Lux SE - Search Results

1

Large numbers of alternatively spliced isoforms of the regulatory region of human erythrocyte ankyrin.

Gallagher PG, Tse WT, Scarpa AL, Lux SE, Forget BG. Gallagher PG, et al. Among authors: lux se. Trans Assoc Am Physicians. 1992;105:268-77. Trans Assoc Am Physicians. 1992. PMID: 1309004 No abstract available.

2

Demonstration of the deletion of a copy of the ankyrin gene in a patient with hereditary spherocytosis by in situ hybridization.

Tse WT, Menninger JC, Ward DC, Chilcote RR, John KM, Lux SE, Forget BG. Tse WT, et al. Among authors: lux se. Trans Assoc Am Physicians. 1990;103:242-8. Trans Assoc Am Physicians. 1990. PMID: 2151901 No abstract available.

3

Structure and organization of the human ankyrin-1 gene. Basis for complexity of pre-mRNA processing.

Gallagher PG, Tse WT, Scarpa AL, Lux SE, Forget BG. Gallagher PG, et al. Among authors: lux se. J Biol Chem. 1997 Aug 1;272(31):19220-8. doi: 10.1074/jbc.272.31.19220. J Biol Chem. 1997. PMID: 9235914 Free article.

4

The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter.

Gallagher PG, Romana M, Tse WT, Lux SE, Forget BG. Gallagher PG, et al. Among authors: lux se. Blood. 2000 Aug 1;96(3):1136-43. Blood. 2000. PMID: 10910934 Free article.

5

Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin.

Costa FF, Agre P, Watkins PC, Winkelmann JC, Tang TK, John KM, Lux SE, Forget BG. Costa FF, et al. Among authors: lux se. N Engl J Med. 1990 Oct 11;323(15):1046-50. doi: 10.1056/NEJM199010113231507. N Engl J Med. 1990. PMID: 1977081 Free article. No abstract available.

6

Beta spectrin kissimmee: a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1.

Becker PS, Tse WT, Lux SE, Forget BG. Becker PS, et al. Among authors: lux se. J Clin Invest. 1993 Aug;92(2):612-6. doi: 10.1172/JCI116628. J Clin Invest. 1993. PMID: 8102379 Free PMC article.

7

A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis.

Jenkins PB, Abou-Alfa GK, Dhermy D, Bursaux E, Féo C, Scarpa AL, Lux SE, Garbarz M, Forget BG, Gallagher PG. Jenkins PB, et al. Among authors: lux se. J Clin Invest. 1996 Jan 15;97(2):373-80. doi: 10.1172/JCI118425. J Clin Invest. 1996. PMID: 8567957 Free PMC article.

8

Isolation and chromosomal localization of a novel nonerythroid ankyrin gene.

Tse WT, Menninger JC, Yang-Feng TL, Francke U, Sahr KE, Lux SE, Ward DC, Forget BG. Tse WT, et al. Among authors: lux se. Genomics. 1991 Aug;10(4):858-66. doi: 10.1016/0888-7543(91)90173-c. Genomics. 1991. PMID: 1833308

9

Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.

Eber SW, Gonzalez JM, Lux ML, Scarpa AL, Tse WT, Dornwell M, Herbers J, Kugler W, Ozcan R, Pekrun A, Gallagher PG, Schröter W, Forget BG, Lux SE. Eber SW, et al. Among authors: lux se, lux ml. Nat Genet. 1996 Jun;13(2):214-8. doi: 10.1038/ng0696-214. Nat Genet. 1996. PMID: 8640229

10

A widely expressed betaIII spectrin associated with Golgi and cytoplasmic vesicles.

Stankewich MC, Tse WT, Peters LL, Ch'ng Y, John KM, Stabach PR, Devarajan P, Morrow JS, Lux SE. Stankewich MC, et al. Among authors: lux se. Proc Natl Acad Sci U S A. 1998 Nov 24;95(24):14158-63. doi: 10.1073/pnas.95.24.14158. Proc Natl Acad Sci U S A. 1998. PMID: 9826670 Free PMC article.

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