asparagine has been researched along with Bullous Congenital Ichthyosiform Erythroderma in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Affolter, VK; Jagannathan, V; Kiener, S; Leeb, T; Nagle, T | 1 |
| Arin, MJ; Hohl, D; Huber, M; Küster, W; Longley, MA; Roop, DR; Rothnagel, JA | 1 |
2 other study(ies) available for asparagine and Bullous Congenital Ichthyosiform Erythroderma
| Article | Year |
|---|---|
A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosis.
Topics: Animals; Asparagine; China; Dogs; Humans; Hyperkeratosis, Epidermolytic; Ichthyosis; Infant; Keratin-1; Keratin-10; Keratins; Mutation | 2022 |
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 |