tetraethyleneglycol dimethacrylate and Skin Diseases

tetraethyleneglycol dimethacrylate has been researched along with Skin Diseases in 13 studies

Research

Studies (13)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (15.38)	29.6817
2010's	11 (84.62)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Franzke, CW; Kiritsi, D; Pampalakis, G; Sotiropoulou, G; Valari, M; Zingkou, E	1
Baty, D; Browne, F; Greenblatt, DT; Has, C; Kowalewski, C; Liu, L; McGrath, JA; Mellerio, JE; Morton, J; Moss, C; Nesteruk, D; Ozoemena, L; Szczecinska, W; Terron-Kwiatkowski, A; Wertheim-Tysarowska, K; Woźniak, K	1
Azzouzi, S; Benchat, L; Mernissi, FZ; Mikou, O; Soughi, M	1
Bruckner-Tuderman, L; Has, C; Kiritsi, D; Mileounis, K; Valari, M	1
Álvarez-Cuesta, CC; Bueno, E; Cañueto, J; González-Sarmiento, R; Gonzalvo-Rodríguez, P; Rodríguez-Diaz, E; Vicente-Díaz, MA	1
Cassidy, AJ; Jonkman, MF; McGrath, JA; McLean, WH; Nanda, A; Nellen, RG; Sprecher, E; van der Velden, JJ; van Geel, M; van Steensel, MA	1
Campos Dominguez, M; Parra Blanco, V; Ruiz Rivero, J; Suárez Fernández, R	1
Ammar, D; El Fekih, N; Fazaa, B; Fischer, J; Jaafoura, H; Kamoun, MR; Kharfi, M; Schwonbeck, S; van Steensel, MA	1
Bruckner-Tuderman, L; Cosgarea, I; Franzke, CW; Has, C; Kiritsi, D; Kohlhase, J; Oji, V; Schumann, H	1
Bowden, PE	1
Hamm, H; Jonkman, MF; McLean, WH; Steijlen, PM; van der Velden, JJ; van Geel, M; van Steensel, MA	1
Aho, H; Bruckner-Tuderman, L; Cobzaru, C; Faletra, F; Has, C; Kern, JS; Kiritsi, D; Mäkelä, L; Pigors, M; Schwieger-Briel, A; Suárez, J	1
Candi, E; Cassidy, AJ; McLean, WH; Melino, G; Morley, SM; Steijlen, PM; Terrinoni, A; van der Velden, J; van Geel, M; van Steensel, MA	1

Reviews

2 review(s) available for tetraethyleneglycol dimethacrylate and Skin Diseases

Article	Year
'Double trouble': diagnostic challenges in genetic skin disorders. The British journal of dermatology, 2015, Volume: 172, Issue:1 Topics: Anodontia; Breast; Child; Dermatitis, Exfoliative; Ectodermal Dysplasia; Female; Heterozygote; Humans; Lacrimal Duct Obstruction; Limb Deformities, Congenital; Male; Mutation; Nails, Malformed; Pigmentation Disorders; Skin Diseases; Transcription Factors; Transglutaminases; Tumor Suppressor Proteins	2015
Acral Peeling Skin Syndrome: A Case Report and Literature Review. Actas dermo-sifiliograficas, 2016, Volume: 107, Issue:8 Topics: Biopsy; Child, Preschool; Foot Dermatoses; Genes, Dominant; Hand Dermatoses; Homozygote; Humans; Male; Mutation, Missense; Skin; Skin Diseases; Transglutaminases	2016

Article

Year

'Double trouble': diagnostic challenges in genetic skin disorders.

The British journal of dermatology, 2015, Volume: 172, Issue:1

Topics: Anodontia; Breast; Child; Dermatitis, Exfoliative; Ectodermal Dysplasia; Female; Heterozygote; Humans; Lacrimal Duct Obstruction; Limb Deformities, Congenital; Male; Mutation; Nails, Malformed; Pigmentation Disorders; Skin Diseases; Transcription Factors; Transglutaminases; Tumor Suppressor Proteins

2015

Acral Peeling Skin Syndrome: A Case Report and Literature Review.

Actas dermo-sifiliograficas, 2016, Volume: 107, Issue:8

Topics: Biopsy; Child, Preschool; Foot Dermatoses; Genes, Dominant; Hand Dermatoses; Homozygote; Humans; Male; Mutation, Missense; Skin; Skin Diseases; Transglutaminases

2016

Other Studies

11 other study(ies) available for tetraethyleneglycol dimethacrylate and Skin Diseases

Article	Year
Enhanced Proteolytic Activities in Acral Peeling Skin Syndrome: A Role of Transglutaminase 5 in Epidermal Homeostasis. The Journal of investigative dermatology, 2017, Volume: 137, Issue:8 Topics: Epidermis; Homeostasis; Humans; Proteolysis; Skin Diseases; Transglutaminases	2017
Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations. The British journal of dermatology, 2014, Volume: 171, Issue:5 Topics: Child; Dermatitis, Exfoliative; Diagnosis, Differential; Epidermolysis Bullosa Simplex; Founder Effect; Genetic Testing; Germany; Heterozygote; Homozygote; Humans; Keratin-14; Keratin-5; Mutation; Pigmentation Disorders; Poland; Skin Diseases; Transglutaminases; United Kingdom	2014
[Acral peeling skin syndrome]. Annales de dermatologie et de venereologie, 2014, Volume: 141, Issue:4 Topics: Administration, Cutaneous; Biomarkers; Child; Child, Preschool; Dermatitis, Exfoliative; Education, Medical, Continuing; Emollients; Female; Foot; Hand; Humans; Hyperhidrosis; Male; Mutation; Pigmentation Disorders; Siblings; Skin Diseases; Transglutaminases	2014
Acral peeling skin syndrome resulting from mutations in TGM5. Journal of the European Academy of Dermatology and Venereology : JEADV, 2016, Volume: 30, Issue:3 Topics: Biopsy; Child, Preschool; DNA; DNA Mutational Analysis; Female; Humans; Male; Mutation, Missense; Skin; Skin Diseases; Transglutaminases	2016
Novel TGM5 mutations in acral peeling skin syndrome. Experimental dermatology, 2015, Volume: 24, Issue:4 Topics: Alternative Splicing; Amino Acid Sequence; Amino Acid Substitution; Cells, Cultured; Child; Child, Preschool; DNA Mutational Analysis; Europe; Female; HEK293 Cells; Humans; INDEL Mutation; Infant; Kuwait; Male; Molecular Sequence Data; Mutant Proteins; Mutation; Mutation, Missense; Netherlands; Recombinant Proteins; Sequence Homology, Amino Acid; Skin Diseases; Transfection; Transglutaminases	2015
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: genetic defects in late terminal differentiation of the epidermis. The Journal of investigative dermatology, 2011, Volume: 131, Issue:3 Topics: Dermatitis, Exfoliative; Diagnosis, Differential; Glycoproteins; Humans; Intercellular Signaling Peptides and Proteins; Mutation, Missense; Pigmentation Disorders; Skin Diseases; Transglutaminases	2011
A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome. Journal of dermatological science, 2012, Volume: 65, Issue:1 Topics: Dermatitis, Exfoliative; DNA Mutational Analysis; Europe; Family Health; Haplotypes; Homozygote; Humans; Models, Genetic; Mutation; Pigmentation Disorders; Skin Diseases; Skin Diseases, Vesiculobullous; Transglutaminases	2012
TGM5 mutations impact epidermal differentiation in acral peeling skin syndrome. The Journal of investigative dermatology, 2012, Volume: 132, Issue:10 Topics: Adult; Biopsy; Case-Control Studies; Cell Differentiation; Cells, Cultured; Child; Child, Preschool; Dermatitis, Exfoliative; Epidermis; Glycoproteins; Humans; Infant; Intercellular Signaling Peptides and Proteins; Keratin-1; Keratin-10; Keratinocytes; Mutation; Pigmentation Disorders; Protein Precursors; Skin Diseases; Transglutaminases	2012
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