Compounds > cysteine

cysteine and Hyperkeratosis Palmaris et Plantaris

cysteine has been researched along with Hyperkeratosis Palmaris et Plantaris in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's2 (50.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ben Khalifa, Y; Bollen, M; Bonnard, C; Boussofara, L; Chourabi, M; Common, JE; Dai, L; Denguezli, M; Denil, S; Foo, JN; H'mida-Ben Brahim, D; Liew, MS; Lim, S; Liu, J; Mamaï, O; Reversade, B; Robinson, KS; Saad, A; Sriha, B; Wong, PM1
Audebert, S; Bouadjar, B; Cure, S; Fischer, J; Has, C; Hohl, D; Jobard, F; Lefèvre, C; Marrakchi, S; Morlot, S; Munro, C; Prud'homme, JF; Turki, H; Zahaf, A1
Kang, HJ; Lee, ES; Lee, JH; Lee, S; Park, KB; Son, IY; Steinert, PM; Yang, JM; Yeo, UC1
Cleaver, JE; Gardner, RJ; McDowell, M; Savarirayan, R; Sinclair, RD1

Other Studies

4 other study(ies) available for cysteine and Hyperkeratosis Palmaris et Plantaris

ArticleYear
ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis.
    The Journal of investigative dermatology, 2018, Volume: 138, Issue:2

    Topics: Biopsy; Cysteine; DNA Mutational Analysis; Exome Sequencing; Female; Fibroblasts; Germ-Line Mutation; HEK293 Cells; Homozygote; Humans; Hypopigmentation; Keratinocytes; Keratoderma, Palmoplantar; Male; Melanins; Melanocytes; Pedigree; Phosphoric Diester Hydrolases; Primary Cell Culture; Pyrophosphatases; Severity of Illness Index; Skin

2018
Novel mutations in the gene encoding secreted lymphocyte antigen-6/urokinase-type plasminogen activator receptor-related protein-1 (SLURP-1) and description of five ancestral haplotypes in patients with Mal de Meleda.
    The Journal of investigative dermatology, 2003, Volume: 120, Issue:3

    Topics: Aged; Antigens, Ly; Base Sequence; Conserved Sequence; Cysteine; Female; Founder Effect; Haplotypes; Heterozygote; Homozygote; Humans; Infant; Infant, Newborn; Keratoderma, Palmoplantar; Male; Molecular Sequence Data; Mutation; Pedigree; Protein Sorting Signals; Tyrosine; Urokinase-Type Plasminogen Activator

2003
Mutations in the 1A rod domain segment of the keratin 9 gene in epidermolytic palmoplantar keratoderma.
    Acta dermato-venereologica, 1998, Volume: 78, Issue:6

    Topics: Arginine; Base Sequence; Child, Preschool; Conserved Sequence; Cysteine; Epidermolysis Bullosa Simplex; Female; Genes, Dominant; Genes, Recessive; Glutamic Acid; Humans; Keratins; Keratoderma, Palmoplantar; Korea; Male; Microscopy, Electron; Pedigree; Point Mutation; Polymerase Chain Reaction; Sequence Analysis, DNA; Tryptophan

1998
Rough skin, brittle hair, and photosensitivity: a mild phenotypic variant of trichothiodystrophy.
    Journal of medical genetics, 2000, Volume: 37, Issue:4

    Topics: Abnormalities, Multiple; Alleles; Child, Preschool; Cysteine; DNA Helicases; DNA-Binding Proteins; Drosophila Proteins; Female; Hair; Humans; Keratoderma, Palmoplantar; Mutation; Photosensitivity Disorders; Proteins; Skin Abnormalities; Transcription Factors; Xeroderma Pigmentosum Group D Protein

2000