asparagine has been researched along with bromochloroacetic acid in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (14.29) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 3 (42.86) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Merz, WG; Silva-Hutner, M; Weitzman, I | 1 |
| Arin, MJ; Hohl, D; Huber, M; Küster, W; Longley, MA; Roop, DR; Rothnagel, JA | 1 |
| Felix, DH; Lane, EB; McLean, WH; Melino, G; Munro, CS; Rugg, EL; Terrinoni, A | 1 |
| Feng, YG; Li, L; Ren, XR; Shi, YZ; Tan, SS; Wang, JM; Xiao, SX | 1 |
| Bowden, PE; Komel, R; Liovic, M; Marks, R | 1 |
| Singh, CJ | 1 |
| Affolter, VK; Jagannathan, V; Kiener, S; Leeb, T; Nagle, T | 1 |
7 other study(ies) available for asparagine and bromochloroacetic acid
| Article | Year |
|---|---|
Characterization and mating reactions of clinical isolates of Trychophyton mentagrophytes and T. rubrum which produce a diffusible brownish pigment.
Topics: Agar; Ascomycota; Asparagine; Conjugation, Genetic; Culture Media; Hair; Humans; Keratins; Phenylalanine; Pigments, Biological; Quinic Acid; Shikimic Acid; Stereoisomerism; Tinea; Trichophyton; Tyrosine; Urease | 1974 |
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 |
A novel mutation in the keratin 13 gene causing oral white sponge nevus.
Topics: Adenine; Adolescent; Asparagine; Chromosome Mapping; Chromosomes, Human, Pair 12; Chromosomes, Human, Pair 17; Codon; Epithelium; Exons; Genetic Linkage; Guanine; Hamartoma; Humans; Keratins; Leukoplakia, Oral; Male; Mouth Diseases; Mutation, Missense; Protein Structure, Tertiary; Scotland; Serine | 2001 |
A novel mutation in the second half of the keratin 17 1A domain in a large pedigree with delayed-onset pachyonychia congenita type 2.
Topics: Adenine; Age of Onset; Amino Acid Substitution; Asparagine; Aspartic Acid; Base Sequence; Codon; Female; Guanine; Heterozygote; Humans; Keratins; Male; Middle Aged; Mutation; Nail Diseases; Pedigree; Protein Structure, Tertiary | 2004 |
A mutation (N177S) in the structurally conserved helix initiation peptide motif of keratin 5 causes a mild EBS phenotype.
Topics: Adult; Amino Acid Motifs; Asparagine; Base Sequence; DNA; DNA Mutational Analysis; Epidermolysis Bullosa Simplex; Female; Heterozygote; Humans; Keratin-5; Keratins; Mutation, Missense; Pedigree; Phenotype; Polymerase Chain Reaction; Serine | 2004 |
Extracellular protease expression in Microsporum gypseum complex, its regulation and keratinolytic potential.
Topics: Asparagine; Catabolite Repression; Culture Media; Enzyme Inhibitors; Gelatin; Gene Expression Regulation, Enzymologic; Gene Expression Regulation, Fungal; Glucose; Keratins; Microsporum; Peptide Hydrolases; Soil Microbiology | 2011 |
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 |