Human Genetics Unit: Staff Papers 2009

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1. Anastasaki, C.; Estep, A.L.; Marais, R.; Rauen, K.A. and Patton, E.E. Kinase-activating and kinase-impaired cardio-facio-cutaneous syndrome alleles have activity during zebrafish development, and are sensitive to small molecule inhibitors. Hum.Mol.Genet 18(14):2543-2554, 2009 PubMed Abstract
   
   
2. Andersen, K.M.; Madsen, L.; Prag, S.; Johnsen, A.H.; Semple, C.A.; Hendil, K.B. and Hartmann-Petersen, R. Thioredoxin Txnl1/TRP32 is a redox active co-factor of the 26S proteasome. Journal of Biological Chemistry, 284(22):15246-54, 2009
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3. Asai-Coakwell, M.; French, C.R.; Ye, M.; Garcha, K.; Bigot, K.; Perera, A.G.; Staehling-Hampton, K.; Mema, S.C.; Chanda, B.; Mushegian, A.; Bamforth, S.; Doschak, M.R.; Li, G.; Dobbs, M.B.; Giampietro, P.F.; Brooks, B.P.; Vijayalakshmi, P.; Sauve, Y.; Abitbol, M.; Sundaresan, P.; van Heyningen, V.; Pourquie, O.; Underhill, T.M.; Waskiewicz, A.J., and Lehmann, O.J. Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes. Hum Mol Genet 18(6):1110-21, 2009
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4. Aulchenko, Y.S.; Ripatti, S.; Lindqvist, I.; Boomsma, D.; Heid, I.M.; Pramstaller, P.P.; Penninx, B.W.; Janssens, A.C.; Wilson, J.F.; Spector, T.; Martin, N.G.; Pedersen, N.L.; Kyvik, K.O.; Kaprio, J.; Hofman, A.; Freimer, N.B.; Jarvelin, M.R.; Gyllensten, U.; Campbell, H.; Rudan, I.; Johansson, A.; Marroni, F.; Hayward, C.; Vitart, V.; Jonasson, I.; Pattaro, C.; Wright, A.; Hastie, N.; Pichler, I.; Hicks, A.A.; Falchi, M.; Willemsen, G.; Hottenga, J.J.; de Geus, E.J.; Montgomery, G.W.; Whitfield, J.; Magnusson, P.; Saharinen, J.; Perola, M.; Silander, K.; Isaacs, A.; Sijbrands, E.J.; Uitterlinden, A.G.; Witteman, J.C.; Oostra, B.A.; Elliott, P.; Ruokonen, A.; Sabatti, C.; Gieger, C.; Meitinger, T.; Kronenberg, F.; Doring, A.; Wichmann, H.E.; Smit, J.H.; McCarthy, M.I.; van Duijn, C.M. and Peltonen, L. Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
   Nat Genet 41(1):47-55, 2009
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5. Barbalic, M.; Narancic, N.S.; Skaric-Juric, T.; Salihovic, M.P.; Klaric, I.M.; Lauc, L.B.; Janicijevic, B.; Farrall, M.; Rudan, I.; Campbell, H.; Wright, A.F.; Hastie, N.D. and Rudan, P. A quantitative trait locus for SBP maps near KCNB1 and PTGIS in a population isolate.
   Am.J Hypertens. 22(6):663-668, 2009 PubMed Abstract
   
   
6. Benko, S.; Fantes, J.A.; Amiel, J.; Kleinjan, D.J.; Thomas, S.; Ramsay, J.; Jamshidi, N.; Essafi, A.; Heaney, S.; Gordon, C.T.; McBride, D.; Golzio, C.; Fisher, M.; Perry, P.; Abadie, V.; Ayuso, C.; Holder-Espinasse, M.; Kilpatrick, N.; Lees, M.M.; Picard, A.; Temple, I.K.; Thomas, P.; Vazquez, M.P.; Vekemans, M.; Crollius, H.R.; Hastie, N.D.; Munnich, A.; Etchevers, H.C.; Pelet, A.; Farlie, P.G.; Fitzpatrick, D.R. and Lyonnet, S. Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence. Nat.Genet. 41(3):359-364, 2009 PubMed Abstract
   
   
7. Best, D. and Adams, I.R. Sdmg1 is a component of secretory granules in mouse secretory exocrine tissues.
   Dev Dyn 238(1):223-231, 2009
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8. Biamonti, G. and Caceres, J.F. Cellular stress and RNA splicing.
   Trends in Biochem Sci 34(3):146-53, 2009
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9. Biloglav, Z.; Zgaga, L.; Smoljanovic, M.; Hayward, C.; Polasek, O.; Kolcic, I.; Vitart, V.; Zemunik, T.; Boraska, V.; Torlak, V.; Mulic, R.; Ropac, D.; Grkovic, I.; Rudan, D.; Ristic, S.; Barbalic, M.; Campbell, H.; Wright, A.F. and Rudan, I. Historic, demographic, and genetic evidence for increased population frequencies of CCR5Delta32 mutation in Croatian Island isolates after lethal 15th century epidemics. Croat Med J 50(1):34-42, 2009 PubMed Abstract
   
   
10. Bolcun-Filas, E.; Speed, R.; Taggart, M.; Grey, C.;de Massy, B.; Benavente, R. and Cooke, H.J. Mutation of the Mouse Syce1 Gene Disrupts Synapsis and Suggests a Link Between Synaptonemal Complex Structural Components and DNA Repair. PLoS Genetics 5(2):e1000393, 2009 PubMed Abstract
    
    
11. Borooah, S.; Collins, C.; Wright, A. and Dhillon, B. Late-onset retinal macular degeneration: clinical insights into an inherited retinal degeneration.
    Br.J Ophthalmol. 93(3):284-289, 2009 PubMed Abstract
    
    
12. Brady, R. R. W.; McDermott, C.; Graham, C.; Harrison, E. H.; Eunson, G. J.; Fraise, A. P.; Dunlop, M. G., and Gibb, A. P. A prevalence screen of MRSA Nasal Colonisation amongst UK Doctors in a Non-Clinical Environment. Eur J Clin Microbiol Infect Dis 28(8):991-5, 2009
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13. Briers, S.; Crawford, C.; Bickmore, W.A. and Sutherland, H.G. KRAB zinc-finger proteins localise to novel KAP1-containing foci that are adjacent to PML nuclear bodies. J Cell Sci 122:937-946, 2009
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14. Brook, M.; Smith, J.W. and Gray, N.K. The DAZL and PABP families: RNA-binding proteins with interrelated roles in translational control in oocytes. Reproduction 137(4):595-617, 2009 PubMed Abstract
    
    
15. Burn, S.F. and Hill, R.E. Left-right asymmetry in gut development: what happens next?
    BioEssays 31(10):1026-1037, 2009
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16. Burger, A.; Romano, P.; Paschke, A. and Splendiani, A. Semantic Web Applications and Tools for Life Sciences, 2008--preface. BMC Bioinformatics 10 Suppl 10:S1, 2009 PubMed Abstract
    
    
17. Campbell, H.; Rudan, I.; Bittles, A.H. and Wright, A.F. Human population structure, genome autozygosity and human health. Genome Med 1(9):91, 2009
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18. Carpenter, J.A.; Keegan, L.; Wilfert, L.; O'Connell, M.A. and Jiggins, F.M. Evidence for ADAR-induced hypermutation of the Drosophila sigma virus (Rhabdoviridae)
    BMC Genet 10(1):75, 2009
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19. Chanas, S.A.; Collinson, J.M.; Ramaesh, T.; Dora, N.; Kleinjan, D.A.; Hill, R.E. and West, J.D. Effects of elevated Pax6 expression and genetic background on mouse eye development. Invest Ophthalmol Vis.Sci. 50(9):4045-4059, 2009 PubMed Abstract
    
    
20. Christiansen, J.H.; Davidson, D. and Baldock, R.A. Management of Spatially Organized Biological Data using EMAGE. In: Bioinformatics for Systems Biology. Krawetz, S. (Ed.) Humana Press, New York, 2nd edition, 461-476, 2009
    
    
21. Church, D.M.; Goodstadt, L..... and the Mouse Genome Sequencing Consortium (Jackson, I.J.) Lineage-Specific Biology Revealed by a Finished Genome Assembly of the Mouse. PLoS Biol. 7(5):e1000112, 2009
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22. Clayton-Smith, J.; Walters, S.; Hobson, E.; Burkitt-Wright, E.; Smith, R.; Toutain, A.; Amiel, J.; Lyonnet, S.; Mansour, S.; Fitzpatrick, D.; Ciccone, R.; Ricca, I.; Zuffardi, O. and Donnai, D. Xq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearance.
    Eur.J.Hum.Genet. 17(4):434-443, 2009 PubMed Abstract
    
    
23. Deniaud, E. and Bickmore, W.A. Transcription and the nuclear periphery: edge of darkness? Curr Opin Genet Dev 19(2):187-191, 2009
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24. Despriet, D.D.; van Duijn, C.M.; Oostra, B.A.; Uitterlinden, A.G.; Hofman, A.; Wright, A.F.; ten Brink, J.B.; Bakker, A.; de Jong, P.T.; Vingerling, J.R.; Bergen, A.A. and Klaver, C.C. Complement component C3 and risk of age-related macular degeneration.
    Ophthalmology 116(3):474-480, 2009 PubMed Abstract
    
    
25. Dovey, M.; Patton, E.E.; Bowman, T.; North, T.; Goessling, W.; Zhou, Y. and Zon, L.I. Topoisomerase II alpha is required for embryonic development and liver regeneration in zebrafish Mol.Cell Biol 29(13):3746-3753, 2009
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26. Dunlop, M.G. and Farrington, S.M. MUTYH-associated polyposis and colorectal cancer. Surg.Oncol.Clin N.Am 18(4):599-610, 2009
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27. Elstner, M.; Morris, C.M.; Heim, K.; Lichtner, P.; Bender, A.; Mehta, D.; Schulte, C.; Sharma, M.; Hudson, G.; Goldwurm, S.; Giovanetti, A.; Zeviani, M.; Burn, D.J.; McKeith, I.G.; Perry, R.H.; Jaros, E.; Kruger, R.; Wichmann, H.E.; Schreiber, S.; Campbell, H.; Wilson, J.F.; Wright, A.F.; Dunlop, M.; Pistis, G.; Toniolo, D.; Chinnery, P.F.; Gasser, T.; Klopstock, T.; Meitinger, T.; Prokisch, H. and Turnbull, D.M. Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease gene. Ann.Neurol. 66(6):792-798, 2009 PubMed Abstract
    
    
28. FANTOM Consortium: Suzuki, H.; Forrest, A.R.; van Nimwegen, E.; .....Semple, C.A.;....and Hayashizaki, Y. The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line.
    Nat Genet 41(5):553-562, 2009
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29. Gao, Y.; Du, Z.Q.; Wei, W.H.; Yu, X.J.; Deng, X.M.; Feng, C.G.; Fei, J.; Feng, J.D.; Li, N. and Hu, X.X. Mapping quantitative trait loci regulating chicken body composition traits.
    Anim Genet 40(6):952-954, 2009
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30. Gordon, C.T.; Tan, T.Y.; Benko, S.; Fitzpatrick, D.; Lyonnet, S. and Farlie, P.G. Long-range regulation at the SOX9 locus in development and disease.
    J Med Genet. 46(10):649-656, 2009 PubMed Abstract
    
    
31. Guo, Y.; Mao, H.; Ren, J.; Yan, X.; Duan, Y.; Yang, G.; Ren, D.; Zhang, Z.; Yang, B.; Ouyang, J.; Brenig, B.; Haley, C. and Huang, L. A linkage map of the porcine genome from a large-scale White Duroc x Erhualian resource population and evaluation of factors affecting recombination rates.
    Anim Genet. 40(1):47-52, 2009
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32. Haley, C. Human and livestock genetics: parallel evolution and horizontal exchange. J Animal Breed Genet 126:413-414, 2009 PubMed Abstract
    
    
33. Heale, B.S.; Keegan, L.P.; McGurk, L.; Michlewski, G.; Brindle, J.; Stanton, C.M.; Caceres, J.F. and O'Connell, M.A. Editing independent effects of ADARs on the miRNA/siRNA pathways.
    EMBO J. 28(20):3145-3156, 2009
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34. Heale, B.S.; Keegan, L.P. and O'Connell, M.A. ADARs have effects beyond RNA editing. Cell Cycle 8(24), 2009
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35. Heard-Costa, N.L.; Zillikens, M.C.; Monda, K.L.; Johansson, A.; Harris, T.B.; Fu, M.; Haritunians, T.; Feitosa, M.F.; Aspelund, T.; Eiriksdottir, G.; Garcia, M.; Launer, L.J.; Smith, A.V.; Mitchell, B.D.; McArdle, P.F.; Shuldiner, A.R.; Bielinski, S.J.; Boerwinkle, E.; Brancati, F.; Demerath, E.W.; Pankow, J.S.; Arnold, A.M.; Chen, Y.D.; Glazer, N.L.; McKnight, B.; Psaty, B.M.; Rotter, J.I.; Amin, N.; Campbell, H.; Gyllensten, U.; Pattaro, C.; Pramstaller, P.P.; Rudan, I.; Struchalin, M.; Vitart, V.; Gao, X.; Kraja, A.; Province, M.A.; Zhang, Q.; Atwood, L.D.; Dupuis, J.; Hirschhorn, J.N.; Jaquish, C.E.; O'Donnell, C.J.; Vasan, R.S.; White, C.C.; Aulchenko, Y.S.; Estrada, K.; Hofman, A.; Rivadeneira, F.; Uitterlinden, A.G.; Witteman, J.C.; Oostra, B.A.; Kaplan, R.C.; Gudnason, V.; O'Connell, J.R.; Borecki, I.B.; van Duijn, C.M.; Cupples, L.A.; Fox, C.S. and North, K.E. NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium.
    PLoS Genet. 5(6):e1000539, 2009
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36. Henderson, R.H.; Williamson, K.A.; Kennedy, J.S.; Webster, A.R.; Holder, G.E.; Robson, A.G.; Fitzpatrick, D.R.; van Heyningen. V. and Moore, A.T. A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction. Mol.Vis. 15:2442-2447, 2009
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37. Hicks, A.A.; Pramstaller, P.P.; Johansson, A.; Vitart, V.; Rudan, I.; Ugocsai, P.; Aulchenko, Y.; Franklin, C.S.; Liebisch, G.; Erdmann, J.; Jonasson, I.; Zorkoltseva, I.V.; Pattaro, C.; Hayward, C.; Isaacs, A.; Hengstenberg, C.; Campbell, S.; Gnewuch, C.; Janssens, A.C.; Kirichenko, A.V.; Konig, I.R.; Marroni, F.; Polasek, O.; Demirkan, A.; Kolcic, I.; Schwienbacher, C.; Igl, W.; Biloglav, Z.; Witteman, J.C.; Pichler, I.; Zaboli, G.; Axenovich, T.I.; Peters, A.; Schreiber, S.; Wichmann, H.E.; Schunkert, H.; Hastie, N.; Oostra, B.A.; Wild, S.H.; Meitinger, T.; Gyllensten, U.; van Duijn, C.M.; Wilson, J.F.; Wright, A.; Schmitz, G. and Campbell, H. Genetic determinants of circulating sphingolipid concentrations in European populations.
    PLoS Genet. 5(10):e1000672, 2009
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38. Hilton, E.; Johnston, J.; Whalen, S.; Okamoto, N.; Hatsukawa, Y.; Nishio, J.; Kohara, H.; Hirano, Y.; Mizuno, S.; Torii, C.; Kosaki, K.; Manouvrier, S.; Boute, O.; Perveen, R.; Law, C.; Moore, A.; Fitzpatrick, D.; Lemke, J.; Fellmann, F.; Debray, F.G.; Dastot-Le-Moal, F.; Gerard, M.; Martin, J.; Bitoun, P.; Goossens, M.; Verloes, A.; Schinzel, A.; Bartholdi, D.; Bardakjian, T.; Hay, B.; Jenny, K.; Johnston, K.; Lyons, M.; Belmont, J.W.; Biesecker, L.G.; Giurgea, I. and Black, G. BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects.
    Eur.J Hum.Genet. 17(10):1325-1335, 2009 PubMed Abstract
    
    
39. Hingorani, M.; Williamson, K.A.; Moore, A.T. and van Heyningen, V. Detailed ophthalmological evaluation of 43 individuals with PAX6 mutations. Invest Ophthalmol Vis Sci 50(6):2581-90, 2009 PubMed Abstract
    
    
40. Jackson, A.P. Diversifying microtubules in brain development.
    Nat.Genet. 41(6):638-640, 2009
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41. Johansson, A.; Marroni, F.; Hayward, C.; Franklin, C.S.; Kirichenko, A.V.; Jonasson, I.; Hicks, A.A.; Vitart, V.; Isaacs, A.; Axenovich, T.; Campbell, S.; Dunlop, M.G.; Floyd, J.; Hastie, N.; Hofman, A.; Knott, S.; Kolcic, I.; Pichler, I.; Polasek, O.; Rivadeneira, F.; Tenesa, A.; Uitterlinden, A.G.; Wild, S.H.; Zorkoltseva, I.V.; Meitinger, T.; Wilson, J.F.; Rudan, I.; Campbell, H.; Pattaro, C.; Pramstaller, P.; Oostra, B.A.; Wright, A.F.; van Duijn, C.M.; Aulchenko, Y.S. and Gyllensten, U. Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis. Hum Mol Genet 18(2):373-380, 2009 PubMed Abstract
    
    
42. Kang, J.; Reynolds, N.L.; Tyrrell, C.; Dorin, J.R. and MacMillan, D. Peptide thioester synthesis through N-->S acyl-transfer: application to the synthesis of a beta-defensin. Org.Biomol.Chem. 7(23):4918-4923, 2009
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43. Kleinjan, D.J. and Coutinho, P. Cis-ruption mechanisms: disruption of cis-regulatory control as a cause of human genetic disease. Brief.Funct.Genomic.Proteomic. 8(4):317-32, 2009
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44. Knezevic, A.; Polasek, O.; Gornik, O.; Rudan, I.; Campbell, H.; Hayward, C.; Wright, A.; Kolcic, I.; O'Donoghue, N.; Bones, J.; Rudd, P.M. and Lauc, G. Variability, heritability and environmental determinants of human plasma N-glycome. J.Proteome.Res 8(2):694-701, 2009 PubMed Abstract
    
    
45. Kocer, A.; Reichmann, J.; Best, D. and Adams, I.R. Germ Cell Sex Determination in Mammals.
    Mol Hum Reprod 15(4):205-213, 2009
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46. Kolz, M.; Johnson, T.; Sanna, S.; Teumer, A.; Vitart, V.; Perola, M.; Mangino, M.; Albrecht, E.; Wallace, C.; Farrall, M.; Johansson, A.; Nyholt, D.R.; Aulchenko, Y.; Beckmann, J.S.; Bergmann, S.; Bochud, M.; Brown, M.; Campbell, H.; Connell, J.; Dominiczak, A.; Homuth, G.; Lamina, C.; McCarthy, M.I.; Meitinger, T.; Mooser, V.; Munroe, P.; Nauck, M.; Peden, J.; Prokisch, H.; Salo, P.; Salomaa, V.; Samani, N.J.; Schlessinger, D.; Uda, M.; Volker, U.; Waeber, G.; Waterworth, D.; Wang-Sattler, R.; Wright, A.F.; Adamski, J.; Whitfield, J.B.; Gyllensten, U.; Wilson, J.F.; Rudan, I.; Pramstaller, P.; Watkins, H.; Doering, A.; Wichmann, H.E.; Spector, T.D.; Peltonen, L.; Volzke, H.; Nagaraja, R.; Vollenweider, P.; Caulfield, M.; Illig, T. and Gieger, C. Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.
    PLoS Genet 5(6):e1000504, 2009
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47. Kong, A.; Steinthorsdottir, V.; Masson, G…..the DIAGRAM Consortium (Navaro, P.); Ferguson-Smith, A.C.; Gudbjartsson, D.F.; Thorsteinsdottir, U. and Stefansson, K. Parental origin of sequence variants associated with complex diseases.
    Nature 462(7275):868-874, 2009
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48. Lam, A.C.; Powell, J.; Wei, W.H.; De Koning, D.J. and Haley, C.S. A combined strategy for quantitative trait loci detection by genome-wide association. BMC Proc. 3 Suppl 1(:S6, 2009
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49. Lemos, M.C.; Harding, B.; Reed, A.; Jeyabalan, J.; Walls, G.; Bowl, M.; Sharpe, J.; Wedden, S.; Moss, J.; Ross, A.; Davidson, D. and Thakker, R. Genetic background influences embryonic lethality and the occurrence of neural tube defects in Men1 null mice: relevance to genetic modifiers. J Endocrinol 203:133-142, 2009 PubMed Abstract
    
    
50. Long, J.C. and Caceres, J.F. The SR protein family of splicing factors: master regulators of gene expression.
    Biochem J 417(1):15-27, 2009
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51. Luciano, M.; Gow, A.J.; Harris, S.E.; Hayward, C.; Allerhand, M.; Starr, J.M.; Visscher, P.M. and Deary, I.J. Cognitive ability at age 11 and 70 years, information processing speed, and APOE variation: the Lothian Birth Cohort 1936 study. Psychol.Aging 24(1):129-138, 2009
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52. Luciano, M.; Gow, A.J.; Taylor, M.D.; Hayward, C.; Harris, S.E.; Campbell, H.; Porteous, D.J.; Starr, J.M.; Visscher, P.M. and Deary, I.J. Apolipoprotein E is not related to memory abilities at 70 years of age. Behav.Genet. 39(1):6-14, 2009 PubMed Abstract
    
    
53. Luciano, M.; Miyajima, F.; Lind, P.A.; Bates, T.C.; Horan, M.; Harris, S.E.; Wright, M.J.; Ollier, W.E.; Hayward, C.; Pendleton, N.; Gow, A.J.; Visscher, P.M.; Starr, J.M.; Deary, I.J.; Martin, N.G. and Payton, A. Variation in the dysbindin gene and normal cognitive function in three independent population samples.
    Genes Brain Behav. 8(2):218-227, 2009 PubMed Abstract
    
    
54. Macias, S.; Michlewski, G. and Caceres, J.F. Hormonal Regulation of MicroRNA Biogenesis.
    Molecular Cell 36:172-173, 2009
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55. Madsen, L.; Seeger, M.; Semple, C.A. and Hartmann-Petersen, R. New ATPase regulators--p97 goes to the PUB. Int.J Biochem.Cell Biol 41(12):2380-2388, 2009 PubMed Abstract
    
    
56. Marcucci, R.; Romano, M.; Feiguin, F.; O'Connell, M.A. and Baralle, F.E. Dissecting the splicing mechanism of the Drosophila editing enzyme; dADAR.
    Nucleic Acids Res 37(5):1663-71, 2009 PubMed Abstract
    
    
57. Mengel-From, J.; Wong, T.H.; Morling, N.; Rees, J.L. and Jackson, I.J. Genetic determinants of hair and eye colour in the Scottish and Danish populations
    BMC Genet. 10(1):88, 2009
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58. Mill, P.; Lee, A.W.; Fukata, Y.; Tsutsumi, R.; Fukata, M.; Keighren, M.; Porter, R.M.; McKie, L.; Smyth, I. and Jackson, I.J. Palmitoylation regulates epidermal homeostasis and hair follicle differentiation
    PLoS Genet. 5(11):e1000748, 2009
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59. Miller, T.D.; Jackson, A.P.; Barresi, R.; Smart, C.M.; Eugenicos, M.; Summers, D.; Clegg, S.; Straub, V. and Stone, J. Inclusion body myopathy with Paget disease and frontotemporal dementia (IBMPFD): clinical features including sphincter disturbance in a large pedigree.
    J Neurol Neurosurg Psychiatry 80(5):583-584, 2009
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60. Morey, C.; Kress, C. and Bickmore, W.A. Lack of bystander activation shows that localization exterior to chromosome territories is not sufficient to up-regulate gene expression.
    Genome Res 19(7):1184-1194, 2009 PubMed Abstract
    
    
61. Mort, R.L.; Ramaesh, T.; Kleinjan, D.A.; Morley, S.D. and West, J.D. Mosaic analysis of stem cell function and wound healing in the mouse corneal epithelium. BMC Dev.Biol. 9:4, 2009
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62. Nagamine, Y.; Pong-Wong, R.; Visscher, P.M. and Haley, C.S. Detection of multiple quantitative trait loci and their pleiotropic effects in outbred pig populations.
    Genet Sel Evol 41:44, 2009
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63. Palavicini, J.P.; O'Connell, M.A. and Rosenthal, J.J. An extra double-stranded RNA binding domain confers high activity to a squid RNA editing enzyme.
    RNA 15(6):1208-1218, 2009
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64. Pattaro, C.; Aulchenko, Y.S.; Isaacs, A.; Vitart, V.; Hayward, C.; Franklin, C.S.; Polasek, O.; Kolcic, I.; Biloglav, Z.; Campbell, S.; Hastie, N.; Lauc, G.; Meitinger, T.; Oostra, B.A.; Gyllensten, U.; Wilson, J.F.; Pichler, I.; Hicks, A.A.; Campbell, H.; Wright, A.F.; Rudan, I.; van Duijn, C.M.; Riegler, P.; Marroni, F. and Pramstaller, P.P. Genome-wide linkage analysis of serum creatinine in three isolated European populations.
    Kidney Int 76(3):297-306, 2009
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65. Peng, G.; Yim, E.K.; Dai, H.; Jackson, A.P.; Burgt, I.; Pan, M.R.; Hu, R.; Li, K. and Lin, S.Y. BRIT1/MCPH1 links chromatin remodelling to DNA damage response. Nat.Cell Biol 11(7):865-872, 2009
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66. Pidoux, A.L.; Choi, E.S.; Abbott, J.K.; Liu, X.; Kagansky, A.; Castillo, A.G.; Hamilton, G.L.; Richardson, W.; Rappsilber, J.; He, X. and Allshire, R.C. Fission yeast Scm3: A CENP-A receptor required for integrity of subkinetochore chromatin.
    Mol.Cell 33(3):299-311, 2009
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67. Polasek, O.; Marusic, A.; Rotim, K.; Hayward, C.; Vitart, V.; Huffman, J.; Campbell, S.; Jankovic, S.; Boban, M.; Biloglav, Z.; Kolcic, I.; Krzelj, V.; Terzic, J.; Matec, L.; Tometic, G.; Nonkovic, D.; Nincevic, J.; Pehlic, M.; Zedelj, J.; Velagic, V.; Juricic, D.; Kirac, I.; Belak, K.S.; Wright, A.F.; Campbell, H. and Rudan, I. Genome-wide association study of anthropometric traits in Korcula Island, Croatia. Croat Med J 50(1):7-16, 2009 PubMed Abstract
    
    
68. Poulton, L.D.; Nolan, K.F.; Anastasaki, C.; Waldmann, H. and Patton, E.E. A novel role for Glucocorticoid-Induced TNF Receptor Ligand (Gitrl) in early embryonic zebrafish development. Int.J Dev.Biol, e-pub July 1, 2009
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69. Riches, P.L.; Wright, A.F. and Ralston, S.H. Recent insights into the pathogenesis of hyperuricaemia and gout.
    Hum.Mol.Genet. 18(R2):R177-R184, 2009 PubMed Abstract
    
    
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