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Proceedings of the National Academy of Sciences of the United States of America
|
December 14, 2006
Gene transfer demonstrates that muscle is not a primary target for non-cell-autonomous toxicity in familial amyotrophic lateral sclerosis
Timothy M Miller, Soo H Kim, Koji Yamanaka, et al.
Nature Communications
|
January 6, 2018
C9ORF72 GGGGCC repeat-associated non-AUG translation is upregulated by stress through eIF2α phosphorylation
Weiwei Cheng, Shaopeng Wang, Alexander A Mestre, et al.
Developmental Cell
|
January 31, 2017
Centrosome Amplification Is Sufficient to Promote Spontaneous Tumorigenesis in Mammals
Michelle S Levine, Bjorn Bakker, Bram Boeckx, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 16, 1994
Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity
D R Borchelt, M K Lee, H S Slunt, et al.
Nature Cell Biology
|
June 23, 2025
Author Correction: A two-step mechanism for epigenetic specification of centromere identity and function
Daniele Fachinetti, H Diego Folco, Yael Nechemia-Arbely, et al.
Neurology
|
October 1, 1996
Mechanisms of selective motor neuron death in transgenic mouse models of motor neuron disease
D W Cleveland, L I Bruijn, P C Wong, et al.
Nature Cell Biology
|
July 23, 2013
A two-step mechanism for epigenetic specification of centromere identity and function
Daniele Fachinetti, H Diego Folco, Yael Nechemia-Arbely, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 20, 2007
Common molecular signature in SOD1 for both sporadic and familial amyotrophic lateral sclerosis
Arie Gruzman, William L Wood, Evgenia Alpert, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 31, 2002
Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS)
David S Howland, Jian Liu, Yijin She, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 5, 2014
Blood-spinal cord barrier disruption contributes to early motor-neuron degeneration in ALS-model mice
Ethan A Winkler, Jesse D Sengillo, Abhay P Sagare, et al.
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of 50
Search research articles
Search
Showing results (411-420 of 499) with videos related to
Sort By:
Page
of 50
Proceedings of the National Academy of Sciences of the United States of America
|
December 14, 2006
Gene transfer demonstrates that muscle is not a primary target for non-cell-autonomous toxicity in familial amyotrophic lateral sclerosis
Timothy M Miller, Soo H Kim, Koji Yamanaka, et al.
Nature Communications
|
January 6, 2018
C9ORF72 GGGGCC repeat-associated non-AUG translation is upregulated by stress through eIF2α phosphorylation
Weiwei Cheng, Shaopeng Wang, Alexander A Mestre, et al.
Developmental Cell
|
January 31, 2017
Centrosome Amplification Is Sufficient to Promote Spontaneous Tumorigenesis in Mammals
Michelle S Levine, Bjorn Bakker, Bram Boeckx, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 16, 1994
Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity
D R Borchelt, M K Lee, H S Slunt, et al.
Nature Cell Biology
|
June 23, 2025
Author Correction: A two-step mechanism for epigenetic specification of centromere identity and function
Daniele Fachinetti, H Diego Folco, Yael Nechemia-Arbely, et al.
Neurology
|
October 1, 1996
Mechanisms of selective motor neuron death in transgenic mouse models of motor neuron disease
D W Cleveland, L I Bruijn, P C Wong, et al.
Nature Cell Biology
|
July 23, 2013
A two-step mechanism for epigenetic specification of centromere identity and function
Daniele Fachinetti, H Diego Folco, Yael Nechemia-Arbely, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 20, 2007
Common molecular signature in SOD1 for both sporadic and familial amyotrophic lateral sclerosis
Arie Gruzman, William L Wood, Evgenia Alpert, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 31, 2002
Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS)
David S Howland, Jian Liu, Yijin She, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 5, 2014
Blood-spinal cord barrier disruption contributes to early motor-neuron degeneration in ALS-model mice
Ethan A Winkler, Jesse D Sengillo, Abhay P Sagare, et al.
Page
of 50