Showing results 1346 to 1365 of 3020
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| Preview | Issue Date | Title | Author(s) |
| 2021 | 'I wish I'd had the option': views about donor human milk among parents with babies born moderate-late preterm | Klein, L.D.; Keir, A.K.; Cruz, M.; Rumbold, A.R. |
| 1995 | Iatrogenic bismuth toxicity | Thomas, D. W. |
| 2013 | Iatrogenic blood-borne viral infections in refugee children from war and transition zones | Goldwater, P. |
| 2003 | Identification and characterization of 13 new mutations in mucopolysaccharidosis type I patients | Matte, U.; Yogalingam, G.; Brooks, D.; Leistner, S.; Schwartz, I.; Lima, L.; Norato, D.; Brum, J.; Beesley, C.; Winchester, B.; Giugliani, R.; Hopwood, J. |
| 2009 | Identification and characterization of Ambroxol as an enzyme enhancement agent for Gaucher Disease | Maegawa, G.; Tropak, M.; Buttner, J.; Rigat, B.; Fuller, M.; Pandit, D.; Tang, L.; Kornhaber, G.; Hamuro, Y.; Clarke, J.; Mahuran, D. |
| 2010 | Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation | Rujirabanjerd, S.; Nelson, J.; Tarpey, P.; Hackett, A.; Edkins, S.; Raymond, F.; Schwartz, C.; Turner, G.; Iwase, S.; Shi, Y.; Futreal, P.; Stratton, M.; Gecz, J. |
| 2012 | Identification and functional characterization of two novel mutations in the α-helical loop (residues 484-503) of CYBB/gp91phox resulting in the rare X91⁺ variant of chronic granulomatous disease | Boog, B.; Quach, A.; Costabile, M.; Smart, J.; Quinn, P.; Singh, H.; Gold, M.; Booker, G.; Choo, S.; Hii, C.; Ferrante, A. |
| 2000 | Identification and immunolocalization of decorin, versican, perlecan, nidogen, and chondroitin sulfate proteoglycans in bovine small-antral ovarian follicles | McArthur, M.; Irving-Rodgers, H.; Byers, S.; Rodgers, R. |
| 2004 | Identification and molecular characterization of α-L-iduronidase mutations present in mucopolysaccharidosis type I patients undergoing enzyme replacement therapy | Yogalingam, G.; Guo, X.; Muller, V.; Brooks, D.; Clements, P.; Kakkis, E.; Hopwood, J. |
| 1997 | Identification of 16 Sulfamidase Gene Mutations Including the Common R74C in Patients With Mucopolysaccharidosis Type IIIa (Sanfilippo A) | Bunge, S.; Ince, H.; Steglich, C.; Kleijer, W.; Beck, M.; Zaremba, J.; van Diggelen, O.; Weber, B.; Hopwood, J.; Gal, A. |
| 1998 | Identification of a common mutation (R245h) in Sanfilippo A patients from the Netherlands | Weber, B.; Vandekamp, J.; Kleijer, W.; Guo, X.H.; Blanch, L.; van Diggelen, O.; Wevers, R.; Poorthuis, B.; Hopwood, J. |
| 1998 | Identification of a human HECT family protein with homology to the Drosophila tumor suppressor gene hyperplastic discs | Callaghan, M.; Russell, A.; Woollatt, E.; Sutherland, G.; Sutherland, R.; Watts, C. |
| 2011 | Identification of a microRNA that activates gene expression by repressing nonsense-mediated RNA decay | Bruno, I.; Karam, R.; Huang, L.; Bhardwaj, A.; Lou, C.; Shum, E.; Song, H.; Corbett, M.; Gifford, W.; Gecz, J.; Pfaff, S.; Wilkinson, M. |
| 2002 | Identification of a mutation causing mucopolysaccharidosis type IIIA in New Zealand Huntaway dogs | Yogalingam, G.; Pollard, T.; Gliddon, B.; Jolly, R.; Hopwood, J. |
| 2000 | Identification of a mutation in the XNP/ATR-X gene in a family reported as Smith-Fineman-Myers syndrome | Villard, L.; Fontes, M.; Ades, L.; Gecz, J. |
| 2006 | Identification of a novel FcγRIII receptor that is up-regulated in fetal wound healing | Teusner, J.; Goddard, C.; Belford, D.; Dunaiski, V.; Powell, B. |
| 2001 | Identification of a novel human tankyrase through its interaction with the adaptor protein Grb14 | Lyons, R.; Deane, R.; Lynch, D.; Ye, Z.; Sanderson, G.; Eyre, H.; Sutherland, G.; Daly, R. |
| 2004 | Identification of a SEDL gene mutation in an individual with Leber hereditary optic neuropathy and spondyloepiphyseal dysplasia | Shaw, M.; Gecz, J.; McDonough, B.; Hodess, A.; Harter, D. |
| 2012 | Identification of cases with adverse neonatal outcome monitored by cardiotocography versus ST analysis: secondary analysis of a randomized trial | Westerhuis, M.; Porath, M.; Becker, J.; Van den Akker, E.; van Beek, E.; van Dessel, H.; Drogtrop, A.; van Geijn, H.; Graziosi, G.; Groenendaal, F.; van Lith, J.; Mol, B.; Moons, K.; Nijhuis, J.; Oei, S.; Oosterbaan, H.; Rijnders, R.; Schuitemaker, N.; Wijnberger, L.; Willekes, C.; et al. |
| 2008 | Identification of genes differentially expressed by prematurely fused human sutures using a novel in vivo-in vitro approach | Coussens, A.; Hughes, I.; Wilkinson, C.; Morris, C.; Anderson, P.; Powell, B.; Van Daal, A. |
