genetics|September 3, 2013
De Novo mutations in GNAO1, encoding a Gαo subunit of heterotrimeric G proteins, cause epileptic encephalopathyKazuyuki Nakamura, Hirofumi Kodera, Tenpei Akita, et al.
American Journal of Human Genetics|May 25, 2010
Dominant-negative mutations in alpha-II spectrin cause West syndrome with severe cerebral hypomyelination, spastic quadriplegia, and developmental delayHirotomo Saitsu, Jun Tohyama, Tatsuro Kumada, et al.
Pageof 13