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Proceedings of the National Academy of Sciences of the United States of America
|
June 3, 2025
<i>CACNA1D</i> is a circadian gene and causes familial advanced sleep phase
John M Webb, Fayal Abderemane-Ali, Liza Ashbrook, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids
|
January 8, 2021
Deletion of the gene encoding prostamide/prostaglandin F synthase reveals an important role in regulating intraocular pressure
Jacques A Bertrand, David F Woodward, Joseph M Sherwood, et al.
Nephron. Physiology
|
November 21, 2007
Functional characterization of a novel missense CLCN5 mutation causing alterations in proximal tubular endocytic machinery in Dent's disease
Atsuhito Tanuma, Hiroyoshi Sato, Tetsuro Takeda, et al.
Cell Reports
|
December 24, 2014
Cytoskeletal regulation by AUTS2 in neuronal migration and neuritogenesis
Kei Hori, Taku Nagai, Wei Shan, et al.
European Journal of Immunology
|
February 6, 2015
RASAL3, a novel hematopoietic RasGAP protein, regulates the number and functions of NKT cells
Suguru Saito, Toshihiko Kawamura, Masaya Higuchi, et al.
Eneuro
|
October 28, 2016
Involvement of Brain-Enriched Guanylate Kinase-Associated Protein (BEGAIN) in Chronic Pain after Peripheral Nerve Injury
Tayo Katano, Masafumi Fukuda, Hidemasa Furue, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 26, 2018
Deficiency of AMPAR-Palmitoylation Aggravates Seizure Susceptibility
Masayuki Itoh, Mariko Yamashita, Masaki Kaneko, et al.
Journal of Cell Science
|
November 9, 2014
Proteasome dysfunction induces muscle growth defects and protein aggregation
Yasuo Kitajima, Yoshitaka Tashiro, Naoki Suzuki, et al.
Nature Communications
|
December 15, 2015
A CDC42EP4/septin-based perisynaptic glial scaffold facilitates glutamate clearance
Natsumi Ageta-Ishihara, Maya Yamazaki, Kohtarou Konno, et al.
The Journal of Biological Chemistry
|
October 19, 2013
Point mutation in syntaxin-1A causes abnormal vesicle recycling, behaviors, and short term plasticity
Yumi Watanabe, Norikazu Katayama, Kosei Takeuchi, et al.
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of 8
Search research articles
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Showing results (61-70 of 72) with videos related to
Sort By:
Page
of 8
Proceedings of the National Academy of Sciences of the United States of America
|
June 3, 2025
<i>CACNA1D</i> is a circadian gene and causes familial advanced sleep phase
John M Webb, Fayal Abderemane-Ali, Liza Ashbrook, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids
|
January 8, 2021
Deletion of the gene encoding prostamide/prostaglandin F synthase reveals an important role in regulating intraocular pressure
Jacques A Bertrand, David F Woodward, Joseph M Sherwood, et al.
Nephron. Physiology
|
November 21, 2007
Functional characterization of a novel missense CLCN5 mutation causing alterations in proximal tubular endocytic machinery in Dent's disease
Atsuhito Tanuma, Hiroyoshi Sato, Tetsuro Takeda, et al.
Cell Reports
|
December 24, 2014
Cytoskeletal regulation by AUTS2 in neuronal migration and neuritogenesis
Kei Hori, Taku Nagai, Wei Shan, et al.
European Journal of Immunology
|
February 6, 2015
RASAL3, a novel hematopoietic RasGAP protein, regulates the number and functions of NKT cells
Suguru Saito, Toshihiko Kawamura, Masaya Higuchi, et al.
Eneuro
|
October 28, 2016
Involvement of Brain-Enriched Guanylate Kinase-Associated Protein (BEGAIN) in Chronic Pain after Peripheral Nerve Injury
Tayo Katano, Masafumi Fukuda, Hidemasa Furue, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 26, 2018
Deficiency of AMPAR-Palmitoylation Aggravates Seizure Susceptibility
Masayuki Itoh, Mariko Yamashita, Masaki Kaneko, et al.
Journal of Cell Science
|
November 9, 2014
Proteasome dysfunction induces muscle growth defects and protein aggregation
Yasuo Kitajima, Yoshitaka Tashiro, Naoki Suzuki, et al.
Nature Communications
|
December 15, 2015
A CDC42EP4/septin-based perisynaptic glial scaffold facilitates glutamate clearance
Natsumi Ageta-Ishihara, Maya Yamazaki, Kohtarou Konno, et al.
The Journal of Biological Chemistry
|
October 19, 2013
Point mutation in syntaxin-1A causes abnormal vesicle recycling, behaviors, and short term plasticity
Yumi Watanabe, Norikazu Katayama, Kosei Takeuchi, et al.
Page
of 8