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FA2H gene

Known as: FATTY ACID HYDROXYLASE DOMAIN-CONTAINING PROTEIN 1, FAAH, FAH1 
National Institutes of Health

Papers overview

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2018
2018
Insulation by myelin lipids is essential to fast action potential conductivity: changes in their quality or amount can cause… 
2014
2014
To the Editor : Fatty acid hydroxylase-associated neurodegeneration (FAHN) is caused by mutations in FA2H (OMIM 612319) and… 
Review
2014
Review
2014
We demonstrate CRISPR-Cas9–mediated correction of a Fah mutation in hepatocytes in a mouse model of the human disease hereditary… 
2013
2013
Hereditary spastic paraplegias and related genetically heterogeneous disorders may be difficult to distinguish clinically. The… 
2013
2013
To investigate gene(s) being regulated by ∆(9)-tetrahydrocannabinol (∆(9)-THC), we performed DNA microarray analysis of human… 
2013
2013
Haplotype information could lead to more powerful tests of genetic association than single‐locus analyses but it is not easy to… 
2010
2010
BackgroundHepatic stellate cells (HSC) are involved in hepatic fibrogenesis. Cell signaling associated with an insult to the… 
Highly Cited
2001
Highly Cited
2001
The chemical structures and accumulation kinetics of several major soluble as well as wall-bound, alkali-hydrolyzable compounds… 
Highly Cited
1997
Highly Cited
1997
A search of the Saccharomyces cerevisiae genome data base for cytochromeb 5-like sequences identified a 1.152-kilobase pair open…