| 31945647 | Biological sulfur in the blood cells of Ascidia ceratodes: XAS spectroscopy and a cellular-enzymatic hypothesis for vanadium reduction in the ascidians. | J Inorg Biochem | 2020 |
| 21705752 | A flexible estimating equations approach for mapping function-valued traits. | Genetics | 2011 |
| 20668102 | Genetic variants of human organic anion transporter 4 demonstrate altered transport of endogenous substrates. | Am J Physiol Renal Physiol | 2010 |
| 18234345 | The uptake and fate of vanadyl ion in ascidian blood cells and a detailed hypothesis for the mechanism and location of biological vanadium reduction. A visible and X-ray absorption spectroscopic study. | J Inorg Biochem | 2008 |
| 17700366 | Functional effects of protein sequence polymorphisms in the organic cation/ergothioneine transporter OCTN1 (SLC22A4). | Pharmacogenet Genomics | 2007 |
| 17602178 | Large-scale SNP genotyping with canine buccal swab DNA. | J Hered | 2007 |
| 16291576 | The human organic anion transporter 3 (OAT3; SLC22A8): genetic variation and functional genomics. | Am J Physiol Renal Physiol | 2006 |
| 17123974 | Validation of microsatellite markers for use in genotyping polyclonal Plasmodium falciparum infections. | Am J Trop Med Hyg | 2006 |
| 16702441 | Interaction of methotrexate with organic-anion transporting polypeptide 1A2 and its genetic variants. | J Pharmacol Exp Ther | 2006 |
| 16931768 | Functional genetic diversity in the high-affinity carnitine transporter OCTN2 (SLC22A5). | Mol Pharmacol | 2006 |
| 16507879 | PharmGKB submission update: VI. PMT submissions of genetic variations in neurotransmitter transporters (SLC6, SLC17, and SLC18) to the PharmGKB network. | Pharmacol Rev | 2006 |
| 16507878 | PharmGKB submission update: V. PMT submissions of genetic variation in SLC22 family transporters. | Pharmacol Rev | 2006 |
| 16507877 | PharmGKB submission update: IV. PMT submissions of genetic variations in ATP-Binding cassette transporters to the PharmGKB network. | Pharmacol Rev | 2006 |
| 16497723 | Genetic modifiers of the phenotype of mice deficient in mitochondrial superoxide dismutase. | Hum Mol Genet | 2006 |
| 16641106 | Reversal of Alzheimer's-like pathology and behavior in human APP transgenic mice by mutation of Asp664. | Proc Natl Acad Sci U S A | 2006 |
| 15738947 | Functional analysis of genetic variants in the human concentrative nucleoside transporter 3 (CNT3; SLC28A3). | Pharmacogenomics J | 2005 |
| 16266434 | Analysis of four DLX homeobox genes in autistic probands. | BMC Genet | 2005 |
| 15864112 | Functional analysis of polymorphisms in the organic anion transporter, SLC22A6 (OAT1). | Pharmacogenet Genomics | 2005 |
| 15861032 | Genetic analysis and functional characterization of polymorphisms in the human concentrative nucleoside transporter, CNT2. | Pharmacogenet Genomics | 2005 |
| 14644997 | Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis. | Blood | 2004 |
| 15188443 | Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes. | Dev Dyn | 2004 |
| 15385933 | PTPN11 mutations in pediatric patients with acute myeloid leukemia: results from the Children's Cancer Group. | Leukemia | 2004 |
| 14978229 | Functional and genetic diversity in the concentrative nucleoside transporter, CNT1, in human populations. | Mol Pharmacol | 2004 |
| 15169925 | PharmGKB update: III. Genetic variants of SLC22A1, solute carrier family 22 (organic cation transporter), member 1. | Pharmacol Rev | 2004 |
| 12719533 | Natural variation in human membrane transporter genes reveals evolutionary and functional constraints. | Proc Natl Acad Sci U S A | 2003 |
| 12893986 | Sequence diversity and haplotype structure in the human ABCB1 (MDR1, multidrug resistance transporter) gene. | Pharmacogenetics | 2003 |
| 12890772 | App gene dosage modulates endosomal abnormalities of Alzheimer's disease in a segmental trisomy 16 mouse model of down syndrome. | J Neurosci | 2003 |
| 12620674 | The vanadium environment in blood cells of Ascidia ceratodes is divergent at all organismal levels: an XAS and EPR spectroscopic study. | J Inorg Biochem | 2003 |
| 12603056 | SNP analysis and presentation in the Pharmacogenetics of Membrane Transporters Project. | Pac Symp Biocomput | 2003 |
| 12719534 | Evolutionary conservation predicts function of variants of the human organic cation transporter, OCT1. | Proc Natl Acad Sci U S A | 2003 |
| 11796207 | Increased sensitivity of homozygous Sod2 mutant mice to oxygen toxicity. | Free Radic Biol Med | 2002 |
| 12376353 | Sequential targeted deficiency of SP-A and -D leads to progressive alveolar lipoproteinosis and emphysema. | Am J Physiol Lung Cell Mol Physiol | 2002 |
| 11840489 | Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome. | Am J Med Genet | 2002 |
| 11161607 | Mice with a partial deficiency of manganese superoxide dismutase show increased vulnerability to the mitochondrial toxins malonate, 3-nitropropionic acid, and MPTP. | Exp Neurol | 2001 |
| 11309310 | Mouse intestinal goblet cells expressing SV40 T antigen directed by the MUC2 mucin gene promoter undergo apoptosis upon migration to the villi. | Cancer Res | 2001 |
| 11677043 | Genetic modification of prenatal lethality and dilated cardiomyopathy in Mn superoxide dismutase mutant mice. | Free Radic Biol Med | 2001 |
| 11595386 | Strain-dependent high-level expression of a transgene for manganese superoxide dismutase is associated with growth retardation and decreased fertility. | Free Radic Biol Med | 2001 |
| 11536434 | Cardiomyopathy in mice with paternal uniparental disomy for chromosome 12. | Genesis | 2001 |
| 11514315 | Knockout mice heterozygous for Sod2 show alterations in cardiac mitochondrial function and apoptosis. | Am J Physiol Heart Circ Physiol | 2001 |
| 11504920 | Failed retrograde transport of NGF in a mouse model of Down's syndrome: reversal of cholinergic neurodegenerative phenotypes following NGF infusion. | Proc Natl Acad Sci U S A | 2001 |
| 11035038 | Neonatal mortality in an aquaporin-2 knock-in mouse model of recessive nephrogenic diabetes insipidus. | J Biol Chem | 2001 |
| 10737773 | Nephrogenic diabetes insipidus in mice lacking aquaporin-3 water channels. | Proc Natl Acad Sci U S A | 2000 |
| 10890606 | Role of CuZn superoxide dismutase in regulating lymphocyte apoptosis during sepsis. | Crit Care Med | 2000 |
| 10837894 | Overexpression of mSim2 gene in the zona limitans of the diencephalon of segmental trisomy 16 Ts1Cje fetuses, a mouse model for trisomy 21: a novel whole-mount based RNA hybridization study. | Brain Res Dev Brain Res | 2000 |
| 11044479 | Genetic dissection of region associated with behavioral abnormalities in mouse models for Down syndrome. | Pediatr Res | 2000 |
| 10719757 | Ubiquitous overexpression of CuZn superoxide dismutase does not extend life span in mice. | J Gerontol A Biol Sci Med Sci | 2000 |
| 10476683 | Targeted expression of human CuZn superoxide dismutase gene in mouse central nervous system. | J Neurosci Methods | 1999 |
| 10400615 | Defective secretion of saliva in transgenic mice lacking aquaporin-5 water channels. | J Biol Chem | 1999 |
| 10672232 | The use of transgenic and mutant mice to study oxygen free radical metabolism. | Ann N Y Acad Sci | 1999 |
| 10070043 | Goblet cell-specific expression mediated by the MUC2 mucin gene promoter in the intestine of transgenic mice. | Am J Physiol | 1999 |