Abstract P4-05-02: Conditional inactivation of the 25-hydroxyvitamin D-24-hydroxylase (Cyp24a1) in the mouse mammary epithelium alters mammary gland development von Sheng, L, Turner, AG, Tarulli, GA, Barratt, K, Kremer, R, Morris, HA, Callen, DF, Anderson, PH

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A complex rearrangement involving simultaneous translocation and inversion is associated with a change in chromatin compaction von Callen, D F, Eyre, H, McDonnell, S, Schuffenhauer, S, Bhalla, K

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A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis von Hoff, William van't, Bates, Gillian P, Antignac, Corinne, Jean, Geneviève, Forestier, Lionel, Gribouval, Olivier, Whitmore, Scott A, Town, Margaret, Broyer, Michel, Cherqui, Stèphanie, Attard, Marlene, Callen, David F

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FBXO31 is the chromosome 16q24.3 senescence gene, a candidate breast tumor suppressor, and a component of an SCF complex von KUMAR, Raman, NEILSEN, Paul M, CLETON-JANSEN, Anne-Marie, CALLEN, David F, CRAWFORD, Joanne, MCKIRDY, Ross, LEE, Jaclyn, POWELL, Jason A, SAIF, Zarqa, MARTIN, Julie M, LOMBAERTS, Marc, CORNELISSE, Cees J

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The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene von Bhalla, Kavita, Phillips, Hilary A, Crawford, Joanna, McKenzie, Olivia L D, Mulley, John C, Eyre, Helen, Gardner, Alison E, Kremmidiotis, Gabriel, Callen, David F

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Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene von BELL, R, BRICE, G, MORTIMER, P, JEFFERY, S, CHILD, A. H, MURDAY, V. A, MANSOUR, S, SANDY, C. J, COLLIN, J. R. O, BRADY, A. F, CALLEN, D. F, BURNAND, K

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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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Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA von Kruyt, Frank A.E, Buchwald, Manuel, Lightfoot, Jeff, Joenje, Hans, Strunk, Mark H.P, Cheng, Ngan C, Pronk, Jan C, Gille, Johan J.P, Pals, Gerard, Arwert, Fré, Alon, Noa, Savoia, Anna, Parker, Linda, Carreau, Madeleine, van Berkel, Carola G.M, Rooimans, Martin A, Wijker, Mario, Lo Ten Foe, Jerome R, Bosnoyan-Collins, Lucine, Callen, David F

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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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Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions von CLETON-JANSEN, Anne-Marie, CALLEN, David F, SMIT, Vincent T. B. H. M, HARRIS, William H, MILLIS, Rosemary, MORGAN, Neil V, BARNES, Diana, MATHEW, Christopher G, CORNELISSE, Cees J, SESHADRI, Ram, GOLDUP, Sandra, MCCALLUM, Brett, CRAWFORD, Joanna, POWELL, Jason A, SETTASATIAN, Chatri, VAN BEERENDONK, Hetty, MOERLAND, Elna W

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Positional cloning of the Fanconi anaemia group A gene von Jansen, Stander, Easton, Douglas F, Memeo, Elena, Deaven, Larry L, D'Apolito, Maria, Pronk, Jan C, Cleton-Jansen, Anne-Marie, Verlander, Peter C, Batish, Sat Dev, Mathew, Christopher G, Notarangeio, Angelo, Cornelisse, Cees J, Moyzis, Robert K, Auerbach, Arleen D, Lennon, Gregory, lanzano, Leonarda, Whitmore, Scott A, Callen, David F, Sutherland, Grant R, Doggett, Norman A, Savino, Maria, Apostolou, Sinoula, Morgan, Neil V, de Ravel, Thomy J, Gibson, Rachel A, Crawford, Joanna, Zelante, Leopoldo, Tipping, Alex J, Moerland, Elna W, Levran, Orna, Savoia, Anna, Van Berkell, Carola, Piemontese, Maria Rosaria, Hassock, Sheila, Erlich, Tamar

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CARD15/NOD2 Risk Alleles in the Development of Crohn's Disease in the Australian Population von Cavanaugh, J. A., Adams, K. E., Quak, E. J., Bryce, M. E., O'Callaghan, N. J., Rodgers, H. J., Magarry, G. R., Butler, W. J., Eaden, J. A., Roberts‐Thomson, I. C., Pavli, P., Wilson, S. R., Callen, D. F.

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Isolation of a novel gene underlying batten disease, CLN3 von Lerner, Terry J, Boustany, Rose-Mary N, Anderson, John W, D'Arigo, Kenneth L, Schlumpf, Karen, Buckler, Alan J, Gusella, James F, Haines, Jonathan L

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CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3 von KOCHETKOVA, Marina, MCKENZIE, Olivia L. D, O'CALLAGHAN, Nathan J, CLETON-JANSEN, Anne-Marie, CORNELISSE, Cees, WHITMORE, Scott A, CRAWFORD, Joanna, KREMMIDIOTIS, Gabriel, SUTHERLAND, Grant R, CALLEN, David F, BAIS, Anthony J, MARTIN, Julie M, SECKER, Genevieve A, SESHADRI, Ram, POWELL, Jason A, HINZE, Susan J, GARDNER, Alison E, SPENDLOVE, Hayley E

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Localization of Human Cadherin Genes to Chromosome Regions Exhibiting Cancer-Related Loss of Heterozygosity von Kremmidiotis, Gabriel, Baker, Elizabeth, Crawford, Joanna, Eyre, Helen J., Nahmias, Joseph, Callen, David F.

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Sequencing, Transcript Identification, and Quantitative Gene Expression Profiling in the Breast Cancer Loss of Heterozygosity Region 16q24.3 Reveal Three Potential Tumor-Suppressor... von Powell, Jason A., Gardner, Alison E., Bais, Anthony J., Hinze, Susan J., Baker, Elizabeth, Whitmore, Scott, Crawford, Joanna, Kochetkova, Marina, Spendlove, Hayley E., Doggett, Norman A., Sutherland, Grant R., Callen, David F., Kremmidiotis, Gabriel

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Allele loss on chromosome 16q24.2-qter occurs frequently in breast cancers irrespectively of differences in phenotype and extent of spread von Tsuda, H, Callen, D F, Fukutomi, T, Nakamura, Y, Hirohashi, S

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Molecular and Functional Analyses of the Human and Mouse Genes Encoding AFG3L1, a Mitochondrial Metalloprotease Homologous to the Human Spastic Paraplegia Protein von Kremmidiotis, Gabriel, Gardner, Alison E., Settasatian, Chatri, Savoia, Anna, Sutherland, Grant R., Callen, David F.

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A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene : implications for mutation analysis in pseudoxanthoma elasticum von LI CAI, LUMSDEN, Amanda, LINDPAINTNER, Klaus, RICHARDS, Robert I, STRUK, Berthold, GUENTHER, Ulf P, NELDNER, Sarah A, ZÄCH, Stéphanie, KNOBLAUCH, Hans, RAMESAR, Raj, HOHL, Daniel, CALLEN, David F, NELDNER, Kenneth H

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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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