Search research articles
Contact Us
Filters
Showing results (31-40 of 176) with videos related to
Page
of 18
Sort By:
The European Journal of Neuroscience
|
October 1, 1991
The Gene for Ciliary Neurotrophic Factor (CNTF) Maps to Murine Chromosome 19 and its Expression is Not Affected in the Hereditary Motoneuron Disease 'Wobbler' of the Mouse
Klemens Kaupmann, Michael Sendtner, Kurt A. Stöckli, et al.
Neurobiology of Disease
|
February 26, 2024
hnRNP R regulates mitochondrial movement and membrane potential in axons of motoneurons
Sophia Dithmar, Abdolhossein Zare, Saeede Salehi, et al.
RNA (New York, N.Y.)
|
September 24, 2014
Subcellular transcriptome alterations in a cell culture model of spinal muscular atrophy point to widespread defects in axonal growth and presynaptic differentiation
Lena Saal, Michael Briese, Susanne Kneitz, et al.
Histochemistry and Cell Biology
|
July 20, 2012
Laminin induced local axonal translation of β-actin mRNA is impaired in SMN-deficient motoneurons
Reena Rathod, Steven Havlicek, Nicolas Frank, et al.
Frontiers in Molecular Neuroscience
|
September 9, 2024
Ptbp2 re-expression rescues axon growth defects in Smn-deficient motoneurons
Saeede Salehi, Abdolhossein Zare, Gayatri Gandhi, et al.
Genes & Development
|
April 27, 2004
The Notch target genes Hey1 and Hey2 are required for embryonic vascular development
Andreas Fischer, Nina Schumacher, Manfred Maier, et al.
Journal of Neuroscience Methods
|
January 22, 2005
Optical assessment of motoneuron function in a "twenty-four-hour" acute spinal cord slice model from fetal rats
Friedrich Metzger, Nadine Klapproth, Anna Kulik, et al.
Neuro-Degenerative Diseases
|
June 29, 2007
Differential modulation of neurite growth by the S- and the L-forms of bag1, a co-chaperone of Hsp70
Karin Frebel, Stefan Wiese, Natalja Funk, et al.
Neurobiology of Aging
|
December 19, 2009
C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany
Carsten Drepper, Thomas Herrmann, Carsten Wessig, et al.
The Journal of Cell Biology
|
October 10, 2007
Defective Ca2+ channel clustering in axon terminals disturbs excitability in motoneurons in spinal muscular atrophy
Sibylle Jablonka, Marcus Beck, Barbara Dorothea Lechner, et al.
Page
of 18
Search research articles
Search
Showing results (31-40 of 176) with videos related to
Sort By:
Page
of 18
The European Journal of Neuroscience
|
October 1, 1991
The Gene for Ciliary Neurotrophic Factor (CNTF) Maps to Murine Chromosome 19 and its Expression is Not Affected in the Hereditary Motoneuron Disease 'Wobbler' of the Mouse
Klemens Kaupmann, Michael Sendtner, Kurt A. Stöckli, et al.
Neurobiology of Disease
|
February 26, 2024
hnRNP R regulates mitochondrial movement and membrane potential in axons of motoneurons
Sophia Dithmar, Abdolhossein Zare, Saeede Salehi, et al.
RNA (New York, N.Y.)
|
September 24, 2014
Subcellular transcriptome alterations in a cell culture model of spinal muscular atrophy point to widespread defects in axonal growth and presynaptic differentiation
Lena Saal, Michael Briese, Susanne Kneitz, et al.
Histochemistry and Cell Biology
|
July 20, 2012
Laminin induced local axonal translation of β-actin mRNA is impaired in SMN-deficient motoneurons
Reena Rathod, Steven Havlicek, Nicolas Frank, et al.
Frontiers in Molecular Neuroscience
|
September 9, 2024
Ptbp2 re-expression rescues axon growth defects in Smn-deficient motoneurons
Saeede Salehi, Abdolhossein Zare, Gayatri Gandhi, et al.
Genes & Development
|
April 27, 2004
The Notch target genes Hey1 and Hey2 are required for embryonic vascular development
Andreas Fischer, Nina Schumacher, Manfred Maier, et al.
Journal of Neuroscience Methods
|
January 22, 2005
Optical assessment of motoneuron function in a "twenty-four-hour" acute spinal cord slice model from fetal rats
Friedrich Metzger, Nadine Klapproth, Anna Kulik, et al.
Neuro-Degenerative Diseases
|
June 29, 2007
Differential modulation of neurite growth by the S- and the L-forms of bag1, a co-chaperone of Hsp70
Karin Frebel, Stefan Wiese, Natalja Funk, et al.
Neurobiology of Aging
|
December 19, 2009
C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany
Carsten Drepper, Thomas Herrmann, Carsten Wessig, et al.
The Journal of Cell Biology
|
October 10, 2007
Defective Ca2+ channel clustering in axon terminals disturbs excitability in motoneurons in spinal muscular atrophy
Sibylle Jablonka, Marcus Beck, Barbara Dorothea Lechner, et al.
Page
of 18