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Cell Death and Differentiation
|
July 17, 2004
Apoptosome inactivation rescues proneural and neural cells from neurodegeneration
M Cozzolino, E Ferraro, A Ferri, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 10, 2018
Faulty neuronal determination and cell polarization are reverted by modulating HD early phenotypes
P Conforti, D Besusso, V D Bocchi, et al.
The Journal of Biological Chemistry
|
April 20, 2000
Inhibiting caspase cleavage of huntingtin reduces toxicity and aggregate formation in neuronal and nonneuronal cells
C L Wellington, R Singaraja, L Ellerby, et al.
Science (New York, N.Y.)
|
June 16, 2001
Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease
C Zuccato, A Ciammola, D Rigamonti, et al.
Nature Communications
|
February 23, 2026
Investigation of bile salt hydrolase activity in human gut bacteria reveals production of conjugated secondary bile acids
Lauren N Lucas, Mallikarjun Jillella, Lea E Cattaneo, et al.
Neuroscience Letters
|
March 17, 2011
Whole body cholesterol metabolism is impaired in Huntington's disease
V Leoni, C Mariotti, L Nanetti, et al.
Neuromuscular Disorders : NMD
|
December 18, 2003
Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2)
G Meola, V Sansone, D Perani, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 11, 2000
Wild-type huntingtin protects from apoptosis upstream of caspase-3
D Rigamonti, J H Bauer, C De-Fraja, et al.
Neurobiology of Disease
|
May 22, 2007
Biological abnormalities of peripheral A(2A) receptors in a large representation of polyglutamine disorders and Huntington's disease stages
K Varani, A-C Bachoud-Lévi, C Mariotti, et al.
Page
of 11
Search research articles
Search
Showing results (101-110 of 109) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 109 results.
Cell Death and Differentiation
|
July 17, 2004
Apoptosome inactivation rescues proneural and neural cells from neurodegeneration
M Cozzolino, E Ferraro, A Ferri, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 10, 2018
Faulty neuronal determination and cell polarization are reverted by modulating HD early phenotypes
P Conforti, D Besusso, V D Bocchi, et al.
The Journal of Biological Chemistry
|
April 20, 2000
Inhibiting caspase cleavage of huntingtin reduces toxicity and aggregate formation in neuronal and nonneuronal cells
C L Wellington, R Singaraja, L Ellerby, et al.
Science (New York, N.Y.)
|
June 16, 2001
Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease
C Zuccato, A Ciammola, D Rigamonti, et al.
Nature Communications
|
February 23, 2026
Investigation of bile salt hydrolase activity in human gut bacteria reveals production of conjugated secondary bile acids
Lauren N Lucas, Mallikarjun Jillella, Lea E Cattaneo, et al.
Neuroscience Letters
|
March 17, 2011
Whole body cholesterol metabolism is impaired in Huntington's disease
V Leoni, C Mariotti, L Nanetti, et al.
Neuromuscular Disorders : NMD
|
December 18, 2003
Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2)
G Meola, V Sansone, D Perani, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 11, 2000
Wild-type huntingtin protects from apoptosis upstream of caspase-3
D Rigamonti, J H Bauer, C De-Fraja, et al.
Neurobiology of Disease
|
May 22, 2007
Biological abnormalities of peripheral A(2A) receptors in a large representation of polyglutamine disorders and Huntington's disease stages
K Varani, A-C Bachoud-Lévi, C Mariotti, et al.
Page
of 11