Publications from the Laboratory
Publications
From the Laboratory
Publications (1994-1998)
- Pulver, A., Karayiorgou, M., Wolyniec, P., Lasseter, V.K., Kasch, L., Antonarakis, S., Housman, D., Kazazian, H.H., Meyers, D., Nestadt, G., Ott, J., Lamacz, M., Liang, K-L., Hanfelt, J., Ullrich, G., DeMarchi, N., Ramu, E., McHugh, P.R., Adler, L., Thomas, M., Carpender, W.T., Manschreck, T., Gordon, C.T., Kimberland, M., Babb, R., Puck, J. and Childs, B. (1994) A Sequential Strategy to Identify a Susceptibility Gene for Schizophrenia: Report of a Potential Linkage on Chromosome 22q12-q13.1 Part 1. Amer. J. of Med. Gen. 54: 36-43.
- Munroe, D.M., Haas, M., Bric, E., Whitton, T., Aburatani, H., Hunter, K., Ward, D. and D.E. Housman. (1994) IRE-Bubble PCR: A Rapid Method for Efficient and Reproductive Amplification of Human Genomic DNA Sequences and Complex Sources. Genomics 19: 506-514.
- Pulver, A., Karayiorgou, M., Lasseter, V.K., Wolyniec, P., Kasch, L., Antonarakis, S., Housman, D., Kazazian, H.H., Meyers, D., Nestadt, G., Ott, J., Liang, K-L., Lamacz, M., Thomas, M., and Childs, B. (1994) Follow-up of A Report of a Potential Linkage for Schizophrenia on Chromosome 22q12-q13.1, Part 2. Amer. J. of Med. Gen. 54: 44-50.
- Hunter, K.W., Ontiveros, S.D., Watson, M.L., Stanton, V.P., Guttierez, P., Bhat, D., Rochelle, J., Graw, S., Ton, C.,, Schalling, M., Aburatani, H., Brown, S.D.M., Seldin, M. and Housman, D.E. (1994) Rapid and Efficient Construction of Yeast Artificial Chromosome Contigs in the Mouse Genome Utilizing Interspersed Repetitive Sequence PCR (IRS-PCR): Generation of a 5cM, >5 Megabase Contig on Mouse Chromosome 1. Mammalian Genome 5:597-607
- Ambrose, C., James, M., Barnes, G., Lin, C., Bates, G., Altherr, M., Duyao, Mabel, Groot, N., Church, D., Wasmuth, J., Lerach, H., Housman, D., Buckler, A., Gusella, J.F. and MacDonald, M. (1994) A Novel G Protein-Coupled Receptor Kinase Cloned from 4p16.3. Human Molecular Genetics 1:697-703.
- Lowe, S.W., Bodis, S., Bardeesy, N., McClatchey, A., Remington, L., Ruley, H.E., Fisher, D.E., Jacks, T., Pelletier, J. and Housman, D.E. (1994) Apoptosis and the Prognostic Significance of p53 Mutation. Cold Spring Harbor Sym. Quant. Bio. 59:419-426.
- Lowe, S.W., Bodis, S., McClatchey, A., Remington, L., Ruley. H.E., Fisher, D.E., Housman, D.E. and Jacks, T. (1994) p53 Status and the Efficacy of Cancer Therapy in Vivo. Science 266:807-810.
- Polakiewicz, R.D., Munroe, D.J., Jani Sait, S.N., Tycowski, K.T., Nowak, N.J., Shows, T.B., Housman, D.E., Page, D.C. Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3q13.5. Genomics. 25:577-580.
- Higgins, M.J., Smilinich, N.J., Sait, S., Koenig, A., Pongratz, J., Gessler, M., Richard III, C.W., James, M.R., Sanford, J.P., Kim, B.-W., Cattelane, J., Nowak, N.J., Winterpacht, A., Zabel, B.U., Munroe, D.J., Bric, E., Housman, D.E., Jones, C., Nakamura, Y., Gerhard, D.S., Shows, T.B. (1994) An Ordered NotI Fragment Map of Human Chromosome Band 11p15. Genomics 23: 211-222.
- Coleman, A., Fountain, J.W., Nobori, T., Olopade, O.I., Robertson, G., Housman, D.E., Lugo, T.G. (1994) Distinct deletions of chromosome 9p associated with melanoma versus glioma, lung cancer, and leukemia. Cancer Research 54:344-348.
- Glaser, T., Ton, C.C., Mueller, R., Petzl-Erler, M.L., Oliver, C., Nevin, N.C., Housman, D.E., Maas, R.L. (1994) Absence of PAX6 gene mutations in Gillespie syndrome (partial aniridia, cerebellar ataxia, and mental retardation). Genomics, 19:145-148.
- Taneja, K.L., McCurrach, M., Schalling, M., Housman, D.E., Singer, R.H. (1995). Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues. Journal of Cell Biology 128:995-1002.
- McCarthy, L., Hunter, K., Schalkwyk, L., Riba, L., Anson, S. Mott, R., Newell, W., Bruley, C., Bar, I., Ramu, E., Housman, D.E., Cox, R., Lehrach, H. (1995) Efficient high resolution genetic mapping of mouse IRS-PCR products, towards integrated genetic and physical mapping of the mouse genome. Proc. Natl. Acad. Sci. USA 92:5302-5306.
- Munroe, D.J., Loebbert, R., Bric, E., Whitton, T., Prawitt, D., Vu, D., Buckler, A., Winterpacht, A., Zabel, B. and Housman, D.E. (1995) Systematic screening of an arrayed cDNA library by PCR. Proc. Natl. Acad. Sci.92:2209-2213.
- Cai, W., Aburatani, H., Housman, D.E., Wang, Y-K. and Schwartz, D.C. (1995). Ordered restriction endonuclease maps of yeast artificial chromsomes created by optical mapping on surfaces. Proc. Natl. Acad. Sci. USA 92:5164-5168
- Nakagama, H., Heinrich, G., Pelletier, J., and Housman, D.E. (1995). Sequence and structural requirements for high affinity DNA binding by the WT1 gene product. Molecular and Cellular Biology 15:1489-1498.
- Russell, M.W., Dick III, M., Campbell, R. M., Munroe, D.J., Bric, E., Housman, E.E., Collins F.S., and L.C.Brody (1995). Recombination analysis in two 11p15-linked Romano-Ward Long QT Syndrome (RWLQTS) families: localization of the RWLQTS gene to the interval between tyrosone hydroxylase (TH) and D11S1349. American Journal of Human Genetics 57:503-507.
- Housman, D.E. (1995) Human DNA Polymorphism. New England Journal of Medicine 332: 318-320.
- Housman, D.E. (1995) DNA on trial - The molecular basis of DNA fingerprinting. New England Journal of Medicine 332:534-535.
- Karayiorgou, M., Morris, M.A., Morrow, B., Shprintzen, R.J., Goldberg, R., Borrow, J., Gos, A., Nestadt, G., Wolyniec, P.S., Lasseter, V.K., Eisen, H., Childs, B., Kazazian, H.H., Kucherlapati, R., Antonarkis, S.E., Pulver, A.E., and D.E. Housman. (1995). Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc. Natl. Acad. Sci. 92:7612-7616.
- Haluska, F.G. and David E. Housman. (1995) Recent advances in the molecular genetics of malignant melanoma. Cancer Surveys 25: 277-292.
- Moffett, P., Bruening, W., Nakagama, H., Bardeesy, N., Housman, D., Housman, D.E., and J.Pelletier. (1995) Antagonism of WT1 activity by self-association. Proc.Natl.Acad.Sci. USA 92:11105-11109.
- Flores, J.F., Walker, G.J., Glendening, J.M., Haluska, F.G., Castresana, J.S., Rubio, M-P., Pastorfide, G.C., Boyer, L.A., Kao, W.H., Bulyk, M.L., Barnhill, R.L., Hayward, N.K., Housman, D.E., and Fountain, J.W. Loss of the p16INK4a and p15INK4b genes, as well as neighboring 9p21 markers, in sporadic melanoma. Cancer Research 56 (in press).
- Munroe, D. J., Prawitt, D., Bric, E., Byrd, P., Whitton, T., Vu, D, Loebbert, R., Sait, S.N., Nowak, N.J., Winterpacht, A., Zabel, B. U., Shows, T. B., Deaven, L., Evans, G., and David E. Housman (1995). Rapid assembly of cosmid contigs from YACs. Genome Research, (Submitted)
- Dong, W-F., Xu, Y., Hu, Q., Munroe, D., Minowada, J., Housman, D., and M.D. Minden. Molecular characterization of a chromosome translocation breakpoint t(11;14)(p13;q11) from the cell line KOPT-K1. Leukemia 9:1812-7.
- Hsu, S.Y., Kubo, M., Chun, S.Y., Haluska, F.G., Housman, D.E., Hsueh, A.J. (1995) Wilms' tumor protein WT1 as an ovarian transcription factor: decreases in expression during follicle development and repression of inhibin-alpha gene promoter. Mol. Endocrinol. 9: 1356-66
- Qin, S., Sait, S., Zhang, J., Nowak, N., Cheng, Y., Li, L., Higgens, M., Munroe, D. J., Bric, E., Housman, D., Gerhardt, D., Evans, G., Weber, B., Gaudary, P., and T. Shows. A YAC contig of human chromosome 11. Proc.Natl.Acad.Sci.USA 93:3149-3154.
- Liu, J., Stanton, V.P. Jr., Fujiwara, T.M., Wang, J.X., Rezonzew, R., Crumley, M.J., Morgan, K., Gros, P., Housman, D.E., Schurr, E. (1995) Large-scale cloning of human chromosome 2-specific yeast artificial chromosomes (YACs) using an interspersed repetitive sequences (IRS)-PCR approach. Genomics 26:178-191.
- Housman, D.E. (1995) Gain of glutamines, gain of function? Nature Genetics 10:3-4.
- Reddy, S., Smith, D.B.J., Rich, M.M., Leferovich, J.M., Reilly, P., Davis, B., Tran, K., Rayburn, H., Bronson, R., Cros, D., Balice-Gordon, R.J. and D.E. Housman. (1996) Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy. Nature Genetics 13:325-35.
- Graeber, T.G., Osmanian, C., Jacks, T., Housman, D.E., Koch, C.J., Lowe, S.W. and A.J. Giaccia. (1996) Hypoxia, apoptosis and p53 tumor development. Nature 379: 88-91
- Aburatani, H., Stanton, V.P. Jr., and Housman, D.E. (1996) High resolution physical mapping by combined Alu-hybridization/PCR screening: construction of a Yeast Artificial Chromosome map covering 31 cM in 3p21-p14. Proc. Natl. Acad. Sci. USA 93: 4474-4479.
- Manenti, G., Gariboldi, M., Elango, R., Fiorino, A., De Gregorio, L., Falvella, F.S., Hunter, K., Housman, D., Pierotti, M.A., and Dragani, T.A. (1996) Genetic mapping of a pulmonary adenoma resistance locus (Par1) in the mouse. Nature Genetics 12/4: 455-457.
- Hunter, K., Riba, L.,Schalkwyk, L., Clark, M., Resenchuk,S., Beeghly, A., Su, J., Tinkov, F., Lee, P., Elango, R., Lehrach, H., and Housman, D.E. (1996) Towards the construction of integrated physical and genetic maps of the mouse genome utilizing interspersed repetitive sequence PCR (IRS-PCR) genomics. Genome Research 6:290-299
- Haluska, F.G., Fountain, J.W., Alberta, J., Rivera, M., Stanton, V.P., and Housman, D.E. Construction of a 5 megabase YAC contig on chromosome 9p21-22. (Submitted)
- Borrow, J., Shearman, A.M., Stanton, V.P., Jr., Becher, R., Collins, T., Williams, A.J., Dube, I., Katz, F., Kwong, Y.L., Morris, C., Kazuma, Ohyashiki, Toyama, K., Rowley, J., and Housman, D.E. (1996) The t(7;11)(p15;p15) translocation in acute myeoloid leukaemia fuses the genes for nucleoporin NUP98 to class I homeoprotein HOXA9. Nature Genetics 12:159-167.
- Russell, M.W., Munroe, D.J., Bric, E., Housman, D.E., Dietz-Band, J., Riethman, H.C., Collins, F.S., and Brody, L.C. (1996) A 500 kb physical map from the Harvey ras-1 gene to the 11p telomere. Genomics 35:353-360
- Shearman, A.M., Hudson, T.J., Andresen, J.M., Wu, X., Sohn, R.L., Haluska, F., Housman, D.E. and Weiss, J.S. (1996) The gene for Schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36. Human Molecular Genetics 5:1667-1672.
- Haluska, F.G., Thiele, Carol, Goldstein, A., Fountain, J.W. and Housman, D.E. Lack of phospholipase A2 mutations in colon cancer, melanoma and neuroblastoma cell lines. (submitted)
- Dackowski, W.R., Connors, T.D., Bowe, A.E., Stanton, V.P. Jr., Housman, D.E., Doggett, N.A., Landes, G.M., and Klinger, K.W. (1996) The region surrounding the PKD1 gene: A 700kb P1 contig from a YAC-deficient interval. Genome Research 6: 515-524.
- Elango, R., Riba, L., Housman, D.E. and Hunter, K. (1996) Generation and mapping of M.spretus strain-specific markers for rapid genomic scanning. Mammalian Genome 7:340-343.
- Pulver, A.E., Wolyniec, P.S., Housman, D.E., Kazazian, H.H., Anonarakis, S.E., Nestadt, G., Lasseter, V.K., McGrath, J.A., Dombroski, B., Karayiorgou, M., Ton, C., Blouin, J-L., and L. Kempf. (1996) The Johns Hopkins University Collaborative Schizophrenia Study: an Epidemiologic-genetic approach to test the heterogeneity hypothesis and identify schizophrenia susceptibility genes. (submitted)
- Borrow, J., Stanton, V.P.Jr., Andresen, J.M., Becher, R., Behm., F.G., Chaganti, R.S.K., Civin, C.I., Disteche, C., Dube, I., Frischauf, I., Horsman, D., Mitelman, F., Volinia, S., Watmore, A.E.and D.E. Housman (1996) The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein. Nature Genetics 14:33-41.
- Karayiorgou, M., Gogos, J.A., Galke, B.L., Woyniec, P.S., Nestadt, G., Anonarakis, S.E., Kazazian, H.H., Housman, D.E. and A.E. Pulver Identification of sequence variants and of the role of the COMT gene in schizophrenia susceptibility. Biological Psychiatry (submitted)
- Reddy, P.S. and D.E. Housman (1997) The complex pathology of trinucleotide repeats. Curr. Opin. Cell Biol. 9: 364-372
- Davis, B.M., McCurrach, M.E., Taneja, K.L., Singer, R.H. and D.E. Housman (1997) Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts. Proc. Natl. Acad. Sci. USA 94:7388-7393
- Sobulu, O.M., Borrow, J., Tornek, R., Reshmi, S., Harden, A., Schlegelberger, B., Housman, D.E., Doggett, N.A., Rowley J.D. and J. Zeleznik-Le (1997) MLL is fused to CBP, a histone acetyltransferase, in therapy-related acute. Proc. Natl. Acad. Sci. USA 94 (8732-7).
- Haluska, F.G., Thiele, C., Goldstein, A., Tsao, H., Benoit, E.P., and D.E. Housman. (1997) Lack of phospholipase A2 mutations in neuroblastoma, melanoma, and colon-cancer cell lines. Int. J. Cancer 72:337-339.
- Rodriguez, P., Munroe, D., Prawitt, D. Chu, LL, Bric, E., Kim, J., Reid, L.H., Davies, C., Nakagama, H., Loebbert, R., Winterpacht, A., Petruzzi, MJ., Higgins, M.J., Nowak, N., Evans, G., Shows, T., Weissman, B.E., Zabel, B., Housman, D.E. and J. Pelletier. (1997) Functional characterization of human nucleosome assembly protein -2 (NAP1L4) suggests a role as a histone chaperone. Genomics 44: 253-65
- Das, M., Chu, L.L., Ghahremani, M., Abrams-Ogg, T., Roy, M.S., Housman, D.E., and J. Pelletier. (1998) Characterization of an abundant short interspersed nuclear element (SINE) present in Canis familiaris. Mammalian Genome 9:64-69.
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