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Results 61-70 of 246 (Search time: 0.01 seconds).
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PreviewIssue DateTitleAuthor(s)
2017Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsyEwans, L.; Field, M.; Zhu, Y.; Turner, G.; Leffler, M.; Dinger, M.; Cowley, M.; Buckley, M.; Scheffer, I.; Jackson, M.; Roscioli, T.; Shoubridge, C.
2016Evolutionary novelty in a butterfly wing pattern through enhancer shufflingWallbank, R.; Baxter, S.; Pardo-Diaz, C.; Hanly, J.; Martin, S.; Mallet, J.; Dasmahapatra, K.; Salazar, C.; Joron, M.; Nadeau, N.; McMillan, W.; Jiggins, C.
2016Major improvements to the Heliconius melpomene genome assembly used to confirm 10 chromosome fusion events in 6 million years of butterfly evolutionDavey, J.; Chouteau, M.; Barker, S.; Maroja, L.; Baxter, S.; Simpson, F.; Merrill, R.; Joron, M.; Mallet, J.; Dasmahapatra, K.; Jiggins, C.
2018A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiencyJansen, S.; Hoischen, A.; Coe, B.; Carvill, G.; van Esch, H.; Bosch, D.; Andersen, U.; Baker, C.; Bauters, M.; Bernier, R.; van Bon, B.; Claahsen-van der Grinten, H.; Gecz, J.; Gilissen, C.; Grillo, L.; Hackett, A.; Kleefstra, T.; Koolen, D.; Kvarnung, M.; Larsen, M.; et al.
2013The Guinea Pig as a model for sporadic Alzheimer's Disease (AD): the impact of cholesterol intake on expression of AD-related genesSharman, M.; Moussavi Nik, S.; Chen, M.; Ong, D.; Wijaya, L.; Laws, S.; Taddei, K.; Newman, M.; Lardelli, M.; Martins, R.; Verdile, G.
2017Unravelling mummies: cryptic diversity, host specificity, trophic and coevolutionary interactions in psyllid-parasitoid food websHall, A.; Steinbauer, M.; Taylor, G.; Johnson, S.; Cook, J.; Riegler, M.
2015Abrupt warming events drove Late Pleistocene Holarctic megafaunal turnoverCooper, A.; Turney, C.; Hughen, K.; Brook, B.; McDonald, H.; Bradshaw, C.
2015Chromosomal instability triggers cell death via local signalling through the innate immune receptor TollLiu, D.; Shaukat, Z.; Saint, R.; Gregory, S.
2012Robust homeostasis of Presenilin1 protein levels by transcript regulationNewman, M.; Nornes, S.; Martins, R.; Lardelli, M.
2013Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disordersNguyen, L.; Kim, H.; Rosenfeld, J.; Shen, Y.; Gusella, J.; Lacassie, Y.; Layman, L.; Shaffer, L.; Gecz, J.