Weissman SM - Search Results

1

Molecular studies of mutations that increase Hb F production in man.

Forget BG, Tuan D, Newman MV, Feingold EA, Collins F, Fukumaki Y, Jagadeeswaran P, Weissman SM. Forget BG, et al. Among authors: weissman sm. Prog Clin Biol Res. 1983;134:65-76. Prog Clin Biol Res. 1983. PMID: 6198666 No abstract available.

2

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: weissman sm. Prog Clin Biol Res. 1985;191:107-24. Prog Clin Biol Res. 1985. PMID: 2413468 No abstract available.

3

Support for the causal relationship between gamma globin gene promoter mutations and nondeletion forms of hereditary persistence of fetal hemoglobin.

Metherall JE, Stoeckert CJ Jr, Gillespie FP, Weissman SM, Forget BG. Metherall JE, et al. Among authors: weissman sm. Prog Clin Biol Res. 1987;251:347-61. Prog Clin Biol Res. 1987. PMID: 2448805 No abstract available.

4

Interspersed repetitive DNA sequences of the human genome: are they transposons?

Jagadeeswaran P, Biro PA, Tuan D, Pan J, Forget BG, Weissman SM. Jagadeeswaran P, et al. Among authors: weissman sm. Prog Clin Biol Res. 1982;103 Pt A:29-35. Prog Clin Biol Res. 1982. PMID: 6298805 No abstract available.

5

The molecular genetics of human hemoglobin.

Collins FS, Weissman SM. Collins FS, et al. Among authors: weissman sm. 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.

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: weissman sm. 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

A gene deletion ending at the midpoint of a repetitive DNA sequence in one form of hereditary persistence of fetal haemoglobin.

Jagadeeswaran P, Tuan D, Forget BG, Weissman SM. Jagadeeswaran P, et al. Among authors: weissman sm. Nature. 1982 Apr 1;296(5856):469-70. doi: 10.1038/296469a0. Nature. 1982. PMID: 6174873 No abstract available.

8

Structural features of the DNA flanking the human non-alpha globin genes: implications in the control of fetal hemoglobin switching.

Forget BG, Tuan D, Biro PA, Jagadeeswaran PO, Weissman SM. Forget BG, et al. Among authors: weissman sm. Trans Assoc Am Physicians. 1981;94:204-10. Trans Assoc Am Physicians. 1981. PMID: 6178203 No abstract available.

9

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.

Tuan D, Feingold E, Newman M, Weissman SM, Forget BG. Tuan D, et al. Among authors: weissman sm. Proc Natl Acad Sci U S A. 1983 Nov;80(22):6937-41. doi: 10.1073/pnas.80.22.6937. Proc Natl Acad Sci U S A. 1983. PMID: 6196781 Free PMC article.

10

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. Among authors: weissman sm. Nature. 1985 Jan 24-30;313(6000):325-6. doi: 10.1038/313325a0. Nature. 1985. PMID: 2578620

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