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Results 1-10 of 40 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2017A novel embryo culture media supplement that improves pregnancy rates in miceHighet, A.; Bianco-Miotto, T.; Pringle, K.; Peura, A.; Bent, S.; Zhang, J.; Nottle, M.; Thompson, J.; Roberts, C.
2014Placental restriction of fetal growth reduces cutaneous responses to antigen after sensitization in sheepWooldridge, A.; Bischof, R.; Meeusen, E.; Liu, H.; Heinemann, G.; Hunter, D.; Giles, L.; Kind, K.; Owens, J.; Clifton, V.; Gatford, K.
2014Rapidly alternating photoperiods disrupt central and peripheral rhythmicity and decrease plasma glucose, but do not affect glucose tolerance or insulin secretion in sheepVarcoe, T.; Gatford, K.; Voultsios, A.; Salkeld, M.; Boden, M.; Rattanatray, L.; Kennaway, D.
2017Targeted insertion of an anti-CD2 monoclonal antibody transgene into the GGTA1 locus in pigs using FokI-dCas9Nottle, M.; Salvaris, E.; Fisicaro, N.; McIlfatrick, S.; Vassiliev, I.; Hawthorne, W.; O'Connell, P.; Brady, J.; Lew, A.; Cowan, P.
2014Modifications of human growth differentiation factor 9 to improve the generation of embryos from low competence oocytesLi, J.; Sugimura, S.; Mueller, T.; White, M.; Martin, G.; Ritter, L.; Liang, X.; Gilchrist, R.; Mottershead, D.
2016Prenatal fish oil supplementation and allergy: 6-year follow-up of a randomized controlled trialBest, K.P.; Sullivan, T.; Palmer, D.; Gold, M.; Kennedy, D.J.; Martin, J.; Makrides, M.
2013A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndromeBuchovecky, C.; Turley, S.; Brown, H.; Kyle, S.; McDonald, J.; Liu, B.; Pieper, A.; Huang, W.; Katz, D.; Russell, D.; Shendure, J.; Justice, M.
2012A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disabilityHuang, L.; Jolly, L.; Willis-Owen, S.; Gardner, A.; Sharma, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M.; Hackett, A.; Field, M.; Froyen, G.; Hu, H.; Haas, S.; Ropers, H.; Kalscheuer, V.; Corbett, M.; Gecz, J.
2015HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.Jolly, L.; Nguyen, L.; Domingo, D.; Sun, Y.; Barry, S.; Hancarova, M.; Plevova, P.; Vlckova, M.; Havlovicova, M.; Kalscheuer, V.; Graziano, C.; Pippucci, T.; Bonora, E.; Sedlacek, Z.; Gecz, J.
2013Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndromeAoki, Y.; Niihori, T.; Banjo, T.; Okamoto, N.; Mizuno, S.; Kurosawa, K.; Ogata, T.; Takada, F.; Yano, M.; Ando, T.; Hoshika, T.; Barnett, C.; Ohashi, H.; Kawame, H.; Hasegawa, T.; Okutani, T.; Nagashima, T.; Hasegawa, S.; Funayama, R.; Nagashima, T.; et al.