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Tuan, D., Feingold, E., Newman, M., Weissman, S. M., Forget, B. G. (1983) Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man. Proceedings of the National Academy of Sciences, 80 (22) 6937-6941 doi:10.1073/pnas.80.22.6937

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Reference TypeJournal (article/letter/editorial)
TitleDifferent 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man.
JournalProceedings of the National Academy of Sciences
AuthorsTuan, D.Author
Feingold, E.Author
Newman, M.Author
Weissman, S. M.Author
Forget, B. G.Author
Year1983 (November 1)Volume80
Issue22
PublisherProceedings of the National Academy of Sciences
DOIdoi:10.1073/pnas.80.22.6937Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID1431531Long-form Identifiermindat:1:5:1431531:0
GUID0
Full ReferenceTuan, D., Feingold, E., Newman, M., Weissman, S. M., Forget, B. G. (1983) Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man. Proceedings of the National Academy of Sciences, 80 (22) 6937-6941 doi:10.1073/pnas.80.22.6937
Plain TextTuan, D., Feingold, E., Newman, M., Weissman, S. M., Forget, B. G. (1983) Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man. Proceedings of the National Academy of Sciences, 80 (22) 6937-6941 doi:10.1073/pnas.80.22.6937
In(1983, November) Proceedings of the National Academy of Sciences Vol. 80 (22) Proceedings of the National Academy of Sciences

See Also

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Collins, F. S., Stoeckert, C. J., Serjeant, G. R., Forget, B. G., Weissman, S. M. (1984) G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene. Proceedings of the National Academy of Sciences, 81 (15) 4894-4898 doi:10.1073/pnas.81.15.4894
FEINGOLD, ELISE A., COLLINS, FRANCIS S., METHERALL, JAMES E., STOECKERT, CHRISTIAN J., WEISSMAN, SHERMAN M., FORGET, BERNARD G. (1985) Molecular Analysis of Deletion and Nondeletion Hereditary Persistence of Fetal Hemoglobin and Identification of a New Mutation Causing ?-Thalassemia. Annals of the New York Academy of Sciences, 445 (1) 159-169 doi:10.1111/j.1749-6632.1985.tb17185.x
Charache, S., Dover, G., Smith, K., Talbot, C. C., Moyer, M., Boyer, S. (1983) Treatment of sickle cell anemia with 5-azacytidine results in increased fetal hemoglobin production and is associated with nonrandom hypomethylation of DNA around the gamma-delta-beta-globin gene complex. Proceedings of the National Academy of Sciences, 80 (15) 4842-4846 doi:10.1073/pnas.80.15.4842
Ottolenghi, S., Giglioni, B., Taramelli, R., Comi, P., Mazza, U., Saglio, G., Camaschella, C., Izzo, P., Cao, A., Galanello, R., Gimferrer, E., Baiget, M., Gianni, A. M. (1982) Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?. Proceedings of the National Academy of Sciences, 79 (7) 2347-2351 doi:10.1073/pnas.79.7.2347
Groudine, M., Kohwi-Shigematsu, T., Gelinas, R., Stamatoyannopoulos, G., Papayannopoulou, T. (1983) Human fetal to adult hemoglobin switching: changes in chromatin structure of the beta-globin gene locus. Proceedings of the National Academy of Sciences, 80 (24) 7551-7555 doi:10.1073/pnas.80.24.7551
Driscoll, M. C., Dobkin, C. S., Alter, B. P. (1989) Gamma delta beta-thalassemia due to a de novo mutation deleting the 5' beta-globin gene activation-region hypersensitive sites. Proceedings of the National Academy of Sciences, 86 (19) 7470-7474 doi:10.1073/pnas.86.19.7470
TANAKA, MINORU, NOLAN, JUDITH A., BHARGAVA, AJAY K., ROOD, KIRSTEN, COLLINS, FRANCIS S., WEISSMAN, SHERMAN M., FORGET, BERNARD G., CHAMBERLAIN, JOHN W. (1990) Expression of Human Globin Genes in Transgenic Mice Carrying the ?-Globin Gene Cluster with a Mutation CausingG??+Hereditary Persistence of Fetal Hemoglobin. Annals of the New York Academy of Sciences, 612 (1) 167-178 doi:10.1111/j.1749-6632.1990.tb24303.x
Kafatos, F. C., Efstratiadis, A., Forget, B. G., Weissman, S. M. (1977) Molecular evolution of human and rabbit beta-globin mRNAs. Proceedings of the National Academy of Sciences, 74 (12) 5618-5622 doi:10.1073/pnas.74.12.5618
Ottolenghi, S., Lanyon, W. G., Williamson, R., Weatherall, D. J., Clegg, J. B., Pitcher, C. S. (1975) Human globin gene analysis for a patient with beta-o/delta beta-thalassemia. Proceedings of the National Academy of Sciences, 72 (6) 2294-2299 doi:10.1073/pnas.72.6.2294
Perkins, A. C., Gaensler, K. M., Orkin, S. H. (1996) Silencing of human fetal globin expression is impaired in the absence of the adult beta-globin gene activator protein EKLF. Proceedings of the National Academy of Sciences, 93 (22) 12267-12271 doi:10.1073/pnas.93.22.12267
Forget, B. G., Marotta, C. A., Weissman, S. M., Cohen-Solal, M. (1975) Nucleotide sequences of the 3'-terminal untranslated region of messenger RNA for human beta globin chain. Proceedings of the National Academy of Sciences, 72 (9) 3614-3618 doi:10.1073/pnas.72.9.3614
 
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