threonine 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 | 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 |
|---|---|
| Hasegawa, T; Kohroh, K; Matsuba, S; Mizuno, Y; Muramatsu, S; Ogawa, H; Suga, Y; Tsuchihashi, H; Yaguchi, H | 1 |
| Bang, HD; Kim, WS; Lee, ES; Lee, S; Steinert, PM; Yang, JM | 1 |
| Arin, MJ; Hohl, D; Huber, M; Küster, W; Longley, MA; Roop, DR; Rothnagel, JA | 1 |
3 other study(ies) available for threonine and Bullous Congenital Ichthyosiform Erythroderma
| Article | Year |
|---|---|
A novel threonine to proline mutation in the helix termination motif of keratin 1 in epidermolytic hyperkeratosis with severe palmoplantar hyperkeratosis and contractures of the digits.
Topics: Adult; Base Sequence; Contracture; Fingers; Humans; Hyperkeratosis, Epidermolytic; Keratins; Male; Mutation; Proline; Threonine | 2005 |
A novel threonine --> proline mutation at the end of 2B rod domain in the keratin 2e chain in ichthyosis bullosa of Siemens.
Topics: Biopsy; Exons; Humans; Hyperkeratosis, Epidermolytic; Ichthyosis; Keratins; Point Mutation; Proline; Protein Structure, Tertiary; Skin; Threonine | 1997 |
An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosis.
Topics: Amino Acid Sequence; Amino Acid Substitution; Asparagine; Base Sequence; Female; Follow-Up Studies; Humans; Hyperkeratosis, Epidermolytic; Infant, Newborn; Keratins; Male; Pedigree; Point Mutation; Threonine | 1999 |