136 related articles for article (PubMed ID: 12488505)
1. The effect of GPI-anchor deficiency on apoptosis in mice carrying a Piga gene mutation in hematopoietic cells.
Kulkarni S; Bessler M
J Leukoc Biol; 2002 Dec; 72(6):1228-33. PubMed ID: 12488505
[TBL] [Abstract][Full Text] [Related]
2. Paroxysmal nocturnal hemoglobinuria: insights from recent advances in molecular biology.
Bessler M; Schaefer A; Keller P
Transfus Med Rev; 2001 Oct; 15(4):255-67. PubMed ID: 11668433
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. The molecular basis of paroxysmal nocturnal hemoglobinuria.
Rosti V
Haematologica; 2000 Jan; 85(1):82-7. PubMed ID: 10629597
[TBL] [Abstract][Full Text] [Related]
5. The pathophysiology of paroxysmal nocturnal hemoglobinuria.
Parker CJ
Exp Hematol; 2007 Apr; 35(4):523-33. PubMed ID: 17379062
[TBL] [Abstract][Full Text] [Related]
6. Molecular cloning of murine pig-a, a gene for GPI-anchor biosynthesis, and demonstration of interspecies conservation of its structure, function, and genetic locus.
Kawagoe K; Takeda J; Endo Y; Kinoshita T
Genomics; 1994 Oct; 23(3):566-74. PubMed ID: 7851884
[TBL] [Abstract][Full Text] [Related]
7. Glycosylphosphatidylinositol-linked proteins are required for maintenance of a normal peripheral lymphoid compartment but not for lymphocyte development.
Bessler M; Rosti V; Peng Y; Cattoretti G; Notaro R; Ohsako S; Elkon KB; Luzzatto L
Eur J Immunol; 2002 Sep; 32(9):2607-16. PubMed ID: 12207345
[TBL] [Abstract][Full Text] [Related]
8. Clonal Cell Proliferation in Paroxysmal Nocturnal Hemoglobinuria: Evaluation of
Park J; Kim M; Kim Y; Han K; Chung NG; Cho B; Lee SE; Lee JW
Ann Lab Med; 2019 Sep; 39(5):438-446. PubMed ID: 31037862
[TBL] [Abstract][Full Text] [Related]
9. Glycophosphatidylinositol-anchored protein deficiency as a marker of mutator phenotypes in cancer.
Chen R; Eshleman JR; Brodsky RA; Medof ME
Cancer Res; 2001 Jan; 61(2):654-8. PubMed ID: 11212264
[TBL] [Abstract][Full Text] [Related]
10. FES-Cre targets phosphatidylinositol glycan class A (PIGA) inactivation to hematopoietic stem cells in the bone marrow.
Keller P; Payne JL; Tremml G; Greer PA; Gaboli M; Pandolfi PP; Bessler M
J Exp Med; 2001 Sep; 194(5):581-9. PubMed ID: 11535627
[TBL] [Abstract][Full Text] [Related]
11. Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency.
Almeida AM; Murakami Y; Layton DM; Hillmen P; Sellick GS; Maeda Y; Richards S; Patterson S; Kotsianidis I; Mollica L; Crawford DH; Baker A; Ferguson M; Roberts I; Houlston R; Kinoshita T; Karadimitris A
Nat Med; 2006 Jul; 12(7):846-51. PubMed ID: 16767100
[TBL] [Abstract][Full Text] [Related]
12. Structures and chromosomal localizations of the glycosylphosphatidylinositol synthesis gene PIGC and its pseudogene PIGCP1.
Hong Y; Ohishi K; Inoue N; Endo Y; Fujita T; Takeda J; Kinoshita T
Genomics; 1997 Sep; 44(3):347-9. PubMed ID: 9325057
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. GATA1-Cre mediates Piga gene inactivation in the erythroid/megakaryocytic lineage and leads to circulating red cells with a partial deficiency in glycosyl phosphatidylinositol-linked proteins (paroxysmal nocturnal hemoglobinuria type II cells).
Jasinski M; Keller P; Fujiwara Y; Orkin SH; Bessler M
Blood; 2001 Oct; 98(7):2248-55. PubMed ID: 11568013
[TBL] [Abstract][Full Text] [Related]
16. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria.
Takeda J; Miyata T; Kawagoe K; Iida Y; Endo Y; Fujita T; Takahashi M; Kitani T; Kinoshita T
Cell; 1993 May; 73(4):703-11. PubMed ID: 8500164
[TBL] [Abstract][Full Text] [Related]
17. Glycosyl phosphatidylinositol (GPI)-anchored molecules and the pathogenesis of paroxysmal nocturnal hemoglobinuria.
Boccuni P; Del Vecchio L; Di Noto R; Rotoli B
Crit Rev Oncol Hematol; 2000 Jan; 33(1):25-43. PubMed ID: 10714960
[TBL] [Abstract][Full Text] [Related]
18. G-CSF induced progenitor mobilization in mice with PIGA- blood cells.
Han B; Unsinger J; Liu F; Link DC; Bessler M
Hematol J; 2004; 5(4):347-52. PubMed ID: 15297852
[TBL] [Abstract][Full Text] [Related]
19. [Differentiation of hematopoietic stem cell and expression of GPI-anchor protein in paroxysmal nocturnal hemoglobinuria].
Kanamaru A; Nishimura T; Kawaguchi K; Wada H; Kakishita E
Nihon Naika Gakkai Zasshi; 1996 Jul; 85(7):1160-4. PubMed ID: 8926479
[No 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]