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Journal of Immunology (Baltimore, Md. : 1950)|August 20, 2013
Contributions of the three CYP1 monooxygenases to pro-inflammatory and inflammation-resolution lipid mediator pathwaysSenad Divanovic, Jesmond Dalli, Lucia F Jorge-Nebert, et al.Biorxiv : the Preprint Server for Biology|July 3, 2023
Endocrine pancreas-specific Gclc gene deletion causes a severe diabetes phenotypeEmily A Davidson, Ying Chen, Surendra Singh, et al.Pharmacogenetics and Genomics|April 13, 2006
Search for an association between the human CYP1A2 genotype and CYP1A2 metabolic phenotypeZhengwen Jiang, Nadine Dragin, Lucia F Jorge-Nebert, et al.Journal of Lipid Research|August 5, 2004
Revised nomenclature for the mammalian long-chain acyl-CoA synthetase gene familyDouglas G Mashek, Karin E Bornfeldt, Rosalind A Coleman, et al.American Journal of Human Genetics|December 7, 2015
SLC39A8 Deficiency: A Disorder of Manganese Transport and GlycosylationJulien H Park, Max Hogrebe, Marianne Grüneberg, et al.American Journal of Human Genetics|December 7, 2015
Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8Kym M Boycott, Chandree L Beaulieu, Kristin D Kernohan, et al.Nature|September 24, 2005
DNA sequence and analysis of human chromosome 18Chad Nusbaum, Michael C Zody, Mark L Borowsky, et al.Pageof 16