1 - 25 of
82
results
for author:"Palmer L."
in Literature Citations
| RRD1, a component of the TORC1 signalling pathway, affects anaesthetic response in Saccharomyces cerevisiae. Palmer L.K., Baptiste B.A., Fester J.C., Perkins J.C., Keil R.L. Yeast 0:0-0(2009) · Mapped (6) |
| Complement factor H Y402H and C-reactive protein polymorphism and photodynamic therapy response in age-related macular degeneration. Feng X., Xiao J., Longville B., Tan A.X., Wu X.N., Cooper M.N., McAllister I.L., Isaacs T., Palmer L.J., Constable I.J. Ophthalmology 116:1908-12.e1(2009) · Mapped (7) |
| Matrix metalloproteinase-2 gene variants and abdominal aortic aneurysm. Smallwood L., Warrington N., Allcock R., van Bockxmeer F., Palmer L.J., Iacopetta B., Golledge J., Norman P.E. Eur J Vasc Endovasc Surg 38:169-171(2009) · Mapped (3) |
| Possible association between genetic polymorphisms in transforming growth factor beta receptors, serum transforming growth factor beta1 concentration and abdominal aortic aneurysm. Golledge J., Clancy P., Jones G.T., Cooper M., Palmer L.J., van Rij A.M., Norman P.E. Br J Surg 96:628-632(2009) · Mapped (5) |
| The PHF11 gene is not associated with asthma or asthma phenotypes in two independent populations. McClenaghan J., Warrington N.M., Jamrozik E.F., Hui J., Beilby J.P., Hansen J., de Klerk N.H., James A.L., Musk A.W., Palmer L.J. Thorax 64:620-625(2009) · Mapped (4) |
| Up-regulating BDNF with an ampakine rescues synaptic plasticity and memory in Huntington's disease knockin mice. Simmons D.A., Rex C.S., Palmer L., Pandyarajan V., Fedulov V., Gall C.M., Lynch G. Proc. Natl. Acad. Sci. U.S.A. 106:4906-4911(2009) · Mapped (1) |
| Analyses of associations with asthma in four asthma population samples from Canada and Australia. Daley D., Lemire M., Akhabir L., Chan-Yeung M., He J.Q., McDonald T., Sandford A., Stefanowicz D., Tripp B., Zamar D. et al. Hum. Genet. 125:445-459(2009) · Mapped (561) |
| Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Gudbjartsson D.F., Bjornsdottir U.S., Halapi E., Helgadottir A., Sulem P., Jonsdottir G.M., Thorleifsson G., Helgadottir H., Steinthorsdottir V., Stefansson H. et al. Nat. Genet. 41:342-347(2009) · Mapped (29) |
| Moving the pH gate of the Kir1.1 inward rectifier channel. Nanazashvili M., Li H., Palmer L.G., Walters D.E., Sackin H. Channels (Austin) 1:21-28(2007) · Mapped (3) |
| The association of common genetic variants in the APOA5, LPL and GCK genes with longitudinal changes in metabolic and cardiovascular traits. Webster R.J., Warrington N.M., Weedon M.N., Hattersley A.T., McCaskie P.A., Beilby J.P., Palmer L.J., Frayling T.M. Diabetologia 52:106-114(2009) · Mapped (17) |
| Hypoxia-inducible factor-1alpha is constitutively expressed in murine Leydig cells and regulates 3beta-hydroxysteroid dehydrogenase type 1 promoter activity. Lysiak J.J., Kirby J.L., Tremblay J.J., Woodson R.I., Reardon M.A., Palmer L.A., Turner T.T. J. Androl. 30:146-156(2009) · Mapped (3) |
| Polymorphisms of the matrix metalloproteinase 9 gene and abdominal aortic aneurysm. Smallwood L., Allcock R., van Bockxmeer F., Warrington N., Palmer L.J., Iacopetta B., Golledge J., Norman P.E. Br J Surg 95:1239-1244(2008) · Mapped (6) |
| Association of PARL rs3732581 genetic variant with insulin levels, metabolic syndrome and coronary artery disease. Powell B.L., Wiltshire S., Arscott G., McCaskie P.A., Hung J., McQuillan B.M., Thompson P.L., Carter K.W., Palmer L.J., Beilby J.P. Hum. Genet. 124:263-270(2008) · Mapped (1) |
| Association of Interleukin-1 gene polymorphisms with central obesity and metabolic syndrome in a coronary heart disease population. Carter K.W., Hung J., Powell B.L., Wiltshire S., Foo B.T., Leow Y.C., McQuillan B.M., Jennens M., McCaskie P.A., Thompson P.L. et al. Hum. Genet. 124:199-206(2008) · Mapped (5) |
| The association of C-reactive protein and CRP genotype with coronary heart disease: findings from five studies with 4,610 cases amongst 18,637 participants. Lawlor D.A., Harbord R.M., Timpson N.J., Lowe G.D., Rumley A., Gaunt T.R., Baker I., Yarnell J.W., Kivimaki M., Kumari M. et al. PLoS ONE 3:e3011-e3011(2008) · Mapped (3) |
| Surface expression of epithelial Na channel protein in rat kidney. Frindt G., Ergonul Z., Palmer L.G. J. Gen. Physiol. 131:617-627(2008) · Mapped (3) |
| Angiotensinogen gene T235 variant: a marker for the development of persistent microalbuminuria in children and adolescents with type 1 diabetes mellitus. Gallego P.H., Shephard N., Bulsara M.K., van Bockxmeer F.M., Powell B.L., Beilby J.P., Arscott G., Le Page M., Palmer L.J., Davis E.A. et al. J. Diabetes Complicat. 22:191-198(2008) · Mapped (20) |
| 15-Lipoxygenase gene variants are associated with carotid plaque but not carotid intima-media thickness. McCaskie P.A., Beilby J.P., Hung J., Chapman C.M., McQuillan B.M., Powell B.L., Thompson P.L., Palmer L.J. Hum. Genet. 123:445-453(2008) · Mapped (7) |
| Epithelial Na+ channel activation and processing in mice lacking SGK1. Fejes-Toth G., Frindt G., Naray-Fejes-Toth A., Palmer L.G. Am. J. Physiol. Renal Physiol. 294:F1298-305(2008) · Mapped (2) |
| Disruption of contactin 4 in three subjects with autism spectrum disorder. Roohi J., Montagna C., Tegay D.H., Palmer L.E., DeVincent C., Pomeroy J.C., Christian S.L., Nowak N., Hatchwell E. J. Med. Genet. 46:176-182(2009) · Mapped (5) |
| Comprehensive analysis of tagging sequence variants in DTNBP1 shows no association with schizophrenia or with its composite neurocognitive endophenotypes. Peters K., Wiltshire S., Henders A.K., Dragovic M., Badcock J.C., Chandler D., Howell S., Ellis C., Bouwer S., Montgomery G.W. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 147B:1159-1166(2008) · Mapped (2) |
| Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease. Wiltshire S., Powell B.L., Jennens M., McCaskie P.A., Carter K.W., Palmer L.J., Thompson P.L., McQuillan B.M., Hung J., Beilby J.P. Hum. Genet. 123:307-313(2008) · Mapped (2) |
| The apolipoprotein AII rs5082 variant is associated with reduced risk of coronary artery disease in an Australian male population. Xiao J., Zhang F., Wiltshire S., Hung J., Jennens M., Beilby J.P., Thompson P.L., McQuillan B.M., McCaskie P.A., Carter K.W. et al. Atherosclerosis 199:333-339(2008) · Mapped (2) |
| TNFR-associated factor-2 (TRAF-2) in Alzheimer's disease. Culpan D., Cram D., Chalmers K., Cornish A., Palmer L., Palmer J., Hughes A., Passmore P., Craigs D., Wilcock G.K. et al. Neurobiol. Aging 30:1052-1060(2009) · Mapped (9) |
| Polymorphisms of the interleukin-6 gene promoter and abdominal aortic aneurysm. Smallwood L., Allcock R., van Bockxmeer F., Warrington N., Palmer L.J., Iacopetta B., Norman P.E. Eur J Vasc Endovasc Surg 35:31-36(2008) · Mapped (6) |
