Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Yo-Tsen Liu

Showing results (21-30 of 54) with videos related to

Pageof 6
Sort By:
Cellular and Molecular Life Sciences : CMLS|November 16, 2019
Cellular secretion and cytotoxicity of transthyretin mutant proteins underlie late-onset amyloidosis and neurodegenerationRidwan Babatunde Ibrahim, Ssu-Yu Yeh, Kon-Ping Lin, et al.
Human Mutation|July 12, 2019
Novel SCA19/22-associated KCND3 mutations disrupt human K<sub>V</sub> 4.3 protein biosynthesis and channel gatingCheng-Tsung Hsiao, Ssu-Ju Fu, Yo-Tsen Liu, et al.
Neurology|May 10, 2013
Hereditary sensory and autonomic neuropathy type 1 (HSANI) caused by a novel mutation in SPTLC2Sinéad M Murphy, Daniela Ernst, Yu Wei, et al.
Epilepsia|February 25, 2022
Novel lissencephaly-associated DCX variants in the C-terminal DCX domain affect microtubule binding and dynamicsJun-Ru Lin, Ju-Fang Cheng, Yo-Tsen Liu, et al.
Epilepsy & Behavior : E&B|February 24, 2021
Acute withdrawal of new-generation antiepileptic drugs in epilepsy monitoring units: Safety and efficacyChien-Chen Chou, Po-Tso Lin, Der-Jen Yen, et al.
Neurobiology of Aging|January 26, 2016
Mutational analysis of TBK1 in Taiwanese patients with amyotrophic lateral sclerosisPei-Chien Tsai, Yi-Chien Liu, Kon-Ping Lin, et al.
Molecular Neurobiology|July 13, 2022
Plasma Matrix Metalloproeteinase-9 Is Associated with Seizure and Angioarchitecture Changes in Brain Arteriovenous MalformationsYo-Tsen Liu, Cheng-Chia Lee, Chun-Fu Lin, et al.
Neuromolecular Medicine|January 9, 2015
Novel HSAN1 mutation in serine palmitoyltransferase resides at a putative phosphorylation site that is involved in regulating substrate specificityDaniela Ernst, Sinéad M Murphy, Karthik Sathiyanadan, et al.
Epilepsia|April 14, 2019
PRRT2 missense mutations cluster near C-terminus and frequently lead to protein mislocalizationMeng-Han Tsai, Fang-Shin Nian, Mei-Hsin Hsu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 13, 2013
Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisationYo-Tsen Liu, Joshua Hersheson, Vincent Plagnol, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Cellular and Molecular Life Sciences : CMLS|November 16, 2019
Cellular secretion and cytotoxicity of transthyretin mutant proteins underlie late-onset amyloidosis and neurodegenerationRidwan Babatunde Ibrahim, Ssu-Yu Yeh, Kon-Ping Lin, et al.
Human Mutation|July 12, 2019
Novel SCA19/22-associated KCND3 mutations disrupt human K<sub>V</sub> 4.3 protein biosynthesis and channel gatingCheng-Tsung Hsiao, Ssu-Ju Fu, Yo-Tsen Liu, et al.
Neurology|May 10, 2013
Hereditary sensory and autonomic neuropathy type 1 (HSANI) caused by a novel mutation in SPTLC2Sinéad M Murphy, Daniela Ernst, Yu Wei, et al.
Epilepsia|February 25, 2022
Novel lissencephaly-associated DCX variants in the C-terminal DCX domain affect microtubule binding and dynamicsJun-Ru Lin, Ju-Fang Cheng, Yo-Tsen Liu, et al.
Epilepsy & Behavior : E&B|February 24, 2021
Acute withdrawal of new-generation antiepileptic drugs in epilepsy monitoring units: Safety and efficacyChien-Chen Chou, Po-Tso Lin, Der-Jen Yen, et al.
Neurobiology of Aging|January 26, 2016
Mutational analysis of TBK1 in Taiwanese patients with amyotrophic lateral sclerosisPei-Chien Tsai, Yi-Chien Liu, Kon-Ping Lin, et al.
Molecular Neurobiology|July 13, 2022
Plasma Matrix Metalloproeteinase-9 Is Associated with Seizure and Angioarchitecture Changes in Brain Arteriovenous MalformationsYo-Tsen Liu, Cheng-Chia Lee, Chun-Fu Lin, et al.
Neuromolecular Medicine|January 9, 2015
Novel HSAN1 mutation in serine palmitoyltransferase resides at a putative phosphorylation site that is involved in regulating substrate specificityDaniela Ernst, Sinéad M Murphy, Karthik Sathiyanadan, et al.
Epilepsia|April 14, 2019
PRRT2 missense mutations cluster near C-terminus and frequently lead to protein mislocalizationMeng-Han Tsai, Fang-Shin Nian, Mei-Hsin Hsu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 13, 2013
Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisationYo-Tsen Liu, Joshua Hersheson, Vincent Plagnol, et al.
Pageof 6