BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

353 related articles for article (PubMed ID: 8844207)

  • 21. Hereditary Red Cell Membrane Disorders in Japan: Their Genotypic and Phenotypic Features in 1014 Cases Studied.
    Yawata Y; Kanzaki A; Yawata A; Nakanishi H; Kaku M
    Hematology; 2001; 6(6):399-422. PubMed ID: 27405697
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Variations in both α-spectrin (SPTA1) and β-spectrin ( SPTB ) in a neonate with prolonged jaundice in a family where nine individuals had hereditary elliptocytosis.
    Christensen RD; Nussenzveig RH; Reading NS; Agarwal AM; Prchal JT; Yaish HM
    Neonatology; 2014; 105(1):1-4. PubMed ID: 24193021
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Molecular pathology of the erythrocyte membrane].
    Delaunay J
    Rev Prat; 1993 Jun; 43(11):1392-6. PubMed ID: 8235389
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. 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]  

  • 26. Three Novel Spectrin Variants in Jaundiced Neonates.
    Christensen RD; Agarwal AM; Yaish HM; Reading NS; O'Brien EA; Prchal JT
    Clin Pediatr (Phila); 2018 Jan; 57(1):19-26. PubMed ID: 28090778
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Red cell membrane disorders.
    Narla J; Mohandas N
    Int J Lab Hematol; 2017 May; 39 Suppl 1():47-52. PubMed ID: 28447420
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mild elliptocytosis associated with the alpha 34 Arg-->Trp mutation in spectrin Genova (alpha I/74).
    Perrotta S; Miraglia del Giudice E; Alloisio N; Sciarratta G; Pinto L; Delaunay J; Cutillo S; Iolascon A
    Blood; 1994 Jun; 83(11):3346-9. PubMed ID: 8193371
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Advances in understanding the pathogenesis of red cell membrane disorders.
    Iolascon A; Andolfo I; Russo R
    Br J Haematol; 2019 Oct; 187(1):13-24. PubMed ID: 31364155
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Novel mutations in patients with hereditary red blood cell membrane disorders using next-generation sequencing.
    He Y; Jia S; Dewan RK; Liao N
    Gene; 2017 Sep; 627():556-562. PubMed ID: 28694211
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis.
    Park J; Jeong DC; Yoo J; Jang W; Chae H; Kim J; Kwon A; Choi H; Lee JW; Chung NG; Kim M; Kim Y
    Clin Genet; 2016 Jul; 90(1):69-78. PubMed ID: 26830532
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Hereditary red cell membrane disorders and laboratory diagnostic testing.
    King MJ; Zanella A
    Int J Lab Hematol; 2013 Jun; 35(3):237-43. PubMed ID: 23480868
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Clinical and gene mutation characteristics of patients with hereditary ellipsocytosis: nine cases report and literature review].
    Liu X; Li Y; Zhao X; Yang Y; Zhang L; Jing LP; Ye L; Zhou K; Li JP; Peng GX; Fan HH; Yang WR; Xiong YZ; Zhang FK
    Zhonghua Xue Ye Xue Za Zhi; 2023 Apr; 44(4):316-320. PubMed ID: 37357001
    [No Abstract]   [Full Text] [Related]  

  • 34. A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrin.
    Gallagher PG; Tse WT; Coetzer T; Lecomte MC; Garbarz M; Zarkowsky HS; Baruchel A; Ballas SK; Dhermy D; Palek J
    J Clin Invest; 1992 Mar; 89(3):892-8. PubMed ID: 1541680
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Hereditary red cell membrane disorders in Japan: comparison with other countries].
    Nakanishi H; Wada H; Suemori S; Sugihara T
    Rinsho Ketsueki; 2015 Jul; 56(7):760-70. PubMed ID: 26251138
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. 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]  

  • 38. Spectrin oligomerization is cooperatively coupled to membrane assembly: a linkage targeted by many hereditary hemolytic anemias?
    Giorgi M; Cianci CD; Gallagher PG; Morrow JS
    Exp Mol Pathol; 2001 Jun; 70(3):215-30. PubMed ID: 11418000
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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
    Am J Hum Genet; 1996 Aug; 59(2):351-9. PubMed ID: 8755921
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 18.