Forget BG - Search Results

1

Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.

Sahr KE, Tobe T, Scarpa A, Laughinghouse K, Marchesi SL, Agre P, Linnenbach AJ, Marchesi VT, Forget BG. Sahr KE, et al. Among authors: forget bg. J Clin Invest. 1989 Oct;84(4):1243-52. doi: 10.1172/JCI114291. J Clin Invest. 1989. PMID: 2794061 Free PMC article.

2

Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide.

Floyd PB, Gallagher PG, Valentino LA, Davis M, Marchesi SL, Forget BG. Floyd PB, et al. Among authors: forget bg. Blood. 1991 Sep 1;78(5):1364-72. Blood. 1991. PMID: 1878597 Free article.

3

Molecular cloning of the cDNA for human erythrocyte beta-spectrin.

Winkelmann JC, Leto TL, Watkins PC, Eddy R, Shows TB, Linnenbach AJ, Sahr KE, Kathuria N, Marchesi VT, Forget BG. Winkelmann JC, et al. Among authors: forget bg. Blood. 1988 Jul;72(1):328-34. Blood. 1988. PMID: 3390609 Free article.

4

Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.

Gallagher PG, Weed SA, Tse WT, Benoit L, Morrow JS, Marchesi SL, Mohandas N, Forget BG. Gallagher PG, et al. Among authors: forget bg. J Clin Invest. 1995 Mar;95(3):1174-82. doi: 10.1172/JCI117766. J Clin Invest. 1995. PMID: 7883966 Free PMC article.

5

The exon-intron organization of the human erythroid beta-spectrin gene.

Amin KM, Scarpa AL, Winkelmann JC, Curtis PJ, Forget BG. Amin KM, et al. Among authors: forget bg. Genomics. 1993 Oct;18(1):118-25. doi: 10.1006/geno.1993.1434. Genomics. 1993. PMID: 8276395 Free article.

6

Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion.

Gallagher PG, Roberts WE, Benoit L, Speicher DW, Marchesi SL, Forget BG. Gallagher PG, et al. Among authors: forget bg. Blood. 1993 Oct 1;82(7):2210-5. Blood. 1993. PMID: 8400271 Free article.

7

Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis.

Gallagher PG, Kotula L, Wang Y, Marchesi SL, Curtis PJ, Speicher DW, Forget BG. Gallagher PG, et al. Among authors: forget bg. Am J Hum Genet. 1996 Aug;59(2):351-9. Am J Hum Genet. 1996. PMID: 8755921 Free PMC article.

8

Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.

Gallagher PG, Petruzzi MJ, Weed SA, Zhang Z, Marchesi SL, Mohandas N, Morrow JS, Forget BG. Gallagher PG, et al. Among authors: forget bg. J Clin Invest. 1997 Jan 15;99(2):267-77. doi: 10.1172/JCI119155. J Clin Invest. 1997. PMID: 9005995 Free PMC article.

9

Amino-acid substitution in alpha-spectrin commonly coinherited with nondominant hereditary spherocytosis.

Tse WT, Gallagher PG, Jenkins PB, Wang Y, Benoit L, Speicher D, Winkelmann JC, Agre P, Forget BG, Marchesi SL. Tse WT, et al. Among authors: forget bg. Am J Hematol. 1997 Mar;54(3):233-41. doi: 10.1002/(sici)1096-8652(199703)54:3<233::aid-ajh10>3.0.co;2-e. Am J Hematol. 1997. PMID: 9067503 Free article.

10

A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain.

Gallagher PG, Tse WT, Costa F, Scarpa A, Boivin P, Delaunay J, Forget BG. Gallagher PG, et al. Among authors: forget bg. J Biol Chem. 1991 Aug 15;266(23):15154-9. J Biol Chem. 1991. PMID: 1840591 Free article.

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