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Kevin B Boylan

Showing results (11-20 of 50) with videos related to

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Acta Neuropathologica|April 29, 2015
A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degenerationMasataka Nakamura, Kevin F Bieniek, Wen-Lang Lin, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 3, 2013
Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementiaMarka van Blitterswijk, Matthew C Baker, Kevin F Bieniek, et al.
Neuron|February 19, 2013
Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALSPeter E A Ash, Kevin F Bieniek, Tania F Gendron, et al.
Acta Neuropathologica|November 1, 2015
Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bankKevin F Bieniek, Owen A Ross, Kerry A Cormier, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 6, 2012
Clinical and electrophysiologic variability in amyotrophic lateral sclerosis within a kindred harboring the C9ORF72 repeat expansionElizabeth A Coon, Jasper R Daube, Mariely Dejesus-Hernandez, et al.
Human Molecular Genetics|June 23, 2017
Repetitive element transcripts are elevated in the brain of C9orf72 ALS/FTLD patientsMercedes Prudencio, Patrick K Gonzales, Casey N Cook, et al.
Acta Neuropathologica|October 17, 2013
Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALSTania F Gendron, Kevin F Bieniek, Yong-Jie Zhang, et al.
Annals of Neurology|June 20, 2017
Phosphorylated neurofilament heavy chain: A biomarker of survival for C9ORF72-associated amyotrophic lateral sclerosisTania F Gendron, , Lillian M Daughrity, et al.
Acta Neuropathologica Communications|December 9, 2017
Clinical and neuropathological features of ALS/FTD with TIA1 mutationsVeronica Hirsch-Reinshagen, Cyril Pottier, Alexandra M Nicholson, et al.
Acta Neuropathologica|August 16, 2017
Conserved DNA methylation combined with differential frontal cortex and cerebellar expression distinguishes C9orf72-associated and sporadic ALS, and implicates SERPINA1 in diseaseMark T W Ebbert, Christian A Ross, Luc J Pregent, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
Acta Neuropathologica|April 29, 2015
A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degenerationMasataka Nakamura, Kevin F Bieniek, Wen-Lang Lin, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 3, 2013
Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementiaMarka van Blitterswijk, Matthew C Baker, Kevin F Bieniek, et al.
Neuron|February 19, 2013
Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALSPeter E A Ash, Kevin F Bieniek, Tania F Gendron, et al.
Acta Neuropathologica|November 1, 2015
Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bankKevin F Bieniek, Owen A Ross, Kerry A Cormier, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 6, 2012
Clinical and electrophysiologic variability in amyotrophic lateral sclerosis within a kindred harboring the C9ORF72 repeat expansionElizabeth A Coon, Jasper R Daube, Mariely Dejesus-Hernandez, et al.
Human Molecular Genetics|June 23, 2017
Repetitive element transcripts are elevated in the brain of C9orf72 ALS/FTLD patientsMercedes Prudencio, Patrick K Gonzales, Casey N Cook, et al.
Acta Neuropathologica|October 17, 2013
Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALSTania F Gendron, Kevin F Bieniek, Yong-Jie Zhang, et al.
Annals of Neurology|June 20, 2017
Phosphorylated neurofilament heavy chain: A biomarker of survival for C9ORF72-associated amyotrophic lateral sclerosisTania F Gendron, , Lillian M Daughrity, et al.
Acta Neuropathologica Communications|December 9, 2017
Clinical and neuropathological features of ALS/FTD with TIA1 mutationsVeronica Hirsch-Reinshagen, Cyril Pottier, Alexandra M Nicholson, et al.
Acta Neuropathologica|August 16, 2017
Conserved DNA methylation combined with differential frontal cortex and cerebellar expression distinguishes C9orf72-associated and sporadic ALS, and implicates SERPINA1 in diseaseMark T W Ebbert, Christian A Ross, Luc J Pregent, et al.
Pageof 5