Page last updated: 2024-08-21

myristic acid and Familial Turner Syndrome

myristic acid has been researched along with Familial Turner Syndrome in 1 studies

Research

Studies (1)

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

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

Other Studies

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. Nature genetics, 2009, Volume: 41, Issue:9 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

Article

Year

Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair.

Nature genetics, 2009, Volume: 41, Issue:9

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