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Human Molecular Genetics|August 14, 2003
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2Caroline Lefévre, Stéphanie Audebert, Florence Jobard, et al.Particle and Fibre Toxicology|September 14, 2010
Mechanisms of oxidative stress and alterations in gene expression by Libby six-mix in human mesothelial cellsJedd M Hillegass, Arti Shukla, Maximilian B MacPherson, et al.The Lancet. Public Health|January 27, 2018
The Zika Contraception Access Network: a feasibility programme to increase access to contraception in Puerto Rico during the 2016-17 Zika virus outbreakEva Lathrop, Lisa Romero, Stacey Hurst, et al.Particle and Fibre Toxicology|February 4, 2012
Differences in gene expression and cytokine production by crystalline vs. amorphous silica in human lung epithelial cellsTimothy N Perkins, Arti Shukla, Paul M Peeters, et al.Human Molecular Genetics|May 2, 2001
Trans-ethnic fine mapping of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE)C A McKenzie, G R Abecasis, B Keavney, et al.Scientific Reports|May 9, 2025
CpG methylation changes associated with hyperglycemia in type 1 diabetes occur at angiogenic glomerular and retinal gene lociXiaojian Shao, Sophie Le Fur, Warren Cheung, et al.Plos Genetics|June 12, 2013
Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humansFranz P W Radner, Slaheddine Marrakchi, Peter Kirchmeier, et al.Plos Genetics|January 30, 2019
Regeneration of the zebrafish retinal pigment epithelium after widespread genetic ablationNicholas J Hanovice, Lyndsay L Leach, Kayleigh Slater, et al.European Journal of Orthodontics|October 29, 2022
Impacts of anterior-posterior jaw disproportions on speech of dentofacial disharmony patientsSteven Oliver, Mary Morgan Bitler Keyser, Samantha Jhingree, et al.Human Molecular Genetics|April 4, 2001
Mutations in the gene encoding SLURP-1 in Mal de MeledaJ Fischer, B Bouadjar, R Heilig, et al.Pageof 139