107 related articles for article (PubMed ID: 9398536)
1. Structural and functional analysis of the Pig-a protein that is mutated in paroxysmal nocturnal hemoglobinuria.
Norris ER; Howard TA; Marcus SJ; Ware RE
Blood Cells Mol Dis; 1997 Dec; 23(3):350-60. PubMed ID: 9398536
[TBL] [Abstract][Full Text] [Related]
2. Genetic instability and the etiology of somatic PIG-A mutations in paroxysmal nocturnal hemoglobinuria.
Purow DB; Howard TA; Marcus SJ; Rosse WF; Ware RE
Blood Cells Mol Dis; 1999 Apr; 25(2):81-91. PubMed ID: 10389589
[TBL] [Abstract][Full Text] [Related]
3. The molecular basis of paroxysmal nocturnal hemoglobinuria.
Rosti V
Haematologica; 2000 Jan; 85(1):82-7. PubMed ID: 10629597
[TBL] [Abstract][Full Text] [Related]
4. [Paroxysmal nocturnal hemoglobinuria].
Wada H; Kanamaru A
Nihon Rinsho; 1996 Sep; 54(9):2507-12. PubMed ID: 8890586
[TBL] [Abstract][Full Text] [Related]
5. Genotypic and phenotypic implications in paroxysmal nocturnal hemoglobinuria (PNH): a preliminary investigation.
Pakdeesuwan K; Siripanyaphinyo U; Pramoonjago P; Pattanapanyasat K; Wilairat P; Kinoshita T; Wanachiwanawin W
Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():58-63. PubMed ID: 9640601
[TBL] [Abstract][Full Text] [Related]
6. A cohort study of the nature of paroxysmal nocturnal hemoglobinuria clones and PIG-A mutations in patients with aplastic anemia.
Wanachiwanawin W; Siripanyaphinyo U; Piyawattanasakul N; Kinoshita T
Eur J Haematol; 2006 Jun; 76(6):502-9. PubMed ID: 16529603
[TBL] [Abstract][Full Text] [Related]
7. Paroxysmal nocturnal hemoglobinuria: new insights from murine Pig-a-deficient hematopoiesis.
Devetten MP; Liu JM; Ling V; Weichold FF; Yu J; Medof ME; Young NS; Dunn DE
Proc Assoc Am Physicians; 1997 Mar; 109(2):99-110. PubMed ID: 9069578
[TBL] [Abstract][Full Text] [Related]
8. The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplications.
Nafa K; Bessler M; Castro-Malaspina H; Jhanwar S; Luzzatto L
Blood Cells Mol Dis; 1998 Sep; 24(3):370-84. PubMed ID: 10087994
[TBL] [Abstract][Full Text] [Related]
9. PIG-A gene abnormalities in Thai patients with paroxysmal nocturnal hemoglobinuria.
Pramoonjago P; Wanachiwanawin W; Chinprasertsuk S; Pattanapanyasat K; Takeda J; Kinoshita T
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():322-4. PubMed ID: 8629134
[TBL] [Abstract][Full Text] [Related]
10. Frequent HPRT mutations in paroxysmal nocturnal haemoglobinuria reflect T cell clonal expansion, not genomic instability.
Chen G; Zeng W; Green S; Young NS
Br J Haematol; 2004 May; 125(3):383-91. PubMed ID: 15086421
[TBL] [Abstract][Full Text] [Related]
11. Altered lipid raft composition and defective cell death signal transduction in glycosylphosphatidylinositol anchor-deficient PIG-A mutant cells.
Szpurka H; Schade AE; Jankowska AM; Maciejewski JP
Br J Haematol; 2008 Jul; 142(3):413-22. PubMed ID: 18544084
[TBL] [Abstract][Full Text] [Related]
12. Somatic mutation and clonal selection in the pathogenesis and in the control of paroxysmal nocturnal hemoglobinuria.
Bessler M; Hillmen P
Semin Hematol; 1998 Apr; 35(2):149-67. PubMed ID: 9565157
[TBL] [Abstract][Full Text] [Related]
13. Detailed immunophenotypic characterization of different major and minor subsets of peripheral blood cells in patients with paroxysmal nocturnal hemoglobinuria.
Hernández-Campo PM; Almeida J; Acevedo MJ; Sánchez ML; Alberca I; Vidriales B; Martínez E; Romero JR; Orfao A
Transfusion; 2008 Jul; 48(7):1403-14. PubMed ID: 18422849
[TBL] [Abstract][Full Text] [Related]
14. Mutations in the PIG-A gene causing partial deficiency of GPI-linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuria.
Bessler M; Mason PJ; Hillmen P; Luzzatto L
Br J Haematol; 1994 Aug; 87(4):863-6. PubMed ID: 7986731
[TBL] [Abstract][Full Text] [Related]
15. [Mutations in the PIG-A gene lead to GPI-deficiency in paroxysmal nocturnal hemoglobinuria].
Ostendorf T; Schubert J; Schmidt RE
Immun Infekt; 1994 Aug; 22(4):154-5. PubMed ID: 7927481
[TBL] [Abstract][Full Text] [Related]
16. Structure and chromosomal localization of the GPI-anchor synthesis gene PIGF and its pseudogene psi PIGF.
Ohishi K; Inoue N; Endo Y; Fujita T; Takeda J; Kinoshita T
Genomics; 1995 Oct; 29(3):804-7. PubMed ID: 8575782
[TBL] [Abstract][Full Text] [Related]
17. Paroxysmal nocturnal hemoglobinuria: molecular pathogenesis and molecular therapeutic approaches.
Nishimura J; Smith CA; Phillips KL; Ware RE; Rosse WF
Hematopathol Mol Hematol; 1998; 11(3-4):119-46. PubMed ID: 9844822
[TBL] [Abstract][Full Text] [Related]
18. Genotypic, immunophenotypic and clinical features of Thai patients with paroxysmal nocturnal haemoglobinuria.
Pramoonjago P; Pakdeesuwan K; Siripanyaphinyo U; Chinprasertsuk S; Kinoshita T; Wanachiwanawin W
Br J Haematol; 1999 May; 105(2):497-504. PubMed ID: 10233427
[TBL] [Abstract][Full Text] [Related]
19. Recent insights into the pathophysiology of paroxysmal nocturnal hemoglobinuria.
Meletis J; Terpos E
Med Sci Monit; 2003 Jul; 9(7):RA161-72. PubMed ID: 12883466
[TBL] [Abstract][Full Text] [Related]
20. Paroxysmal nocturnal hemoglobinuria and complement-mediated erythrocyte damage.
Parker CJ
Curr Opin Hematol; 1994 Mar; 1(2):151-6. PubMed ID: 9371274
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]