Page last updated: 2024-09-05

biotin and Genetic Skin Diseases

biotin has been researched along with Genetic Skin Diseases in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Anand, A; Chatterjee, A; Hiremagalore, R; Mani, RS; Pandey, N; Rajashekhar, B; Tharakan, A; Xavier, DF	1
Dobrowolski, R; Kretz, M; Markopoulos, C; Schnichels, M; Schwarz, G; Willecke, K; Winterhager, E; Wörsdörfer, P	1

Other Studies

2 other study(ies) available for biotin and Genetic Skin Diseases

Article	Year
Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma. Annals of human genetics, 2016, Volume: 80, Issue:1 Topics: Biotin; Connexin 30; Connexins; DNA Mutational Analysis; Female; Genetic Linkage; Hearing Loss, Sensorineural; Humans; Ichthyosis; Keratoderma, Palmoplantar, Diffuse; Male; Pedigree; Phenotype; Skin Diseases, Genetic	2016
The connexin31 F137L mutant mouse as a model for the human skin disease erythrokeratodermia variabilis (EKV). Human molecular genetics, 2007, May-15, Volume: 16, Issue:10 Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Base Sequence; Biotin; Connexin 26; Connexin 43; Connexins; Disease Models, Animal; DNA Primers; HeLa Cells; Humans; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Mice, Transgenic; Molecular Sequence Data; Point Mutation; Recombinant Proteins; Sequence Homology, Amino Acid; Skin Diseases, Genetic; Transfection	2007

Article

Year

Functional Analysis of a Novel Connexin30 Mutation in a Large Family with Hearing Loss, Pesplanus, Ichthyosis, Cutaneous Nodules, and Keratoderma.

Annals of human genetics, 2016, Volume: 80, Issue:1

Topics: Biotin; Connexin 30; Connexins; DNA Mutational Analysis; Female; Genetic Linkage; Hearing Loss, Sensorineural; Humans; Ichthyosis; Keratoderma, Palmoplantar, Diffuse; Male; Pedigree; Phenotype; Skin Diseases, Genetic

2016

The connexin31 F137L mutant mouse as a model for the human skin disease erythrokeratodermia variabilis (EKV).

Human molecular genetics, 2007, May-15, Volume: 16, Issue:10

Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Base Sequence; Biotin; Connexin 26; Connexin 43; Connexins; Disease Models, Animal; DNA Primers; HeLa Cells; Humans; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Mice, Transgenic; Molecular Sequence Data; Point Mutation; Recombinant Proteins; Sequence Homology, Amino Acid; Skin Diseases, Genetic; Transfection

2007