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PreviewIssue DateTitleAuthor(s)
2008Deletion of Glu155 causes a deficiency of glutathione transferase Omega 1-1 but does not alter sensitivity to arsenic trioxide and other cytotoxic drugsSchmuck, E.; Cappello, J.; Coggan, M.; Brew, J.; Cavanaugh, J.; Blackburn, A.; Baker, R.; Eyre, H.; Sutherland, G.; Board, P.
2000Fca/m receptor mediates endocytosis of IgM-coated microbesShibuya, A.; Sakamoto, N.; Shimizu, Y.; Shibuya, K.; Osawa, M.; Hiroyama, T.; Eyre, H.; Sutherland, G.; Endo, Y.; Fujita, T.; Miyabayashi, T.; Sakana, S.; Tsuji, T.; Nakayama, E.; Phillips, J.; Lanier, L.; Nakauchi, H.
2001Isolation, tissue distribution, and chromosomal localization of a novel testis-specific human four-transmembrane gene related to CD20 and FcRI-bHulett, M.; Pagler, E.; Hornby, J.; Hogarth, P.; Eyre, H.; Baker, E.; Crawford, J.; Sutherland, G.; Ohms, S.; Parish, C.
2001HPP1: A transmembrane protein-encoding gene commonly methylated in colorectal polyps and cancersYoung, J.; Biden, K.; Simms, L.; Huggard, P.; Karamatic, R.; Eyre, H.; Sutherland, G.; Herath, N.; Barker, M.; Anderson, G.; Fitzpatrick, D.; Ramm, G.; Jass, J.; Leggett, B.
2003Disruption of the Serine/Threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardationKalscheuer, V.; Tao, J.; Donnelly, A.; Hollway, G.; Schwinger, E.; Kubart, S.; Menzel, C.; Hoeltzenbein, M.; Tommerup, N.; Eyre, H.; Harbord, M.; Haan, E.; Sutherland, G.; Ropers, H.; Gecz, J.
2002Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomaliesBaker, E.; Hinton, L.; Callen, D.; Altree, M.; Dobbie, A.; Eyre, H.; Sutherland, G.; Thompson, E.; Thompson, P.; Woollatt, E.; Haan, E.
2005Frequency of truly cryptic subtelomere abnormalities - a study of 534 patients and literature reviewYu, S.; Baker, E.; Hinton, L.; Eyre, H.; Waters, W.; Higgins, S.; Sutherland, G.; Haan, E.
1999C160rf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brainBhalla, K.; Eyre, H.; Whitmore, S.; Sutherland, G.; Callen, D.
1997Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeatYu, S.; Mangelsdorf, M.; Hewett, D.; Hobson, L.; Baker, E.; Eyre, H.; Lapsys, N.; Le Paslier, D.; Doggett, N.; Sutherland, G.; Richards, R.
1998Construction of a high-resolution physical and transcription map of chromosome 16q24.3 - a region of frequent loss of heterozygosity in sporadic breast cancerWhitmore, S.; Crawford, J.; Apostolou, S.; Eyre, H.; Baker, E.; Lower, K.; Settasatian, C.; Goldup, S.; Seshadri, R.; Gibson, R.; Mathew, C.; Cleton-Jansen, A.; Savoia, A.; Pronk, J.; Auerbach, A.; Doggett, N.; Sutherland, G.; Callen, D.