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PreviewIssue DateTitleAuthor(s)
2021'I wish I'd had the option': views about donor human milk among parents with babies born moderate-late pretermKlein, L.D.; Keir, A.K.; Cruz, M.; Rumbold, A.R.
1995Iatrogenic bismuth toxicityThomas, D. W.
2013Iatrogenic blood-borne viral infections in refugee children from war and transition zonesGoldwater, P.
2006ICAM-1 expression in adipose tissue: effects of diet-induced obesity in miceBrake, D.; O'Brian Smith, E.; Mersmann, H.; Smith, C.; Robker, R.
2003Identification and characterization of 13 new mutations in mucopolysaccharidosis type I patientsMatte, U.; Yogalingam, G.; Brooks, D.; Leistner, S.; Schwartz, I.; Lima, L.; Norato, D.; Brum, J.; Beesley, C.; Winchester, B.; Giugliani, R.; Hopwood, J.
1995Identification and characterization of a corticotrophin-releasing hormone recptor in human placentaClifton, V.; Robinson, P.; Owens, P.; Smith, R.
2009Identification and characterization of Ambroxol as an enzyme enhancement agent for Gaucher DiseaseMaegawa, G.; Tropak, M.; Buttner, J.; Rigat, B.; Fuller, M.; Pandit, D.; Tang, L.; Kornhaber, G.; Hamuro, Y.; Clarke, J.; Mahuran, D.
2010Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlationRujirabanjerd, 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.
2012Identification 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 diseaseBoog, B.; Quach, A.; Costabile, M.; Smart, J.; Quinn, P.; Singh, H.; Gold, M.; Booker, G.; Choo, S.; Hii, C.; Ferrante, A.
2000Identification and immunolocalization of decorin, versican, perlecan, nidogen, and chondroitin sulfate proteoglycans in bovine small-antral ovarian folliclesMcArthur, M.; Irving-Rodgers, H.; Byers, S.; Rodgers, R.
2004Identification and molecular characterization of α-L-iduronidase mutations present in mucopolysaccharidosis type I patients undergoing enzyme replacement therapyYogalingam, G.; Guo, X.; Muller, V.; Brooks, D.; Clements, P.; Kakkis, E.; Hopwood, J.
1997Identification 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.
1998Identification of a common mutation (R245h) in Sanfilippo A patients from the NetherlandsWeber, B.; Vandekamp, J.; Kleijer, W.; Guo, X.H.; Blanch, L.; van Diggelen, O.; Wevers, R.; Poorthuis, B.; Hopwood, J.
1998Identification of a human HECT family protein with homology to the Drosophila tumor suppressor gene hyperplastic discsCallaghan, M.; Russell, A.; Woollatt, E.; Sutherland, G.; Sutherland, R.; Watts, C.
2011Identification of a microRNA that activates gene expression by repressing nonsense-mediated RNA decayBruno, I.; Karam, R.; Huang, L.; Bhardwaj, A.; Lou, C.; Shum, E.; Song, H.; Corbett, M.; Gifford, W.; Gecz, J.; Pfaff, S.; Wilkinson, M.
2002Identification of a mutation causing mucopolysaccharidosis type IIIA in New Zealand Huntaway dogsYogalingam, G.; Pollard, T.; Gliddon, B.; Jolly, R.; Hopwood, J.
2000Identification of a mutation in the XNP/ATR-X gene in a family reported as Smith-Fineman-Myers syndromeVillard, L.; Fontes, M.; Ades, L.; Gecz, J.
2021Identification of a novel distension-evoked motility pattern in the mouse uterusDodds, K.N.; Travis, L.; Beckett, E.A.; Spencer, N.J.
2006Identification of a novel FcγRIII receptor that is up-regulated in fetal wound healingTeusner, J.; Goddard, C.; Belford, D.; Dunaiski, V.; Powell, B.
2001Identification of a novel human tankyrase through its interaction with the adaptor protein Grb14Lyons, R.; Deane, R.; Lynch, D.; Ye, Z.; Sanderson, G.; Eyre, H.; Sutherland, G.; Daly, R.