Publications from the Laboratory

Publications
From the Laboratory

Publications (1990-1993)
  1. Lichter, P., Tang, C.C., Call., K., Hermanson, G., Evans, G.A., Housman, D. Ward, D.C. (1990) High resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. Science 247: 64-69.
  2. Rose, E.A., Glaser, T.M., Jones, C.a., Smith, C.L., Lewis, W.H., Call, K.M., Minden, M., Champagne, C., Bonetta, L., Yeger, H. Housman, D.E. (1990) Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene. Cell 60: 495-508.
  3. Warburton, D., Gersen, S., Yu, M.-T., Jackson, C., Handelin, B. Housman, D. (1990) Monochromosomal rodent-human hybrids from microcell fusion of human lymphoblastoid cells containing an inserted dominant selectable marker. Genomics 6: 358-366.
  4. Hensold, J.O., Hunt, C.R., Calderwood, S.K., Housman, D.E. Kingston, R.E. (1990) DNA binding of heat shock factor to the heat shock element is insufficient for transcriptional activation in murine erythroleukemia cells. Mol. & Cell. Biol. 10: 1600-1608.
  5. Raymond, M., Rose, E., Housman, D.E. Gros, P. (1990) Physical mapping, amplification, and overexpression of the mouse mdr gene family in multidrug-resistant cells. Mol. & Cell. Biol. 10: 1642-1651.
  6. Wilson, S.D., Billings, P.R., D'Eustachio, P., Fournier, R.E.K., Geissler, E., Lalley, P.A., Burd, P.R., Housman, D.E., Taylor, B. Dort, M. (1990) Clustering of cytokine genes on mouse chromosome 11. J. Exp. Med. 171: 1301-1314.
  7. 144. Haber, D.A., Buckler, A.J., Glaser, T. , Call, K., Pelletier, J., Douglass, E., Housman, D.E. (1990) A 25 bp internal deletion identifies the 11p13 Wilms' tumor gene. Cell 61: 1257-1269.
  8. Pritchard-Jones, K., Fleming, S., Davidson, D., Bickmore., W., Portious, D., Gosden, C., Bard, J., Buckler, A., Pelletier, J., Housman, D., van Heyningen, V. Hastie, N. (1990) The candidate Wilms' gene is involved in genitourinary development. Nature 346: 194-197.
  9. Glaser, T., Lane, J. Housman D. (1990) A mouse model of the Aniridia-Wilms' tumor deletion syndrome. Science 250: 823-827.
  10. Tam, S-Y., Geissler, E.N., Graw, S.L., Housman, (1990) Functional Expression of the Genomic DNA Sequences Encoding Muse Na,K-ATPase a 1 Gene by CoTransfection of Overlapping Genomic DNA Segments. Mol. & Cel. Biol. 10: 6619-6623.
  11. Housman, D.E. (1990) The Human Gene Map: An Overview of Strategies, Status, and Application Mapping the Genomes of Agriculturally Important Animals, ed. James Womack. Texas A&M University by Cold Spring Harbor Laboratory Press. pp. 3-12.
  12. Matsumoto, A., Naito, M., Itakura, H., Ikemoto, S., Asaoka, H., Hayakawa, I., Kanamori, H., Aburatani, H., Takaku, F., Suzuki, H., Kobari, Y., Miyai, T., Takahashi, K., Cohen, E.H., Wydro, R., Housman, D.E. Kodama, T., (1990) Human macrophage scavenger receptors: Primary structure, expression and localization in atherosclerotic lesions. PNAS 87: 9133-9137.
  13. Fountain, J.W., Bale, S.J., Housman, D.E. and Dracopoli, N.C. (1990) Genetics of melanoma. Cancer Surveys 9(4): 645-671.
  14. Geissler, E.N., Liao, M., Brook, J.D., Martin, F.H., Zsebo, K.M., Housman, D.E. Galli, S.J. (1991) Stem Cell Factor (SCF), a Novel Hematopoietic Growth Factor and a Ligand for the c-kit Tyrosine Kinase Receptor, Maps on Human Chromosome 12 between 12q14.3 and 12qter. Som. Cell & Mol. Genet. 17: 207-214..
  15. Hunter, K., Housman, D. Hopkins, N. (1991) Isolation and Characterization of Irradiation Fusion Hybrids from Mouse Chromosome 1 for the Mapping Rmc, a Gene that Encodes a Cellular Receptor for the MCF Class of Murine Retroviruses. Som. Cell & Mol. Genet. 17: 169-183.
  16. Haber, D. Housman, D.E. (1991) Rate-Limiting Steps: The genetics of pediatric cancers. Cell 64: 5-8.
  17. Buckler, A.J., Pelletier, J., Haber, D.A., Glaser, T. Housman, D.E. (1991) The murine Wilms' tumor gene (WT1): Isolation, characterization, and expression during kidney development. Mol. & Cell. Biol. 11: 1707-1712.
  18. Wexler, N.S., Rose, E.A., Housman, D.E. (1991) Molecular Approaches to hereditary Diseases of the Nervous System: Huntington's Disease as a Paradigm. Annual Review of Neuroscience 14: 503-29.
  19. Hensold, J.O., Dubyak, G. Housman, D.E. (1991) Calcium Ionophore, A23187, Induces Commitment to Differentiation But Inhibits the Subsequent Expression of Erythroid Genes in Murine Erythroleukemia Cells. Blood. 6: 1362-1370.
  20. Huff, V., Miwa, H. Haber, D., Call, K.M., Housman, D.E., Strong, L.C. Saunders, G.F. (1991) Evidence of WT1 as a Wilms' tumor (WT) gene: Intragenic Germinal Deletion in Bilateral WT. Am. J. of Hum. Genet. 48: 997-1003.
  21. Fountain, J.W., Dracopoli, N.C., Housman, D.E. Baldwin, A.S. (1991) MspI RFLP detected by a MBP-1 cDNA Sequence. Nuc.Acids Res. 19: 2514.
  22. Buckler, A.J., Chang, D.D., Graw, S.L., Brook, J.D., Haber, D.A. Sharp, P.A., Housman, D.E. (1991) Exon Amplification: A Strategy to isolate mammalian genes based on RNA splicing. PNAS 88: 4005-4009.
  23. Pelletier, J., Brook, J.D. Housman, D.E. (1991) Assignment of Two of the Translation Initiation Factor-4E (eIF-4E) Genes to Human Chromosomes 4 and 20. Genomics 10: 1079-1082.
  24. Ton, C.T., Huff, V., Call, K.M., Cohn, S., Strong, L.C., Housman, D.E. Saunders, G.F. (1991) Smallest region of overlap in Wilms' tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus. Genomics 10: 293-297.
  25. Goradia, T.M ., Stanton, V.P., Jr., Cui, X., Aburatani, H., Li, H., Lange, D., Housman, D.E. Arnheim, N. (1991) Ordering three DNA polymorphisms on human chromosome 3 by sperm typing. Genomics 10: 748-755.
  26. Royer-Pokoroa, B., Ragg, S., Heckl-Ostreicher, B., Held. M., Loos, U., Call, K.M., Glaser, T., Housman, D., Saunders, G., Zabel, B., Williams, B., Poustka. (1991) Direct pulsed field gel electrophoresis of Wilms' tumor material shows that DNA deletions in 11p13 are rare. Genes, Chromosomes & Cancer 3: 89-100.
  27. Davis, L.M., Zabel, B., Senger, G., Ludecke, H-J., Metzroth, B., Call, K., Housman, D. Claussen, U., Horsthemke, B. Shows, T.B. (1991) A tumor chromosome rearrangement further defines the 11p13 Wilms' tumor locus. Genomics 10: 588-592.
  28. Cowell, J.K., Wadey, R.B., Haber, D.A., Call, K.M., Housman, D.E., Strong, L.C. and Saunders, G.F. (1991) Structural Rearrangements of the WT1 gene in Wilms' Tumor Cells. Oncogene 6: 595-600.
  29. Schwartz, C.E., Haber, D.A., Stanton, V.P., Strong, L.C., Skolnick, M.H., Housman, D.E. (1991) Familial Predisposition to Wilms' Tumor Does Not Segregate with the WT1 Gene. Genomics 10: 927-930.
  30. Pelletier, J., Schalling, M., Buckler, A.J., Rogers, A., Haber, D.A., Housman, D.E. (1991) Expression of the Wilms' tumor gene WT1 in the murine urogenital system. Genes & Dev. 5: 1345-1356.
  31. Haber, D.A., Buckler, A.J., Glaser, T., Call, C.K., Pelletier, J., Sohn, R.L., Douglass, E.C., Housman, D.E. (1991) An Internal Deletion within an 11p13 Zinc Finger Gene Contributes to the Development of Wilms' Tumor. Cell 61: 1257-1269.
  32. Pelletier, J., Bruening, W., Kashtan, C.E., Mauer, S.M., Manivel, J.C., Striegel, J.E., Houghton, D.C., Junien, C., Habib, R., Fouser, L., Fine, R.N., Silverman, B.L., Haber, D.A., Housman, D.E. (1991) Germline Mutations in the Wilms' Tumor Suppressor Gene Are Associated with Abnormal Urogenital Development in Denys-Drash Syndrome. Cell 67: 437-447.
  33. Pelletier, J., Bruening, W., Li, F.P., Haber, D.A., Glaser, T., Housman, D.E. (1991) WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumor. Nature, 353: 431-434.
  34. Haber, D.A., Sohn, R., Buckler, A.J., Pelletier, J., Call, K., Housman, D.E. (1991) Alternative splicing and genomic structure of the Wilms' tumor gene, WT1. Proc. Natl. Acad. Sci. USA, 88: 9618-9622.
  35. Pelletier, J., Munroe, D., Housman, D.E. (1991) Molecular genetics of Wilms' tumor. In Genome Analysis, Genes and Phenotypes, (Cold Spring Harbor Laboratory Press NY: Cold Spring Harbor), 3: 135-169.
  36. Doucette-Stamm, L., Riba, L., Handelin, B., Housman, D. (1991) Generation and Characterization of Irradiation Hybrids of Chromosome 4. Somatic Cell and Molecular Genetics, 17, 5: 471-480.
  37. Strobel, S., Doucette-Stamm, L., Riba, L., Housman, D., Dervan, P. (1991) Site-Specific Cleavage of Human Chromosome 4 Mediated by Triple Helix. Science, 254: 1639-1642.
  38. Pelletier, J. , Haber, D.A. , Housman, D.E. (1991). Genetics of Wilms' Tumor. In Origins of Human Cancer: A Comprehensive Review, (Cold Spring Harbor Laboratory Press NY: Cold Spring Harbor), 1: 433-441
  39. Brook, J.D., Zemelman, B.V., Haddingham, K., Siciliano, M.J., Crow, S., Harley, H.G., Rundle, S.A., Buxton, J., Johnson, K., Almond, J.W., Housman, D.E., Shaw, D.J. (1991) Radiation Reduced Hybrids for the Myotonic Dystrophy Locus. Genomics 13 (2): 243-250.
  40. Thompson, L.M., Plummer, S., Schalling, M., Altherr, M.R., Gusella, J.F., Housman, D.E. Wasmuth, J.J. (1991) A Gene Encoding a Fibroblast Growth Factor Receptor Isolated from the Huntington Disease Gene Region of Human Chromosome 4. Genomics 11: 1133-1142.
  41. Hudson, T.J., Engelstein, M., Lee, M.K., Ho, E.C., Rubenfield, M.J., Adams, C.P., Housman, D.E. and Dracopoli, N.C. Isolation and Chromosomal Assignment of 100 Highly Informative Human Simple Sequence Repeat Polymorphisms. (1991) Genomics. 48: 29-35.
  42. Fountain, J.W., Karayiorgou, M., Graw, S.L., Buckler, A.J., Taruscio, D., Ward, D.C., Ernstoff, M.S., Kirkwood, J.M., Andersen, L.B., Collins, F.S., Dracopoli, N.C. and Housman, D.E. (1991). Chromsome 9p Involvement in Melanoma. Am. J. Hum. Genet. Suppl., 49: A45.
  43. Gusella, J.F., Altherr, M.R., McClatchey, A.I., Doucette-Stamm, L.A., Tagle, D.A., Plummer, S., Groot, N., Collins, F.S., Housman, D.E., Lerach, H., MacDonald, M.E., Bates, G., Wasmuth, J.J. (1992) Sequence Tagged Sites (STSs) Spanning 4P16.3 and the Huntington's Disease Candidate Region. Genomics, 13:75-80.
  44. Harley, H.G., Brook, J.D., Rundle, S.A., Crow, S., Reardon, W., Buckler, A.J., Harper, P.S., Housman, D.E. and Shaw, D.J. (1992) Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy. Nature 355: 545-546.
  45. Brook, D.J., McCurrach, M.E., Harley, H.G., Buckler, A.J., Church, D., Aburantani, H., Hunter, K., Stanton, V.P., Thirion, J-P., Hudson, T., Sohn, R., Zemelman, B., Snell, R.G., Shelbourne, P., Buxton, J., Jones, C., Juvonen, V., Johnson, K., Harper, P.S., Shaw, D.J. and Housman, D.E. (1992). Molecular Basis of Myotonic Dystrophy Expansion of a Trinucleotide (CTG) Repeat at the 3' End of a Transcript Encoding a Protein Kinase Family Member. Cell 68: 799-808.
  46. Graw, S.L., Buckler, A.J., Britt, D.E., Jackson, C.L., Tarucsio, D., Baldini, A., Ward, D.C. and Housman, D.E.(1992) Generation and Characterization of a Human Chromosome 9 Cosmid Library. Som. Cell & Mol. Gen. 18: 269-284.
  47. Jackson, C.L.,. Britt, D.E., Graw, S.L., Potts, A., Santoro, K., Buckler, A.J., Housman, D.E. and Mark, H.F.L. (1992) Construction and Characterization of Radiation Hybrids for Chromosome 9, and their use in Mapping Cosmid Probes on the Chromosome. Som. Cell & Mol. Gen. 18: 285-301.
  48. Valentijin, L.J., Bolhuis, P.A., Zorn, I., Hoogendijk, J.E., van den Bosch, N., Hensels, G.W., Stanton, V.P., Jr., Housman, D.E., Fischbeck, K.H., Ross, D.A., Nickolson, G.A., Meershoek, E.J., Dauwerse, H.G., van Ommen, G-J.B. and Baas, F. (1992) The Peripheral Myelin Protein Gene PMP-22/GAS-3 is Duplicated in Charcot-Marie-Tooth Disease Type 1A. Nature Genetics. 1: 166-170.
  49. Boyle, A.L., Feltquate, D.M., Dracopoli, N.C., Housman, D.E. and Ward, D.C. (1992) Rapid Physical Mapping of Cloned DNA on Banded Mouse Chromosomes by Flourescence in Situ Hybridization. Genomics. 12: 106-115.
  50. Oettinger, M.A., Stanger, B., Schatz, D.G., Glaser, T. , Call, K., Housman, D. and Baltimore, D. (1992). The Recomination of Activating Genes, RAG-1 and RAG-2, are on Chromsome 11p in Humans and 2p in Mice. Immunogenetics, 35: 97-101.
  51. Haber, D.A. and Housman, D.E. (1992) The Genetics of Wilms' Tumor. Advances in Cancer Research, 59: 41-68.
  52. Haber, D.A. and Housman, D.E. (1992) Role of the WT1 Gene in Wilms' Tumor. Cancer Surveys, 12: 105-117.
  53. Breuning, W. Bardeesy, N., Silverman, B.L., Cohn, R.A., Machin, G.A., Aronson, A.J., Housman, D. and Pelletier, J. (1992) Germline Intronic and Exonic Mutations in the Wilms' Tumor Gene (WT1) Affecting Urogenital Development. Nature Genetics, 1: 144-148.
  54. Call, K.M., Ito, C.Y., Lindberg, C., Memisoglu, A., Petrou, C., Glaser, T., Jones, C. and Housman, D.E. (1992) Mapping and Characterization of 129 Cosmids on Human Chromsome 11p. Som. Cell & Mol. Gen. Vol. 18, 5: 463-475.
  55. Krolewski, A.S., Krolewski, B., Gray, M., Stanton, V., Warram, J.H. and Housman, D.E. (1992) High-Frequency DNA Sequence Polymorphisms in the Insulin Receptor Gene Detected by Denaturing Gradient Gel Blots. Genomics. 12: 705-709.
  56. Fountain, W.J., Karayiorgou, M., Taruscio, D., Graw, S.L., Buckler, A.J., Ward, D.C., Dracopoli, N.C. and Housman, D.E. (1992) Genetic and Physical map of the 'Interferon Region' on Chromosome 9p. Genomics 14: 105-112.
  57. Fountain, J.W., Karayiorgou, M., ERnstoff, M.S., Kirkwood, J.M., Vlock, D.R., Titus-Ernstoff, L., Bouchard, B., Vijayasaradhi, S., Houghton, A.N., Lahti, J., Kidd, V., Housman, D.E. and Dracopoli, N.C. (1992) Homozygous Deletions within Human Chromosome Band 9p21 in Melanoma. Proc. Natl. Acad. Sci. USA, 89: 10557-10561.
  58. Fountain, J.W., Graw, S.L., Kao, W., Stanton, V.P., Aburantani, H., Munroe, D.J., Dracopoli, N.C. and Housman, D.E. (1992) Further Characterization of the Region of Chromosome 9p Deleted in Cutaneous Malignant Melanoma. Am. J. Hum. Genet., Suppl. 51: A51.
  59. Haber, D.A., Timmers, H.Th.M., Pelletier, J., Sharp, P.A. and Housman, D.E. (1992) A Dominant Mutation in the Wilm's Tumor Gene WT1 Cooperates with E1A in Transforming Primary Kidney Cells. PNAS 89:10984-10988.
  60. Shaw, D.J., McCurrach, M., Rundle, S.A., Harley, H.G., Crow, S.R., Sohn, R., Thirion, J-P, Harper, P.S., Housman, D.E. and Brook, J.D. (1992) Genomic organization and Transcription Units at the Myotonic Dystrophy Locus. Genomics 18: 673-679.
  61. Taruscio, D., Graw, S., Ladanyi, T., Buckler, A.J., Housman, D.E. and D.C. Ward (1992) Mapping of 105 Cosmid Clones to Human Chromosome 9 by Fluorescence in Situ Hybridization. ????
  62. Takahara, Y., Hamada, K. and D.E. Housman (1992) A New Retrovirus Packaging Cell for Gene Transfer Constructed from Amplified Long Terminal Repeat-Free Chimeric Proviral Genes. J. of Virology, June 1992: 3725-3732.
  63. Krolewski, A.S., Doria, A., Magre, J., Warram, J.H. and D.E. Housman. (1992) Molecular Genetic Approaches to the Identification of Genes Involved in the Development of Nephroopathy in Insulin-Dependent Diabetes Mellitus. J. of Am. S. of Nephrology, vol. 3, Supplement 1, S9-S17.
  64. Housman, D.E. (1992) Role of Wilms' Tumor 1 Tumor-Suppressor Gene in the Etiology of Wilms' Tumor. in Nuclear Processes and Oncogenes, Academic Press, 147-160.
  65. Bruhn, S.L., Pil, P.M., Essignmann, J.M., Housman, D.E. and Lippard, S.J. (1992) Isolation and Characterization of Human cDNA Clones Encoding an HMG-box Protein that Recognized Structural Distortions to DNA Caused by Binding of the Anticancer Agent Cisplatin, Proc. Natl. Acad. Sci., USA 98:2307.
  66. Lerner, T., Graw, S., Landes, G., Klinger, K., Callen, D., Housman, D., Buckler, A. Isolation and Transciptional Characterization of Cosmid Clones from the region of the PKD1 Gene on Human Chromosome 16. Bio/Technology. (in press)
  67. Graw, S.L., Schalling, M., Callen, D.F., Klinger, K., Landes, G. and Lerner, T. (1992) Isolation and Characterization of a Candidate Gene for Autosomal Dominant Polycystic Kidney Disease. Contributions to Nephrology 97:110-117.
  68. Bruhn, S.L., Housman, D.E. and Lippard, S.L. (1993) Isolation and characterization of cDNA clones encoding the Drosophila homolog of the HMG-box SSRP family that recognizes specific DNA structures. Nucl. Acids Res. 21:1643.
  69. Snell, R.G., Doucette-Stamm, L.A., Gillespie, S.A.M. Riba, L. Bates, G.P. Altherr, M.R., MacDonald, M.E., Gusella, J.F., Wasmuth, J.J., Lehrach, H., Housman, D.E. Harper, P.S. and Shaw, D.J. The isolation of cDNAs within the Huntington disease region by hybridization of yeast artificial chromosomes to a cDNA library. (1993) Human Mol. Gen. Vol. 2, 3: 305-309.
  70. Andersen, L.B., Fountain, J.W., Gutmann, D.H. , Tarle, S.A., Glover, T.W., Dracopoli, N.C., Housman, D.E. and Collins, F.S. (1993) Neurofibromatosis I DNA, RNA, and Protein Abnormalities in Malignant Melanoma. Nature Genetics 3: 118-121.
  71. Hinds, H.L., Ashley, C.T., Sutcliffe, J.S., Nelson, D.L., Warren, S.T., Housman, D.H. and Schalling, M. (1993) Tissue Specific Expression of FMR-1 Provides Evidence for a Functional Role in Fragile X Syndrome. Nature Genetics, 3: 36-43.
  72. The Huntington's Disease Collaborative Research Group (1993) A Novel Gene Containing a Trinucleotide Repeat that is expanded and Unstable on Huntington's Disease Chromosomes. Cell, 72: 971-983.
  73. Schalling, M., Hudson, T.J., Buetow, K.H. and Housman, D.E. (1993) Direct Detection of Novel Expanded Trinucleotide Repeats in the Human Genome. Nature Genetics, 4: 135-139
  74. Galson, D.L., Hensold, J.O., Bishop, T.R., Schalling, M., D'Andrea, A.D., Jones, C., Auron, P.E. and Housman, D.E. (1993) Mouse b-Globin DNA-Binding Protein B1 is Identical to a Proto-oncogene, the Transcription Factor Spi-1/PU.1, and is Restricted in Expression to Hemotopoietic Cells and the Testis. MCB, May, 2929-2941.
  75. Kreidberg, J.A., Sariola, H., Loring, J.M., Maeda, M., Pelletier, J., Housman, D. and R. Jaenisch. (1993). WT-1 is Required for Early Kidney Development. Cell 74: 679-693.
  76. Lowe, S.W., Ruley, H.E., Jacks, T. and Housman, D.E. (1993). p53-dependent apoptosis modulates the cytoxicity of anticancer agents. Cell 74: 957-967.
  77. Hunter, K.W., Watson, M.L., Rochelle, J., Ontiveros, S., Munroe, D., Seldin, M. and Housman, D.E. (1993). Single Strand Conformational Polymorphism (SSCP) Mapping the Mouse Genome: Integration of the SSCP, Microsatellite and Gene Maps of Mouse Chromosome 1. Genomics 18: 510-519.
  78. Lowe, S.W., Jacks, T., Housman, D.E. and Ruley, H.E., (1993). Abrogation of oncogene-associated apoptosis allows transformation of p53-deficient cells. Proc. Natl. Acad. Sci. USA, 91: 2026-2030.
  79. Church, D., Rogers, A.C., Graw, S.L., Housman, D.E., Gusella, J.F. and Buckler, A.J. Identification of Human Chromosome 9 Specific Genes using Exon Amplification. (1993) Human Molecular Genetics Vol. 2, 11: 1915-1920.
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