Skip to Main Content

Author Details

Elaine J Carlson
University of California san francisco
1990
101
55
Andrej Sali (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
31945647Biological sulfur in the blood cells of Ascidia ceratodes: XAS spectroscopy and a cellular-enzymatic hypothesis for vanadium reduction in the ascidians.J Inorg Biochem2020
21705752A flexible estimating equations approach for mapping function-valued traits.Genetics2011
20668102Genetic variants of human organic anion transporter 4 demonstrate altered transport of endogenous substrates.Am J Physiol Renal Physiol2010
18234345The 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 Biochem2008
17700366Functional effects of protein sequence polymorphisms in the organic cation/ergothioneine transporter OCTN1 (SLC22A4).Pharmacogenet Genomics2007
17602178Large-scale SNP genotyping with canine buccal swab DNA.J Hered2007
16291576The human organic anion transporter 3 (OAT3; SLC22A8): genetic variation and functional genomics.Am J Physiol Renal Physiol2006
17123974Validation of microsatellite markers for use in genotyping polyclonal Plasmodium falciparum infections.Am J Trop Med Hyg2006
16702441Interaction of methotrexate with organic-anion transporting polypeptide 1A2 and its genetic variants.J Pharmacol Exp Ther2006
16931768Functional genetic diversity in the high-affinity carnitine transporter OCTN2 (SLC22A5).Mol Pharmacol2006
16507879PharmGKB submission update: VI. PMT submissions of genetic variations in neurotransmitter transporters (SLC6, SLC17, and SLC18) to the PharmGKB network.Pharmacol Rev2006
16507878PharmGKB submission update: V. PMT submissions of genetic variation in SLC22 family transporters.Pharmacol Rev2006
16507877PharmGKB submission update: IV. PMT submissions of genetic variations in ATP-Binding cassette transporters to the PharmGKB network.Pharmacol Rev2006
16497723Genetic modifiers of the phenotype of mice deficient in mitochondrial superoxide dismutase.Hum Mol Genet2006
16641106Reversal of Alzheimer's-like pathology and behavior in human APP transgenic mice by mutation of Asp664.Proc Natl Acad Sci U S A2006
15738947Functional analysis of genetic variants in the human concentrative nucleoside transporter 3 (CNT3; SLC28A3).Pharmacogenomics J2005
16266434Analysis of four DLX homeobox genes in autistic probands.BMC Genet2005
15864112Functional analysis of polymorphisms in the organic anion transporter, SLC22A6 (OAT1).Pharmacogenet Genomics2005
15861032Genetic analysis and functional characterization of polymorphisms in the human concentrative nucleoside transporter, CNT2.Pharmacogenet Genomics2005
14644997Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis.Blood2004
15188443Down syndrome mouse models Ts65Dn, Ts1Cje, and Ms1Cje/Ts65Dn exhibit variable severity of cerebellar phenotypes.Dev Dyn2004
15385933PTPN11 mutations in pediatric patients with acute myeloid leukemia: results from the Children's Cancer Group.Leukemia2004
14978229Functional and genetic diversity in the concentrative nucleoside transporter, CNT1, in human populations.Mol Pharmacol2004
15169925PharmGKB update: III. Genetic variants of SLC22A1, solute carrier family 22 (organic cation transporter), member 1.Pharmacol Rev2004
12719533Natural variation in human membrane transporter genes reveals evolutionary and functional constraints.Proc Natl Acad Sci U S A2003
12893986Sequence diversity and haplotype structure in the human ABCB1 (MDR1, multidrug resistance transporter) gene.Pharmacogenetics2003
12890772App gene dosage modulates endosomal abnormalities of Alzheimer's disease in a segmental trisomy 16 mouse model of down syndrome.J Neurosci2003
12620674The vanadium environment in blood cells of Ascidia ceratodes is divergent at all organismal levels: an XAS and EPR spectroscopic study.J Inorg Biochem2003
12603056SNP analysis and presentation in the Pharmacogenetics of Membrane Transporters Project.Pac Symp Biocomput2003
12719534Evolutionary conservation predicts function of variants of the human organic cation transporter, OCT1.Proc Natl Acad Sci U S A2003
11796207Increased sensitivity of homozygous Sod2 mutant mice to oxygen toxicity.Free Radic Biol Med2002
12376353Sequential targeted deficiency of SP-A and -D leads to progressive alveolar lipoproteinosis and emphysema.Am J Physiol Lung Cell Mol Physiol2002
11840489Craniofacial phenotypes in segmentally trisomic mouse models for Down syndrome.Am J Med Genet2002
11161607Mice with a partial deficiency of manganese superoxide dismutase show increased vulnerability to the mitochondrial toxins malonate, 3-nitropropionic acid, and MPTP.Exp Neurol2001
11309310Mouse intestinal goblet cells expressing SV40 T antigen directed by the MUC2 mucin gene promoter undergo apoptosis upon migration to the villi.Cancer Res2001
11677043Genetic modification of prenatal lethality and dilated cardiomyopathy in Mn superoxide dismutase mutant mice.Free Radic Biol Med2001
11595386Strain-dependent high-level expression of a transgene for manganese superoxide dismutase is associated with growth retardation and decreased fertility.Free Radic Biol Med2001
11536434Cardiomyopathy in mice with paternal uniparental disomy for chromosome 12.Genesis2001
11514315Knockout mice heterozygous for Sod2 show alterations in cardiac mitochondrial function and apoptosis.Am J Physiol Heart Circ Physiol2001
11504920Failed 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 A2001
11035038Neonatal mortality in an aquaporin-2 knock-in mouse model of recessive nephrogenic diabetes insipidus.J Biol Chem2001
10737773Nephrogenic diabetes insipidus in mice lacking aquaporin-3 water channels.Proc Natl Acad Sci U S A2000
10890606Role of CuZn superoxide dismutase in regulating lymphocyte apoptosis during sepsis.Crit Care Med2000
10837894Overexpression 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 Res2000
11044479Genetic dissection of region associated with behavioral abnormalities in mouse models for Down syndrome.Pediatr Res2000
10719757Ubiquitous overexpression of CuZn superoxide dismutase does not extend life span in mice.J Gerontol A Biol Sci Med Sci2000
10476683Targeted expression of human CuZn superoxide dismutase gene in mouse central nervous system.J Neurosci Methods1999
10400615Defective secretion of saliva in transgenic mice lacking aquaporin-5 water channels.J Biol Chem1999
10672232The use of transgenic and mutant mice to study oxygen free radical metabolism.Ann N Y Acad Sci1999
10070043Goblet cell-specific expression mediated by the MUC2 mucin gene promoter in the intestine of transgenic mice.Am J Physiol1999
  • 1 - 50 of 101

Recommended Authors

Mary Lyon Centre at Medical Research Council
Career Start Year 2007
Number of shared co-authors 0
Mary Lyon Centre at Medical Research Council
Career Start Year 2004
Number of shared co-authors 0
Beth Israel Deaconess Medical Center
Career Start Year 1999
Number of shared co-authors 0
Institute of Experimental Genetics, German Mouse Clinic
Career Start Year 1999
Number of shared co-authors 0
University of California
Career Start Year 1996
Number of shared co-authors 0
The Hospital for Sick Children
Career Start Year 1996
Number of shared co-authors 0
Institute of Experimental Genetics, German Mouse Clinic
Career Start Year 1996
Number of shared co-authors 0
Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
Career Start Year 1995
Number of shared co-authors 0
Wellcome Trust Sanger Institute
Career Start Year 1994
Number of shared co-authors 0
Center for Global Infectious Disease Research, Seattle Children's Research Institute
Career Start Year 1993
Number of shared co-authors 1
North Carolina State University, USA Center for Human Health and the Environment
Career Start Year 1993
Number of shared co-authors 0
German Center for Diabetes Research (DZD e.V.)
Career Start Year 1993
Number of shared co-authors 1
National Institute on Aging, National Institutes of Health
Career Start Year 1992
Number of shared co-authors 1
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
Career Start Year 1991
Number of shared co-authors 1
JAX Center for Precision Genetics
Career Start Year 1990
Number of shared co-authors 0
National Centre for Biotechnology (CNB-CSIC)
Career Start Year 1989
Number of shared co-authors 0
College Station
Career Start Year 1988
Number of shared co-authors 1
Institute for Cell Engineering, Johns Hopkins University School of Medicine
Career Start Year 1988
Number of shared co-authors 3
National Institute of Environmental Health Sciences
Career Start Year 1985
Number of shared co-authors 0
Institute of Developmental Genetics, German Research Center for Environmental Health
Career Start Year 1984
Number of shared co-authors 6
University of Kentucky
Career Start Year 1982
Number of shared co-authors 1
Duke University Medical Center
Career Start Year 1981
Number of shared co-authors 0
Mayo Clinic
Career Start Year 1981
Number of shared co-authors 2
Howard Hughes Medical Institute, The Rockefeller University
Career Start Year 1980
Number of shared co-authors 2
Icahn School of Medicine at Mount Sinai
Career Start Year 1980
Number of shared co-authors 1
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Career Start Year 1980
Number of shared co-authors 0
Lunenfeld Tanenbaum Research Institute, Mount Sinai Hospital
Career Start Year 1975
Number of shared co-authors 1
University of British Columbia
Career Start Year 1972
Number of shared co-authors 0
Oregon Health & Science University
Career Start Year 1970
Number of shared co-authors 0
Baylor College of Medicine
Career Start Year 1968
Number of shared co-authors 0

Collaborators

University of California San Francisco
Co-authored papers 17
Department of Pharmaceutical Chemistry, University of California San Francisco
Co-authored papers 17
Center for Visualization, Washington State University
Co-authored papers 16
University of California San Francisco
Co-authored papers 16
Co-authored papers 16
Department of Pharmaceutical Chemistry, University of California San Francisco
Co-authored papers 15
University of Toledo
Co-authored papers 12
University of California San Francisco (UCSF)
Co-authored papers 8
University of California san francisco
Co-authored papers 7
Eshelman School of Pharmacy, University of North Carolina
Co-authored papers 6
University of California San Francisco
Co-authored papers 5
Co-authored papers 5
University of California San Diego
Co-authored papers 4
Children's Hospital Oakland Research Institute
Co-authored papers 4
Stanford University
Co-authored papers 3
University of California Davis
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
University of California san francisco
Co-authored papers 2
Fred Hutchinson Cancer Research Centre
Co-authored papers 2
University of Washington
Co-authored papers 2
University of California San Francisco
Co-authored papers 1
Institute on Aging, University of Florida
Co-authored papers 1
University of California san francisco
Co-authored papers 1
University of Pittsburgh
Co-authored papers 1
University of California san francisco
Co-authored papers 1
University of Tennessee Health Science Center
Co-authored papers 1
University of California San Francisco
Co-authored papers 1