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The European Journal of Neuroscience
|
January 19, 2005
A rat model of slow Wallerian degeneration (WldS) with improved preservation of neuromuscular synapses
Robert Adalbert, Thomas H Gillingwater, Jane E Haley, et al.
Brain : a Journal of Neurology
|
January 13, 2005
The slow Wallerian degeneration gene, WldS, inhibits axonal spheroid pathology in gracile axonal dystrophy mice
Weiqian Mi, Bogdan Beirowski, Thomas H Gillingwater, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 28, 2011
Sir-two-homolog 2 (Sirt2) modulates peripheral myelination through polarity protein Par-3/atypical protein kinase C (aPKC) signaling
Bogdan Beirowski, Jason Gustin, Sean M Armour, et al.
Kidney International
|
June 18, 2004
DDR1-deficient mice show localized subepithelial GBM thickening with focal loss of slit diaphragms and proteinuria
Oliver Gross, Bogdan Beirowski, Scott J Harvey, et al.
Experimental Neurology
|
June 10, 2026
Aged oligodendrocyte progenitors retain the capacity to respond to an inflammatory insult
Emily E Fresenko, Kaitlin E Kaiser, Benjamin J Burson, et al.
Molecular and Cellular Neurosciences
|
May 13, 2008
VCP binding influences intracellular distribution of the slow Wallerian degeneration protein, Wld(S)
Anna L Wilbrey, Jane E Haley, Thomas M Wishart, et al.
The Journal of Cell Biology
|
February 25, 2009
Wld S protein requires Nmnat activity and a short N-terminal sequence to protect axons in mice
Laura Conforti, Anna Wilbrey, Giacomo Morreale, et al.
Molecular Biology of the Cell
|
December 24, 2005
The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleus
Heike Laser, Laura Conforti, Giacomo Morreale, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 38) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 38 results.
The European Journal of Neuroscience
|
January 19, 2005
A rat model of slow Wallerian degeneration (WldS) with improved preservation of neuromuscular synapses
Robert Adalbert, Thomas H Gillingwater, Jane E Haley, et al.
Brain : a Journal of Neurology
|
January 13, 2005
The slow Wallerian degeneration gene, WldS, inhibits axonal spheroid pathology in gracile axonal dystrophy mice
Weiqian Mi, Bogdan Beirowski, Thomas H Gillingwater, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 28, 2011
Sir-two-homolog 2 (Sirt2) modulates peripheral myelination through polarity protein Par-3/atypical protein kinase C (aPKC) signaling
Bogdan Beirowski, Jason Gustin, Sean M Armour, et al.
Kidney International
|
June 18, 2004
DDR1-deficient mice show localized subepithelial GBM thickening with focal loss of slit diaphragms and proteinuria
Oliver Gross, Bogdan Beirowski, Scott J Harvey, et al.
Experimental Neurology
|
June 10, 2026
Aged oligodendrocyte progenitors retain the capacity to respond to an inflammatory insult
Emily E Fresenko, Kaitlin E Kaiser, Benjamin J Burson, et al.
Molecular and Cellular Neurosciences
|
May 13, 2008
VCP binding influences intracellular distribution of the slow Wallerian degeneration protein, Wld(S)
Anna L Wilbrey, Jane E Haley, Thomas M Wishart, et al.
The Journal of Cell Biology
|
February 25, 2009
Wld S protein requires Nmnat activity and a short N-terminal sequence to protect axons in mice
Laura Conforti, Anna Wilbrey, Giacomo Morreale, et al.
Molecular Biology of the Cell
|
December 24, 2005
The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleus
Heike Laser, Laura Conforti, Giacomo Morreale, et al.
Page
of 4