Wilms' tumor-aniridia association: Segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin gene
dc.contributor.author | Kimmel, Kathryn A. | en_US |
dc.contributor.author | Sparkes, Robert S. | en_US |
dc.contributor.author | Miller, York E. | en_US |
dc.contributor.author | Fisher, James H. | en_US |
dc.contributor.author | Bateman, J. Brownwyn | en_US |
dc.contributor.author | Carey, Thomas E. | en_US |
dc.contributor.author | Rodell, Timothy | en_US |
dc.contributor.author | Shoemaker, Steven A. | en_US |
dc.contributor.author | Scoggin, Charles H. | en_US |
dc.date.accessioned | 2006-09-11T16:10:23Z | |
dc.date.available | 2006-09-11T16:10:23Z | |
dc.date.issued | 1984-09 | en_US |
dc.identifier.citation | Fisher, James H.; Miller, York E.; Sparkes, Robert S.; Bateman, J. Brownwyn; Kimmel, Kathryn A.; Carey, Thomas E.; Rodell, Timothy; Shoemaker, Steven A.; Scoggin, Charles H.; (1984). "Wilms' tumor-aniridia association: Segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin gene." Somatic Cell and Molecular Genetics 10(5): 455-464. <http://hdl.handle.net/2027.42/45533> | en_US |
dc.identifier.issn | 0740-7750 | en_US |
dc.identifier.issn | 1572-9931 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/45533 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6089356&dopt=citation | en_US |
dc.description.abstract | Fusion of an auxotrophic mutant hamster cell with the skin fibroblasts of a child with the Wilms' tumor-aniridia association produced clones which, on the one hand, contained the child's normal chromosome 11 and, on the other, the chromosome 11 with the 11p13 deletion associated with the syndrome. Both hybrids were positive for human LDH-A by enzymatic assay. Clones containing the normal human chromosome 11 were killed by a cytotoxic monoclonal antibody to a cell surface antigen previously mapped to the 11p13→ 11pter region of chromosome 11. Clones with the abnormal 11 were not killed. Thus, we have produced hybrids from the same patient distinct from each other on the basis of their chromosome 11. These hybrids have been used to map the locus for a cell surface antigen to the deleted region on chromosome 11 of a patient with the Wilms tumor-aniridia association. The linkage between this antigen and the syndrome should be helpful in further study of the genetics of this disease. In addition, we have found that the c-Ha-ras-1 oncogene is distal to the p13 region of chromosome 11 and the position of insulin and beta-globin on the chromosome. Finally, by producing segregants of the hybrids containing the abnormal chromosome 11, we have provided evidence that chromosome 11-associated c-Ha-ras-1 is syntenic with chromosome 11 and not moved to a different portion of the genome . | en_US |
dc.format.extent | 1537235 bytes | |
dc.format.extent | 3115 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Kluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Media | en_US |
dc.subject.other | Biochemistry, General | en_US |
dc.subject.other | Biomedicine | en_US |
dc.subject.other | Human Genetics | en_US |
dc.subject.other | Plant Sciences | en_US |
dc.subject.other | Animal Anatomy / Morphology / Histology | en_US |
dc.title | Wilms' tumor-aniridia association: Segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin gene | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Natural Resources and Environment | en_US |
dc.subject.hlbsecondlevel | Molecular, Cellular and Developmental Biology | en_US |
dc.subject.hlbsecondlevel | Ecology and Evolutionary Biology | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | The Cancer Research Laboratory in the Department of Otorhinolaryngology and Department of Microbiology and Immunology, University of Michigan, 48109, Ann Arbor, Michigan | en_US |
dc.contributor.affiliationum | The Cancer Research Laboratory in the Department of Otorhinolaryngology and Department of Microbiology and Immunology, University of Michigan, 48109, Ann Arbor, Michigan | en_US |
dc.contributor.affiliationother | Eleanor Roosevelt Institute for Cancer Research (contribution number 427), Webb-Waring Lung Institute and Division of Pulmonary Sciences, Section on Human Genetics, Department of Medicine, University of Colorado Health, 80262, Denver, Colorado | en_US |
dc.contributor.affiliationother | Eleanor Roosevelt Institute for Cancer Research (contribution number 427), Webb-Waring Lung Institute and Division of Pulmonary Sciences, Section on Human Genetics, Department of Medicine, University of Colorado Health, 80262, Denver, Colorado | en_US |
dc.contributor.affiliationother | Eleanor Roosevelt Institute for Cancer Research (contribution number 427), Webb-Waring Lung Institute and Division of Pulmonary Sciences, Section on Human Genetics, Department of Medicine, University of Colorado Health, 80262, Denver, Colorado | en_US |
dc.contributor.affiliationother | Eleanor Roosevelt Institute for Cancer Research (contribution number 427), Webb-Waring Lung Institute and Division of Pulmonary Sciences, Section on Human Genetics, Department of Medicine, University of Colorado Health, 80262, Denver, Colorado | en_US |
dc.contributor.affiliationother | Division of Medical Genetics, Departments of Medicine, Pediatrics, and Psychiatry, UCLA Center for the Health Sciences, 90024, Los Angeles, California | en_US |
dc.contributor.affiliationother | Division of Medical Genetics, Departments of Medicine, Pediatrics, and Psychiatry, UCLA Center for the Health Sciences, 90024, Los Angeles, California | en_US |
dc.contributor.affiliationother | Eleanor Roosevelt Institute for Cancer Research (contribution number 427), Webb-Waring Lung Institute and Division of Pulmonary Sciences, Section on Human Genetics, Department of Medicine, University of Colorado Health, 80262, Denver, Colorado | en_US |
dc.contributor.affiliationumcampus | Ann Arbor | en_US |
dc.identifier.pmid | 6089356 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/45533/1/11188_2005_Article_BF01534850.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1007/BF01534850 | en_US |
dc.identifier.source | Somatic Cell and Molecular Genetics | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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