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Results 1-10 of 18 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2010
Genome-wide identification of human FOXP3 target genes in natural regulatory T cells
Sadlon, T.
;
Wilkinson, B.
;
Pederson, S.
;
Brown, C.
;
Bresatz, S.
;
Gargett, T.
;
Melville, E.
;
Peng, K.
;
D'Andrea, R.
;
Glonek, G.
;
Goodall, G.
;
Zola, H.
;
Shannon, F.
;
Barry, S.
2010
Imaging blood vessels in the zebrafish
Kamei, M.
;
Isogai, S.
;
Pan, W.
;
Weinstein, B.M.
;
Detrich, H.W.
;
Westerfield, M.
;
Zon, L.I.
2010
Augmented currents of an HCN2 variant in patients with febrile seizure syndromes
Dibbens, L.
;
Reid, C.
;
Hodgson, B.
;
Thomas, E.
;
Phillips, A.
;
Gazina, E.
;
Cromer, B.
;
Clarke, A.
;
Barram, T.
;
Scheffer, I.
;
Berkovic, S.
;
Petrou, S.
2010
Lessons learnt from animal models: pathophysiology of neuropathic lysosomal storage disorders
Hemsley, K.
;
Hopwood, J.
2010
Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes
Dimasi, D.
;
Chen, J.
;
Hewitt, A.
;
Klebe, S.
;
Davey, R.
;
Stirling, J.
;
Thompson, E.
;
Forbes, R.
;
Tan, T.
;
Savarirayan, R.
;
Mackey, D.
;
Healey, P.
;
Mitchell, P.
;
Burdon, K.
;
Craig, J.
2010
Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly
Giannandrea, M.
;
Bianchi, V.
;
Mignogna, M.
;
Sirri, A.
;
Carrabino, S.
;
D'Elia, E.
;
Vecellio, M.
;
Russo, S.
;
Cogliati, F.
;
Larizza, L.
;
Ropers, H.
;
Tzschach, A.
;
Kalscheuer, V.
;
Oehl-Jaschkowitz, B.
;
Skinner, C.
;
Schwartz, C.
;
Gecz, J.
;
Van Esch, H.
;
Raynaud, M.
;
Chelly, J.
;
et al.
2010
Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome
Gecz, J.
2010
Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination
Pearlman, A.
;
Loke, J.
;
Le Caignec, C.
;
White, S.
;
Chin, L.
;
Friedman, A.
;
Warr, N.
;
Willan, J.
;
Brauer, D.
;
Farmer, C.
;
Brooks, E.
;
Oddoux, C.
;
Riley, B.
;
Shajahan, S.
;
Camerino, G.
;
Homfray, T.
;
Crosby, A.
;
Couper, J.
;
David, A.
;
Greenfield, A.
;
et al.
2010
Iminochromene inhibitors of dynamins I and II GTPase activity and endocytosis
Hill, T.
;
Mariana, A.
;
Gordon, C.
;
Odell, L.
;
Robertson, M.
;
McGeachie, A.
;
Chau, N.
;
Daniel, J.
;
Gorgani, N.
;
Robinson, P.
;
McCluskey, A.
2010
High-spatial resolution matrix-assisted laser desorption ionization imaging analysis of glucosylceramide in spleen sections from a mouse model of Gaucher Disease
Snel, M.
;
Fuller, M.
Discover
Author
3
Gecz, J.
2
Barry, S.
2
Brown, C.
2
et al.
2
Gargett, T.
2
Melville, E.
2
Sadlon, T.
1
Anson, D.
1
Barram, T.
1
Berkovic, S.
.
next >
Subject
13
Humans
10
Female
9
Male
9
Mice
4
Disease Models, Animal
4
Mutation
3
Pedigree
3
Sheep
2
Adult
2
Amino Acid Sequence
.
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