Compounds > cysteine

cysteine and Autosomal Dominant Hereditary Spastic Paraplegia

cysteine has been researched along with Autosomal Dominant Hereditary Spastic Paraplegia in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Battini, R; Catania, A; Chiapparini, ML; Garavaglia, B; Ghezzi, D; Nardocci, N; Pasquariello, R; Pippucci, T; Seri, M; Tiranti, V; Zorzi, G1
Baas, PW; D'Rozario, M; Davidson, MW; Jean, DC; Marenda, DR; Solowska, JM1
Dam, M; Eiberg, H; Grønbech-Jensen, M; Hasholt, L; Johnsen, B; Koefoed, P; Krabbe, K; Krarup, C; Law, I; Nielsen, JE; Nørremølle, A; Paulson, OB; Rehfeld, JF; Scheuer, KH; Søndergård, H; Sørensen, SA1
Bernardi, G; Hase, Y; Iseki, K; Kawarai, T; Matsui, M; Orlacchio, A; Rogaeva, E; St George-Hyslop, P; Takahashi, R; Tomimoto, H1

Other Studies

4 other study(ies) available for cysteine and Autosomal Dominant Hereditary Spastic Paraplegia

ArticleYear
R106C TFG variant causes infantile neuroaxonal dystrophy "plus" syndrome.
    Neurogenetics, 2018, Volume: 19, Issue:3

    Topics: Adult; Amino Acid Substitution; Arginine; Case-Control Studies; Cells, Cultured; Child; Child, Preschool; Consanguinity; Cysteine; Female; Follow-Up Studies; Genetic Predisposition to Disease; Humans; Male; Middle Aged; Mutation, Missense; Neuroaxonal Dystrophies; Pedigree; Proteins; Siblings; Spastic Paraplegia, Hereditary

2018
Pathogenic mutation of spastin has gain-of-function effects on microtubule dynamics.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014, Jan-29, Volume: 34, Issue:5

    Topics: Adenosine Triphosphatases; Animals; Animals, Genetically Modified; Cells, Cultured; Cysteine; Disease Models, Animal; Drosophila; Drosophila Proteins; Female; Gene Expression Regulation; Green Fluorescent Proteins; Haploinsufficiency; Humans; Locomotion; Male; Microtubules; Mutation; Neurons; Nocodazole; Rats; Spastic Paraplegia, Hereditary; Spastin; Transfection; Tubulin Modulators; Tyrosine

2014
Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.
    European journal of neurology, 2004, Volume: 11, Issue:12

    Topics: Adenosine Triphosphatases; Adult; Brain Mapping; Case-Control Studies; Cerebellar Ataxia; Cognition; Cysteine; DNA Mutational Analysis; Electroencephalography; Electromyography; Evoked Potentials; Family Health; Female; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Neural Conduction; Neuropsychological Tests; Phenotype; Positron-Emission Tomography; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Spastic Paraplegia, Hereditary; Spastin; Threonine

2004
A novel mutation in the SPG3A gene (atlastin) in hereditary spastic paraplegia.
    Journal of neurology, 2007, Volume: 254, Issue:7

    Topics: Adult; Cysteine; DNA Mutational Analysis; Family Health; Female; Genetic Linkage; GTP Phosphohydrolases; GTP-Binding Proteins; Humans; Japan; Membrane Proteins; Polymorphism, Genetic; Spastic Paraplegia, Hereditary; Tyrosine

2007