David Housman - Publications

Massachusetts Institute of Technology, Cambridge, MA, United States 
Human Genetics, Huntington's disease, Myotonic dystrophy, Fragile-X syndrome

109 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Crittenden JR, Zhai S, Sauvage M, Kitsukawa T, Burguière E, Thomsen M, Zhang H, Costa C, Martella G, Ghiglieri V, Picconi B, Pescatore KA, Unterwald EM, Jackson WS, Housman DE, et al. CalDAG-GEFI mediates striatal cholinergic modulation of dendritic excitability, synaptic plasticity and psychomotor behaviors. Neurobiology of Disease. 105473. PMID 34371144 DOI: 10.1016/j.nbd.2021.105473  0.689
2021 Crittenden JR, Gipson TA, Smith AC, Bowden HA, Yildirim F, Fischer KB, Yim M, Housman DE, Graybiel AM. Striatal transcriptome changes linked to drug-induced repetitive behaviors. The European Journal of Neuroscience. PMID 33759265 DOI: 10.1111/ejn.15116  0.701
2018 Wang ET, Treacy D, Eichinger K, Struck A, Estabrook J, Olafson H, Wang TT, Bhatt K, Westbrook T, Sedehizadeh S, Ward A, Day J, Brook D, Berglund JA, Cooper T, ... Housman D, et al. Transcriptome alterations in myotonic dystrophy skeletal muscle and heart. Human Molecular Genetics. PMID 30561649 DOI: 10.1093/Hmg/Ddy432  0.668
2018 Fratta P, Sivakumar P, Humphrey J, Lo K, Ricketts T, Oliveira H, Brito-Armas JM, Kalmar B, Ule A, Yu Y, Birsa N, Bodo C, Collins T, Conicella AE, Mejia Maza A, ... ... Housman DE, et al. Mice with endogenous TDP-43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis. The Embo Journal. PMID 29764981 DOI: 10.15252/Embj.201798684  0.511
2018 Sivakumar P, Humphrey J, Lo K, Ricketts T, Oliveira H, Kalmar B, Wang E, Housman D, Baralle F, Greensmith L, Buratti E, Plagnol V, Fisher EMC, Arozena AA, Fratta P. Dissecting TDP-43 gain- and loss-of-function in neurodegeneration Neuromuscular Disorders. 28. DOI: 10.1016/S0960-8966(18)30366-3  0.498
2017 McGinty RJ, Puleo F, Aksenova AY, Hisey JA, Shishkin AA, Pearson EL, Wang ET, Housman DE, Moore C, Mirkin SM. A Defective mRNA Cleavage and Polyadenylation Complex Facilitates Expansions of Transcribed (GAA)n Repeats Associated with Friedreich's Ataxia. Cell Reports. 20: 2490-2500. PMID 28877480 DOI: 10.1016/J.Celrep.2017.08.051  0.505
2017 Sivakumar P, Humphrey J, Ule A, Bodo C, Emmett W, Ricketts T, Oliveira H, Wang E, Housman D, Greensmith L, Buratti E, Baralle F, Plagnol V, Acevedo-Arozena A, Fisher E, et al. Investigating dysfunctional RNA processing in TDP-43 mouse mutants Neuromuscular Disorders. 27: S32. DOI: 10.1016/S0960-8966(17)30314-0  0.527
2016 Crittenden JR, Tillberg PW, Riad MH, Shima Y, Gerfen CR, Curry J, Housman DE, Nelson SB, Boyden ES, Graybiel AM. Striosome-dendron bouquets highlight a unique striatonigral circuit targeting dopamine-containing neurons. Proceedings of the National Academy of Sciences of the United States of America. PMID 27647894 DOI: 10.1073/Pnas.1613337113  0.682
2014 Bugiardini E, Meola G, Alvarez C, Angeard N, Bassez G, Day JW, Dent G, Ekström AB, Eymard B, Fossati B, Gagnon C, Gomes-Pereira M, Gourdon G, Heatwole C, Housman DE, et al. Consensus on cerebral involvement in myotonic dystrophy. Workshop report: May 24-27, 2013, Ferrere (AT), Italy Neuromuscular Disorders. 24: 445-452. PMID 24613228 DOI: 10.1016/J.Nmd.2014.01.013  0.436
2013 Gipson TA, Neueder A, Wexler NS, Bates GP, Housman D. Aberrantly spliced HTT, a new player in Huntington's disease pathogenesis. Rna Biology. 10: 1647-52. PMID 24256709 DOI: 10.4161/rna.26706  0.33
2013 van Blitterswijk M, Wang ET, Friedman BA, Keagle PJ, Lowe P, Leclerc AL, van den Berg LH, Housman DE, Veldink JH, Landers JE. Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-Seq. Plos One. 8: e60788. PMID 23577159 DOI: 10.1371/Journal.Pone.0060788  0.521
2012 Wang ET, Cody NA, Jog S, Biancolella M, Wang TT, Treacy DJ, Luo S, Schroth GP, Housman DE, Reddy S, Lécuyer E, Burge CB. Transcriptome-wide regulation of pre-mRNA splicing and mRNA localization by muscleblind proteins. Cell. 150: 710-24. PMID 22901804 DOI: 10.1016/J.Cell.2012.06.041  0.651
2012 Janas MM, Wang E, Love T, Harris AS, Stevenson K, Semmelmann K, Shaffer JM, Chen PH, Doench JG, Yerramilli SV, Neuberg DS, Iliopoulos D, Housman DE, Burge CB, Novina CD. Reduced expression of ribosomal proteins relieves microRNA-mediated repression. Molecular Cell. 46: 171-86. PMID 22541556 DOI: 10.1016/J.Molcel.2012.04.008  0.624
2012 Parkesh R, Childs-Disney JL, Nakamori M, Kumar A, Wang E, Wang T, Hoskins J, Tran T, Housman D, Thornton CA, Disney MD. Design of a bioactive small molecule that targets the myotonic dystrophy type 1 RNA via an RNA motif-ligand database and chemical similarity searching. Journal of the American Chemical Society. 134: 4731-42. PMID 22300544 DOI: 10.1021/Ja210088V  0.54
2010 Crittenden JR, Dunn DE, Merali FI, Woodman B, Yim M, Borkowska AE, Frosch MP, Bates GP, Housman DE, Lo DC, Graybiel AM. CalDAG-GEFI down-regulation in the striatum as a neuroprotective change in Huntington's disease. Human Molecular Genetics. 19: 1756-65. PMID 20147317 DOI: 10.1093/Hmg/Ddq055  0.698
2009 Weiss A, Abramowski D, Bibel M, Bodner R, Chopra V, DiFiglia M, Fox J, Kegel K, Klein C, Grueninger S, Hersch S, Housman D, Régulier E, Rosas HD, Stefani M, et al. Single-step detection of mutant huntingtin in animal and human tissues: a bioassay for Huntington's disease. Analytical Biochemistry. 395: 8-15. PMID 19664996 DOI: 10.1016/J.Ab.2009.08.001  0.3
2009 Brocklebank D, Gayán J, Andresen JM, Roberts SA, Young AB, Snodgrass SR, Penney JB, Ramos-Arroyo MA, Cha JJ, Rosas HD, Hersch SM, Feigin A, Cherny SS, Wexler NS, Housman DE, et al. Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 425-9. PMID 18712713 DOI: 10.1002/Ajmg.B.30826  0.516
2008 Gayán J, Brocklebank D, Andresen JM, Alkorta-Aranburu G, Zameel Cader M, Roberts SA, Cherny SS, Wexler NS, Cardon LR, Housman DE. Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds. Genetic Epidemiology. 32: 445-53. PMID 18481795 DOI: 10.1002/Gepi.20317  0.544
2007 Bergmeier W, Goerge T, Wang HW, Crittenden JR, Baldwin AC, Cifuni SM, Housman DE, Graybiel AM, Wagner DD. Mice lacking the signaling molecule CalDAG-GEFI represent a model for leukocyte adhesion deficiency type III. The Journal of Clinical Investigation. 117: 1699-707. PMID 17492052 DOI: 10.1172/Jci30575  0.693
2007 Andresen JM, Gayán J, Djoussé L, Roberts S, Brocklebank D, Cherny SS, Cardon LR, Gusella JF, MacDonald ME, Myers RH, Housman DE, Wexler NS. The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset. Annals of Human Genetics. 71: 295-301. PMID 17181545 DOI: 10.1111/J.1469-1809.2006.00335.X  0.591
2007 Andresen JM, Gayán J, Cherny SS, Brocklebank D, Alkorta-Aranburu G, Addis EA, Cardon LR, Housman DE, Wexler NS. Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds. Journal of Medical Genetics. 44: 44-50. PMID 17018562 DOI: 10.1136/Jmg.2006.045153  0.509
2007 Goerge T, Bergmeier W, Wang H, Crittenden J, Baldwin A, Cifuni S, Housman D, Graybiel A, Wagner D. CALDAG-GEFI-DEFICIENCY CAUSES IMPAIRED BETA1, BETA2, AND BETA3 INTEGRIN ACTIVATION IN NEUTROPHILS AND PLATELETS: A MODEL FOR LEUKOCYTE ADHESION DEFICIENCY-III (LAD-III) Journal of Thrombosis and Haemostasis. 5: P-T-278-P-T-278. DOI: 10.1111/J.1538-7836.2007.Tb02036.X  0.673
2004 Crittenden JR, Bergmeier W, Zhang Y, Piffath CL, Liang Y, Wagner DD, Housman DE, Graybiel AM. CalDAG-GEFI integrates signaling for platelet aggregation and thrombus formation. Nature Medicine. 10: 982-6. PMID 15334074 DOI: 10.1038/Nm1098  0.686
2004 Wexler NS, Lorimer J, Porter J, Gomez F, Moskowitz C, Shackell E, Marder K, Penchaszadeh G, Roberts SA, Gayán J, Brocklebank D, Cherny SS, Cardon LR, Gray J, Dlouhy SR, ... ... Housman DE, et al. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. Proceedings of the National Academy of Sciences of the United States of America. 101: 3498-503. PMID 14993615 DOI: 10.1073/Pnas.0308679101  0.6
2004 Bergmeier W, Crittenden JR, Piffath CL, Wagner DD, Housman DE, Graybiel AM. CalDAG-GEFI Is a Key Signal Integrator in Platelet Activation and Thrombus Formation. Blood. 104: 326-326. DOI: 10.1182/Blood.V104.11.326.326  0.695
2004 Crittenden JR, Bergmeier W, Zhang Y, Piffath CL, Liang Y, Wagner DD, Housman DE, Graybiel AM. Erratum: CalDAG-GEFI integrates signaling for platelet aggregation and thrombus formation Nature Medicine. 10: 1139-1139. DOI: 10.1038/Nm1004-1139A  0.67
2003 Charest A, Lane K, McMahon K, Park J, Preisinger E, Conroy H, Housman D. Fusion of FIG to the receptor tyrosine kinase ROS in a glioblastoma with an interstitial del(6)(q21q21). Genes, Chromosomes & Cancer. 37: 58-71. PMID 12661006 DOI: 10.1002/Gcc.10207  0.305
2000 Chattopadhyay S, Kaul R, Charest A, Housman D, Chen J. SMAR1, a novel, alternatively spliced gene product, binds the Scaffold/Matrix-associated region at the T cell receptor beta locus. Genomics. 68: 93-6. PMID 10950932 DOI: 10.1006/geno.2000.6279  0.312
1999 Kazantsev A, Preisinger E, Dranovsky A, Goldgaber D, Housman D. Insoluble detergent-resistant aggregates form between pathological and nonpathological lengths of polyglutamine in mammalian cells. Proceedings of the National Academy of Sciences of the United States of America. 96: 11404-9. PMID 10500189 DOI: 10.1073/Pnas.96.20.11404  0.304
1999 Ashworth A, Lloyd S, Brown J, Gydesen S, Sorensen SA, Brun A, Englund E, Humphreys C, Housman D, Badura M, Stanton V, Taylor K, Cameron J, Munroe D, Johansson J, et al. Molecular genetic characterisation of frontotemporal dementia on chromosome 3. Dementia and Geriatric Cognitive Disorders. 10: 93-101. PMID 10436350 DOI: 10.1159/000051222  0.322
1998 Nichols KE, Harkin DP, Levitz S, Krainer M, Kolquist KA, Genovese C, Bernard A, Ferguson M, Zuo L, Snyder E, Buckler AJ, Wise C, Ashley J, Lovett M, Valentine MB, ... ... Housman DE, et al. Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome. Proceedings of the National Academy of Sciences of the United States of America. 95: 13765-70. PMID 9811875 DOI: 10.1073/Pnas.95.23.13765  0.475
1998 Heesen M, Berman MA, Charest A, Housman D, Gerard C, Dorf ME. Cloning and chromosomal mapping of an orphan chemokine receptor: mouse RDC1. Immunogenetics. 47: 364-70. PMID 9510554 DOI: 10.1007/S002510050371  0.303
1997 Beckers MC, Ernst E, Diez E, Morissette C, Gervais F, Hunter K, Housman D, Yoshida S, Skamene E, Gros P. High-resolution linkage map of mouse chromosome 13 in the vicinity of the host resistance locus Lgn1. Genomics. 39: 254-63. PMID 9119362 DOI: 10.1006/Geno.1996.4489  0.316
1996 Shearman AM, Hudson TJ, Andresen JM, Wu X, Sohn RL, Haluska F, Housman DE, Weiss JS. The gene for schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36. Human Molecular Genetics. 5: 1667-72. PMID 8894705  0.521
1996 Dackowski WR, Connors TD, Bowe AE, Stanton V, Housman D, Doggett NA, Landes GM, Klinger KW. The region surrounding the PKD1 gene: a 700-kb P1 contig from a YAC-deficient interval. Genome Research. 6: 515-24. PMID 8828040 DOI: 10.1101/Gr.6.6.515  0.319
1996 Borrow J, Stanton VP, Andresen JM, Becher R, Behm FG, Chaganti RS, Civin CI, Disteche C, Dubé I, Frischauf AM, Horsman D, Mitelman F, Volinia S, Watmore AE, Housman DE. 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. PMID 8782817 DOI: 10.1038/Ng0996-33  0.521
1995 Moffett P, Bruening W, Nakagama H, Bardeesy N, Housman D, Housman DE, Pelletier J. Antagonism of WT1 activity by protein self-association. Proceedings of the National Academy of Sciences of the United States of America. 92: 11105-9. PMID 7479946 DOI: 10.1073/Pnas.92.24.11105  0.32
1993 Hinds HL, Ashley CT, Sutcliffe JS, Nelson DL, Warren ST, Housman DE, Schalling M. Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. Nature Genetics. 3: 36-43. PMID 8490651 DOI: 10.1038/Ng0193-36  0.766
1993 Haas M, Aburatani H, Stanton VP, Bhatt M, Housman D, Ward DC. Isolation and FISH mapping of 80 cosmid clones on the short arm of human chromosome 3. Genomics. 16: 90-6. PMID 8486389 DOI: 10.1006/Geno.1993.1145  0.304
1993 Park S, Schalling M, Bernard A, Maheswaran S, Shipley GC, Roberts D, Fletcher J, Shipman R, Rheinwald J, Demetri G, Griffin J, Minden M, Housman DE, Haber DA. The Wilms tumour gene WT1 is expressed in murine mesoderm-derived tissues and mutated in a human mesothelioma Nature Genetics. 4: 415-420. PMID 8401592 DOI: 10.1038/ng0893-415  0.461
1993 Kreidberg JA, Sariola H, Loring JM, Maeda M, Pelletier J, Housman D, Jaenisch R. WT-1 is required for early kidney development. Cell. 74: 679-91. PMID 8395349 DOI: 10.1016/0092-8674(93)90515-R  0.307
1993 Skare J, Wu B, Madan S, Pulijaal V, Purtilo D, Haber D, Nelson D, Sylla B, Grierson H, Nitowsky H, Glaser J, Wissink J, White B, Holden J, Housman D, et al. Characterization of three overlapping deletions causing X-linked lymphoproliferative disease Genomics. 16: 254-255. PMID 8387453 DOI: 10.1006/Geno.1993.1169  0.508
1993 Moir DT, Dorman TE, Xue F, Ma NS, Stanton VP, Housman D, Bowden DW, Noll WW, Mao J. Rapid identification of overlapping YACs in the MEN2 region of human chromosome 10 by hybridization with Alu element-mediated PCR products. Gene. 136: 177-83. PMID 7904972 DOI: 10.1016/0378-1119(93)90461-B  0.314
1993 Church DM, Banks LT, Rogers AC, Graw SL, Housman DE, Gusella JF, Buckler AJ. Identification of human chromosome 9 specific genes using exon amplification. Human Molecular Genetics. 2: 1915-20. PMID 7506603 DOI: 10.1093/hmg/2.11.1915  0.408
1992 Oettinger MA, Stanger B, Schatz DG, Glaser T, Call K, Housman D, Baltimore D. The recombination activating genes, RAG 1 and RAG 2, are on chromosome 11p in humans and chromosome 2p in mice. Immunogenetics. 35: 97-101. PMID 1735560 DOI: 10.1007/Bf00189518  0.335
1992 Ambrose C, James M, Barnes G, Lin C, Bates G, Altherr M, Duyao M, Groot N, Church D, Wasmuth JJ, Lehrach H, Housman D, Buckler A, Gusella JF, MacDonald ME. A novel G protein-coupled receptor kinase gene cloned from 4p16.3 Human Molecular Genetics. 1: 697-703. PMID 1338872 DOI: 10.1093/Hmg/1.9.697  0.319
1992 Baird PN, Groves N, Haber DA, Housman DE, Cowell JK. Identification of mutations in the WT1 gene in tumours from patients with the WAGR syndrome. Oncogene. 7: 2141-9. PMID 1331933  0.468
1992 Haber DA, Housman DE. The genetics of Wilms' tumor. Advances in Cancer Research. 59: 41-68. PMID 1325734 DOI: 10.1016/S0065-230X(08)60302-4  0.423
1992 Haber DA, Housman DE. Role of the WT1 gene in Wilms' tumour. Cancer Surveys. 12: 105-17. PMID 1322241  0.466
1992 Haber DA, Timmers HT, Pelletier J, Sharp PA, Housman DE. A dominant mutation in the Wilms tumor gene WT1 cooperates with the viral oncogene E1A in transformation of primary kidney cells. Proceedings of the National Academy of Sciences of the United States of America. 89: 6010-4. PMID 1321431 DOI: 10.1073/Pnas.89.13.6010  0.469
1992 Bruening W, Bardeesy N, Silverman BL, Cohn RA, Machin GA, Aronson AJ, Housman D, Pelletier J. Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development. Nature Genetics. 1: 144-8. PMID 1302008 DOI: 10.1038/Ng0592-144  0.31
1991 Hunter K, Housman D, Hopkins N. Isolation and characterization of irradiation fusion hybrids from mouse chromosome 1 for mapping Rmc-1, a gene encoding a cellular receptor for MCF class murine retroviruses. Somatic Cell and Molecular Genetics. 17: 169-83. PMID 2011795 DOI: 10.1007/Bf01232974  0.311
1991 Cowell JK, Wadey RB, Haber DA, Call KM, Housman DE, Pritchard J. Structural rearrangements of the WT1 gene in Wilms' tumour cells. Oncogene. 6: 595-9. PMID 1851548  0.462
1991 Buckler AJ, Chang DD, Graw SL, Brook JD, Haber DA, Sharp PA, Housman DE. Exon amplification: a strategy to isolate mammalian genes based on RNA splicing. Proceedings of the National Academy of Sciences of the United States of America. 88: 4005-9. PMID 1850845 DOI: 10.1073/Pnas.88.9.4005  0.468
1991 Haber DA, Housman DE. Rate-limiting steps: the genetics of pediatric cancers. Cell. 64: 5-8. PMID 1846091 DOI: 10.1016/0092-8674(91)90200-I  0.374
1991 Doucette-Stamm LA, Riba L, Handelin B, Difilippantonio M, Ward DC, Wasmuth JJ, Gusella JF, Housman DE. Generation and characterization of irradiation hybrids of human chromosome 4. Somatic Cell and Molecular Genetics. 17: 471-80. PMID 1837181 DOI: 10.1007/Bf01233171  0.426
1991 Huff V, Miwa H, Haber DA, Call KM, Housman D, Strong LC, Saunders GF. Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT. American Journal of Human Genetics. 48: 997-1003. PMID 1673293  0.478
1991 Buckler AJ, Pelletier J, Haber DA, Glaser T, Housman DE. Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development. Molecular and Cellular Biology. 11: 1707-12. PMID 1671709 DOI: 10.1128/Mcb.11.3.1707  0.467
1991 Thompson LM, Plummer S, Schalling M, Altherr MR, Gusella JF, Housman DE, Wasmuth JJ. A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4. Genomics. 11: 1133-42. PMID 1664411 DOI: 10.1016/0888-7543(91)90041-C  0.452
1991 Haber DA, Sohn RL, Buckler AJ, Pelletier J, Call KM, Housman DE. Alternative splicing and genomic structure of the Wilms tumor gene WT1. Proceedings of the National Academy of Sciences of the United States of America. 88: 9618-22. PMID 1658787 DOI: 10.1073/Pnas.88.21.9618  0.48
1991 Schwartz CE, Haber DA, Stanton VP, Strong LC, Skolnick MH, Housman DE. Familial predisposition to Wilms tumor does not segregate with the WT1 gene. Genomics. 10: 927-30. PMID 1655633 DOI: 10.1016/0888-7543(91)90181-D  0.45
1991 Pelletier J, Bruening W, Kashtan CE, Mauer SM, Manivel JC, Striegel JE, Houghton DC, Junien C, Habib R, Fouser L, Fine RN, Silverman BL, Haber DA, Housman D. Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Cell. 67: 437-447. PMID 1655284 DOI: 10.1016/0092-8674(91)90194-4  0.499
1991 Pelletier J, Bruening W, Li FP, Haber DA, Glaser T, Housman DE. WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour. Nature. 353: 431-4. PMID 1654525 DOI: 10.1038/353431A0  0.473
1991 Pelletier J, Schalling M, Buckler AJ, Rogers A, Haber DA, Housman D. Expression of the Wilms' tumor gene WT1 in the murine urogenital system. Genes & Development. 5: 1345-56. PMID 1651275 DOI: 10.1101/Gad.5.8.1345  0.523
1991 Royer-Pokora B, Ragg S, Heckl-Ostreicher B, Held M, Loos U, Call K, Glaser T, Housman D, Saunders G, Zabel B. Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare. Genes, Chromosomes & Cancer. 3: 89-100. PMID 1648959 DOI: 10.1002/Gcc.2870030203  0.308
1990 Warburton D, Gersen S, Yu MT, Jackson C, Handelin B, Housman D. Monochromosomal rodent-human hybrids from microcell fusion of human lymphoblastoid cells containing an inserted dominant selectable marker. Genomics. 6: 358-66. PMID 2307476 DOI: 10.1016/0888-7543(90)90577-H  0.314
1990 Lichter P, Tang CJ, Call K, Hermanson G, Evans GA, Housman D, Ward DC. High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. Science (New York, N.Y.). 247: 64-9. PMID 2294592 DOI: 10.1126/Science.2294592  0.306
1990 Glaser T, Lane J, Housman D. A mouse model of the aniridia-Wilms tumor deletion syndrome. Science (New York, N.Y.). 250: 823-7. PMID 2173141 DOI: 10.1126/Science.2173141  0.333
1990 Pritchard-Jones K, Fleming S, Davidson D, Bickmore W, Porteous D, Gosden C, Bard J, Buckler A, Pelletier J, Housman D. The candidate Wilms' tumour gene is involved in genitourinary development. Nature. 346: 194-7. PMID 2164159 DOI: 10.1038/346194A0  0.342
1990 Haber DA, Buckler AJ, Glaser T, Call KM, Pelletier J, Sohn RL, Douglass EC, Housman DE. An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor. Cell. 61: 1257-69. PMID 2163761 DOI: 10.1016/0092-8674(90)90690-G  0.482
1990 Glaser T, Rose E, Morse H, Housman D, Jones C. A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex. Genomics. 6: 48-64. PMID 2154397 DOI: 10.1016/0888-7543(90)90447-3  0.348
1990 Arceci RJ, Baas F, Raponi R, Horwitz SB, Housman D, Croop JM. Multidrug resistance gene expression is controlled by steroid hormones in the secretory epithelium of the uterus. Molecular Reproduction and Development. 25: 101-9. PMID 1968749 DOI: 10.1002/mrd.1080250202  0.302
1989 Glaser T, Housman D, Lewis WH, Gerhard D, Jones C. A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids. Somatic Cell and Molecular Genetics. 15: 477-501. PMID 2595451 DOI: 10.1007/Bf01534910  0.342
1989 Glaser T, Driscoll DJ, Antonarakis S, Valle D, Housman D. A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome. Genomics. 5: 880-93. PMID 2574149 DOI: 10.1016/0888-7543(89)90130-4  0.344
1989 Emanuel JR, Graw S, Housman D, Levenson R. Identification of a region within the Na,K-ATPase alpha subunit that contributes to differential ouabain sensitivity. Molecular and Cellular Biology. 9: 3744-9. PMID 2550800 DOI: 10.1128/Mcb.9.9.3744  0.445
1989 Haber DA, Housman DE. MspI/HpaII polymorphism in the human multidrug resistance gene 1. Nucleic Acids Research. 17: 10142. PMID 2481261 DOI: 10.1093/Nar/17.23.10142  0.418
1989 Croop JM, Raymond M, Haber D, Devault A, Arceci RJ, Gros P, Housman DE. The three mouse multidrug resistance (mdr) genes are expressed in a tissue-specific manner in normal mouse tissues. Molecular and Cellular Biology. 9: 1346-50. PMID 2471060 DOI: 10.1128/Mcb.9.3.1346  0.46
1988 Geissler EN, Cheng SV, Gusella JF, Housman DE. Genetic analysis of the dominant white-spotting (W) region on mouse chromosome 5: identification of cloned DNA markers near W. Proceedings of the National Academy of Sciences of the United States of America. 85: 9635-9. PMID 3200849  0.381
1987 Kent RB, Emanuel JR, Ben Neriah Y, Levenson R, Housman DE. Ouabain resistance conferred by expression of the cDNA for a murine Na+, K+-ATPase alpha subunit. Science (New York, N.Y.). 237: 901-3. PMID 3039660 DOI: 10.1126/Science.3039660  0.537
1987 Weis JH, Seidman JG, Housman DE, Nelson DL. Eucaryotic chromosome transfer: production of a murine-specific cosmid library from a neor-linked fragment of murine chromosome 17. Molecular and Cellular Biology. 6: 441-51. PMID 3023847 DOI: 10.1128/MCB.6.2.441  0.334
1987 Kent RB, Fallows DA, Geissler E, Glaser T, Emanuel JR, Lalley PA, Levenson R, Housman DE. Genes encoding alpha and beta subunits of Na,K-ATPase are located on three different chromosomes in the mouse. Proceedings of the National Academy of Sciences of the United States of America. 84: 5369-73. PMID 2885848 DOI: 10.1073/Pnas.84.15.5369  0.495
1987 Fallows D, Kent RB, Nelson DL, Emanuel JR, Levenson R, Housman DE. Chromosome-mediated transfer of the murine Na,K-ATPase alpha subunit confers ouabain resistance. Molecular and Cellular Biology. 7: 2985-7. PMID 2823111 DOI: 10.1128/Mcb.7.8.2985  0.47
1985 Wexler NS, Conneally PM, Housman D, Gusella JF. A DNA Polymorphism for Huntington's Disease Marks the Future Archives of Neurology. 42: 20-24. PMID 3155610 DOI: 10.1001/Archneur.1985.04060010026009  0.455
1984 Weis JH, Nelson DL, Przyborski MJ, Chaplin DD, Mulligan RC, Housman DE, Seidman JG. Eukaryotic chromosome transfer: linkage of the murine major histocompatibility complex to an inserted dominant selectable marker. Proceedings of the National Academy of Sciences of the United States of America. 81: 4879-83. PMID 6589632 DOI: 10.1073/Pnas.81.15.4879  0.35
1984 Levenson R, Racaniello V, Albritton L, Housman D. Molecular cloning of the mouse ouabain-resistance gene. Proceedings of the National Academy of Sciences of the United States of America. 81: 1489-93. PMID 6324196 DOI: 10.1073/Pnas.81.5.1489  0.532
1984 Minden M, Gusella J, Housman D. Chromosome-mediated transfer of the malignant phenotype by human acute myelogenous leukemic cells Blood. 64: 842-846. DOI: 10.1182/Blood.V64.4.842.Bloodjournal644842  0.455
1982 Gusella JF, Jones C, Kao FT, Housman D, Puck TT. Genetic fine-structure mapping in human chromosome 11 by use of repetitive DNA sequences. Proceedings of the National Academy of Sciences of the United States of America. 79: 7804-8. PMID 6961451 DOI: 10.1073/Pnas.79.24.7804  0.488
1982 Gusella JF, Tsiftsoglou AS, Volloch V, Weil SC, Neumann J, Housman DE. Dissociation of hemoglobin accumulation and commitment during murine erythroleukemia cell differentiation by treatment with imidazole. Journal of Cellular Physiology. 113: 179-85. PMID 6957412 DOI: 10.1002/JCP.1041130127  0.381
1982 Housman D, Kidd K, Gusella JF. Recombinant DNA approach to neurogenetic disorders Trends in Neurosciences. 5: 320-323. DOI: 10.1016/0166-2236(82)90192-8  0.477
1981 Levenson R, Housman D. Commitment: how do cells make the decision to differentiate? Cell. 25: 5-6. PMID 7023699 DOI: 10.1016/0092-8674(81)90225-7  0.496
1981 Levenson R, Housman D. Erasure of the memory response in MEL cells. Developmental Biology. 86: 81-6. PMID 6974666 DOI: 10.1016/0012-1606(81)90317-1  0.506
1981 Housman D, Levenson R, Volloch V, Tsiftsoglou A, Gusella J, Parker D, Kernen J, Mitrani A, Weeks V, Witte O, Besmer P. Control of proliferation and differentiation in cells transformed by Friend virus. Cold Spring Harbor Symposia On Quantitative Biology. 1177-85. PMID 6933050 DOI: 10.1101/Sqb.1980.044.01.127  0.583
1981 Bridges K, Levenson R, Housman D, Cantley L. Calcium regulates the commitment of murine erythroleukemia cells to terminal erythroid differentiation. The Journal of Cell Biology. 90: 542-4. PMID 6793600 DOI: 10.1083/Jcb.90.2.542  0.514
1981 Bruns GAP, Gusella JF, Keys C, Housman D, Gerald PS. 704 ISOLATION OF DNA SEGMENTS FROM THE HUMAN X CHROMOSOME Pediatric Research. 15: 559-559. DOI: 10.1203/00006450-198104001-00727  0.455
1980 Gusella JF, Keys C, VarsanyiBreiner A, Kao FT, Jones C, Puck TT, Housman D. Isolation and localization of DNA segments from specific human chromosomes. Proceedings of the National Academy of Sciences of the United States of America. 77: 2829-33. PMID 6930670 DOI: 10.1073/Pnas.77.5.2829  0.485
1980 Levenson R, Kernen J, Mitrani A, Housman D. DNA synthesis is not required for the commitment of murine erythroleukemia cells. Developmental Biology. 74: 224-30. PMID 6444216 DOI: 10.1016/0012-1606(80)90064-0  0.52
1980 Levenson R, Kernen J, Housman D. Synchronization of MEL cell commitment with cordycepin. Cell. 18: 1073-8. PMID 316363 DOI: 10.1016/0092-8674(79)90220-4  0.526
1980 Gusella J, Weil S, Tsiftsoglou A, Volloch V, Neumann J, Keys C, Housman D. Hemin does not cause commitment of murine erythroleukemia (MEL) cells to terminal differentiation Blood. 56: 481-487. DOI: 10.1182/Blood.V56.3.481.481  0.455
1980 Gusella J, Weil S, Tsiftsoglou A, Volloch V, Neumann J, Keys C, Housman D. Hemin does not cause commitment of murine erythroleukemia (MEL) cells to terminal differentiation Blood. 56: 481-487. DOI: 10.1182/BLOOD.V56.3.481.481  0.381
1979 Gusella J, Varsanyi-Breiner A, Kao FT, Jones C, Puck TT, Keys C, Orkin S, Housman D. Precise localization of human beta-globin gene complex on chromosome 11. Proceedings of the National Academy of Sciences of the United States of America. 76: 5239-42. PMID 291941 DOI: 10.1073/Pnas.76.10.5239  0.511
1979 Varsanyi-Breiner A, Gusella JF, Keys C, Housman DE, Sullivan D, Brisson N, Verma DP. The organization of a nuclear DNA sequence from a higher plant: molecular cloning and characterization of soybean ribosomal DNA. Gene. 7: 317-34. PMID 160361 DOI: 10.1016/0378-1119(79)90051-9  0.381
1978 Geller R, Levenson R, Housman D. Significance of the cell cycle in commitment of murine erythroleukemia cells to erythroid differentiation. Journal of Cellular Physiology. 95: 213-22. PMID 274446 DOI: 10.1002/Jcp.1040950211  0.512
1976 Gusella J, Geller R, Clarke B, Weeks V, Housman D. Commitment to erythroid differentiation by friend erythroleukemia cells: a stochastic analysis Cell. 9: 221-229. PMID 975244 DOI: 10.1016/0092-8674(76)90113-6  0.455
1976 Gusella JF, Housman D. Induction of erythroid differentiation in vitro by purines and purine analogues. Cell. 8: 263-9. PMID 971485 DOI: 10.1016/0092-8674(76)90010-6  0.455
1973 Jacobson A, Housman D, Prensky W. Oligonucleotide fingerprinting of Hela cell 5 S RNA labeled in vitro with (125)I. Molecular Biology Reports. 1: 209-213. PMID 24197568 DOI: 10.1007/Bf00357643  0.537
1972 Nathan DG, Lodish HF, Kan YW, Housman D. Beta thalassemia and translation of globin messenger RNA. Proceedings of the National Academy of Sciences of the United States of America. 68: 2514-8. PMID 5289885 DOI: 10.1073/Pnas.68.10.2514  0.448
1972 Pemberton RE, Housman D, Lodish HF, Baglioni C. Isolation of duck haemoglobin messenger RNA and its translation by rabbit reticulocyte cell free system. Nature: New Biology. 235: 99-102. PMID 4501199 DOI: 10.1038/Newbio235099A0  0.441
1971 Lodish HF, Housman D, Jacobsen M. Initiation of hemoglobin synthesis. Specific inhibition by antibiotics and bacteriophage ribonucleic acid. Biochemistry. 10: 2348-2356. PMID 5114993 DOI: 10.1021/Bi00788A027  0.421
1970 Housman D, Jacobs-lorena M, Rajbhandary UL, Lodish HF. Initiation of haemoglobin synthesis by methionyl-tRNA Nature. 227: 913-918. PMID 4915406 DOI: 10.1038/227913A0  0.438
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