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Maternally transmitted partial direct tandem duplication of mitochondrial DNA associated with diabetes mellitus. Hum Mol Genet. 1993;2(10):1619-24.
Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes. Proc Natl Acad Sci USA. 1995;92(14):6562-6.
Complex I deficiency is associated with 3243G:C mitochondrial DNA in osteosarcoma cell cybrids. Hum Mol Genet. 1996;5(1):123-29.
In situ hybridisation mapping of genomic clones for five human respiratory chain complex I genes. Cytogenet Cell Genet. 1997;78(1):21-4.
A tRNA suppressor mutation in human mitochondria. Nat Genet. 1998;18(4):350-3.
Sex-specific association between bipolar affective disorder in women and GPR50, an X-linked orphan G protein-coupled receptor. Mol Psychiatry. 2005;10(5):470-8.
Identification of a human ortholog of the mouse Dcpp gene locus, encoding a novel member of the CSP-1/Dcpp salivary protein family. Physiological genomics. 2006;28:129-40.
Cryptic loxP sites in mammalian genomes: genome-wide distribution and relevance for the efficiency of BAC/PAC recombineering techniques. Nucleic acids research. 2007;35:1402-10.
Class III antiarrhythmic methanesulfonanilides inhibit leukocyte recruitment in zebrafish. Journal of leukocyte biology. 2007;82:79-84.
Automated seeding of specialised wiki knowledgebases with BioKb. BMC bioinformatics. 2009;10:291.
IUPHAR-DB: the IUPHAR database of G protein-coupled receptors and ion channels. Nucleic acids research. 2009;37:D680-5.
Angiotensin-converting enzyme is a modifier of hypertensive end organ damage. The Journal of biological chemistry. 2009;284:15564-72.
Human dendritic cells produce TGF-beta 1 under the influence of lung carcinoma cells and prime the differentiation of CD4+CD25+Foxp3+ regulatory T cells. Journal of immunology (Baltimore, Md. : 1950). 2009;182:2795-807.
In silico structure-function analysis of pathological variation in the HSD11B2 gene sequence. Physiological genomics. 2010;42:319-30.
Underestimated and under-recognized: the late consequences of acute coronary syndrome (GRACE UK-Belgian Study). European heart journal. 2010.
Transcriptional and physiological responses to chronic ACTH treatment by the mouse kidney. Physiological genomics. 2010;40:158-66.
A variant at chromosome 9p21 is associated with recurrent myocardial infarction and cardiac death after acute coronary syndrome: the GRACE Genetics Study. European heart journal. 2010;31:1132-41.
Hyperglycemia and Renin-Dependent Hypertension Synergize to Model Diabetic Nephropathy. Journal of the American Society of Nephrology : JASN. 2011.