arginine and Abnormalities, Skin

arginine has been researched along with Abnormalities, Skin in 2 studies

Research

Studies (2)

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

Authors

AuthorsStudies
Arveiler, B; Bessis, D; Boralevi, F; Lasseaux, E; Leauté-Labrèze, C; Michaud, V; Morice-Picard, F; Plaisant, C; Rezvani, HR; Taieb, A; Trimouille, A1
Kanzaki, T; Mori, M; Murakami, T; Noda, T; Saheki, T; Shimada, T; Takiguchi, M; Tashiro, M; Yamamura, K1

Other Studies

2 other study(ies) available for arginine and Abnormalities, Skin

ArticleYear
Hereditary Mucoepithelial Dysplasia Results from Heterozygous Variants at p.Arg557 Mutational Hotspot in SREBF1, Encoding a Transcription Factor Involved in Cholesterol Homeostasis.
    The Journal of investigative dermatology, 2020, Volume: 140, Issue:6

    Topics: Alopecia; Arginine; Cholesterol; DNA Mutational Analysis; Female; Heterozygote; Humans; Keratosis; Lipid Metabolism; Male; Mucous Membrane; Mutation; Pedigree; Polymorphism, Single Nucleotide; Skin; Skin Abnormalities; Sterol Regulatory Element Binding Protein 1

2020
Normalization of hair growth in sparse fur-abnormal skin and hair (SPF-ASH) mice by introduction of the rat ornithine transcarbamylase (OTC) gene.
    Journal of dermatological science, 1994, Volume: 7 Suppl

    Topics: Animals; Arginine; Citrulline; Crosses, Genetic; Disease Models, Animal; Female; Genetic Linkage; Hair; Intestine, Small; Liver; Male; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Mice, Transgenic; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid; Phenotype; Rats; Skin Abnormalities; X Chromosome

1994