Global ETD Search

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Showing 1 to 3 of 3 for “"amytrophic lateral sclerosis"”.

  1. MACROPHAGE RESPONSE TO INITIAL MUSCLE DENERVATION IN THE SOD1-G93A MOUSE MODEL OF AMYTROPHIC LATERAL SCLEROSIS.

    Amyotrophic lateral sclerosis (ALS) is a fatal adult-onset motor neuron (MN) disease characterized by dysfunction, degeneration and death of upper and lower MNs. Loss of the connections of MN to muscle at the neuromuscular junction (NMJ) underlies the characteristic muscle weakness seen in ALS. …

    wfu Repository record for MACROPHAGE RESPONSE TO INITIAL MUSCLE DENERVATION IN THE SOD1-G93A MOUSE MODEL OF AMYTROPHIC LATERAL SCLEROSIS. (opens in a new tab)

  2. Investigating the effect of amyotrophic lateral sclerosis-associated mutant vesicle-associated membrane protein B on axonal transport

    Amytrophic lateral sclerosis (ALS) is a fatal neurodegenrative disease characterised by selective degeneration and death of motor neurons. The architecture of neurons makes them dependent upon the proper transport of protein and organelle cargoes, especially through axons (axonal transport). …

    kings Repository record for Investigating the effect of amyotrophic lateral sclerosis-associated mutant vesicle-associated membrane protein B on axonal transport (opens in a new tab)

  3. Molecular mechanisms underlying morphological effects of protein kinase C under normal conditions and cellular stress.

    … behind the neurodegenerative disease amyotrophic lateral sclerosis (ALS), where aggregates containing peripherin are essentially always seen in afflicted tissues. The RNA-binding proteins were found to localize to specific RNA-granules, formed when cells are exposed to stress. PKCalpha, rather …

    lund Repository record for Molecular mechanisms underlying morphological effects of protein kinase C under normal conditions and cellular stress. (opens in a new tab)