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Cell Stem Cell
|
September 8, 2009
Neuroprotection of host cells by human central nervous system stem cells in a mouse model of infantile neuronal ceroid lipofuscinosis
Stanley J Tamaki, Yakop Jacobs, Monika Dohse, et al.
Scientific Reports
|
November 24, 2020
Central nervous system pathology in preclinical MPS IIIB dogs reveals progressive changes in clinically relevant brain regions
Martin T Egeland, Marta M Tarczyluk-Wells, Melissa M Asmar, et al.
Molecular Therapy. Methods & Clinical Development
|
March 5, 2021
Intracranial delivery of AAV9 gene therapy partially prevents retinal degeneration and visual deficits in CLN6-Batten disease mice
Katherine A White, Hemanth R Nelvagal, Timothy A Poole, et al.
JCI Insight
|
August 21, 2025
GABAergic interneurons contribute to the fatal seizure phenotype of CLN2 disease mice
Keigo Takahashi, Nicholas R Rensing, Elizabeth M Eultgen, et al.
Optics Express
|
September 24, 2016
Origin of terminal voltage variations due to self-mixing in terahertz frequency quantum cascade lasers
Andrew Grier, Paul Dean, Alexander Valavanis, et al.
JCI Insight
|
November 30, 2023
Neuronal deletion of the circadian clock gene Bmal1 induces cell-autonomous dopaminergic neurodegeneration
Michael F Kanan, Patrick W Sheehan, Jessica N Haines, et al.
Biochimica Et Biophysica Acta
|
June 29, 2015
Guidelines for incorporating scientific knowledge and practice on rare diseases into higher education: neuronal ceroid lipofuscinoses as a model disorder
Inés Adriana Cismondi, Romina Kohan, Heather Adams, et al.
Molecular and Cellular Neurosciences
|
June 23, 2004
p38alpha stress-activated protein kinase phosphorylates neurofilaments and is associated with neurofilament pathology in amyotrophic lateral sclerosis
Steven Ackerley, Andrew J Grierson, Steven Banner, et al.
Molecular Genetics and Metabolism
|
August 25, 2016
Diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2 disease): Expert recommendations for early detection and laboratory diagnosis
Michael Fietz, Moeenaldeen AlSayed, Derek Burke, et al.
Acta Neuropathologica Communications
|
July 23, 2025
Gene therapy ameliorates neuromuscular pathology in CLN3 disease
Ewa A Ziółkowska, Albina Jablonka-Shariff, Letitia L Williams, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 144) with videos related to
Sort By:
Page
of 15
Cell Stem Cell
|
September 8, 2009
Neuroprotection of host cells by human central nervous system stem cells in a mouse model of infantile neuronal ceroid lipofuscinosis
Stanley J Tamaki, Yakop Jacobs, Monika Dohse, et al.
Scientific Reports
|
November 24, 2020
Central nervous system pathology in preclinical MPS IIIB dogs reveals progressive changes in clinically relevant brain regions
Martin T Egeland, Marta M Tarczyluk-Wells, Melissa M Asmar, et al.
Molecular Therapy. Methods & Clinical Development
|
March 5, 2021
Intracranial delivery of AAV9 gene therapy partially prevents retinal degeneration and visual deficits in CLN6-Batten disease mice
Katherine A White, Hemanth R Nelvagal, Timothy A Poole, et al.
JCI Insight
|
August 21, 2025
GABAergic interneurons contribute to the fatal seizure phenotype of CLN2 disease mice
Keigo Takahashi, Nicholas R Rensing, Elizabeth M Eultgen, et al.
Optics Express
|
September 24, 2016
Origin of terminal voltage variations due to self-mixing in terahertz frequency quantum cascade lasers
Andrew Grier, Paul Dean, Alexander Valavanis, et al.
JCI Insight
|
November 30, 2023
Neuronal deletion of the circadian clock gene Bmal1 induces cell-autonomous dopaminergic neurodegeneration
Michael F Kanan, Patrick W Sheehan, Jessica N Haines, et al.
Biochimica Et Biophysica Acta
|
June 29, 2015
Guidelines for incorporating scientific knowledge and practice on rare diseases into higher education: neuronal ceroid lipofuscinoses as a model disorder
Inés Adriana Cismondi, Romina Kohan, Heather Adams, et al.
Molecular and Cellular Neurosciences
|
June 23, 2004
p38alpha stress-activated protein kinase phosphorylates neurofilaments and is associated with neurofilament pathology in amyotrophic lateral sclerosis
Steven Ackerley, Andrew J Grierson, Steven Banner, et al.
Molecular Genetics and Metabolism
|
August 25, 2016
Diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2 disease): Expert recommendations for early detection and laboratory diagnosis
Michael Fietz, Moeenaldeen AlSayed, Derek Burke, et al.
Acta Neuropathologica Communications
|
July 23, 2025
Gene therapy ameliorates neuromuscular pathology in CLN3 disease
Ewa A Ziółkowska, Albina Jablonka-Shariff, Letitia L Williams, et al.
Page
of 15