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2. 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]
3. 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]
4. Somatic mutations of the PIG-A gene found in Japanese patients with paroxysmal nocturnal hemoglobinuria. Yamada N; Miyata T; Maeda K; Kitani T; Takeda J; Kinoshita T Blood; 1995 Feb; 85(4):885-92. PubMed ID: 7531514 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. Somatic mutations of PIG-A in Thai patients with paroxysmal nocturnal hemoglobinuria. Pramoonjago P; Wanachiwanawin W; Chinprasertsak S; Pattanapanayasat K; Takeda J; Kinoshita T Blood; 1995 Sep; 86(5):1736-9. PubMed ID: 7655005 [TBL] [Abstract][Full Text] [Related]
7. The distribution of PIG-A gene abnormalities in paroxysmal nocturnal hemoglobinuria granulocytes and cultured erythroblasts. Noji H; Shichishima T; Saitoh Y; Kai T; Yamamoto T; Ogawa K; Okamoto M; Ikeda K; Maruyama Y Exp Hematol; 2001 Apr; 29(4):391-400. PubMed ID: 11301179 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Heterogeneous PIG-A mutations in different cell lineages in paroxysmal nocturnal hemoglobinuria. Ostendorf T; Nischan C; Schubert J; Grussenmeyer T; Scholz C; Zielinska-Skowronek M; Schmidt RE Blood; 1995 Mar; 85(6):1640-6. PubMed ID: 7888683 [TBL] [Abstract][Full Text] [Related]
10. Efficient retrovirus-mediated PIG-A gene transfer and stable restoration of GPI-anchored protein expression in cells with the PNH phenotype. Nishimura Ji ; Phillips KL; Ware RE; Hall S; Wilson L; Gentry TL; Howard TA; Murakami Y; Shibano M; Machii T; Gilboa E; Kanakura Y; Takeda J; Kinoshita T; Rosse WF; Smith CA Blood; 2001 May; 97(10):3004-10. PubMed ID: 11342424 [TBL] [Abstract][Full Text] [Related]
11. Glycosylphosphatidylinositol-anchor-deficient mice: implications for clonal dominance of mutant cells in paroxysmal nocturnal hemoglobinuria. Kawagoe K; Kitamura D; Okabe M; Taniuchi I; Ikawa M; Watanabe T; Kinoshita T; Takeda J Blood; 1996 May; 87(9):3600-6. PubMed ID: 8611683 [TBL] [Abstract][Full Text] [Related]
12. Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene. Bessler M; Mason PJ; Hillmen P; Miyata T; Yamada N; Takeda J; Luzzatto L; Kinoshita T EMBO J; 1994 Jan; 13(1):110-7. PubMed ID: 8306954 [TBL] [Abstract][Full Text] [Related]
13. Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria. Miyata T; Yamada N; Iida Y; Nishimura J; Takeda J; Kitani T; Kinoshita T N Engl J Med; 1994 Jan; 330(4):249-55. PubMed ID: 8272086 [TBL] [Abstract][Full Text] [Related]
14. Characterization of genomic PIG-A gene: a gene for glycosylphosphatidylinositol-anchor biosynthesis and paroxysmal nocturnal hemoglobinuria. Iida Y; Takeda J; Miyata T; Inoue N; Nishimura J; Kitani T; Maeda K; Kinoshita T Blood; 1994 Jun; 83(11):3126-31. PubMed ID: 8193350 [TBL] [Abstract][Full Text] [Related]
15. Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals. Araten DJ; Nafa K; Pakdeesuwan K; Luzzatto L Proc Natl Acad Sci U S A; 1999 Apr; 96(9):5209-14. PubMed ID: 10220445 [TBL] [Abstract][Full Text] [Related]
16. The small population of PIG-A mutant cells in myelodysplastic syndromes do not arise from multipotent hematopoietic stem cells. Pu JJ; Hu R; Mukhina GL; Carraway HE; McDevitt MA; Brodsky RA Haematologica; 2012 Aug; 97(8):1225-33. PubMed ID: 22315493 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Paroxysmal nocturnal hemoglobinuria: the price for a chance. Bessler M Schweiz Med Wochenschr; 1996 Nov; 126(45):1912-21. PubMed ID: 8946596 [TBL] [Abstract][Full Text] [Related]
19. [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]
20. 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] [Next] [New Search]