Related Experiment Videos
Fine-scale mapping of CYP gene clusters: an example from human CYP4 family
Susan M G Hoffman1, Diane S Keeney
1Department of Zoology, Miami University, Oxford, Ohio 45056, USA.
Methods in Enzymology
|November 12, 2002
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
The importance of the lipoxygenase-hepoxilin pathway in the mammalian epidermal barrier.
Biochimica et biophysica acta·2013
Gene regulation of CYP4F11 in human keratinocyte HaCaT cells.
Drug metabolism and disposition: the biological fate of chemicals·2009
20-Hydroxylation is the CYP-dependent and retinoid-inducible leukotriene B4 inactivation pathway in human and mouse skin cells.
Archives of biochemistry and biophysics·2009
Inflammation resolved by retinoid X receptor-mediated inactivation of leukotriene signaling pathways.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2007
Mechanistic insights on HDAC6 ZnF UBP-Tau interaction through biophysical and computational approaches.
Methods in enzymology·2026
Methodological approach to investigate peroxiredoxin 1 deacetylation by histone deacetylase 6.
Methods in enzymology·2026
Protocols for in vitro analysis of liquid-liquid phase separation of proteins.
Methods in enzymology·2026
Experimental approaches to study histone deacetylation in Caenorhabditis elegans.
Methods in enzymology·2026
Histone deacetylases: From acetylation homeostasis to oncogenic and neurodegenerative disorders.
Methods in enzymology·2026
[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].
Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences·2026
Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.
Biology of sex differences·2026
Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.
Journal of assisted reproduction and genetics·2026
Monoallelic loss-of-function variants in ZNF536 are associated with a neurodevelopmental disorder with prominent behavioral features.
American journal of human genetics·2026