Compounds > tyrosine

tyrosine and Anhidrotic Ectodermal Dysplasia

tyrosine has been researched along with Anhidrotic Ectodermal Dysplasia in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19902 (50.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Biedziak, B; Kobielak, A; Kobielak, K; Trzeciak, WH1
Agou, F; Chaffotte, A; Courtois, G; Israël, A; Sebban, H; Véron, M; Vinolo, E1
Gold, RJ; Tenenhouse, HS1
Gold, MB; Reynold, JM; Scriver, CR1

Other Studies

4 other study(ies) available for tyrosine and Anhidrotic Ectodermal Dysplasia

ArticleYear
A novel mutation A1270G of the EDA1 gene causing Tyr343Cys substitution in ectodysplasin-A in a family with anhidrotic ectodermal dysplasia.
    Acta biochimica Polonica, 2003, Volume: 50, Issue:1

    Topics: Adenine; Amino Acid Substitution; Base Sequence; Cysteine; Ectodermal Dysplasia; Ectodysplasins; Exons; Female; Guanine; Humans; Infant; Male; Membrane Proteins; Mutation, Missense; Pedigree; Tyrosine

2003
A point mutation in NEMO associated with anhidrotic ectodermal dysplasia with immunodeficiency pathology results in destabilization of the oligomer and reduces lipopolysaccharide- and tumor necrosis factor-mediated NF-kappa B activation.
    The Journal of biological chemistry, 2006, Mar-10, Volume: 281, Issue:10

    Topics: Amino Acid Sequence; Animals; Cell Line; Circular Dichroism; Ectodermal Dysplasia; Humans; I-kappa B Kinase; Immunologic Deficiency Syndromes; Lipopolysaccharides; Mice; Molecular Sequence Data; NF-kappa B; Point Mutation; Recombinant Proteins; Temperature; Tumor Necrosis Factor-alpha; Tyrosine; Zinc Fingers

2006
Loss of a homologous group of proteins in a dominantly inherited ectodermal malformation.
    The Biochemical journal, 1976, Oct-01, Volume: 159, Issue:1

    Topics: Amino Acids; Animals; Chromatography, Gel; Ectodermal Dysplasia; Electrophoresis, Polyacrylamide Gel; Genes; Glycine; Hair; Keratins; Mice; Mice, Inbred Strains; Molecular Weight; Mutation; Protein Deficiency; Proteins; Tyrosine

1976
The characterization of hereditary abnormalities of keratin: Clouston's ectodermal dysplasia.
    Birth defects original article series, 1971, Volume: 7, Issue:8

    Topics: Ectodermal Dysplasia; Genes, Dominant; Hair; Humans; Keratosis; Nails, Malformed; Phenylalanine; Proline; Serine; Sulfur; Tyrosine; Urea; Water

1971