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Teepu Siddique

Showing results (71-80 of 86) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 24, 2014
Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2George H Gorrie, Faisal Fecto, Daniel Radzicki, et al.
American Journal of Human Genetics|February 7, 2008
Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degenerationMaria K Tsaousidou, Karim Ouahchi, Tom T Warner, et al.
American Journal of Human Genetics|July 15, 2003
Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosisPeter C Sapp, Betsy A Hosler, Diane McKenna-Yasek, et al.
Neurology. Genetics|August 6, 2020
Disease-modifying effects of an <i>SCAF4</i> structural variant in a predominantly <i>SOD1</i> ALS cohortJulia Pytte, Loren L Flynn, Ryan S Anderton, et al.
Neuron|February 16, 2020
Nucleocytoplasmic Proteomic Analysis Uncovers eRF1 and Nonsense-Mediated Decay as Modifiers of ALS/FTD C9orf72 ToxicityJuan A Ortega, Elizabeth L Daley, Sukhleen Kour, et al.
Human Molecular Genetics|April 22, 2008
Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approachHan-Xiang Deng, Deng Han-Xiang, Hujun Jiang, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2020
ALS/FTD mutations in UBQLN2 impede autophagy by reducing autophagosome acidification through loss of functionJosephine J Wu, Ashley Cai, Jessie E Greenslade, et al.
Brain : a Journal of Neurology|May 4, 2024
Hippocampal aggregation signatures of pathogenic UBQLN2 in amyotrophic lateral sclerosis and frontotemporal dementiaKyrah M Thumbadoo, Birger V Dieriks, Helen C Murray, et al.
Neuron|June 21, 2016
Activation of HIPK2 Promotes ER Stress-Mediated Neurodegeneration in Amyotrophic Lateral SclerosisSebum Lee, Yulei Shang, Stephanie A Redmond, et al.
Annals of Neurology|May 1, 2007
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutationsIan R A Mackenzie, Eileen H Bigio, Paul G Ince, et al.
Pageof 9

Showing results (71-80 of 86) with videos related to

Sort By:
Pageof 9
Proceedings of the National Academy of Sciences of the United States of America|September 24, 2014
Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2George H Gorrie, Faisal Fecto, Daniel Radzicki, et al.
American Journal of Human Genetics|February 7, 2008
Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degenerationMaria K Tsaousidou, Karim Ouahchi, Tom T Warner, et al.
American Journal of Human Genetics|July 15, 2003
Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosisPeter C Sapp, Betsy A Hosler, Diane McKenna-Yasek, et al.
Neurology. Genetics|August 6, 2020
Disease-modifying effects of an <i>SCAF4</i> structural variant in a predominantly <i>SOD1</i> ALS cohortJulia Pytte, Loren L Flynn, Ryan S Anderton, et al.
Neuron|February 16, 2020
Nucleocytoplasmic Proteomic Analysis Uncovers eRF1 and Nonsense-Mediated Decay as Modifiers of ALS/FTD C9orf72 ToxicityJuan A Ortega, Elizabeth L Daley, Sukhleen Kour, et al.
Human Molecular Genetics|April 22, 2008
Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approachHan-Xiang Deng, Deng Han-Xiang, Hujun Jiang, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2020
ALS/FTD mutations in UBQLN2 impede autophagy by reducing autophagosome acidification through loss of functionJosephine J Wu, Ashley Cai, Jessie E Greenslade, et al.
Brain : a Journal of Neurology|May 4, 2024
Hippocampal aggregation signatures of pathogenic UBQLN2 in amyotrophic lateral sclerosis and frontotemporal dementiaKyrah M Thumbadoo, Birger V Dieriks, Helen C Murray, et al.
Neuron|June 21, 2016
Activation of HIPK2 Promotes ER Stress-Mediated Neurodegeneration in Amyotrophic Lateral SclerosisSebum Lee, Yulei Shang, Stephanie A Redmond, et al.
Annals of Neurology|May 1, 2007
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutationsIan R A Mackenzie, Eileen H Bigio, Paul G Ince, et al.
Pageof 9