Mutant p53 drives invasion in breast tumors through up-regulation of miR-155 von Neilsen, P M, Noll, J E, Mattiske, S, Bracken, C P, Gregory, P A, Schulz, R B, Lim, S P, Kumar, R, Suetani, R J, Goodall, G J, Callen, D F

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Mutant p53 drives multinucleation and invasion through a process that is suppressed by ANKRD11 von Noll, J E, Jeffery, J, Al-Ejeh, F, Kumar, R, Khanna, K K, Callen, D F, Neilsen, P M

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Systematic characterisation of the rat and human CYP24A1 promoter von Kumar, R., Iachini, D.N., Neilsen, P.M., Kaplan, J., Michalakas, J., Anderson, P.H., May, B.K., Morris, H.A., Callen, D.F.

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Mapping of Two Phenol Sulfotransferase Genes, STP and STM, to 16p: Candidate Genes for Batten Disease von Dooley, T.P., Mitchison, H.M., Munroe, P.B., Probst, P., Neal, M., Siciliano, M.J., Deng, Z.M., Doggett, N.A., Callen, D.F., Gardiner, R.M., Mole, S.E.

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Incidence and origin of null alleles in the (AC)n microsatellite markers von CALLEN, D. F, THOMPSON, A. D, YANG SHEN, PHILLIPS, H. A, RICHARDS, R. I, MULLEY, J. C, SUTHERLAND, G. R

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Human chemokines fractalkine (SCYD1), MDC (SCYA22) and TARC (SCYA17) are clustered on chromosome 16q13 1 von Nomiyama, H., Imai, T., Kusuda, J., Miura, R., Callen, D.F., Yoshie, O.

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Implications of FRA16A Structure for the Mechanism of Chromosomal Fragile Site Genesis von Nancarrow, J. K., Kremer, E., Holman, K., Eyre, H., Doggett, N. A., Le Paslier, D., Callen, D. F., Sutherland, G. R., Richards, R. I.

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Mapping the short arm of human chromosome 16 von Callen, D.F., Hyland, V.J., Baker, E.G., Fratini, A., Gedeon, A.K., Mulley, J.C., Fernandez, K.E.W., Breuning, M.H., Sutherland, G.R.

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Deletion of gene for multidrug resistance in acute myeloid leukaemia with inversion in chromosome 16: prognostic implications von Kuss, B.J, Eyre, H.J, Lane, S.A, Nancarrow, J.K, Whitmore, S.A, Callen, D.F, Deeley, R.G, Cole, S.P.C, Willman, C.L, Kopecky, K.L, Willman, C.L, Kopecky, Kj, Wolman, S.R, Willman, C.L, Kopecky, Kj, Wolman, S.R

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Partial Androgen Insensitivity Syndrome and t(X;5): Are There Upstream Regulatory Elements of the Androgen Receptor Gene? von Lower, K.M., Kumar, R., Woollatt, E., Villard, L., Gecz, J., Sutherland, G.R., Callen, D.F.

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Isolation and characterisation of (AC) n microsatellite genetic markers from human chromosome 16 von Thompson, A.D., Shen, Y., Holman, K., Sutherland, G.R., Callen, D.F., Richards, R.I.

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Genomic structure and expression analysis of the spastic paraplegia gene, SPG7 von SETTASATIAN, C, WHITMORE, S. A, CRAWFORD, J, BILTON, R. L, CLETON-JANSEN, A.-M, SUTHERLAND, G. R, CALLEN, D. F

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ARA,a Novel ABC Transporter, Is Located at 16p13.1, Is Deleted in inv(16) Leukemias, and Is Shown To Be Expressed in Primitive Hematopoietic Precursors von Kuss, B.J, O'Neill, G.M, Eyre, H, Doggett, N.A, Callen, D.F, Davey, R.A

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Integration of Transcript and Genetic Maps of Chromosome 16 at Near-1-Mb Resolution: Demonstration of a “Hot Spot” for Recombination at 16p12 von CALLEN, D.F., LANE, S.A., KOZMAN, H., KREMMIDIOTIS, G., WHITMORE, S.A., LOWENSTEIN, M., DOGGETT, N.A., KENMOCHI, N., PAGE, D.C., MAGLOTT, D.R., NIERMAN, W.C., MURAKAWA, K., BERRY, R., SIKELA, J.M., HOULGATTE, R., AUFFRAY, C., SUTHERLAND, G.R.

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Structure and chromosomal localization of the human renal kallikrein gene von Evans, Bronwyn A, Yun, Zhang Xiao, Close, Jacqueline A, Tregear, Geoffrey W, Kitamura, Naomi, Nakanishi, Shigetada, Callen, David F, Baker, Elizabeth, Hyland, Valentine J

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Genomic structure and expression analysis of the spastic paraplegia gene, SPG7 von Settasatian, C., Whitmore, S.A., Crawford, J., Bilton, R.L., Cleton-Jansen, A.-M., Sutherland, G.R., Callen, D.F.

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High-resolution cytogenetic-based physical map of human chromosome 16 von Callen, D.F., Doggett, N.A., Stallings, R.L., Chen, L.Z., Whitmore, S.A., Lane, S.A., Nancarrow, J.K., Apostolou, S., Thompson, A.D., Lapsys, N.M., Eyre, H.J., Baker, E.G., Shen, Y., Holman, K., Phillips, H., Richards, R.I., Sutherland, G.R.

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THE GENE FOR THE HUMAN-IGA FC RECEPTOR MAPS TO 19Q13.4 von KREMER, EJ, KALATZIS, BAKER, E, CALLEN, DF, SUTHERLAND, GR, MALISZEWSKI, CR

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Fine Genetic Mapping of the Batten Disease Locus (CLN3) by Haplotype Analysis and Demonstration of Allelic Association with Chromosome 16p Microsatellite Loci von Mitchison, Hannah M., Thompson, Andrew D., Mulley, John C., Kozman, Helen M., Richards, Rob I., Callen, David F., Stallings, Ray L., Doggett, Norman A., Attwood, John, McKay, Tristan R., Sutherland, Grant R., Gardiner, R.Mark

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A PCR-Based Genetic Linkage Map of Human Chromosome 16 von Shen, Y., Kozman, H.M., Thompson, A., Phillips, H.A., Holman, K., Nancarrow, J., Lane, S., Chen, L.-Z., Apostolou, S., Doggett, N.A., Callen, D.F., Mulley, J.C., Sutherland, G.R., Richards, R.I.

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