lysine has been researched along with Bullous Congenital Ichthyosiform Erythroderma in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Christiano, AM; Djabali, K; Green, J; Horev, L; Ingber, A; Martinez-Mir, A; Sinclair, R; Zlotogorski, A | 1 |
| Berbis, P; Calvas, P; Chassaing, N; Claudy, A; Cordier-Alex, MP; Hovnanian, A; Kanitakis, J; Sportich, S; Titeux, M | 1 |
| Choi, GS; Jung, SY; Kang, HJ; Lee, ES; Park, KB; Steinert, PM; Yang, JM; Yoneda, K | 1 |
3 other study(ies) available for lysine and Bullous Congenital Ichthyosiform Erythroderma
| Article | Year |
|---|---|
De novo mutations in monilethrix.
Topics: Amino Acid Motifs; DNA Mutational Analysis; Exons; Genotype; Hair Diseases; Heterozygote; Homozygote; Humans; Hyperkeratosis, Epidermolytic; Keratins; Lysine; Microsatellite Repeats; Mutation; Pedigree; Phenotype; Protein Structure, Tertiary; Sequence Analysis, DNA | 2003 |
Generalized epidermolytic hyperkeratosis in two unrelated children from parents with localized linear form, and prenatal diagnosis.
Topics: Adult; DNA Mutational Analysis; Female; Glutamic Acid; Humans; Hyperkeratosis, Epidermolytic; Infant, Newborn; Isoleucine; Keratin-1; Keratin-10; Lysine; Mutation; Phenylalanine; Prenatal Diagnosis; Skin | 2006 |
A glutamate to lysine mutation at the end of 2B rod domain of keratin 2e gene in ichthyosis bullosa of Siemens.
Topics: Amino Acid Substitution; Base Sequence; Child, Preschool; Codon; Conserved Sequence; Epidermis; Exons; Glutamic Acid; Humans; Hyperkeratosis, Epidermolytic; Ichthyosis; Keratin-2; Keratins; Lysine; Male; Microscopy, Electron; Point Mutation; Polymerase Chain Reaction; Sequence Analysis, DNA | 1998 |