Compounds > arginine

arginine and Amyoplasia Congenita

arginine has been researched along with Amyoplasia Congenita in 3 studies

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's0 (0.00)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Hu, L; Li, H; Lin, Z; Lou, Y; Lu, J; Luan, Z; Tang, S; Xu, C; Xu, X; Zhang, H1
Altin, E; Ashley, CC; Lipscomb, S; Preston, LC; Redwood, CS; Robinson, P; Watkins, H1
Holmgren, D; Kimber, E; Oldfors, A; Tajsharghi, H; Tulinius, M1

Other Studies

3 other study(ies) available for arginine and Amyoplasia Congenita

ArticleYear
The distal arthrogryposis-linked p.R63C variant promotes the stability and nuclear accumulation of TNNT3.
    Journal of clinical laboratory analysis, 2021, Volume: 35, Issue:12

    Topics: Amino Acid Substitution; Arginine; Arthrogryposis; Case-Control Studies; Cell Nucleus; Child; Cysteine; Female; HEK293 Cells; Humans; Male; Point Mutation; Pregnancy; Protein Stability; Troponin T

2021
Mutations in fast skeletal troponin I, troponin T, and beta-tropomyosin that cause distal arthrogryposis all increase contractile function.
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2007, Volume: 21, Issue:3

    Topics: Actins; Amino Acid Substitution; Animals; Arginine; Arthrogryposis; Calcium; Glycine; Humans; Muscle Contraction; Muscle, Skeletal; Mutation; Myosins; Rabbits; Tropomyosin; Troponin I; Troponin T

2007
Distal arthrogryposis and muscle weakness associated with a beta-tropomyosin mutation.
    Neurology, 2007, Mar-06, Volume: 68, Issue:10

    Topics: Adult; Aged; Arginine; Arthrogryposis; DNA Mutational Analysis; Exons; Family Health; Female; Humans; Muscle Weakness; Mutation, Missense; Tropomyosin; Tryptophan

2007