These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 2040699)

  • 1. Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans.
    Alloisio N; Morlé L; Maréchal J; Roux AF; Ducluzeau MT; Guetarni D; Pothier B; Baklouti F; Ghanem A; Kastally R; Delaunay J
    J Clin Invest; 1991 Jun; 87(6):2169-77. PubMed ID: 2040699
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular basis of clinical and morphological heterogeneity in hereditary elliptocytosis (HE) with spectrin alpha I variants.
    Lecomte MC; Garbarz M; Gautero H; Bournier O; Galand C; Boivin P; Dhermy D
    Br J Haematol; 1993 Nov; 85(3):584-95. PubMed ID: 8136282
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expression of spectrin alpha I/65 hereditary elliptocytosis in patients from Brazil.
    Pranke PH; Basseres DS; Costa FF; Saad ST
    Br J Haematol; 1996 Sep; 94(3):470-5. PubMed ID: 8790144
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity].
    Eber SW
    Klin Padiatr; 1991; 203(4):284-95. PubMed ID: 1942935
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An alpha-spectrin mutation responsible for hereditary elliptocytosis associated in cis with the alpha v/41 polymorphism.
    Dalla Venezia N; Wilmotte R; Morlé L; Forissier A; Parquet N; Garbarz M; Rousset T; Dhermy D; Alloisio N; Delaunay J
    Hum Genet; 1993 Feb; 90(6):641-4. PubMed ID: 8444470
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Abnormal tryptic peptide from the spectrin alpha-chain resulting from alpha- or beta-chain mutations: two genetically distinct forms of the Sp alpha I/74 variant.
    Lecomte MC; Gautero H; Garbarz M; Boivin P; Dhermy D
    Br J Haematol; 1990 Nov; 76(3):406-13. PubMed ID: 2261350
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spectrin Cosenza: a novel beta chain variant associated with Sp alphaI/74 hereditary elliptocytosis.
    Qualtieri A; Pasqua A; Bisconte MG; Le Pera M; Brancati C
    Br J Haematol; 1997 May; 97(2):273-8. PubMed ID: 9163587
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Point mutation in the beta-spectrin gene associated with alpha I/74 hereditary elliptocytosis. Implications for the mechanism of spectrin dimer self-association.
    Tse WT; Lecomte MC; Costa FF; Garbarz M; Feo C; Boivin P; Dhermy D; Forget BG
    J Clin Invest; 1990 Sep; 86(3):909-16. PubMed ID: 1975598
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin allele.
    Guetarni D; Roux AF; Alloisio N; Morlé F; Ducluzeau MT; Forget BG; Colonna P; Delaunay J; Godet J
    Hum Genet; 1990 Oct; 85(6):627-30. PubMed ID: 2227954
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Assignment of Sp alpha I/74 hereditary elliptocytosis to the alpha- or beta-chain of spectrin through in vitro dimer reconstitution.
    Pothier B; Alloisio N; Maréchal J; Morlé L; Ducluzeau MT; Caldani C; Philippe N; Delaunay J
    Blood; 1990 May; 75(10):2061-9. PubMed ID: 2337674
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel exon 2 α spectrin mutation and intragenic crossover: three morphological phenotypes associated with four distinct α spectrin defects.
    Swierczek S; Agarwal AM; Naidoo K; Lorenzo FR; Whisenant J; Nussenzveig RH; Agarwal N; Coetzer TL; Prchal JT
    Haematologica; 2013 Dec; 98(12):1972-9. PubMed ID: 24077844
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular basis of Sp alpha I/65 hereditary elliptocytosis in North Africa: insertion of a TTG triplet between codons 147 and 149 in the alpha-spectrin gene from five unrelated families.
    Roux AF; Morlé F; Guetarni D; Colonna P; Sahr K; Forget BG; Delaunay J; Godet J
    Blood; 1989 Jun; 73(8):2196-201. PubMed ID: 2567189
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spectrin Tunis (alpha I/78): a new alpha I variant that causes asymptomatic hereditary elliptocytosis in the heterozygous state.
    Morlé L; Alloisio N; Ducluzeau MT; Pothier B; Blibech R; Kastally R; Delaunay J
    Blood; 1988 Feb; 71(2):508-11. PubMed ID: 3337911
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association site.
    Alloisio N; Wilmotte R; Morlé L; Baklouti F; Maréchal J; Ducluzeau MT; Denoroy L; Féo C; Forget BG; Kastally R
    Blood; 1992 Aug; 80(3):809-15. PubMed ID: 1638030
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spectrin Anastasia (alpha I/78): a new spectrin variant (alpha 45 Arg-->Thr) with moderate elliptocytogenic potential.
    Perrotta S; Iolascon A; De Angelis F; Pagano L; Colonna G; Cutillo S; Miraglia del Giudice E
    Br J Haematol; 1995 Apr; 89(4):933-6. PubMed ID: 7772539
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous state.
    Alloisio N; Morlé L; Pothier B; Roux AF; Maréchal J; Ducluzeau MT; Benhadji-Zouaoui Z; Delaunay J
    Blood; 1988 Apr; 71(4):1039-47. PubMed ID: 2895677
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A variant of spectrin low-expression allele alpha LELY carrying a hereditary elliptocytosis mutation in codon 28.
    Randon J; Boulanger L; Marechal J; Garbarz M; Vallier A; Ribeiro L; Tamagnini G; Dhermy D; Delaunay J
    Br J Haematol; 1994 Nov; 88(3):534-40. PubMed ID: 7819065
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary pyropoikilocytosis and elliptocytosis in a white French family with the spectrin alpha I/74 variant related to a CGT to CAT codon change (Arg to His) at position 22 of the spectrin alpha I domain.
    Garbarz M; Lecomte MC; Féo C; Devaux I; Picat C; Lefebvre C; Galibert F; Gautero H; Bournier O; Galand C
    Blood; 1990 Apr; 75(8):1691-8. PubMed ID: 2328319
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis.
    Lane PA; Shew RL; Iarocci TA; Mohandas N; Hays T; Mentzer WC
    J Clin Invest; 1987 Mar; 79(3):989-96. PubMed ID: 3818958
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Family of hereditary elliptocytosis with abnormalities of spectrin function (Sp alpha 1/74)].
    Okino E; Mori C; Yamazaki S; Toyota K; Yamada T; Tachi K; Shike S; Kanzaki A; Ikeda A; Yawata Y
    Rinsho Ketsueki; 1989 Jul; 30(7):1047-51. PubMed ID: 2810789
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.