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 *

157 related articles for article (PubMed ID: 8755921)

  • 21. Clinical expression of alpha spectrin mutants in hereditary elliptocytosis.
    Palek J; Coetzer T
    Blood Cells; 1987; 13(1-2):237-50. PubMed ID: 3311220
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Hereditary elliptocytosis: spectrin and protein 4.1R.
    Gallagher PG
    Semin Hematol; 2004 Apr; 41(2):142-64. PubMed ID: 15071791
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis.
    Hanspal M; Hanspal JS; Sahr KE; Fibach E; Nachman J; Palek J
    Blood; 1993 Sep; 82(5):1652-60. PubMed ID: 8364214
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis.
    Coetzer T; Palek J; Lawler J; Liu SC; Jarolim P; Lahav M; Prchal JT; Wang W; Alter BP; Schewitz G
    Blood; 1990 Jun; 75(11):2235-44. PubMed ID: 2346784
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin.
    Glele-Kakai C; Garbarz M; Lecomte MC; Leborgne S; Galand C; Bournier O; Devaux I; Gautero H; Zohoun I; Gallagher PG; Forget BG; Dhermy D
    Br J Haematol; 1996 Oct; 95(1):57-66. PubMed ID: 8857939
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Hereditary poikilocytic anemia associated with the co-inheritance of two alpha spectrin abnormalities.
    Iarocci TA; Wagner GM; Mohandas N; Lane PA; Mentzer WC
    Blood; 1988 May; 71(5):1390-6. PubMed ID: 3359047
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [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]  

  • 29. Four different mutations in codon 28 of alpha spectrin are associated with structurally and functionally abnormal spectrin alpha I/74 in hereditary elliptocytosis.
    Coetzer TL; Sahr K; Prchal J; Blacklock H; Peterson L; Koler R; Doyle J; Manaster J; Palek J
    J Clin Invest; 1991 Sep; 88(3):743-9. PubMed ID: 1679439
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis.
    Liu SC; Derick LH; Agre P; Palek J
    Blood; 1990 Jul; 76(1):198-205. PubMed ID: 2364170
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Research on genetic abnormality in the hemolytic form of hereditary elliptocytosis with homozygosity for the spectrin alpha I/74 variant].
    Garbarz M; Devaux I; Grandchamp B; Picat C; Dhermy D; Lecomte MC; Boivin P; Sahr KE; Forget B
    C R Acad Sci III; 1989; 308(2):43-8. PubMed ID: 2493313
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis.
    Marchesi SL; Letsinger JT; Speicher DW; Marchesi VT; Agre P; Hyun B; Gulati G
    J Clin Invest; 1987 Jul; 80(1):191-8. PubMed ID: 3597773
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation.
    Harper SL; Sriswasdi S; Tang HY; Gaetani M; Gallagher PG; Speicher DW
    Blood; 2013 Oct; 122(17):3045-53. PubMed ID: 23974198
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Partial spectrin deficiency in hereditary pyropoikilocytosis.
    Coetzer TL; Palek J
    Blood; 1986 Apr; 67(4):919-24. PubMed ID: 3955236
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Location and PCR-based detection of three polymorphisms of the human erythrocyte beta-spectrin gene (SPTB).
    Gallagher PG; Lecomte MC; Galand C; Wang YP; Tse WT; Forget BG
    Br J Haematol; 1994 Oct; 88(2):413-4. PubMed ID: 7803294
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis.
    Niss O; Chonat S; Dagaonkar N; Almansoori MO; Kerr K; Rogers ZR; McGann PT; Quarmyne MO; Risinger M; Zhang K; Kalfa TA
    Blood Cells Mol Dis; 2016 Oct; 61():4-9. PubMed ID: 27667160
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular defect of spectrin in the family of a child with congenital hemolytic poikilocytic anemia.
    Dhermy D; Lecomte MC; Garbarz M; Feo C; Gautero H; Bournier O; Galand C; Herrera A; Gretillat F; Boivin P
    Pediatr Res; 1984 Oct; 18(10):1005-12. PubMed ID: 6493844
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis.
    Maillet P; Alloisio N; Morlé L; Delaunay J
    Hum Mutat; 1996; 8(2):97-107. PubMed ID: 8844207
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.