arginine has been researched along with EBS-DM in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Farrar, GJ; Humphries, MM; Humphries, P; Jordan, SA; Kenna, PF; Kumar-Singh, R; Mansergh, FC; Sheils, DM; Young, M | 1 |
| Kang, HJ; Lee, ES; Lee, JH; Lee, S; Park, KB; Son, IY; Steinert, PM; Yang, JM; Yeo, UC | 1 |
| Glass, I; Klingberg, S; Murrell, D; Premaratne, C; Wright, K | 1 |
3 other study(ies) available for arginine and EBS-DM
| Article | Year |
|---|---|
A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex.
Topics: Amino Acid Sequence; Arginine; Base Sequence; Chromosomes, Human, Pair 1; DNA; DNA Mutational Analysis; Epidermolysis Bullosa Simplex; Female; Genes, Dominant; Genetic Linkage; Humans; Keratins; Male; Methionine; Molecular Sequence Data; Pedigree; Point Mutation | 1993 |
Mutations in the 1A rod domain segment of the keratin 9 gene in epidermolytic palmoplantar keratoderma.
Topics: Arginine; Base Sequence; Child, Preschool; Conserved Sequence; Cysteine; Epidermolysis Bullosa Simplex; Female; Genes, Dominant; Genes, Recessive; Glutamic Acid; Humans; Keratins; Keratoderma, Palmoplantar; Korea; Male; Microscopy, Electron; Pedigree; Point Mutation; Polymerase Chain Reaction; Sequence Analysis, DNA; Tryptophan | 1998 |
Epidermolysis bullosa simplex Dowling-Meara due to an arginine to cysteine substitution in exon 1 of keratin 14.
Topics: Amino Acid Sequence; Arginine; Cysteine; Epidermolysis Bullosa Simplex; Exons; Female; Follow-Up Studies; Humans; Infant, Newborn; Keratin-14; Keratins; Male; Molecular Sequence Data; Mutation, Missense; Pedigree; Pregnancy; Prenatal Diagnosis; Severity of Illness Index; Skin | 2002 |