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The Pharmacogenomics Journal|January 27, 2016
ABCG2 loss-of-function polymorphism predicts poor response to allopurinol in patients with goutR L Roberts, M C Wallace, A J Phipps-Green, et al.
Science Signaling|July 4, 2019
Host mitochondria influence gut microbiome diversity: A role for ROSTal Yardeni, Ceylan E Tanes, Kyle Bittinger, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 6, 2000
Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric miceJ E Sligh, S E Levy, K G Waymire, et al.
Biochimica Et Biophysica Acta|February 7, 2012
Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELASValerie Desquiret-Dumas, Naig Gueguen, Magalie Barth, et al.
BMC Genomics|January 25, 2007
High-density rhesus macaque oligonucleotide microarray design using early-stage rhesus genome sequence information and human genome annotationsJames C Wallace, Marcus J Korth, Bryan Paeper, et al.
Human Mutation|June 21, 2008
MITOMASTER: a bioinformatics tool for the analysis of mitochondrial DNA sequencesMarty C Brandon, Eduardo Ruiz-Pesini, Dan Mishmar, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|February 10, 2016
The National Osteoporosis Foundation's position statement on peak bone mass development and lifestyle factors: a systematic review and implementation recommendationsC M Weaver, C M Gordon, K F Janz, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|October 4, 2000
Cardiac function after eight hour storage by using polyethylene glycol hemoglobin versus crystalloid perfusionD L Serna, L L Powell, C Kahwaji, et al.
Science (New York, N.Y.)|February 16, 2008
A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutationsWeiwei Fan, Katrina G Waymire, Navneet Narula, et al.
Discovery Medicine|January 1, 2013
Mitochondrial disease genetic diagnostics: optimized whole-exome analysis for all MitoCarta nuclear genes and the mitochondrial genomeMarni J Falk, Eric A Pierce, Mark Consugar, et al.
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