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| Preview | Issue Date | Title | Author(s) |
| 2017 | Mitochondrion to endoplasmic reticulum apposition length in zebrafish embryo spinal progenitors is unchanged in response to perturbations associated with Alzheimer’s disease | Newman, M.; Halter, L.; Lim, A.; Lardelli, M.; Lakshmana, M. |
| 2021 | Mitogenomes reveal two major influxes of Papuan ancestry across Wallacea following the last glacial maximum and Austronesian contact | Purnomo, G.A.; Mitchell, K.J.; O'Connor, S.; Kealy, S.; Taufik, L.; Schiller, S.; Rohrlach, A.; Cooper, A.; Llamas, B.; Sudoyo, H.; Teixeira, J.C.; Tobler, R. |
| 2013 | MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype study | Makrythanasis, P.; van Bon, B.; Steehouwer, M.; Rodríguez-Santiago, B.; Simpson, M.; Dias, P.; Anderlid, B.; Arts, P.; Bhat, M.; Augello, B.; Biamino, E.; Bongers, E.; del Campo, M.; Cordeiro, I.; Cueto-González, A.; Cuscó, I.; Deshpande, C.; Frysira, E.; Izatt, L.; Flores, R.; et al. |
| 2017 | Modelling predictors of molecular response to frontline imatinib for patients with chronic myeloid leukaemia | Banjar, H.; Ranasinghe, D.; Brown, F.; Adelson, D.; Kroger, T.; Leclercq, T.; White, D.; Hughes, T.; Chaudhri, N.; Speletas, M. |
| 1997 | Molecular characterisation of mutants of the acetate regulatory gene facB of Aspergillus nidulans | Todd, R.; Kelly, J.; Davis, M.; Hynes, M. |
| 1998 | Molecular systematics of Australian rhinolophid bats (Chiroptera:Rhinolophidae). | Cooper, S.; Reardon, T.; Skilins, J. |
| 2019 | Morphological evolution and modularity of the caecilian skull | Bardua, C.; Marshall, A.; Gower, D.J.; Wilkinson, M.; Sherratt, E.; Goswami, A. |
| 2015 | Morphological phylogenetics in the genomic age | Lee, M.; Palci, A. |
| 1987 | Multiple copies of the amdS gene of Aspergillus nidulans cause titration of trans-acting regulatory proteins | Kelly, J.M.; Hynes, M.J. |
| 1999 | Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3 | Cleton-Jansen, A.M.; Moerland, E.; Pronk, J.; Van Berkel, C.; Apostolou, S.; Crawford, J.; Savoia, A.; Auerbach, A.; Callen, D.; Cornelisse, C. |
| 2017 | Mutations in the Katnb1 gene cause left-right asymmetry and heart defects | Furtado, M.B.; Merriner, D.J.; Berger, S.; Rhodes, D.; Jamsai, D.; O'Bryan, M.K. |
| 2016 | Myth or relict: does ancient DNA detect the enigmatic Upland seal? | Salis, A.T.; Easton, L.J.; Robertson, B.C.; Gemmell, N.; Smith, I.W.G.; Weisler, M.I.; Waters, J.M.; Rawlence, N.J. |
| 2014 | Natural history and galsulfase treatment in mucopolysaccharidosis VI (MPS VI, Maroteaux-Lamy syndrome)-10-year follow-up of patients who previously participated in an MPS VI survey study | Giugliani, R.; Lampe, C.; Guffon, N.; Ketteridge, D.; Leão-Teles, E.; Wraith, J.E.; Jones, S.A.; Piscia-Nichols, C.; Lin, P.; Quartel, A.; Harmatz, P. |
| 2017 | Neanderthal behaviour, diet, and disease inferred from ancient DNA in dental calculus | Weyrich, L.; Duchene, S.; Soubrier, J.; Arriola, L.; Llamas, B.; Breen, J.; Morris, A.; Alt, K.; Caramelli, D.; Dresely, V.; Farrell, M.; Farrer, A.; Francken, M.; Gully, N.; Haak, W.; Hardy, K.; Harvati, K.; Held, P.; Holmes, E.; Kaidonis, J.; et al. |
| 1998 | Neural precursor differentiation into astrocytes requires signaling through the leukemia inhibitory factor receptor. | Koblar, S.; Turnley, A.; Classon, B.; Reid, K.; Ware, C.; Cheema, S.; Murphy, M.; Bartlett, P. |
| 2018 | Neutron scanning reveals unexpected complexity in the enamel thickness of an herbivorous Jurassic reptile | Jones, M.; Lucas, P.; Tucker, A.; Watson, A.; Sertich, J.; Foster, J.; Williams, R.; Garbe, U.; Bevitt, J.; Salvemini, F. |
| 2014 | New Middle Cambrian palaeoscolecid sclerites of Hadimopanella oezgueli from the Cantabrian Mountains, northern Spain | Barragán, T.; Esteve, J.; Garcia-Bellido, D.C.; Zamora, S.; Álvaro, J.J. |
| 2015 | Non-genetic inheritance, fertility and assisted reproductive technologies | Zander-Fox, D.; Mc Pherson, N.; Lane, M. |
| 2017 | Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome) | Javadiyan, S.; Craig, J.; Sharma, S.; Lower, K.; Casey, T.; Haan, E.; Souzeau, E.; Burdon, K. |
| 2014 | Novel mitochondrial DNA primers for identification of population trends in longnose suckers (Catostomus catostomus) and multispecies identification | Langille, B.; Perry, R.; Keefe, D.; Marshall, H. |
