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Results 31-40 of 105 (Search time: 0.005 seconds).
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PreviewIssue DateTitleAuthor(s)
2022Retrotransposon instability dominates the acquired mutation landscape of mouse induced pluripotent stem cells.Gerdes, P.; Lim, S.M.; Ewing, A.D.; Larcombe, M.R.; Chan, D.; Sanchez-Luque, F.J.; Walker, L.; Carleton, A.L.; James, C.; Knaupp, A.S.; Carreira, P.E.; Nefzger, C.M.; Lister, R.; Richardson, S.R.; Polo, J.M.; Faulkner, G.J.
2023Human gene-engineered calreticulin mutant stem cells recapitulate MPN hallmarks and identify targetable vulnerabilitiesFoßelteder, J.; Pabst, G.; Sconocchia, T.; Schlacher, A.; Auinger, L.; Kashofer, K.; Beham-Schmid, C.; Trajanoski, S.; Waskow, C.; Schöll, W.; Sill, H.; Zebisch, A.; Wölfler, A.; Thomas, D.; Reinisch, A.
2013The genomic landscape of hypodiploid acute lymphoblastic leukemiaTo, L.
2016The First Histidine Triad Motif of PhtD Is Critical for Zinc Homeostasis in Streptococcus pneumoniaeEijkelkamp, B.; Pederick, V.; Plumptre, C.; Harvey, R.; Hughes, C.; Paton, J.; McDevitt, C.; Camilli, A.
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.
2013A tudor domain protein SPINDLIN1 interacts with the mRNA-binding protein SERBP1 and is involved in mouse oocyte meiotic resumptionChew, T.; Peaston, A.; Lim, A.; Lorthongpanich, C.; Knowles, B.; Solter, D.; Sun, Q.-Y.
2004Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neuronsColombo, E.; Galli, R.; Cossu, G.; Gecz, J.; Broccoli, V.
2013ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticityHirata, H.; McMichael, G.; Haan, E.; MacLennan, A.; Yap, T.; Nguyen, L.; Shaw, M.; Gecz, J.
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.
2008An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing lossGuipponi, M.; Toh, M.; Tan, J.; Park, D.; Hanson, K.; Ballana, E.; Kwong, D.; Cannon, P.; Wu, Q.; Gout, A.; Delorenzi, M.; Speed, T.; Smith, R.; Dahl, H.; Petersen, M.; Teasdale, R.; Estivill, X.; Park, W.; Scott, H.

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