myristic acid has been researched along with Familial Turner Syndrome in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Anichini, C; Bartholdi, D; Bazzicalupo, P; Cardinale, A; Cecchetti, S; Cordeddu, V; Dallapiccola, B; Di Schiavi, E; Digilio, MC; Ferrero, GB; Flex, E; Fodale, V; Gelb, BD; Iyengar, R; Kutsche, K; Lepri, F; Lipzen, A; Ma'ayan, A; Martin, J; Martinelli, S; Mazzanti, L; Merlo, D; Pennacchio, LA; Rossi, C; Sarkozy, A; Schackwitz, W; Selicorni, A; Tartaglia, M; Tenconi, R; Zampino, G; Zenker, M | 1 |
1 other study(ies) available for myristic acid and Familial Turner Syndrome
Article | Year |
---|---|
Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair.
Topics: Actins; Cell Nucleus; Cytoskeleton; Fluorescent Antibody Technique, Indirect; Fluorescent Dyes; Germ-Line Mutation; Hair; Humans; Indoles; Intracellular Signaling Peptides and Proteins; Mutation; Mutation, Missense; Myristic Acid; Noonan Syndrome | 2009 |