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Results 51-60 of 573 (Search time: 0.009 seconds).
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PreviewIssue DateTitleAuthor(s)
2003Enhanced CXC chemokine responses of human colonic epithelial cells to locus of enterocyte effacement-negative Shiga-toxigenic Escherichia coliRogers, T.; Paton, A.; McColl, S.; Paton, J.
2005Drosophila starvin encodes a tissue-specific BAG-domain protein required for larval food uptakeCoulson, M.; Robert, S.; Saint, R.
2012Dynamic mutations: where are they now?van Eyk, C.; Richards, R.; Hannan, A.
1994Carbon catabolite repressionKelly, J.; Martinelli, S.; Kinghorn, J.
2020Drosophila as a model to understand autophagy deregulation in human disordersDenton, D.; O'Keefe, L.; Kumar, S.; Martinez, A.B.; Galluzzi, L.
2008TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafnessGuipponi, M.; Antonarakis, S.; Scott, H.
2002Biochemical and molecular analysis of mucopolysaccharidoses in TurkeyEmre, S.; Terzioglu, M.; Coskun, T.; Tokatli, A.; Ozalp, I.; Muller, V.; Hopwood, J.
2016Conformational changes in the GM-CSF receptor suggest a molecular mechanism for affinity conversion and receptor signalingBroughton, S.E.; Hercus, T.R.; Nero, T.L.; King-Scott, J.; Lopez, A.F.; Parker, M.W.; Dottore, M.; McClure, B.J.; Dhagat, U.; Taing, H.; Gorman, M.A.
1996Mutations in the androgen receptor gene are associated with progression of human prostate cancer to androgen independenceTilley, W.D.; Buchanan, G.; Hickey, T.E.; Bentel, J.M.
2005A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey Disease) expands the spectrum of collagen-related disordersGensure, R.; Makitie, O.; Barclay, C.; Chan, C.; DePalma, S.; Bastepe, M.; Abuzahra, H.; Couper, R.; Mundlos, S.; Sillence, D.; Kokko, L.; Seidman, J.; Cole, W.; Juppner, H.