BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 8276898)

  • 1. Cell shape and interaction defects in alpha-spectrin mutants of Drosophila melanogaster.
    Lee JK; Coyne RS; Dubreuil RR; Goldstein LS; Branton D
    J Cell Biol; 1993 Dec; 123(6 Pt 2):1797-809. PubMed ID: 8276898
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ankyrin and beta-spectrin accumulate independently of alpha-spectrin in Drosophila.
    Dubreuil RR; Yu J
    Proc Natl Acad Sci U S A; 1994 Oct; 91(22):10285-9. PubMed ID: 7937942
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations of alpha spectrin and labial block cuprophilic cell differentiation and acid secretion in the middle midgut of Drosophila larvae.
    Dubreuil RR; Frankel J; Wang P; Howrylak J; Kappil M; Grushko TA
    Dev Biol; 1998 Feb; 194(1):1-11. PubMed ID: 9473327
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic and molecular analysis of hyperplastic discs, a gene whose product is required for regulation of cell proliferation in Drosophila melanogaster imaginal discs and germ cells.
    Mansfield E; Hersperger E; Biggs J; Shearn A
    Dev Biol; 1994 Oct; 165(2):507-26. PubMed ID: 7958417
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Murine recessive hereditary spherocytosis, sph/sph, is caused by a mutation in the erythroid alpha-spectrin gene.
    Wandersee NJ; Birkenmeier CS; Gifford EJ; Mohandas N; Barker JE
    Hematol J; 2000; 1(4):235-42. PubMed ID: 11920196
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Drosophila melanogaster stranded at second (sas) gene encodes a putative epidermal cell surface receptor required for larval development.
    Schonbaum CP; Organ EL; Qu S; Cavener DR
    Dev Biol; 1992 Jun; 151(2):431-45. PubMed ID: 1339334
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cloning of a portion of the chromosomal gene and cDNA for human beta-fodrin, the nonerythroid form of beta-spectrin.
    Chang JG; Scarpa A; Eddy RL; Byers MG; Harris AS; Morrow JS; Watkins P; Shows TB; Forget BG
    Genomics; 1993 Aug; 17(2):287-93. PubMed ID: 8406479
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Drosophila development requires spectrin network formation.
    Deng H; Lee JK; Goldstein LS; Branton D
    J Cell Biol; 1995 Jan; 128(1-2):71-9. PubMed ID: 7822424
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Drosophila clathrin heavy chain gene: clathrin function is essential in a multicellular organism.
    Bazinet C; Katzen AL; Morgan M; Mahowald AP; Lemmon SK
    Genetics; 1993 Aug; 134(4):1119-34. PubMed ID: 8375651
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Combination of two mutant alpha spectrin alleles underlies a severe spherocytic hemolytic anemia.
    Wichterle H; Hanspal M; Palek J; Jarolim P
    J Clin Invest; 1996 Nov; 98(10):2300-7. PubMed ID: 8941647
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A genetic and molecular characterization of two proximal heterochromatic genes on chromosome 3 of Drosophila melanogaster.
    Schulze SR; Sinclair DA; Fitzpatrick KA; Honda BM
    Genetics; 2005 Apr; 169(4):2165-77. PubMed ID: 15687284
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    J Clin Invest; 1993 Aug; 92(2):612-6. PubMed ID: 8102379
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic studies of spectrin in the larval fat body of Drosophila melanogaster: evidence for a novel lipid uptake apparatus.
    Diaconeasa B; Mazock GH; Mahowald AP; Dubreuil RR
    Genetics; 2013 Nov; 195(3):871-81. PubMed ID: 24037266
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Low expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V/41 polymorphism) and intron 45 and with partial skipping of exon 46.
    Wilmotte R; Maréchal J; Morlé L; Baklouti F; Philippe N; Kastally R; Kotula L; Delaunay J; Alloisio N
    J Clin Invest; 1993 May; 91(5):2091-6. PubMed ID: 8486776
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    J Clin Invest; 1989 Oct; 84(4):1243-52. PubMed ID: 2794061
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The Drosophila Anion Exchanger (DAE) lacks a detectable interaction with the spectrin cytoskeleton.
    Dubreuil RR; Das A; Base C; Mazock GH
    J Negat Results Biomed; 2010 Jun; 9():5. PubMed ID: 20573195
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The murine mutation jaundiced is caused by replacement of an arginine with a stop codon in the mRNA encoding the ninth repeat of beta-spectrin.
    Bloom ML; Kaysser TM; Birkenmeier CS; Barker JE
    Proc Natl Acad Sci U S A; 1994 Oct; 91(21):10099-103. PubMed ID: 7937844
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cloning and chromosomal localization of the human cytoskeletal alpha-actinin gene reveals linkage to the beta-spectrin gene.
    Youssoufian H; McAfee M; Kwiatkowski DJ
    Am J Hum Genet; 1990 Jul; 47(1):62-72. PubMed ID: 2349951
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Drosophila beta spectrin functions independently of alpha spectrin to polarize the Na,K ATPase in epithelial cells.
    Dubreuil RR; Wang P; Dahl S; Lee J; Goldstein LS
    J Cell Biol; 2000 May; 149(3):647-56. PubMed ID: 10791978
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutational effects at the tetramerization site of nonerythroid alpha spectrin.
    Sumandea CA; Fung LW
    Brain Res Mol Brain Res; 2005 May; 136(1-2):81-90. PubMed ID: 15893590
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.