Collins FS - Search Results

1

A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobin.

Collins FS, Metherall JE, Yamakawa M, Pan J, Weissman SM, Forget BG. Collins FS, et al. Nature. 1985 Jan 24-30;313(6000):325-6. doi: 10.1038/313325a0. Nature. 1985. PMID: 2578620

2

G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene.

Collins FS, Stoeckert CJ Jr, Serjeant GR, Forget BG, Weissman SM. Collins FS, et al. Proc Natl Acad Sci U S A. 1984 Aug;81(15):4894-8. doi: 10.1073/pnas.81.15.4894. Proc Natl Acad Sci U S A. 1984. PMID: 6205403 Free PMC article.

3

Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population.

Collins FS, Boehm CD, Waber PG, Stoeckert CJ Jr, Weissman SM, Forget BG, Kazazian HH Jr. Collins FS, et al. Blood. 1984 Dec;64(6):1292-6. Blood. 1984. PMID: 6208955 Free article.

4

Human fetal globin DNA sequences suggest novel conversion event.

Stoeckert CJ Jr, Collins FS, Weissman SM. Stoeckert CJ Jr, et al. Among authors: collins fs. Nucleic Acids Res. 1984 Jun 11;12(11):4469-79. doi: 10.1093/nar/12.11.4469. Nucleic Acids Res. 1984. PMID: 6330670 Free PMC article.

5

Expression of human globin genes in transgenic mice carrying the beta-globin gene cluster with a mutation causing G gamma beta + hereditary persistence of fetal hemoglobin.

Tanaka M, Nolan JA, Bhargava AK, Rood K, Collins FS, Weissman SM, Forget BG, Chamberlain JW. Tanaka M, et al. Among authors: collins fs. Ann N Y Acad Sci. 1990;612:167-78. doi: 10.1111/j.1749-6632.1990.tb24303.x. Ann N Y Acad Sci. 1990. PMID: 2291546 Free article.

6

Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemia.

Feingold EA, Collins FS, Metherall JE, Stoeckert CJ Jr, Weissman SM, Forget BG. Feingold EA, et al. Among authors: collins fs. Ann N Y Acad Sci. 1985;445:159-69. doi: 10.1111/j.1749-6632.1985.tb17185.x. Ann N Y Acad Sci. 1985. PMID: 2409868 No abstract available.

7

Analysis of mutations associated with deletion and nondeletion hereditary persistence of fetal hemoglobin.

Feingold EA, Collins FS, Metherall JE, Stoeckert CJ Jr, Weissman SM, Forget BG. Feingold EA, et al. Among authors: collins fs. Prog Clin Biol Res. 1985;191:107-24. Prog Clin Biol Res. 1985. PMID: 2413468 No abstract available.

8

Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks.

Waber PG, Bender MA, Gelinas RE, Kattamis C, Karaklis A, Sofroniadou K, Stamatoyannopoulos G, Collins FS, Forget BG, Kazazian HH Jr. Waber PG, et al. Among authors: collins fs. Blood. 1986 Feb;67(2):551-4. Blood. 1986. PMID: 2417646 Free article.

9

Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intron.

Metherall JE, Collins FS, Pan J, Weissman SM, Forget BG. Metherall JE, et al. Among authors: collins fs. EMBO J. 1986 Oct;5(10):2551-7. doi: 10.1002/j.1460-2075.1986.tb04534.x. EMBO J. 1986. PMID: 3780671 Free PMC article.

10

The molecular genetics of human hemoglobin.

Collins FS, Weissman SM. Collins FS, et al. Prog Nucleic Acid Res Mol Biol. 1984;31:315-462. doi: 10.1016/s0079-6603(08)60382-7. Prog Nucleic Acid Res Mol Biol. 1984. PMID: 6397774 Review. No abstract available.

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