Page last updated: 2024-08-21

ethylnitrosourea and Amyotrophic Lateral Sclerosis

ethylnitrosourea has been researched along with Amyotrophic Lateral Sclerosis in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Acevedo-Arozena, A; Blanco, G; Brandner, S; de Oliveira, HM; Fisher, EM; Fratta, P; Greensmith, L; Kent, R; McGoldrick, P; Phatak, V; Ricketts, T	1

Other Studies

1 other study(ies) available for ethylnitrosourea and Amyotrophic Lateral Sclerosis

Article	Year
A nonsense mutation in mouse Tardbp affects TDP43 alternative splicing activity and causes limb-clasping and body tone defects. PloS one, 2014, Volume: 9, Issue:1 Topics: Adaptor Proteins, Vesicular Transport; Alternative Splicing; Amyotrophic Lateral Sclerosis; Animals; Behavior, Animal; Body Weight; Codon, Nonsense; DNA-Binding Proteins; Embryo Loss; Ethylnitrosourea; Hand Strength; Hindlimb; Homozygote; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Motor Activity; Mutant Proteins; Phenotype; Point Mutation; RNA, Messenger; Superoxide Dismutase; Superoxide Dismutase-1	2014

Article

Year

A nonsense mutation in mouse Tardbp affects TDP43 alternative splicing activity and causes limb-clasping and body tone defects.

PloS one, 2014, Volume: 9, Issue:1

Topics: Adaptor Proteins, Vesicular Transport; Alternative Splicing; Amyotrophic Lateral Sclerosis; Animals; Behavior, Animal; Body Weight; Codon, Nonsense; DNA-Binding Proteins; Embryo Loss; Ethylnitrosourea; Hand Strength; Hindlimb; Homozygote; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Motor Activity; Mutant Proteins; Phenotype; Point Mutation; RNA, Messenger; Superoxide Dismutase; Superoxide Dismutase-1

2014