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

Mari Yoshida

Showing results (121-130 of 376) with videos related to

Pageof 38
Sort By:
BMC Evolutionary Biology|December 18, 2014
Directed evolution of cell size in Escherichia coliMari Yoshida, Saburo Tsuru, Naoko Hirata, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 28, 2015
An autopsied case of unclassifiable sporadic four-repeat tauopathy presenting with parkinsonism and speech disturbancesYasushi Iwasaki, Keiko Mori, Masumi Ito, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 3, 2019
Clinicopathological differences between the motor onset and psychiatric onset of Huntington's disease, focusing on the nucleus accumbensMitsuaki Hirano, Shuji Iritani, Hiroshige Fujishiro, et al.
Rinsho Shinkeigaku = Clinical Neurology|October 22, 2010
[An autopsy case of senile dementia suspected to be influenced by cerebral amyloid angiopathy with multiple cortical microinfarcts]Yasushi Iwasaki, Keiko Mori, Masumi Ito, et al.
Brain : a Journal of Neurology|September 14, 2017
Reply: Neuronal intranuclear (hyaline) inclusion disease and fragile X-associated tremor/ataxia syndrome: a morphological and molecular dilemmaJun Sone, Tomohiko Nakamura, Haruki Koike, et al.
Molecular Phylogenetics and Evolution|June 29, 2007
Mitochondrial genome structure and evolution in the living fossil vampire squid, Vampyroteuthis infernalis, and extant cephalopodsShin-ichi Yokobori, Dhugal J Lindsay, Mari Yoshida, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|September 29, 2007
Enhanced Aquaporin-4 immunoreactivity in sporadic Creutzfeldt-Jakob diseaseYasushi Iwasaki, Maya Mimuro, Mari Yoshida, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|May 9, 2009
An autopsied case of panencephalopathic-type Creutzfeldt-Jakob disease with mutation in the prion protein gene at codon 232 and type 1 prion proteinTetsuo Hama, Yasushi Iwasaki, Hisayoshi Niwa, et al.
Brain Research|October 10, 2009
Overexpression of hippocampal cholinergic neurostimulating peptide in heterozygous transgenic mice increases the amount of ChAT in the medial septal nucleusNorihiko Uematsu, Noriyuki Matsukawa, Tetsuko Kanamori, et al.
Neuroscience Letters|June 26, 2012
Autophagy-related proteins (p62, NBR1 and LC3) in intranuclear inclusions in neurodegenerative diseasesFumiaki Mori, Kunikazu Tanji, Saori Odagiri, et al.
Pageof 38

Showing results (121-130 of 376) with videos related to

Sort By:
Pageof 38
BMC Evolutionary Biology|December 18, 2014
Directed evolution of cell size in Escherichia coliMari Yoshida, Saburo Tsuru, Naoko Hirata, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 28, 2015
An autopsied case of unclassifiable sporadic four-repeat tauopathy presenting with parkinsonism and speech disturbancesYasushi Iwasaki, Keiko Mori, Masumi Ito, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 3, 2019
Clinicopathological differences between the motor onset and psychiatric onset of Huntington's disease, focusing on the nucleus accumbensMitsuaki Hirano, Shuji Iritani, Hiroshige Fujishiro, et al.
Rinsho Shinkeigaku = Clinical Neurology|October 22, 2010
[An autopsy case of senile dementia suspected to be influenced by cerebral amyloid angiopathy with multiple cortical microinfarcts]Yasushi Iwasaki, Keiko Mori, Masumi Ito, et al.
Brain : a Journal of Neurology|September 14, 2017
Reply: Neuronal intranuclear (hyaline) inclusion disease and fragile X-associated tremor/ataxia syndrome: a morphological and molecular dilemmaJun Sone, Tomohiko Nakamura, Haruki Koike, et al.
Molecular Phylogenetics and Evolution|June 29, 2007
Mitochondrial genome structure and evolution in the living fossil vampire squid, Vampyroteuthis infernalis, and extant cephalopodsShin-ichi Yokobori, Dhugal J Lindsay, Mari Yoshida, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|September 29, 2007
Enhanced Aquaporin-4 immunoreactivity in sporadic Creutzfeldt-Jakob diseaseYasushi Iwasaki, Maya Mimuro, Mari Yoshida, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|May 9, 2009
An autopsied case of panencephalopathic-type Creutzfeldt-Jakob disease with mutation in the prion protein gene at codon 232 and type 1 prion proteinTetsuo Hama, Yasushi Iwasaki, Hisayoshi Niwa, et al.
Brain Research|October 10, 2009
Overexpression of hippocampal cholinergic neurostimulating peptide in heterozygous transgenic mice increases the amount of ChAT in the medial septal nucleusNorihiko Uematsu, Noriyuki Matsukawa, Tetsuko Kanamori, et al.
Neuroscience Letters|June 26, 2012
Autophagy-related proteins (p62, NBR1 and LC3) in intranuclear inclusions in neurodegenerative diseasesFumiaki Mori, Kunikazu Tanji, Saori Odagiri, et al.
Pageof 38