Compounds > cysteine

cysteine and Abnormalities, Musculoskeletal

cysteine has been researched along with Abnormalities, Musculoskeletal in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's2 (66.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Al-Shammary, A; Al-Zaidan, H; Faiyaz-Ul-Haque, M; Faqeih, EA; Zaidi, SH1
Flanagan, S; Glass, IA; Hayes, M; Hyland, VJ; Masel, J; Robertson, SP; Roscioli, T; Savarirayan, R1
Donoghue, DJ; Galvin, BD; Hart, KC; Meyer, AN; Robertson, SC; Webster, MK1

Other Studies

3 other study(ies) available for cysteine and Abnormalities, Musculoskeletal

ArticleYear
Grebe-type chondrodysplasia: a novel missense mutation in a conserved cysteine of the growth differentiation factor 5.
    Journal of bone and mineral metabolism, 2008, Volume: 26, Issue:6

    Topics: Amino Acid Sequence; Animals; Child; Child, Preschool; Cysteine; DNA Mutational Analysis; Female; Growth Differentiation Factor 5; Humans; Male; Molecular Sequence Data; Musculoskeletal Abnormalities; Mutation, Missense; Osteochondrodysplasias; Pedigree; Sequence Alignment

2008
Somatic and germline mosaicism for a R248C missense mutation in FGFR3, resulting in a skeletal dysplasia distinct from thanatophoric dysplasia.
    American journal of medical genetics. Part A, 2003, Jul-15, Volume: 120A, Issue:2

    Topics: Acanthosis Nigricans; Body Height; Bone Diseases, Developmental; Chromatography, High Pressure Liquid; Cysteine; Female; Heterozygote; Humans; Hyperplasia; Middle Aged; Mosaicism; Musculoskeletal Abnormalities; Mutation, Missense; Protein-Tyrosine Kinases; Radiography; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Sequence Analysis, DNA; Thanatophoric Dysplasia

2003
Activating mutations in the extracellular domain of the fibroblast growth factor receptor 2 function by disruption of the disulfide bond in the third immunoglobulin-like domain.
    Proceedings of the National Academy of Sciences of the United States of America, 1998, Apr-14, Volume: 95, Issue:8

    Topics: Amino Acid Sequence; Animals; COS Cells; Craniofacial Dysostosis; Cysteine; Dimerization; Disulfides; Humans; Immunoglobulins; Models, Molecular; Molecular Sequence Data; Musculoskeletal Abnormalities; Point Mutation; Protein Structure, Secondary; Receptor Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 2; Receptors, Fibroblast Growth Factor; Recombinant Fusion Proteins; Recombinant Proteins; Transfection

1998