Showing results 21 to 40 of 446
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| Preview | Issue Date | Title | Author(s) |
| 1998 | A new pineoblastoma cell line, PER-480, with der(10)t(10;17), der(16)t(1;16), & enhanced MYC expression in the absence of gene amplification. | Kees, U.; Spagnolo, D.; Hallam, L.; Ford, J.; Ranford, P.; Baker, D.; Callen, D.; Biegel, J. |
| 2012 | A new species of extinct little owl from the Pleistocene of Mallorca (Balearic Islands) | Guerra, C.; Bover, P.; Alcover, J.A. |
| 2016 | A new species of Rattus (Rodentia: Muridae) from Manus Island, Papua New Guinea | Timm, R.M.; Weijola, V.; Aplin, K.A.; Donnellan, S.C.; Flannery, T.F.; Thomson, V.; Pine, R.H. |
| 2014 | A new vetulicolian from Australia and its bearing on the chordate affinities of an enigmatic Cambrian group | Garcia-Bellido, D.; Lee, M.; Edgecombe, G.; Jago, J.; Gehling, J.; Paterson, J. |
| 2015 | A novel forensic DNA profiling technique for protected species | Ciavaglia, S.; Donnellan, S.; Tobe, S.; Henry, J.; Linacre, A. |
| 1998 | A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis. | Town, M.; Jean, G.; Cherqui, S.; Attard, M.; Forestier, L.; Whitmore, S.; Callen, D.; Gribouval, O.; Broyer, M.; Bates, G.; van't Hoff, W.; Antignac, C. |
| 2021 | A novel GSN variant outside the G2 calcium-binding domain associated with Amyloidosis of the Finnish type | Mullany, S.; Souzeau, E.; Klebe, S.; Zhou, T.; Knight, L.S.W.; Qassim, A.; Berry, E.C.; Marshall, H.; Hussey, M.; Dubowsky, A.; Breen, J.; Hassall, M.M.; Mills, R.A.; Craig, J.E.; Siggs, O.M. |
| 1997 | A novel method for development of species and strain-specific DNA proves and PCR primers for identifying Burkholderia Solanacearum (formerly Pseudomonas Solanacearum) | Opina, N.; Tavner, F.; Hollway, G.; Wang, J.F.; Li, T.H.; Maghirang, R.; Fegan, M.; Hayward, A.; Krishnapillai, V.; Hong, W.; Holloway, B.; Timmis, J. |
| 1996 | A novel mutation in Exon 6 (F236S) of the proteolipid protein gene is associated with spastic paraplegia | Donnelly, A.; Colley, A.; Crimmins, D.; Mulley, J. |
| 1998 | A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy. | Donnelly, A.; Haan, E.; Manson, J.; Mulley, J. |
| 1996 | A novel X-linked gene, G4.5. is responsible for Barth Syndrome | Bione, S.; D'Adamo, P.; Maestrini, E.; Gedeon, A.; Bolhuis, P.; Toniolo, D. |
| 2010 | A p53-dependent mechanism underlies macrocytic anemia in a mouse model of human 5q- syndrome | Barlow, J.; Drynan, L.; Hewett, D.; Holmes, L.; Lorenzo-Abalde, S.; Lane, A.; Jolin, H.; Pannell, R.; Middleton, A.; Wong, S.; Warren, A.; Wainscoat, J.; Boultwood, J.; McKenzie, A. |
| 2017 | A paleogenetic perspective on the early population history of the high altitude Andes | Fehren-Schmitz, L.; Harkins, K.; Llamas, B. |
| 2020 | A paleogenomic reconstruction of the deep population history of the Andes | Nakatsuka, N.; Lazaridis, I.; Barbieri, C.; Skoglund, P.; Rohland, N.; Mallick, S.; Posth, C.; Harkins-Kinkaid, K.; Ferry, M.; Harney, É.; Michel, M.; Stewardson, K.; Novak-Forst, J.; Capriles, J.M.; Durruty, M.A.; Álvarez, K.A.; Beresford-Jones, D.; Burger, R.; Cadwallader, L.; Fujita, R.; et al. |
| 2016 | A predictive computational framework for direct reprogramming between human cell types | Rackham, O.J.L.; Firas, J.; Fang, H.; Oates, M.E.; Holmes, M.L.; Knaupp, A.S.; Suzuki, H.; Nefzger, C.M.; Daub, C.O.; Shin, J.W.; Petretto, E.; Forrest, A.R.R.; Hayashizaki, Y.; Polo, J.M.; Gough, J. |
| 2016 | A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape | Ried, J.; Jeff, J.; Chu, A.; Bragg-Gresham, J.; Van Dongen, J.; Huffman, J.; Ahluwalia, T.; Cadby, G.; Eklund, N.; Eriksson, J.; Esko, T.; Feitosa, M.; Goel, A.; Gorski, M.; Hayward, C.; Heard-Costa, N.; Jackson, A.; Jokinen, E.; Kanoni, S.; Kristiansson, K.; et al. |
| 1999 | A putative exchange factor for Rho1 GTPase is required for initiation of cytokinesis in Drosophila | Prokopenko, S.; Brumby, A.; O'Keefe, L.; Prior, L.; He, Y.; Saint, R.; Bellen, H. |
| 2017 | A recurrent de novo nonsense variant in ZSWIM6 results in severe intellectual disability without frontonasal or limb malformations | Palmer, E.E.; Kumar, R.; Gordon, C.T.; Shaw, M.; Hubert, L.; Carroll, R.; Rio, M.; Murray, L.; Leffler, M.; Dudding-Byth, T.; Oufadem, M.; Lalani, S.R.; Lewis, A.M.; Xia, F.; Tam, A.; Webster, R.; Brammah, S.; Filippini, F.; Pollard, J.; Spies, J.; et al. |
| 1997 | A repetitive DNA sequence common to the different B chromosomes of the genus Brachycome | Houben, A.; Leach, C.; Verlin, D.; Rofe, R.; Timmis, J. |
| 2012 | A type VI secretion system encoding locus is required for bordetella bronchiseptica immunomodulation and persistence in vivo | Weyrich, L.; Rolin, O.; Muse, S.; Park, J.; Spidale, N.; Kennett, M.; Hester, S.; Chen, C.; Dudley, E.; Harvill, E.; Boneca, I. |
