Page last updated: 2024-10-25

dapi and Amyotrophic Lateral Sclerosis

dapi has been researched along with Amyotrophic Lateral Sclerosis in 3 studies

DAPI: RN given refers to parent cpd.

Amyotrophic Lateral Sclerosis: A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)

Research Excerpts

ExcerptRelevanceReference
"Western blot of lysates from FTLD-TDP frontal cortex and TDP-43-positive SALS spinal cord revealed decreased levels of OPTN protein compared to controls (p < 0."1.37Optineurin inclusions occur in a minority of TDP-43 positive ALS and FTLD-TDP cases and are rarely observed in other neurodegenerative disorders. ( Al-Sarraj, S; Hortobágyi, T; King, A; Nishimura, AL; Rogelj, B; Seelaar, H; Shaw, CE; Troakes, C; van Swieten, JC; Vance, C, 2011)
" The possible toxic factor(s) and the exact mode of action (e."1.33Protective effect of metabotropic glutamate receptor inhibition on amyotrophic lateral sclerosis-cerebrospinal fluid toxicity in vitro. ( Anneser, JM; Borasio, GD; Chahli, C, 2006)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Jeong, SY1
Rathore, KI1
Schulz, K1
Ponka, P1
Arosio, P1
David, S1
Hortobágyi, T1
Troakes, C1
Nishimura, AL1
Vance, C1
van Swieten, JC1
Seelaar, H1
King, A1
Al-Sarraj, S1
Rogelj, B1
Shaw, CE1
Anneser, JM1
Chahli, C1
Borasio, GD1

Other Studies

3 other studies available for dapi and Amyotrophic Lateral Sclerosis

ArticleYear
Dysregulation of iron homeostasis in the CNS contributes to disease progression in a mouse model of amyotrophic lateral sclerosis.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009, Jan-21, Volume: 29, Issue:3

    Topics: Age Factors; Aldehydes; Amyotrophic Lateral Sclerosis; Animals; Body Weight; Cation Transport Protei

2009
Optineurin inclusions occur in a minority of TDP-43 positive ALS and FTLD-TDP cases and are rarely observed in other neurodegenerative disorders.
    Acta neuropathologica, 2011, Volume: 121, Issue:4

    Topics: Aged; Aged, 80 and over; Amyotrophic Lateral Sclerosis; Brain; Cell Cycle Proteins; DNA-Binding Prot

2011
Protective effect of metabotropic glutamate receptor inhibition on amyotrophic lateral sclerosis-cerebrospinal fluid toxicity in vitro.
    Neuroscience, 2006, Sep-15, Volume: 141, Issue:4

    Topics: Aged; Amyotrophic Lateral Sclerosis; Animals; Cell Count; Cell Death; Cells, Cultured; Cerebrospinal

2006