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Results 1-10 of 303 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2017DNA barcoding reveals habitual clonal dominance of myeloma plasma cells in the bone marrow microenvironmentHewett, D.; Vandyke, K.; Lawrence, D.; Friend, N.; Noll, J.; Geoghegan, J.; Croucher, P.; Zannettino, A.
2017Reduced CD62L expression on T cells and increased soluble CD62L levels predict molecular response to tyrosine kinase inhibitor therapy in early chronic-phase chronic myelogenous leukemiaSopper, S.; Mustjoki, S.; White, D.; Hughes, T.; Valent, P.; Burchert, A.; Gjertsen, B.; Gastl, G.; Baldauf, M.; Trajanoski, Z.; Giles, F.; Hochhaus, A.; Ernst, T.; Schenk, T.; Janssen, J.; Ossenkoppele, G.; Porkka, K.; Wolf, D.
2017Robotic prostatectomy took off, despite a lack of evidence and risks of inequityHutchison, K.; Carter, D.A.; Johnson, J.
2017A comparison of right unilateral and sequential bilateral repetitive transcranial magnetic stimulation for major depression: a naturalistic clinical Australian studyGalletly, C.A.; Carnell, B.L.; Clarke, P.; Gill, S.
2017Psychotropic pharmacogenetics - distraction or destiny?Singh, A.; Baune, B.; Hamilton, A.; Das, P.; Outhred, T.; Morris, G.; Bassett, D.; Berk, M.; Boyce, P.; Lyndon, B.; Mulder, R.; Parker, G.; Malhi, G.
2017Leptin signals via TGFB1 to promote metastatic potential and stemness in breast cancerMishra, A.; Parish, C.; Wong, M.; Licinio, J.; Blackburn, A.; Ahmad, A.
2017Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signallingHughes, J.; Dawson, R.; Tea, M.; McAninch, D.; Piltz, S.; Jackson, D.; Stewart, L.; Ricos, M.; Dibbens, L.; Harvey, N.; Thomas, P.
2017Effects of postnatal omega-3 fatty acid supplementation on offspring pro-resolving mediators of inflammation at 6 months and 5 years of age: a double blind, randomized controlled clinical trialSee, V.H.L.; Mas, E.; Prescott, S.L.; Beilin, L.J.; Burrows, S.; Barden, A.E.; Huang, R.C.; Mori, T.A.
2017Increased methylation and decreased expression of homeobox genes TLX1, HOXA10 and DLX5 in human placenta are associated with trophoblast differentiationNovakovic, B.; Fournier, T.; Harris, L.; James, J.; Roberts, C.; Yong, H.; Kalionis, B.; Evain-Brion, D.; Ebeling, P.; Wallace, E.; Saffery, R.; Murthi, P.
2017NAD deficiency, congenital malformations, and niacin supplementationShi, H.; Enriquez, A.; Rapadas, M.; Martin, E.; Wang, R.; Moreau, J.; Lim, C.; Szot, J.; Ip, E.; Hughes, J.; Sugimoto, K.; Humphreys, D.; McInerney-Leo, A.; Leo, P.; Maghzal, G.; Halliday, J.; Smith, J.; Colley, A.; Mark, P.; Collins, F.; et al.

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