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PreviewIssue DateTitleAuthor(s)
2014Aberrant GDF9 expression and activation are associated with common human ovarian disordersSimpson, C.; Robertson, D.; Al-Musawi, S.; Heath, D.; McNatty, K.; Ritter, L.; Mottershead, D.; Gilchrist, R.; Harrison, C.; Stanton, P.
2015HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.Jolly, L.; Nguyen, L.; Domingo, D.; Sun, Y.; Barry, S.; Hancarova, M.; Plevova, P.; Vlckova, M.; Havlovicova, M.; Kalscheuer, V.; Graziano, C.; Pippucci, T.; Bonora, E.; Sedlacek, Z.; Gecz, J.
2011Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemiaHahn, C.; Chong, C.; Carmichael, C.; Wilkins, E.; Brautigan, P.; Li, X.; Babic, M.; Lin, M.; Carmagnac, A.; Lee, Y.; Kok, C.; Gagliardi, L.; Friend, K.; Ekert, P.; Butcher, C.; Brown, A.; Lewis, I.; To, L.; Timms, A.; Storek, J.; et al.
2012Activation of latent human GDF9 by a single residue change (Gly³⁹¹Arg) in the mature domainSimpson, C.; Stanton, P.; Walton, K.; Chan, K.; Ritter, L.; Gilchrist, R.; Harrison, C.
2013Identification and functional characterization of a novel monotreme-specific antibacterial protein expressed during lactationBisana, S.; Kumar, S.; Rismiller, P.; Nicol, S.; Lefevre, C.; Nicholas, K.; Sharp, J.; Janke, A.
2014Identification of androgen receptor splice variant transcripts in breast cancer cell lines and human tissuesHu, D.; Hickey, T.; Irvine, C.; Wijayakumara, D.; Lu, L.; Tilley, W.; Selth, L.; MacKenzie, P.