Showing results 4917 to 4936 of 4943
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| Preview | Issue Date | Title | Author(s) |
| 1995 | X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome | Gedeon, A.; Wilson, M.; Colley, A.; Sillence, D.; Mulley, J. |
| 2003 | X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in PAK3 | Gedeon, A.; Nelson, J.; Gecz, J.; Mulley, J. |
| 2002 | X-linked myoclonic epilepsy with spasticity and intellectual disability - Mutation in the homeobox gene ARX | Scheffer, I.; Wallace, R.; Phillips, F.; Hewson, P.; Reardon, K.; Parasivam, G.; Stromme, P.; Berkovic, S.; Gecz, J.; Mulley, J. |
| 1995 | X-Y chromosome dissociation in mice and rats exposed to increased testicular or environmental temperatures | Van Zelst, S.; Zupp, J.; Hayman, D.; Setchell, B. |
| 2012 | Xenobiotics and loss of cell adhesion drive distinct transcriptional outcomes by aryl hydrocarbon receptor signaling | Hao, N.; Lee, K.; Furness, S.; Bosdotter, C.; Poellinger, L.; Whitelaw, M. |
| 2000 | Xenorhabdus bovienii T228 phase variation and virulence are independent of RecA function | Pinyon, R.A.; Hew, F.H.; Thomas, CJ, |
| 2012 | XMRV and prostate cancer - a 'final' perspective | Sfanos, K.S.; Aloia, A.L.; De Marzo, A.M.; Rein, A. |
| 2010 | XMRV: a new virus in prostate cancer? | Aloia, A.; Sfanos, K.; Isaacs, W.; Zheng, Q.; Maldarelli, F.; De Marzo, A.; Rein, A. |
| 2013 | XThe eEF2 kinase confers resistance to nutrient deprivation by blocking translation elongation | Leprivier, G.; Remke, M.; Rotblat, B.; Dubuc, A.; Mateo, A.; Kool, M.; Agnihotri, S.; El-Naggar, A.; Yu, B.; Prakash Somasekharan, S.; Faubert, B.; Bridon, G.; Tognon, C.; Mathers, J.; Thomas, R.; Li, A.; Barokas, A.; Kwok, B.; Bowden, M.; Smith, S.; et al. |
| 2012 | XX male sex reversal with genital abnormalities associated with a de novo SOX3 gene duplication | Moalem, S.; Babul-Hirji, R.; Stavropolous, D.; Wherrett, D.; Bagli, D.; Thomas, P.; Chitayat, D. |
| 2013 | Y-Chromosome and mtDNA genetics reveal significant contrasts in affinities of modern Middle Eastern populations with European and African populations | Badro, D.; Douaihy, B.; Haber, M.; Youhanna, S.; Salloum, A.; Ghassibe-Sabbagh, M.; Johnsrud, B.; Khazen, G.; Matisoo-Smith, E.; Soria-Hernanz, D.; Wells, R.; Tyler-Smith, C.; Platt, D.; Zalloua, P.; Caramelli, D. |
| 1995 | The yeast tribrid system | Osborne, M. A.; Dalton, Stephen; Kochar, J. |
| 2013 | Yunis-Varón Syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase | Campeau, P.; Lenk, G.; Lu, J.; Bae, Y.; Burrage, L.; Turnpenny, P.; Corona-Rivera, J.; Morandi, L.; Mora, M.; Reutter, H.; Vulto-van Silfhout, A.; Faivre, L.; Haan, E.; Gibbs, R.; Meisler, M.; Lee, B. |
| 2017 | YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction | Gabriele, M.; Vulto-van Silfhout, A.; Germain, P.; Vitriolo, A.; Kumar, R.; Douglas, E.; Haan, E.; Kosaki, K.; Takenouchi, T.; Rauch, A.; Steindl, K.; Frengen, E.; Misceo, D.; Pedurupillay, C.; Stromme, P.; Rosenfeld, J.; Shao, Y.; Craigen, W.; Schaaf, C.; Rodriguez-Buritica, D.; et al. |
| 2003 | ZccR-a MerR-like regulator from Bordetella pertussis which responds to zinc, cadmium, and cobalt | Kidd, S.; Brown, N. |
| 2007 | Zebrafish Angiotensin II receptor-like 1a (agtrl1a) is expressed in migrating hypoblast, vasculature, and in multiple embryonic epithelia | Tucker, B.; Hepperle, C.; Kortschak, R.; Rainbird, B.; Wells, S.; Oates, A.; Lardelli, M. |
| 2009 | Zebrafish aplnra functions in epiboly | Nornes, S.; Tucker, B.; Lardelli, M. |
| 2011 | Zebrafish as a tool in Alzheimer's disease research | Newman, M.; Verdile, G.; Martins, R.; Lardelli, M. |
| 2004 | Zebrafish fgfr1 is a member of the fgf8 synexpression group and is required for fgf8 signalling at the midbrain-hindbrain boundary | Scholpp, S.; Groth, C.; Lohs, C.; Lardelli, M.; Brand, M. |
| 2005 | Zinc inhibits human CIC-1 muscle chloride channel by interacting with its common gating mechanism | Duffield, M.; Rychkov, G.; Bretag, A.; Roberts, M. |
