lysine has been researched along with Hair Diseases in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bickers, DR; Christiano, AM; Djabali, K; Garzon, MC; Lalin, T; Longley, BJ; Panteleyev, AA; Zlotogorski, A | 1 |
| Christiano, AM; Djabali, K; Green, J; Horev, L; Ingber, A; Martinez-Mir, A; Sinclair, R; Zlotogorski, A | 1 |
| Krieg, T; Labrèze, C; Langbein, L; Leigh, IM; Rogers, MA; Roul, S; Schweizer, J; Stevens, HP; Taieb, A; Winter, H | 1 |
| Chapalain, V; Labrèze, C; Mercier, M; Rogers, MA; Schweizer, J; Surlève-Bazeille, JE; Taieb, A; Winter, H | 1 |
4 other study(ies) available for lysine and Hair Diseases
| Article | Year |
|---|---|
Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix.
Topics: Colombia; DNA Mutational Analysis; Female; Glutamic Acid; Hair Diseases; Humans; Keratins; Lysine; Male; Mutation, Missense; Pedigree; Russia | 2003 |
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 |
Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix.
Topics: Adolescent; Child; Female; Glutamic Acid; Hair Diseases; Heterozygote; Humans; Keratins; Lysine; Male; Middle Aged; Mutation; Pedigree | 1997 |
A variable monilethrix phenotype associated with a novel mutation, Glu402Lys, in the helix termination motif of the type II hair keratin hHb1.
Topics: Adult; Child, Preschool; Female; Glutamic Acid; Hair Diseases; Humans; Keratins; Lysine; Phenotype; Point Mutation | 1998 |