Compounds > cysteine

cysteine and Cutis Elastica

cysteine has been researched along with Cutis Elastica in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (37.50)18.2507
2000's5 (62.50)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cabral, WA; Fertala, A; Keene, DR; Leikin, S; Letocha, AD; Makareeva, E; Marini, JC; Persikov, AV; Scribanu, N; Steplewski, A1
Coucke, P; De Backer, J; De Paepe, A; Hermanns-Lê, T; Lapière, CM; Malfait, F; Sakalihasan, N; Symoens, S1
Hermanns-Lê, T; Piérard, GE1
Bächinger, HP; Davis, JM1
Anton-Lamprecht, I; De Paepe, A; Hausser, I; Naeyaert, JM; Nuytinck, L1
Cole, WG1
Allen, JD; Murad, S; Overstreet, MA; Thai, SF; Walker, LC; Yeowell, HN1
De Paepe, A; Freund, M; Hermanns-Le, T; Lagae, L; Nuytinck, L; Pierard, GE1

Other Studies

8 other study(ies) available for cysteine and Cutis Elastica

ArticleYear
Y-position cysteine substitution in type I collagen (alpha1(I) R888C/p.R1066C) is associated with osteogenesis imperfecta/Ehlers-Danlos syndrome phenotype.
    Human mutation, 2007, Volume: 28, Issue:4

    Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Cells, Cultured; Child; Collagen Type I; Cysteine; Dimerization; Ehlers-Danlos Syndrome; Humans; Infant; Male; Microscopy, Electron, Transmission; Mutation, Missense; Osteogenesis Imperfecta; Pedigree; Phenotype; Protein Structure, Tertiary; Sequence Analysis, Protein

2007
Three arginine to cysteine substitutions in the pro-alpha (I)-collagen chain cause Ehlers-Danlos syndrome with a propensity to arterial rupture in early adulthood.
    Human mutation, 2007, Volume: 28, Issue:4

    Topics: Adolescent; Adult; Amino Acid Substitution; Arginine; Base Sequence; Bone Diseases, Metabolic; Collagen; Collagen Type I; Collagen Type I, alpha 1 Chain; Collagen Type III; Cysteine; Ehlers-Danlos Syndrome; Female; Femoral Artery; Humans; Iliac Artery; Male; Molecular Sequence Data; Mutation, Missense; Protein Structure, Secondary; RNA, Messenger; Rupture, Spontaneous

2007
Multifaceted dermal ultrastructural clues for Ehlers-Danlos syndrome with arterial rupture and type I collagen R-to-C substitution.
    The American Journal of dermatopathology, 2007, Volume: 29, Issue:5

    Topics: Adult; Aneurysm, Ruptured; Aortic Dissection; Arginine; Biopsy; Collagen Type I; Cysteine; Ehlers-Danlos Syndrome; Humans; Skin

2007
Hysteresis in the triple helix-coil transition of type III collagen.
    The Journal of biological chemistry, 1993, Dec-05, Volume: 268, Issue:34

    Topics: Amino Acid Sequence; Animals; Calorimetry, Differential Scanning; Cattle; Cells, Cultured; Collagen; Cysteine; Ehlers-Danlos Syndrome; Fetus; Fibroblasts; Guanidine; Guanidines; Humans; Kinetics; Methionine; Molecular Sequence Data; Proline; Protein Denaturation; Protein Folding; Skin; Sulfur Radioisotopes; Thermodynamics; Tritium

1993
Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and II.
    American journal of human genetics, 1997, Volume: 60, Issue:3

    Topics: Adolescent; Adult; Amino Acid Sequence; Animals; Cells, Cultured; Collagen; Conserved Sequence; Cysteine; Ehlers-Danlos Syndrome; Female; Genetic Linkage; Humans; Male; Molecular Sequence Data; Mutation; Pedigree; Procollagen; Serine; Skin

1997
The Nicholas Andry Award-1996. The molecular pathology of osteogenesis imperfecta.
    Clinical orthopaedics and related research, 1997, Issue:343

    Topics: 3T3 Cells; Animals; Arginine; Awards and Prizes; Bone and Bones; Cells, Cultured; Child; Collagen; Cysteine; Ehlers-Danlos Syndrome; Extracellular Matrix; Extracellular Matrix Proteins; Fibroblasts; Genotype; Glycine; Humans; Infant; Mice; Mice, Transgenic; Molecular Biology; Mutation; Osteogenesis Imperfecta; Phenotype; Point Mutation; Procollagen; Radiography; RNA; Skin

1997
Deletion of cysteine 369 in lysyl hydroxylase 1 eliminates enzyme activity and causes Ehlers-Danlos syndrome type VI.
    Matrix biology : journal of the International Society for Matrix Biology, 2000, Volume: 19, Issue:1

    Topics: Alleles; Cells, Cultured; Cysteine; Ehlers-Danlos Syndrome; Heterozygote; Humans; Mutagenesis, Site-Directed; Oxidation-Reduction; Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase; Protein Denaturation; Sequence Deletion

2000
Classical Ehlers-Danlos syndrome caused by a mutation in type I collagen.
    American journal of human genetics, 2000, Volume: 66, Issue:4

    Topics: Amino Acid Motifs; Amino Acid Sequence; Amino Acid Substitution; Arginine; Base Sequence; Child; Child, Preschool; Collagen; Cysteine; Dimerization; Disulfides; DNA Mutational Analysis; Ehlers-Danlos Syndrome; Exons; Female; Fibroblasts; Genetic Heterogeneity; Humans; Male; Mutation; Polymorphism, Single-Stranded Conformational

2000