Showing results 1989 to 2008 of 3321
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| Preview | Issue Date | Title | Author(s) |
| 2001 | Mutant GABAA receptor g2-subunit in childhood absence epilepsy and febrile seizures | Wallace, R.; Marini, C.; Petrou, S.; Harkin, L.; Bowser, D.; Panchal, R.; Williams, D.; Sutherland, G.; Mulley, J.; Scheffer, I.; Berkovic, S. |
| 2003 | Mutation induced enhancement of Al tolerance in barley cell lines | Zhu, M.; Pan, J.; Wang, L.; Gu, Q.; Huang, C. |
| 2003 | Mutation of luxS of Streptococcus pneumoniae affects virulence in a mouse model | Stroeher, U.; Paton, A.; Ogunniyi, A.; Paton, J. |
| 2001 | Mutational analysis of protein substrate presentation in the post-translational attachment of biotin to biotin domains | Polyak, S.; Chapman-Smith, A.; Mulhern, T.; Cronan Jr., J.; Wallace, J. |
| 2003 | Mutational analysis of the Acropora millepora PaxD paired domain highlights the importance of the linker region for DNA binding | Nordstrom, K.; Scholten, I.; Nordstrom, J.; Larhammar, D.; Miller, D. |
| 2003 | Mutational analysis of the carboxy-terminal (YGX)4 repeat domain of CpsD, an autophosphorylating tyrosine kinase required for capsule biosynthesis in Streptococcus pneumoniae | Morona, J.; Morona, R.; Miller, D.; Paton, J. |
| 2015 | Mutational analysis of the major periplasmic loops of Shigella flexneri Wzy; identification of the residues affecting O antigen modal chain length control, and Wzz dependent polymerisation activity | Nath, P.; Morona, R. |
| 2013 | Mutations in DEPDC5 cause familial focal epilepsy with variable foci | Dibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al. |
| 2009 | Mutations in genes encoding sorting nexins alter production of intracellular and extracellular proteases in Aspergillus nidulans | Katz, M.; Evans, C.; Heagney, E.; vanKuyk, P.; Kelly, J.; Cheetham, B. |
| 2002 | Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome | Lower, K.; Turner, G.; Kerr, B.; Mathews, K.; Shaw, M.; Gedeon, A.; Schelley, S.; Hoyme, H.; White, S.; Delatycki, M.; Lampe, A.; Clayton-Smith, J.; Stewart, H.; van Ravenswaay, C.; de Vries, B.; Cox, B.; Grompe, M.; Ross, S.; Thomas, P.; Mulley, J.; et al. |
| 2007 | Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly | Field, M.; Tarpey, P.; Smith, R.; Edkins, S.; O'Meara, S.; Stevens, C.; Tofts, C.; Teague, J.; Butler, A.; Dicks, E.; Barthorpe, S.; Buck, G.; Cole, J.; Gray, K.; Halliday, K.; Hills, K.; Jenkinson, A.; Jones, D.; Menzies, A.; Mironenko, T.; et al. |
| 2002 | Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy | Stromme, P.; Mangelsdorf, M.; Shaw, M.; Lower, K.; Lewis, S.; Bruyere, H.; Lutcherath, V.; Gedeon, A.; Wallace, R.; Scheffer, I.; Turner, G.; Partington, M.; Frints, S.; Fryns, J.; Sutherland, G.; Mulley, J.; Gecz, J. |
| 2007 | Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation | Tarpey, P.; Raymond, F.; Nguyen, L.; Rodriguez, J.; Hackett, A.; Vandeleur, L.; Smith, R.; Shoubridge, C.; Edkins, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Hills, K.; Jones, D.; Mironenko, T.; Perry, J.; et al. |
| 2005 | Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD) | Turton, J.; Mehta, A.; Raza, J.; Woods, K.; Tiulpakov, A.; Cassar, J.; Chong, K.; Thomas, P.; Eunice, M.; Ammini, A.; Bouloux, P.; Starzyk, J.; Hindmarsh, P.; Dattani, M. |
| 2010 | My favorite pyruvate carboxylase feature | Wallace, J. |
| 2010 | Myc-modulated miR-9 makes more metastases | Khew-Goodall, Y.; Goodall, G. |
| 2009 | Mycobacterium tuberculosis strains with highly discordant rifampin susceptibility test results | Van Deun, A.; Barrera, L.; Bastian, I.; Fattorini, L.; Hoffmann, H.; Kam, K.; Rigouts, L.; Rusch-Gerdes, S.; Wright, A. |
| 2017 | Mycobacterium tuberculosis subverts negative regulatory pathways in human macrophages to drive immunopathology | Brace, P.; Tezera, L.; Bielecka, M.; Mellows, T.; Garay, D.; Tian, S.; Rand, L.; Green, J.; Jogai, S.; Steele, A.; Millar, T.; Sanchez-Elsner, T.; Friedland, J.; Proud, C.; Elkington, P.; Lewinsohn, D.M. |
| 2023 | Myeloperoxidase creates a permissive microenvironmental niche for the progression of multiple myeloma | Williams, C.M.D.; Noll, J.E.; Bradey, A.L.; Duggan, J.; Wilczek, V.J.; Masavuli, M.G.; Grubor‐Bauk, B.; Panagopoulos, R.A.; Hewett, D.R.; Mrozik, K.M.; Zannettino, A.C.W.; Vandyke, K.; Panagopoulos, V. |
| 2004 | Myogenic reactivity is enhanced in rat radial uterine arteries in a model of maternal undernutrition | Veerareddy, Sukrutha; Campbell, Morag E.; Williams, Sarah J.; Baker, Philip N.; Davidge, Sandra T. |
