Page last updated: 2024-08-22

manganese and Autosomal Dominant Hereditary Spastic Paraplegia

manganese has been researched along with Autosomal Dominant Hereditary Spastic Paraplegia 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
Chenevert, M; Huckaba, TM; Jennings, S; Liu, L; Mottamal, M; Wojcik, EJ	1

Other Studies

1 other study(ies) available for manganese and Autosomal Dominant Hereditary Spastic Paraplegia

Article	Year
Characterization of kinesin switch I mutations that cause hereditary spastic paraplegia. PloS one, 2017, Volume: 12, Issue:7 Topics: Adenosine Triphosphate; Binding Sites; Binding, Competitive; Biocatalysis; Genetic Predisposition to Disease; Humans; Hydrolysis; Kinesins; Magnesium; Manganese; Microtubules; Molecular Dynamics Simulation; Mutation; Protein Binding; Protein Multimerization; Protein Structure, Tertiary; Recombinant Proteins; Spastic Paraplegia, Hereditary; Time-Lapse Imaging	2017

Article

Year

Characterization of kinesin switch I mutations that cause hereditary spastic paraplegia.

PloS one, 2017, Volume: 12, Issue:7

Topics: Adenosine Triphosphate; Binding Sites; Binding, Competitive; Biocatalysis; Genetic Predisposition to Disease; Humans; Hydrolysis; Kinesins; Magnesium; Manganese; Microtubules; Molecular Dynamics Simulation; Mutation; Protein Binding; Protein Multimerization; Protein Structure, Tertiary; Recombinant Proteins; Spastic Paraplegia, Hereditary; Time-Lapse Imaging

2017