1 - 25 of 29 results for author:"Gibson R.A." in Literature citations
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| Functional characterization of the chicken fatty acid elongases. Gregory M.K., Geier M.S., Gibson R.A., James M.J. |
| An alternative n-3 fatty acid elongation pathway utilising 18:3n-3 in barramundi (Lates calcarifer). Tu W.C., Muhlhausler B.S., James M.J., Stone D.A., Gibson R.A. Biochem. Biophys. Res. Commun. 423:176-182(2012) · UniProtKB (1) |
| Association of TMPRSS6 polymorphisms with ferritin, hemoglobin, and type 2 diabetes risk in a Chinese Han population. Gan W., Guan Y., Wu Q., An P., Zhu J., Lu L., Jing L., Yu Y., Ruan S., Xie D. et al. Am. J. Clin. Nutr. 95:626-632(2012) · Mapped (1) |
| Elongase reactions as control points in long-chain polyunsaturated fatty acid synthesis. Gregory M.K., Gibson R.A., Cook-Johnson R.J., Cleland L.G., James M.J. PLoS ONE 6:e29662-e29662(2011) · UniProtKB (2) |
| Translation initiator EIF4G1 mutations in familial Parkinson disease. Chartier-Harlin M.C., Dachsel J.C., Vilarino-Guell C., Lincoln S.J., Lepretre F., Hulihan M.M., Kachergus J., Milnerwood A.J., Tapia L., Song M.S. et al. Am. J. Hum. Genet. 89:398-406(2011) · UniProtKB (1) · Mapped (9) |
| Fatty acid desaturase 2 promoter mutation is not responsible for Delta6-desaturase deficiency. Gregory M.K., Lester S.E., Cook-Johnson R.J., Gibson R.A., Proudman S.M., Cleland L.G., James M.J. Eur. J. Hum. Genet. 19:1202-1204(2011) · Mapped (6) |
| Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa. Jasinska-Myga B., Kachergus J., Vilarino-Guell C., Wider C., Soto-Ortolaza A.I., Kefi M., Middleton L.T., Ishihara-Paul L., Gibson R.A., Amouri R. et al. Mov. Disord. 25:2052-2058(2010) · Mapped (4) |
| Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. Kasperaviciute D., Catarino C.B., Heinzen E.L., Depondt C., Cavalleri G.L., Caboclo L.O., Tate S.K., Jamnadas-Khoda J., Chinthapalli K., Clayton L.M. et al. Brain 133:2136-2147(2010) · Mapped (4) |
| Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa. Nishioka K., Vilarino-Guell C., Cobb S.A., Kachergus J.M., Ross O.A., Wider C., Gibson R.A., Hentati F., Farrer M.J. Neurosci. Lett. 477:57-60(2010) · Mapped (1) |
| Cloning and functional characterisation of a fatty acyl elongase from southern bluefin tuna (Thunnus maccoyii). Gregory M.K., See V.H., Gibson R.A., Schuller K.A. Comp. Biochem. Physiol. B, Biochem. Mol. Biol. 155:178-185(2010) · UniProtKB (2) |
| A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease. Nishioka K., Kefi M., Jasinska-Myga B., Wider C., Vilarino-Guell C., Ross O.A., Heckman M.G., Middleton L.T., Ishihara-Paul L., Gibson R.A. et al. J. Neurol. Neurosurg. Psychiatr. 81:391-395(2010) · Mapped (20) |
| Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. International MS Genetics Consortium Nat. Genet. 41:776-782(2009) · Mapped (1,336) |
| ATP13A2 variability in Parkinson disease. Vilarino-Guell C., Soto A.I., Lincoln S.J., Ben Yahmed S., Kefi M., Heckman M.G., Hulihan M.M., Chai H., Diehl N.N., Amouri R. et al. |
| Anatomically-distinct genetic associations of APOE epsilon4 allele load with regional cortical atrophy in Alzheimer's disease. Filippini N., Rao A., Wetten S., Gibson R.A., Borrie M., Guzman D., Kertesz A., Loy-English I., Williams J., Nichols T. et al. Neuroimage 44:724-728(2009) · Mapped (5) |
| Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. Baranzini S.E., Wang J., Gibson R.A., Galwey N., Naegelin Y., Barkhof F., Radue E.W., Lindberg R.L., Uitdehaag B.M., Johnson M.R. et al. Hum. Mol. Genet. 18:767-778(2009) · Mapped (112) |
| PINK1 mutations and parkinsonism. Ishihara-Paul L., Hulihan M.M., Kachergus J., Upmanyu R., Warren L., Amouri R., Elango R., Prinjha R.K., Soto A., Kefi M. et al. Neurology 71:896-902(2008) · Mapped (1) |
| LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study. Hulihan M.M., Ishihara-Paul L., Kachergus J., Warren L., Amouri R., Elango R., Prinjha R.K., Upmanyu R., Kefi M., Zouari M. et al. Lancet Neurol 7:591-594(2008) · Mapped (4) |
| Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease. Li H., Wetten S., Li L., St Jean P.L., Upmanyu R., Surh L., Hosford D., Barnes M.R., Briley J.D., Borrie M. et al. Arch. Neurol. 65:45-53(2008) · Mapped (14) |
| Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study. Cavalleri G.L., Weale M.E., Shianna K.V., Singh R., Lynch J.M., Grinton B., Szoeke C., Murphy K., Kinirons P., O'Rourke D. et al. Lancet Neurol 6:970-980(2007) · Mapped (19) |
| Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families. Ishihara L., Gibson R.A., Warren L., Amouri R., Lyons K., Wielinski C., Hunter C., Swartz J.E., Elango R., Akkari P.A. et al. Mov. Disord. 22:55-61(2007) · Mapped (4) |
| Interleukin-2 in human milk: a potential modulator of lymphocyte development in the breastfed infant. Bryan D.L., Forsyth K.D., Gibson R.A., Hawkes J.S. Cytokine 33:289-293(2006) · Mapped (12) |
| Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease. van der Walt J.M., Martin E.R., Scott W.K., Zhang F., Nance M.A., Watts R.L., Hubble J.P., Haines J.L., Koller W.C., Lyons K. et al. Neurology 60:1189-1191(2003) · Mapped (24) |
| Variations in transforming growth factor beta in human milk are not related to levels in plasma. Hawkes J.S., Bryan D.L., Gibson R.A. Cytokine 17:182-186(2002) · Mapped (14) |
| Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease. Martin E.R., Scott W.K., Nance M.A., Watts R.L., Hubble J.P., Koller W.C., Lyons K., Pahwa R., Stern M.B., Colcher A. et al. JAMA 286:2245-2250(2001) · Mapped (6) |
| The genomic organization of the Fanconi anemia group A (FAA) gene. Ianzano L., D'Apolito M., Centra M., Savino M., Levran O., Auerbach A.D., Cleton-Jansen A.-M., Doggett N.A., Pronk J.C., Tipping A.J. et al. Genomics 41:309-314(1997) · UniProtKB (1) |