Showing results 393 to 412 of 446
< previous
next >
| Preview | Issue Date | Title | Author(s) |
| 1996 | The first gene for an idiopathic epilepsy: A fruitful collaboration of Australian Clinical Research and Molecular Genetics | Berkovic, S.; Mulley, J. |
| 2015 | The gasteruptiid wasp fauna of New Caledonia, with description of three new species of Gasteruption (Hymenoptera: Evanioidea: Gasteruptiidae) | Jennings, J.; Jourdan, H.; Krogmann, L.; Parslow, B. |
| 2016 | The genetic history of Ice Age Europe | Fu, Q.; Posth, C.; Hajdinjak, M.; Petr, M.; Mallick, S.; Fernandes, D.; Furtwängler, A.; Haak, W.; Meyer, M.; Mittnik, A.; Nickel, B.; Peltzer, A.; Rohland, N.; Slon, V.; Talamo, S.; Lazaridis, I.; Lipson, M.; Mathieson, I.; Schiffels, S.; Skoglund, P.; et al. |
| 2016 | The genetic history of Peruvian Quechua-Lamistas and Chankas: uniparental DNA Patterns among autochthonous Amazonian and Andean populations | Sandoval, J.; Lacerda, D.; Acosta, O.; Jota, M.; Robles-Ruiz, P.; Salazar-Granara, A.; Vieira, P.; Paz-y-Miño, C.; Fujita, R.; Santos, F.; Jin, L.; Li, H.; Li, S.; Swamikrishnan, P.; Javed, A.; Parida, L.; Royyuru, A.; Mitchell, R.; Zalloua, P.; Adhikarla, S.; et al. |
| 1997 | The genome organisation of the Fanconi Anemia Group A (FAA) Gene | Ianzano, L.; d'Apolito, M.; Centra, M.; Savino, M.; Levran, O.; Auerbach, A.; Cleton-Jansen, A.M.; Doggett, N.; Pronk, J.; Tipping, A.; Gibson, R.; Mathew, C.; Whitmore, S.; Apostolou, S.; Callen, D.; Zelante, L.; Savoia, A. |
| 2018 | The genomic history of southeastern Europe | Mathieson, I.; Alpaslan-Roodenberg, S.; Posth, C.; Szécsényi-Nagy, A.; Rohland, N.; Mallick, S.; Olalde, I.; Broomandkhoshbacht, N.; Candilio, F.; Cheronet, O.; Fernandes, D.; Ferry, M.; Gamarra, B.; Fortes, G.G.; Haak, W.; Harney, E.; Jones, E.; Keating, D.; Krause-Kyora, B.; Kucukkalipci, I.; et al. |
| 2013 | The Guinea Pig as a model for sporadic Alzheimer's Disease (AD): the impact of cholesterol intake on expression of AD-related genes | Sharman, M.; Moussavi Nik, S.; Chen, M.; Ong, D.; Wijaya, L.; Laws, S.; Taddei, K.; Newman, M.; Lardelli, M.; Martins, R.; Verdile, G.; Götz, J. |
| 1998 | The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome. | Kortschak, R.; Reimann, H.; Zimmer, M.; Eyre, H.; Saint, R.; Jenne, D. |
| 1998 | The identification and localisation of a human gene with sequence similarity to Polycomblike of Drosophila melanogaster | Coulson, M.; Robert, S.; Eyre, H.; Saint, R. |
| 2016 | The impact of anchored phylogenomics and taxon sampling on phylogenetic inference in narrow-mouthed frogs (Anura, Microhylidae) | Peloso, P.; Frost, D.; Richards, S.; Rodrigues, M.; Donnellan, S.; Matsui, M.; Raxworthy, C.; Biju, S.; Lemmon, E.; Lemmon, A.; Wheeler, W. |
| 2012 | The impact of cholesterol intake on expression of Alzheimer's disease–related genes in the guinea pig brain | Moussavi Nik, S.H.; Verdile, G.; Sharman, M.; Chen, M.; Ong, D.; Wijaya, L.; Newman, M.; Lardelli, M.; Martins, R.; Alzheimer's Association International Conference (14 Jul 2012 - 19 Jul 2012 : Vancouver, British Columbia) |
| 2019 | The impact of genetic adaptation on chimpanzee subspecies differentiation | Schmidt, J.M.; de Manuel, M.; Marques-Bonet, T.; Castellano, S.; Andrés, A.M.; Gojobori, T. |
| 2023 | The impact of the cytoplasmic ubiquitin ligase TNFAIP3 gene variation on transcription factor NF-κB activation in acute kidney injury | Rogers, N.M.; Zammit, N.; Nguyen-Ngo, D.; Souilmi, Y.; Minhas, N.; Meijles, D.N.; Self, E.; Walters, S.N.; Warren, J.; Cultrone, D.; El-Rashid, M.; Li, J.; Chtanova, T.; O'Connell, P.J.; Grey, S.T. |
| 2021 | The inflated significance of neutral genetic diversity in conservation genetics | Teixeira, J.C.; Huber, C.D. |
| 2014 | The ink sac clouds octopod evolutionary history | Strugnell, J.; Norman, M.; Vecchione, M.; Guzik, M.; Allcock, A. |
| 1996 | The molecular organisation of a B chromosome tandem repeat sequence from Brachycome dichromosomatica | Franks, T.; Houben, A.; Leach, C.; Timmis, J. |
| 2021 | The Nestin neural enhancer is essential for normal levels of endogenous Nestin in neuroprogenitors but is not required for embryo development | Thomson, E.; Dawson, R.; H'ng, C.H.; Adikusuma, F.; Piltz, S.; Thomas, P.Q.; Varshney, G. |
| 2010 | The origin, early history and diversification of Lepidosauromorph reptiles | Evans, S.E.; Jones, M.E.; Bandyopadhyay, S. |
| 2007 | The original Lujan syndrome family has a novel missense mutation (p. N1007S) in the MED12 gene | Schwartz, C.; Tarpey, P.; Lubs, H.; Verloes, A.; May, M.; Risheg, H.; Friez, M.; Futreal, P.; Edkins, S.; Teague, J.; Briault, S.; Skinner, C.; Bauer-Carlin, A.; Simensin, R.; Joseph, S.; Jones, J.; Gecz, J.; Stratton, M.; Raymond, F.; Stevenson, R. |
| 1999 | The PISSLRE Gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer | Crawford, J.; Ianzano, L.; Savino, M.; Whitmore, S.; Cleton-Jansen, A.M.; Settasatian, C.; d'Apolito, M.; Seshadri, R.; Pronk, J.; Auerbach, A.; Verlander, P.; Mathew, C.; Tipping, A.; Doggett, N.; Zelante, L.; Callen, D.; Savoia, A. |
