1. Adelaide Research & Scholarship

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Results 31-40 of 61 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1998Motor unit discharge and force tremor in skill- and strength-trained individualsSemmler, J.; Nordstrom, M.
1999Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHMFriend, K.; Crimmins, D.; Phan, T.; Sue, C.; Colley, A.; Fung, V.; Morris, J.; Sutherland, G.; Richards, R.
1997Responses of human single motor units to transcranial magnetic stimulationGarland, S.; Miles, T.
1999Comparison of Three Methods for Estimation of Bone Resoprtion Following Ovariectomy in the Distal Femur and the Proximal Tibia of the RatBaldock, P.; Moore, R.; Durbridge, T.; Morris, H.
1999Isolation and characterisation of zona pellucida A (ZPA) cDNAs from two species of marsupial: regulated oocyte-specific expression of ZPA transcriptsVoyle, R.; Haines, B.; Loffler, K.; Hope, R.; Rathjen, P.; Breed, W.
1998Gene localisation for an autosomal dominant familial periodic fever to 12p13.Mulley, J.; Saar, K.; Hewitt, G.; Rueschendorf, F.; Phillips, H.; Colley, A.; Sillence, D.; Reis, A.; Wilson, M.
1997Genetics heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21-23.2Horwitz, M.; Benson, K.; Li, F.Q.; Wolff, J.; Leppert, M.; Hobson, L.; Mangelsdorf, M.; Yu, S.; Hewett, D.; Richards, R.; Raskind, W.
1996Induction of T cell responses to the invariant chain derived peptide CLIP in mice immunized with the group 1 allergen of house dust miteKristensen, N.; Hoyne, G.; Hayball, J.; Hetzel, C.; Bourne, T.; Lamb, J.
1999Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromesMcDermott, M.; Aksentijevich, I.; Galon, J.; McDermott, E.; Ogunkolade, B.; Centola, M.; Mansfield, E.; Gadina, M.; Karenko, L.; Petterson, T.; McCarthy, J.; Frucht, D.; Aringer, M.; Torosyan, Y.; Teppo, A.M.; Wilson, M.; Karaarslan, H.; Wan, Y.; Todd, I.; Wood, G.; et al.
1996A novel X-linked gene, G4.5. is responsible for Barth SyndromeBione, S.; D'Adamo, P.; Maestrini, E.; Gedeon, A.; Bolhuis, P.; Toniolo, D.

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