Page last updated: 2024-09-03

flag peptide and ALS - Amyotrophic Lateral Sclerosis

flag peptide has been researched along with ALS - Amyotrophic Lateral Sclerosis in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baralle, FE; Buratti, E; Laurents, DV; Mompeán, M; Pantoja-Uceda, D; Romano, V; Stuani, C	1
Doi, K; Fukada, Y; Inoué, T; Kaidoh, T; Kitayama, M; Morino, S; Nakano, T; Nakashima, K; Watanabe, Y; Yasui, K	1

Other Studies

2 other study(ies) available for flag peptide and ALS - Amyotrophic Lateral Sclerosis

Article	Year
Point mutations in the N-terminal domain of transactive response DNA-binding protein 43 kDa (TDP-43) compromise its stability, dimerization, and functions. The Journal of biological chemistry, 2017, 07-14, Volume: 292, Issue:28 Topics: Amino Acid Substitution; Amyotrophic Lateral Sclerosis; Dimerization; DNA-Binding Proteins; Frontotemporal Lobar Degeneration; HEK293 Cells; Humans; Leucine; Models, Molecular; Oligopeptides; Peptide Fragments; Point Mutation; Protein Aggregation, Pathological; Protein Conformation; Protein Folding; Protein Interaction Domains and Motifs; Protein Stability; Protein Transport; Recombinant Fusion Proteins; RNA Stability	2017
Mitochondrial changes in motor neurons of homozygotes of leucine 126 TT deletion SOD1 transgenic mice. Neuropathology : official journal of the Japanese Society of Neuropathology, 2008, Volume: 28, Issue:3 Topics: Amyotrophic Lateral Sclerosis; Animals; Disease Models, Animal; Homozygote; Humans; Leucine; Mice; Mice, Transgenic; Microscopy, Immunoelectron; Mitochondria; Motor Neurons; Oligopeptides; Peptides; Sequence Deletion; Superoxide Dismutase; Superoxide Dismutase-1	2008

Article

Year

Point mutations in the N-terminal domain of transactive response DNA-binding protein 43 kDa (TDP-43) compromise its stability, dimerization, and functions.

The Journal of biological chemistry, 2017, 07-14, Volume: 292, Issue:28

Topics: Amino Acid Substitution; Amyotrophic Lateral Sclerosis; Dimerization; DNA-Binding Proteins; Frontotemporal Lobar Degeneration; HEK293 Cells; Humans; Leucine; Models, Molecular; Oligopeptides; Peptide Fragments; Point Mutation; Protein Aggregation, Pathological; Protein Conformation; Protein Folding; Protein Interaction Domains and Motifs; Protein Stability; Protein Transport; Recombinant Fusion Proteins; RNA Stability

2017

Mitochondrial changes in motor neurons of homozygotes of leucine 126 TT deletion SOD1 transgenic mice.

Neuropathology : official journal of the Japanese Society of Neuropathology, 2008, Volume: 28, Issue:3

Topics: Amyotrophic Lateral Sclerosis; Animals; Disease Models, Animal; Homozygote; Humans; Leucine; Mice; Mice, Transgenic; Microscopy, Immunoelectron; Mitochondria; Motor Neurons; Oligopeptides; Peptides; Sequence Deletion; Superoxide Dismutase; Superoxide Dismutase-1

2008