Showing results 1592 to 1611 of 3020
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| Preview | Issue Date | Title | Author(s) |
| 1995 | Isolation and characterisation of a recombinant precursor form of lysosomal acid α-glucosidase | Fuller, M.; Van der Ploeg, A.; Reuser, A.; Anson, D.; Hopwood, J. |
| 1996 | Isolation and characterization of cDNA clones for Humly9: the human homologue of mouse Ly9 | Sandrin, M.; Henning, M.; Lo, M.; Baker, E.; Sutherland, G.; McKenzie, I. |
| 1994 | Isolation and characterization of ovine IGFBP-4: protein purification and cDNA sequence | CARR, J.M.; GRANT, P.A.; FRANCIS, G.L.; OWENS, J.A.; WALLACE, J.C.; WALTON, P.E. |
| 1997 | Isolation and identification of homeobox genes from the human placenta including a novel member of the Distal-less family, DLX4 | Quinn, L.; Johnson, B.; Nicholl, J.; Sutherland, G.; Kalionis, B. |
| 1995 | Isolation of a novel gene underlying Batten disease, CLN3 | Lerner, Terry J.; Boustany, Rose-Mary N.; Anderson, John W.; D'Arigo, Kenneth L.; Schlumpf, Karen; Buckler, Alan J.; Gusella, James F.; Haines, Jonathan L. |
| 2003 | Isolation of antigen-specific B cells | Kodituwakku, A.; Jessup, C.; Zola, H.; Roberton, D. |
| 1996 | Isolation of the canine alpha-L-fucosidase cDNA and definition of the fucosidosis mutation in English Springer Spaniels | Occhiodoro, T.; Anson, Donald Stewart |
| 2009 | Isolation of whole mononuclear Cells from peripheral blood and cord blood | Fuss, I.; Kanof, M.; Smith, P.; Zola, H. |
| 2012 | Isolation, expansion and characterisation of alloreactive human Th17 and Th1 cells | Ko, K.; Powell, M.; Orlowski, E.; Prickett, S.; Krumbiegel, D.; Hogarth, P. |
| 2007 | Isolation, propagation and characterization of cord blood derived CD4+ CD25+ regulatory T cells | Bresatz, S.; Sadlon, T.; Millard, D.; Zola, H.; Barry, S. |
| 2001 | Isolation, tissue distribution, and chromosomal localization of a novel testis-specific human four-transmembrane gene related to CD20 and FcRI-b | Hulett, M.; Pagler, E.; Hornby, J.; Hogarth, P.; Eyre, H.; Baker, E.; Crawford, J.; Sutherland, G.; Ohms, S.; Parish, C. |
| 2008 | Issues faced by unaffected men with a family history of prostate cancer: A multidisciplinary overview | Wakefield, C.; Meiser, B.; Gaff, C.; Barratt, A.; Patel, M.; Suthers, G.; Lobb, E.; Ramsay, J.; Mann, G. |
| 2000 | Just how long can we live? | Sutherland, G. |
| 2010 | Juvenile idiopathic arthritis | Boros, C.; Whitehead, B. |
| 1996 | Juvenile Psoriatic Arthritis - Followup and Evaluation of Diagnostic Criteria | Roberton, D.; Cabral, D.; Malleson, P.; Petty, R. |
| 1997 | Juvenile rheumatoid arthritis | Roberton, D. |
| 2012 | KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy | Weckhuysen, S.; Mandelstam, S.; Suls, A.; Audenaert, D.; Deconinck, T.; Claes, L.; Deprez, L.; Smets, K.; Hristova, D.; Yordanova, I.; Jordanova, A.; Ceulemans, B.; Jansen, A.; Hasaerts, D.; Roelens, F.; Lagae, L.; Yendle, S.; Stanley, T.; Heron, S.; Mulley, J.; et al. |
| 2014 | KCNT1 gain of function in 2 epilepsy phenotypes is reversed by quinidine | Milligan, C.; Li, M.; Gazina, E.; Heron, S.; Nair, U.; Trager, C.; Reid, C.; Venkat, A.; Younkin, D.; Dlugos, D.; Petrovski, S.; Goldstein, D.; Dibbens, L.; Scheffer, I.; Berkovic, S.; Petrou, S. |
| 2017 | Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signalling | Hughes, J.; Dawson, R.; Tea, M.; McAninch, D.; Piltz, S.; Jackson, D.; Stewart, L.; Ricos, M.; Dibbens, L.; Harvey, N.; Thomas, P. |
| 2022 | Knowledge of Galactagogue Use During Breastfeeding in Australia: A Cross Sectional Online Survey | McBride, G.M.; Stevenson, R.; Zizzo, G.; Rumbold, A.R.; Amir, L.H.; Keir, A.K.; Grzeskowiak, L.E. |
