Query author contributions in Reactome

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Details on Person Pennacchio, LA

Class:Id	Person:174810
_displayName	Pennacchio, LA
_timestamp	2006-02-20 17:48:49
created	[InstanceEdit:174717] D'Eustachio, P, 2006-02-20 17:46:54
firstname	Len A
initial	LA
surname	Pennacchio
(author)	[LiteratureReference:174821] Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment [LiteratureReference:444324] Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy [LiteratureReference:9607285] The liver X receptor ligand T0901317 down-regulates APOA5 gene expression through activation of SREBP-1c [LiteratureReference:9660412] Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair
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No pathways have been reviewed or authored by Pennacchio, LA (174810)