n-formylmethionine leucyl-phenylalanine has been researched along with Genetic Diseases 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 | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Arias, AA; Dinauer, MC; Kellner, JD; Lewis, DB; Li, XJ; Marchal, CC; Matute, JD; Meroueh, SO; Nauseef, WM; Steele, M; Stull, ND; Waterhouse, CC; Wright, NA; Wrobel, I; Yu, W | 1 |
| Boxer, LA; Kindzelskii, AL; Petty, HR; Todd, RF; Xue, W | 1 |
2 other study(ies) available for n-formylmethionine leucyl-phenylalanine and Genetic Diseases
| Article | Year |
|---|---|
A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40 phox and selective defects in neutrophil NADPH oxidase activity.
Topics: Adult; Amino Acid Substitution; Carcinogens; Cell Line, Tumor; Child; Codon, Terminator; DNA Mutational Analysis; Female; Genes, Recessive; Genetic Diseases, Inborn; Granulomatous Disease, Chronic; Heterozygote; Humans; Male; Mutation, Missense; N-Formylmethionine Leucyl-Phenylalanine; NADPH Oxidases; Neutrophils; Phagocytosis; Phorbol Esters; Phosphatidylinositol Phosphates; Superoxides | 2009 |
Aberrant capping of membrane proteins on neutrophils from patients with leukocyte adhesion deficiency.
Topics: Animals; Cell Adhesion; Genetic Diseases, Inborn; Humans; Macrophage-1 Antigen; Membrane Proteins; Mice; N-Formylmethionine Leucyl-Phenylalanine; Neutrophils; Receptors, IgG | 1994 |