Page last updated: 2024-08-18

tetraethyleneglycol dimethacrylate and Syndrome

tetraethyleneglycol dimethacrylate has been researched along with Syndrome in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (40.00)29.6817
2010's3 (60.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ammar, D; El Fekih, N; Fazaa, B; Fischer, J; Jaafoura, H; Kamoun, MR; Kharfi, M; Schwonbeck, S; van Steensel, MA1
Bruckner-Tuderman, L; Cosgarea, I; Franzke, CW; Has, C; Kiritsi, D; Kohlhase, J; Oji, V; Schumann, H1
Ammar, D; El Fekih, N; Ezzine, N; Fazaa, B; Jaafoura, H; Kamoun, MR; Khaled, A; Kharfi, M1
Garg, K; Mishra, D; Singh, D1
Candi, E; Cassidy, AJ; McLean, WH; Melino, G; Morley, SM; Steijlen, PM; Terrinoni, A; van der Velden, J; van Geel, M; van Steensel, MA1

Reviews

1 review(s) available for tetraethyleneglycol dimethacrylate and Syndrome

ArticleYear
Generalized peeling skin syndrome: Case report and review of the literature.
    Dermatology online journal, 2010, Mar-15, Volume: 16, Issue:3

    Topics: Adult; Consanguinity; Female; Humans; Ichthyosis; Syndrome; Transglutaminases

2010

Other Studies

4 other study(ies) available for tetraethyleneglycol dimethacrylate and Syndrome

ArticleYear
A missense mutation in TGM5 causes acral peeling skin syndrome in a Tunisian family.
    The Journal of investigative dermatology, 2009, Volume: 129, Issue:10

    Topics: Child, Preschool; Genetic Predisposition to Disease; Humans; Male; Mutation, Missense; Skin Diseases; Syndrome; Transglutaminases; Tunisia

2009
Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals.
    The Journal of investigative dermatology, 2010, Volume: 130, Issue:6

    Topics: Adolescent; Adult; Blister; Case-Control Studies; Child; Child, Preschool; Diagnosis, Differential; Epidermolysis Bullosa; Erythema; Humans; Infant; Infant, Newborn; Mutation, Missense; Skin; Skin Aging; Skin Diseases; Syndrome; Transglutaminases; Young Adult

2010
Peeling skin syndrome: Current status.
    Dermatology online journal, 2010, Mar-15, Volume: 16, Issue:3

    Topics: Child; Female; Homozygote; Humans; Hyperkeratosis, Epidermolytic; Hypoproteinemia; Immunoglobulin E; Mutation, Missense; Syndrome; Transglutaminases

2010
A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome.
    American journal of human genetics, 2005, Volume: 77, Issue:6

    Topics: Binding Sites; Catalytic Domain; Cell Line; Chromosome Mapping; Consanguinity; Cross Reactions; DNA Mutational Analysis; Epidermis; Female; Genes, Recessive; Genetic Linkage; Genetic Markers; Genetic Vectors; Haplotypes; Homozygote; Humans; Male; Microsatellite Repeats; Models, Molecular; Molecular Sequence Data; Mutation, Missense; Pedigree; Protein Structure, Secondary; Protein Structure, Tertiary; Sequence Analysis, DNA; Skin Diseases; Syndrome; Transglutaminases

2005