110 related articles for article (PubMed ID: 2151901)
1. 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]
2. 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]
3. 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]
4. 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]
5. A de novo interstitial deletion of 8p11.2 including ANK1 identified in a patient with spherocytosis, psychomotor developmental delay, and distinctive facial features.
Miya K; Shimojima K; Sugawara M; Shimada S; Tsuri H; Harai-Tanaka T; Nakaoka S; Kanegane H; Miyawaki T; Yamamoto T
Gene; 2012 Sep; 506(1):146-9. PubMed ID: 22771917
[TBL] [Abstract][Full Text] [Related]
6. Partial ankyrin and spectrin deficiency in severe, atypical hereditary spherocytosis.
Coetzer TL; Lawler J; Liu SC; Prchal JT; Gualtieri RJ; Brain MC; Dacie JV; Palek J
N Engl J Med; 1988 Jan; 318(4):230-4. PubMed ID: 2961992
[No Abstract] [Full Text] [Related]
7. 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]
8. Apparently normal ankyrin content in unsplenectomized hereditary spherocytosis patients with the inactivation of one ankyrin (ANK1) allele.
Miraglia del Giudice E; Francese M; Polito R; Nobili B; Iolascon A; Perrotta S
Haematologica; 1997; 82(3):332-3. PubMed ID: 9234582
[TBL] [Abstract][Full Text] [Related]
9. Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis.
Gallagher PG; Forget BG
Blood Cells Mol Dis; 1997 Dec; 23(3):417-21. PubMed ID: 9446757
[No Abstract] [Full Text] [Related]
10. 4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis.
Perrotta S; Iolascon A; Polito R; d'Urzo G; Conte ML; Miraglia del Giudice E
Haematologica; 1999 Jul; 84(7):660-2. PubMed ID: 10406914
[No Abstract] [Full Text] [Related]
11. (AC)n microsatellite polymorphism and 14-nucleotide deletion in exon 42 ankyrin-1 gene in several families with hereditary spherocytosis in a population of South-Western Poland.
Bogusławska DM; Heger E; Baldy-Chudzik K; Zagulski M; Maciejewska M; Likwiarz A; Sikorski AF
Ann Hematol; 2006 May; 85(5):337-9. PubMed ID: 16518602
[TBL] [Abstract][Full Text] [Related]
12. Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases.
Iolascon A; Miraglia del Giudice E; Camaschella C; Pinto L; Nobili B; Perrotta S; Cutillo S
Br J Haematol; 1991 Aug; 78(4):551-4. PubMed ID: 1832935
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Clinical expression and laboratory detection of red blood cell membrane protein mutations.
Palek J; Jarolim P
Semin Hematol; 1993 Oct; 30(4):249-83. PubMed ID: 8266114
[No Abstract] [Full Text] [Related]
15. 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]
16. [Characteristics of hereditary spherocytosis].
Yawata Y
Nihon Naika Gakkai Zasshi; 1999 Sep; 88(9):1825-33. PubMed ID: 10581770
[No Abstract] [Full Text] [Related]
17. A 2.1 Mb deletion adjacent but distal to a 14q21q23 paracentric inversion in a family with spherocytosis and severe learning difficulties.
Lybaek H; Øyen N; Fauske L; Houge G
Clin Genet; 2008 Dec; 74(6):553-9. PubMed ID: 18717686
[TBL] [Abstract][Full Text] [Related]
18. Genetics of the red cell membrane skeleton.
Palek J; Lambert S
Semin Hematol; 1990 Oct; 27(4):290-332. PubMed ID: 2255917
[No Abstract] [Full Text] [Related]
19. Low frequency of ankyrin mutations in hereditary spherocytosis: identification of three novel mutations.
Leite RC; Basseres DS; Ferreira JS; Alberto FL; Costa FF; Saad ST
Hum Mutat; 2000 Dec; 16(6):529. PubMed ID: 11102985
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
