835 related articles for article (PubMed ID: 14972783)
1. A new aspect of the molecular pathogenesis of paroxysmal nocturnal hemoglobinuria.
Shichishima T; Noji H
Hematology; 2002 Aug; 7(4):211-27. PubMed ID: 14972783
[TBL] [Abstract][Full Text] [Related]
2. Impaired hematopoiesis in paroxysmal nocturnal hemoglobinuria/aplastic anemia is not associated with a selective proliferative defect in the glycosylphosphatidylinositol-anchored protein-deficient clone.
Maciejewski JP; Sloand EM; Sato T; Anderson S; Young NS
Blood; 1997 Feb; 89(4):1173-81. PubMed ID: 9028939
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Heterogeneity in the molecular pathogenesis of paroxysmal nocturnal hemoglobinuria (PNH) syndromes and expansion mechanism of a PNH clone.
Shichishima T; Noji H
Int J Hematol; 2006 Aug; 84(2):97-103. PubMed ID: 16926129
[TBL] [Abstract][Full Text] [Related]
5. Glycosylphosphatidylinositol (GPI)-anchored membrane proteins in clinical pathophysiology of paroxysmal nocturnal hemoglobinuria (PNH).
Shichishima T
Fukushima J Med Sci; 1995 Jun; 41(1):1-13. PubMed ID: 8606038
[TBL] [Abstract][Full Text] [Related]
6. Clinical paroxysmal nocturnal hemoglobinuria is the result of expansion of glycosyl-phosphatidyl-inositol-anchored protein-deficient clone in the condition of deficient hematopoiesis.
Pakdeesuwan K; Muangsup W; Pratya YU; Issaragrisil S; Wanachiwanawin W
Int J Hematol; 2001 Jan; 73(1):64-70. PubMed ID: 11372757
[TBL] [Abstract][Full Text] [Related]
7. Circulating PIG-A mutant T lymphocytes in healthy adults and patients with bone marrow failure syndromes.
Ware RE; Pickens CV; DeCastro CM; Howard TA
Exp Hematol; 2001 Dec; 29(12):1403-9. PubMed ID: 11750098
[TBL] [Abstract][Full Text] [Related]
8. Paroxysmal nocturnal hemoglobinuria: stem cells and clonality.
Brodsky RA
Hematology Am Soc Hematol Educ Program; 2008; ():111-5. PubMed ID: 19074067
[TBL] [Abstract][Full Text] [Related]
9. The PIG-A mutation and absence of glycosylphosphatidylinositol-linked proteins do not confer resistance to apoptosis in paroxysmal nocturnal hemoglobinuria.
Ware RE; Nishimura J; Moody MA; Smith C; Rosse WF; Howard TA
Blood; 1998 Oct; 92(7):2541-50. PubMed ID: 9746796
[TBL] [Abstract][Full Text] [Related]
10. Immune pathogenesis of paroxysmal nocturnal hemoglobinuria.
Tiu R; Maciejewski J
Int J Hematol; 2006 Aug; 84(2):113-7. PubMed ID: 16926131
[TBL] [Abstract][Full Text] [Related]
11. Paroxysmal nocturnal hemoglobinuria clone in bone marrow of patients with pancytopenia.
Nakakuma H; Nagakura S; Iwamoto N; Kawaguchi T; Hidaka M; Horikawa K; Kagimoto T; Shido T; Takatsuki K
Blood; 1995 Mar; 85(5):1371-6. PubMed ID: 7532041
[TBL] [Abstract][Full Text] [Related]
12. [Paroxysmal nocturnal hemoglobinuria (PNH). Pathogenesis, diagnosis and treatment].
Röth A; Dührsen U; Schrezenmeier H; Schubert J
Dtsch Med Wochenschr; 2009 Feb; 134(9):404-9. PubMed ID: 19224425
[TBL] [Abstract][Full Text] [Related]
13. New insights into molecular pathogenesis of bone marrow failure in paroxysmal nocturnal hemoglobinuria.
Kawaguchi T; Nakakuma H
Int J Hematol; 2007 Jul; 86(1):27-32. PubMed ID: 17675263
[TBL] [Abstract][Full Text] [Related]
14. Paroxysmal nocturnal hemoglobinuria (PNH) and primary p.Cys89Tyr mutation in CD59: Differences and similarities.
Mevorach D
Mol Immunol; 2015 Sep; 67(1):51-5. PubMed ID: 25818314
[TBL] [Abstract][Full Text] [Related]
15. The molecular basis of paroxysmal nocturnal hemoglobinuria.
Rosti V
Haematologica; 2000 Jan; 85(1):82-7. PubMed ID: 10629597
[TBL] [Abstract][Full Text] [Related]
16. Molecular basis of paroxysmal nocturnal hemoglobinuria.
Parker CJ
Stem Cells; 1996 Jul; 14(4):396-411. PubMed ID: 8843541
[TBL] [Abstract][Full Text] [Related]
17. The role of Wilms' tumor gene peptide-specific cytotoxic T lymphocytes in immunologic selection of a paroxysmal nocturnal hemoglobinuria clone.
Ikeda K; Shichishima T; Yasukawa M; Nakamura-Shichishima A; Noji H; Akutsu K; Osumi K; Maruyama Y
Exp Hematol; 2007 Apr; 35(4):618-26. PubMed ID: 17379072
[TBL] [Abstract][Full Text] [Related]
18. A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuria.
Mannelli F; Bencini S; Peruzzi B; Cutini I; Sanna A; Benelli M; Magi A; Gianfaldoni G; Rotunno G; Carrai V; Gelli AM; Valle V; Santini V; Notaro R; Luzzatto L; Bosi A
Cytometry B Clin Cytom; 2013 Mar; 84(2):71-81. PubMed ID: 23281097
[TBL] [Abstract][Full Text] [Related]
19. The Role of T Lymphocytes in the Pathogenesis of Paroxysmal Nocturnal Hemoglobinuria.
Li C; Dong X; Wang H; Shao Z
Front Immunol; 2021; 12():777649. PubMed ID: 35003092
[TBL] [Abstract][Full Text] [Related]
20. The dual pathogenesis of paroxysmal nocturnal hemoglobinuria.
Luzzatto L; Bessler M
Curr Opin Hematol; 1996 Mar; 3(2):101-10. PubMed ID: 9372059
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]