Search


Current filters:
Start a new search
Add filters:

Use filters to refine the search results.


Results 61-70 of 173 (Search time: 0.003 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
2015Biochemical effects of mutations in the gene encoding the alpha subunit of eukaryotic initiation factor (eIF) 2B associated with Vanishing White Matter diseaseWortham, N.; Proud, C.
2015DAT isn’t all that: cocaine reward and reinforcement require Toll-like receptor 4 signalingNorthcutt, A.; Hutchinson, M.; Wang, X.; Baratta, M.; Hiranita, T.; Cochran, T.; Pomrenze, M.; Galer, E.; Kopajtic, T.; Li, C.; Amat, J.; Larson, G.; Cooper, D.; Huang, Y.; O'Neill, C.; Yin, H.; Zahniser, N.; Katz, J.; Rice, K.; Maier, S.; et al.
2014Relationship between O-antigen chain length and resistance to colicin E2 in Shigella flexneriTran, N.; Papadopoulos, M.; Morona, R.
2013A transcription factor contributes to pathogenesis and virulence in streptococcus pneumoniaeMahdi, L.; Ebrahimie, E.; Adelson, D.; Paton, J.; Ogunniyi, A.; Skurnik, M.
2003Nova regulates GABA(A) receptor gamma 2 alternative splicing via a distal downstream UCAU-rich intronic splicing enhancerDredge, B.; Darnell, R.
2014Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human diseaseNewman, M.; Wilson, L.; Verdile, G.; Lim, A.; Khan, I.; Nik, S.; Pursglove, S.; Chapman, G.; Martins, R.; Lardelli, M.
1997Dynamic mutation: possible mechanisms and significance in human diseaseRichards, R.; Sutherland, G.
2015Generation of a chimeric hepatitis C replicon encoding a genotype-6a NS3 protease and assessment of boceprevir (SCH503034) sensitivity and drug-associated mutations.Aloia, A.; Eyre, N.; Black, S.; Bent, S.; Gaeguta, A.; Guo, Z.; Narayana, S.; Chase, R.; Locarnini, S.; Carr, J.; Howe, J.; Beard, M.
2013Multicenter Study of Isavuconazole MIC Distributions and Epidemiological Cutoff Values for Aspergillus spp. for the CLSI M38-A2 Broth Microdilution MethodEspinel-Ingroff, A.; Chowdhary, A.; Gonzalez, G.; Lass-Florl, C.; Martin-Mazuelos, E.; Meis, J.; Pelaez, T.; Pfaller, M.; Turnidge, J.
2022Selective ferroptosis vulnerability due to familial Alzheimer's disease presenilin mutations.Greenough, M.A.; Lane, D.J.R.; Balez, R.; Anastacio, H.T.D.; Zeng, Z.; Ganio, K.; McDevitt, C.A.; Acevedo, K.; Belaidi, A.A.; Koistinaho, J.; Ooi, L.; Ayton, S.; Bush, A.I.