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Issue Date	Title	Author(s)
2019	Alternative splicing in a presenilin 2 variant associated with Alzheimer disease	Braggin, J.E.; Bucks, S.A.; Course, M.M.; Smith, C.L.; Sopher, B.; Osnis, L.; Shuey, K.D.; Domoto-Reilly, K.; Caso, C.; Kinoshita, C.; Scherpelz, K.P.; Cross, C.; Grabowski, T.; Nik, S.H.M.; Newman, M.; Garden, G.A.; Leverenz, J.B.; Tsuang, D.; Latimer, C.; Gonzalez-Cuyar, L.F.; et al.
2013	Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features	Bonnefond, A.; Raimondo, A.; Stutzmann, F.; Ghoussaini, M.; Ramachandrappa, S.; Bersten, D.; Durand, E.; Vatin, V.; Balkau, B.; Lantieri, O.; Raverdy, V.; Pattou, F.; Van Hul, W.; Van Gaal, L.; Peet, D.; Weill, J.; Miller, J.; Horber, F.; Goldstone, A.; Driscoll, D.; et al.
2008	Effect of 6-month calorie restriction and exercise on serum and liver lipids and markers of liver function	Larson-Meyer, D.; Newcomer, B.; Heilbronn, L.; Volaufova, J.; Smith, S.; Alfonso, A.; Lefevre, M.; Rood, J.; Williamson, D.; Ravussin, E.; DeLany, J.; de Jonge, L.; Nguyen, T.; Martin, C.; Most, M.; Greenway, F.; York-Crowe, E.; Anton, S.; Champagne, C.; Dahmer, B.; et al.
2013	Mutations in DEPDC5 cause familial focal epilepsy with variable foci	Dibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.