328 related articles for article (PubMed ID: 2141669)
1. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8.
Lux SE; Tse WT; Menninger JC; John KM; Harris P; Shalev O; Chilcote RR; Marchesi SL; Watkins PC; Bennett V
Nature; 1990 Jun; 345(6277):736-9. PubMed ID: 2141669
[TBL] [Abstract][Full Text] [Related]
2. 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
Nat Genet; 1996 Jun; 13(2):214-8. PubMed ID: 8640229
[TBL] [Abstract][Full Text] [Related]
3. Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis.
Garbarz M; Bibas D; Cynober T; Galand C; Bournier O; Devaux I; Tchernia G; Dhermy D
C R Acad Sci III; 1996 Oct; 319(10):913-9. PubMed ID: 8977772
[TBL] [Abstract][Full Text] [Related]
4. Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population.
Yawata Y; Kanzaki A; Yawata A; Doerfler W; Ozcan R; Eber SW
Int J Hematol; 2000 Feb; 71(2):118-35. PubMed ID: 10745622
[TBL] [Abstract][Full Text] [Related]
5. Hereditary spherocytic anemia with deletion of the short arm of chromosome 8.
Okamoto N; Wada Y; Nakamura Y; Nakayama M; Chiyo H; Murayama K; Inoue T; Kanzaki A; Yawata Y; Hirono A
Am J Med Genet; 1995 Sep; 58(3):225-9. PubMed ID: 8533822
[TBL] [Abstract][Full Text] [Related]
6. Hereditary spherocytosis with spectrin deficiency related to null mutations of the beta-spectrin gene.
Dhermy D; Galand C; Bournier O; Cynober T; Méchinaud F; Tchemia G; Garbarz M
Blood Cells Mol Dis; 1998 Jun; 24(2):251-61. PubMed ID: 9714702
[TBL] [Abstract][Full Text] [Related]
7. [Molecular mechanism of hereditary spherocytosis].
Bogusławska DM; Heger E; Sikorski AF
Pol Merkur Lekarski; 2006 Jan; 20(115):112-6. PubMed ID: 16617750
[TBL] [Abstract][Full Text] [Related]
8. 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
Trans Assoc Am Physicians; 1990; 103():242-8. PubMed ID: 2151901
[No Abstract] [Full Text] [Related]
9. Uniquely higher incidence of isolated or combined deficiency of band 3 and/or band 4.2 as the pathogenesis of autosomal dominantly inherited hereditary spherocytosis in the Japanese population.
Inoue T; Kanzaki A; Yawata A; Wada H; Okamoto N; Takahashi M; Sugihara T; Yamada O; Yawata Y
Int J Hematol; 1994 Dec; 60(4):227-38. PubMed ID: 7894027
[TBL] [Abstract][Full Text] [Related]
10. [Cytoskeleton anomalies in disorders of red cell membrane proteins].
Kanzaki A; Wada H; Yawata Y
Rinsho Ketsueki; 1991 Jun; 32(6):573-9. PubMed ID: 1832469
[TBL] [Abstract][Full Text] [Related]
11. Molecular genetics of hereditary elliptocytosis and hereditary spherocytosis.
Delaunay J; Alloisio N; Morle L; Baklouti F; Dalla Venezia N; Maillet P; Wilmotte R
Ann Genet; 1996; 39(4):209-21. PubMed ID: 9037349
[TBL] [Abstract][Full Text] [Related]
12. Hematologically important mutations: ankyrin variants in hereditary spherocytosis.
Gallagher PG
Blood Cells Mol Dis; 2005; 35(3):345-7. PubMed ID: 16223590
[TBL] [Abstract][Full Text] [Related]
13. 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
N Engl J Med; 1990 Oct; 323(15):1046-50. PubMed ID: 1977081
[No Abstract] [Full Text] [Related]
14. 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]
15. [Hereditary spherocytosis: one year study of erythrocyte membrane proteins].
Tshilolo L; Kagambega F; Sztern B; Vertongen F; Gulbis B
Rev Med Brux; 1998 Oct; 19(5 Pt 1):417-23. PubMed ID: 9844481
[TBL] [Abstract][Full Text] [Related]
16. Erythrocyte membrane protein destabilization versus clinical outcome in 160 Portuguese Hereditary Spherocytosis patients.
Rocha S; Costa E; Rocha-Pereira P; Ferreira F; Cleto E; Barbot J; Quintanilha A; Belo L; Santos-Silva A
Br J Haematol; 2010 Jun; 149(5):785-94. PubMed ID: 20346007
[TBL] [Abstract][Full Text] [Related]
17. Hereditary spherocytosis (HS) due to loss of anion exchange transporter.
Iolascon A; Miraglia del Giudice E; Perrotta S; Pinto L; Fiorelli G; Cappellini DM; Vasseur C; Bursaux E; Cutillo S
Haematologica; 1992; 77(6):450-6. PubMed ID: 1289181
[TBL] [Abstract][Full Text] [Related]
18. Band 3Tambaú: a de novo mutation in the AE1 gene associated with hereditary spherocytosis. Implications for anion exchange and insertion into the red blood cell membrane.
Lima PR; Baratti MO; Chiattone ML; Costa FF; Saad ST
Eur J Haematol; 2005 May; 74(5):396-401. PubMed ID: 15813913
[TBL] [Abstract][Full Text] [Related]
19. Molecular basis of spectrin and ankyrin deficiencies in severe hereditary spherocytosis: evidence implicating a primary defect of ankyrin.
Hanspal M; Yoon SH; Yu H; Hanspal JS; Lambert S; Palek J; Prchal JT
Blood; 1991 Jan; 77(1):165-73. PubMed ID: 1702027
[TBL] [Abstract][Full Text] [Related]
20. A dinucleotide deletion in the ankyrin promoter alters gene expression, transcription initiation and TFIID complex formation in hereditary spherocytosis.
Gallagher PG; Nilson DG; Wong C; Weisbein JL; Garrett-Beal LJ; Eber SW; Bodine DM
Hum Mol Genet; 2005 Sep; 14(17):2501-9. PubMed ID: 16037067
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
