benzamidine has been researched along with Netherton Syndrome in 1 studies
benzamidine: RN given refers to parent cpd
benzamidine : A carboxamidine that is benzene carrying an amidino group.
Netherton Syndrome: Rare autosomal recessive disease with variable expressions. Clinical features of the disease include variable ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; bamboo hair (trichorrhexis invaginata); and ATOPIC DERMATITIS. The disease is caused by mutations in the SPINK5 gene.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Walker, AL | 1 |
| Denis, A | 1 |
| Bingham, RP | 1 |
| Bouillot, A | 1 |
| Edgar, EV | 1 |
| Ferrie, A | 1 |
| Holmes, DS | 1 |
| Laroze, A | 1 |
| Liddle, J | 1 |
| Fouchet, MH | 1 |
| Moquette, A | 1 |
| Nassau, P | 1 |
| Pearce, AC | 1 |
| Polyakova, O | 1 |
| Smith, KJ | 1 |
| Thomas, P | 1 |
| Thorpe, JH | 1 |
| Trottet, L | 1 |
| Wang, Y | 1 |
| Hovnanian, A | 1 |
1 other study available for benzamidine and Netherton Syndrome
| Article | Year |
|---|---|
Design and development of a series of borocycles as selective, covalent kallikrein 5 inhibitors.
Topics: Amino Acid Sequence; Benzamidines; Binding Sites; Drug Evaluation, Preclinical; Humans; Isomerism; K | 2019 |