医中誌リンクサービス


文献リスト

1) Nishimura J, Kanakura Y, Ware RE, et al. Clinical course and flow cytometric analysis of paroxysmal nocturnal hemoglobinuria in the United States and Japan. Medicine (Baltimore). 2004; 83: 193-207
PubMed CrossRef
医中誌リンクサービス
2) Parker C, Omine M, Richards S, et al. Diagnosis and management of paroxysmal nocturnal hemoglobinuria. Blood. 2005; 106: 3699-709
PubMed CrossRef
医中誌リンクサービス
3) Almeida AM, Murakami Y, Layton DM, et al. Hypomorphic promoter mutation in PIGM causes inherited glycosylphosphatidylinositol deficiency. Nat Med. 2006; 12: 846-51
PubMed CrossRef
医中誌リンクサービス
4) Tanaka S, Maeda Y, Tashima Y, et al. Inositol deacylation of glycosylphosphatidylinositol-anchored proteins is mediated by mammalian PGAP1 and yeast Bst1p. J Biol Chem. 2004; 279: 14256-63
PubMed CrossRef
医中誌リンクサービス
5) Tashima Y, Taguchi R, Murata C, et al. PGAP2 is essential for correct processing and stable expression of GPI-anchored proteins. Mol Biol Cell. 2006; 17: 1410-20
PubMed
医中誌リンクサービス
6) Maeda Y, Tashima Y, Houjou T, et al. Fatty acid remodeling of GPI-anchored proteins is required for their raft association. Mol Biol Cell. 2007; 18: 1497-506
PubMed CrossRef
医中誌リンクサービス
7) Kawagoe K, Kitamura D, Okabe M, et al. GPI-anchor deficient mice: Implications for clonal dominance of mutant cells in paroxysmal nocturnal hemoglobinuria. Blood. 1996; 87: 3600-6
PubMed
医中誌リンクサービス
8) Takeda J, Miyata T, Kawagoe K, et al. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell. 1993; 73: 703-11
PubMed CrossRef
医中誌リンクサービス
9) Murakami Y, Siripanyaphinyo U, Hong Y, et al. The initial enzyme for glycosylphosphatidylinositol biosynthesis requires PIG-Y, a seventh component. Mol Biol Cell. 2005; 16: 5236-46
PubMed CrossRef
医中誌リンクサービス
10) Maeda Y, Watanabe R, Harris CL, et al. PIG-M transfers the first mannose to glycosylphosphatidylinositol on the lumenal side of the ER. EMBO J. 2001; 20: 250-61
PubMed CrossRef
医中誌リンクサービス
11) Maeda Y, Tanaka S, Hino J, et al. Human dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3. EMBO J. 2000; 19: 2475-82
PubMed CrossRef
医中誌リンクサービス
12) Dancourt J, Vuillaumier-Barrot S, de Baulny HO, et al. A new intronic mutation in the DPM1 gene is associated with a milder form of CDG Ie in two French siblings. Pediatr Res. 2006; 59: 835-9
PubMed CrossRef
医中誌リンクサービス
13) Schenk B, Imbach T, Frank CG, et al. MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If. J Clin Invest. 2001; 108: 1687-95
PubMed CrossRef
医中誌リンクサービス
14) Maeda Y, Ashida H, Kinoshita T. CHO glycosylation mutants: GPI anchor. Methods Enzymol. 2006; 416: 182-205
PubMed CrossRef
医中誌リンクサービス
15) Araten DJ, Nafa K, Pakdeesuwan K, et al. Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals. Proc Natl Acad Sci U S A. 1999; 96: 5209-14
PubMed CrossRef
医中誌リンクサービス
16) Hu R, Mukhina GL, Piantadosi S, et al. PIG-A mutations in normal hematopoiesis. Blood. 2005; 105: 3848-54
PubMed CrossRef
医中誌リンクサービス
17) Rosti V, Tremmi G, Soares V, et al. Murine embryonic stem cells without pig-a gene activity are competent for hematopoiesis with the PNH phenotype but not for clonal expansion. J Clin Invest. 1997; 100: 1028-36
PubMed
医中誌リンクサービス
18) Murakami Y, Kinoshita T, Maeda Y, et al. Different roles of glycosylphosphatidylinositol in various hematopoietic cells as revealed by model mice of paroxysmal nocturnal hemoglobinuria. Blood. 1999; 94: 2963-70
PubMed
医中誌リンクサービス
19) Tremml G, Dominguez C, Rosti V, et al. Increased sensitivity to complement and a decreased red cell life span in mice mosaic for a non-functional Piga gene. Blood. 1999; 94: 2945-54
PubMed
医中誌リンクサービス
20) Keller P, Tremml G, Rosti V, et al. X inactivation and somatic cell selection rescue female mice carrying a Piga-null mutation. Proc Natl Acad Sci U S A. 1999; 96: 7479-83
PubMed CrossRef
医中誌リンクサービス
21) Azenishi Y, Ueda E, Machii T, et al. CD59-deficient blood cells and PIG-A gene abnormalities in Japanese patients with aplastic anaemia. Br J Haematol. 1999; 104: 523-9
PubMed CrossRef
医中誌リンクサービス
22) Dunn DE, Tanawattanacharoen P, Boccuni P, et al. Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes. Ann Intern Med. 1999; 131: 401-8
PubMed
医中誌リンクサービス
23) Wang H, Chuhjo T, Yamazaki H, et al. Relative increase of granulocytes with a paroxysmal nocturnal haemoglobinuria phenotype in aplastic anaemia patients: the high prevalence at diagnosis. Eur J Haematol. 2001; 66: 200-5
PubMed CrossRef
医中誌リンクサービス
24) Wang H, Chuhjo T, Yasue S, et al. Clinical significance of a minor population of paroxysmal nocturnal hemoglobinuria-type cells in bone marrow failure syndrome. Blood. 2002; 100: 3897-902
PubMed CrossRef
医中誌リンクサービス
25) Sugimori C, Chuhjo T, Feng X, et al. Minor population of CD55-CD59- blood cells predicts response to immunosuppressive therapy and prognosis in patients with aplastic anemia. Blood. 2006; 107: 1308-14
PubMed CrossRef
医中誌リンクサービス
26) Maciejewski JP, Follmann D, Nakamura R, et al. Increased frequency of HLA-DR2 in patients with paroxysmal nocturnal hemoglobinuria and the PNH/aplastic anemia syndrome. Blood. 2001; 98: 3513-9
PubMed CrossRef
医中誌リンクサービス
27) Shichishima T, Okamoto M, Ikeda K, et al. HLA class II haplotype and quantitation of WT1 RNA in Japanese patients with paroxysmal nocturnal hemoglobinuria. Blood. 2002; 100: 22-8
PubMed CrossRef
医中誌リンクサービス
28) Karadimitris A, Manavalan JS, Thaler HT, et al. Abnormal T-cell repertoire is consistent with immune process underlying the pathogenesis of paroxysmal nocturnal hemoglobinuria. Blood. 2000; 96: 2613-20
PubMed
医中誌リンクサービス
29) Murakami Y, Kosaka H, Maeda Y, et al. Inefficient response of T lymphocytes to GPI-anchor-negative cells: implications for paroxysmal nocturnal hemoglobinuria. Blood. 2002; 100: 4116-22
PubMed CrossRef
医中誌リンクサービス
30) Feng X, Chuhjo T, Sugimori C, et al. Diazepam-binding inhibitor-related protein 1: a candidate autoantigen in acquired aplastic anemia patients harboring a minor population of paroxysmal nocturnal hemoglobinuria-type cells. Blood. 2004; 104: 2425-31
PubMed CrossRef
医中誌リンクサービス
31) Takamatsu H, Feng X, Chuhjo T, et al. Specific antibodies to moesin, a membrane-cytoskeleton linker protein, are frequently detected in patients with acquired aplastic anemia. Blood. 2007; 109: 2514-20
PubMed CrossRef
医中誌リンクサービス
32) Risitano AM, Kook H, Zeng W, et al. Oligoclonal and polyclonal CD4 and CD8 lymphocytes in aplastic anemia and paroxysmal nocturnal hemoglobinuria measured by V beta CDR3 spectratyping and flow cytometry. Blood. 2002; 100: 178-83
PubMed CrossRef
医中誌リンクサービス
33) Poggi A, Negrini S, Zocchi MR, et al. Patients with paroxysmal nocturnal hemoglobinuria have a high frequency of peripheral-blood T cells expressing activating isoforms of inhibiting superfamily receptors. Blood. 2005; 106: 2399-408
PubMed CrossRef
医中誌リンクサービス
34) Gargiulo L, Lastraioli S, Cerruti G, et al. Highly homologous T-cell receptor beta sequences support a common target for autoreactive T cells in most patients with paroxysmal nocturnal hemoglobinuria. Blood. 2007; 109: 5036-42
PubMed CrossRef
医中誌リンクサービス
35) Nagakura S, Ishihara S, Dunn DE, et al. Decreased susceptibility of leukemic cells with PIG-A mutation to natural killer cells in vitro. Blood. 2002; 100: 1031-7
PubMed CrossRef
医中誌リンクサービス
36) Hanaoka N, Kawaguchi T, Horikawa K, et al. Immunoselection by natural killer cells of PIGA mutant cells missing stress-inducible ULBP. Blood. 2006; 107: 1184-91
PubMed
医中誌リンクサービス
37) Nishimura J, Inoue N, Wada H, et al. A patient with paroxysmal nocturnal hemoglobinuria bearing four independent PIG-A mutant clones. Blood. 1997; 89: 3470-6
PubMed
医中誌リンクサービス
38) Borrmann L, Wilkening S, Bullerdiek J. The expression of HMGA genes is regulated by their 3'UTR. Oncogene. 2001; 20: 4537-41
PubMed CrossRef
医中誌リンクサービス
39) Mayr C, Hemann MT, Bartel DP. Disrupting the pairing between let-7 and Hmga2 enhances oncogenic transformation. Science. 2007; 315: 1576-9
PubMed CrossRef
医中誌リンクサービス
40) Inoue N, Izui-Sarumaru T, Murakami Y, et al. Molecular basis of clonal expansion of hematopoiesis in 2 patients with paroxysmal nocturnal hemoglobinuria (PNH). Blood. 2006; 108: 4232-6
PubMed CrossRef
医中誌リンクサービス
41) Hess JL, Kossev P. Molecular genetics of benign tumors. Cancer Invest. 2002; 20: 362-72
PubMed CrossRef
医中誌リンクサービス
42) Reeves R. Molecular biology of HMGA proteins: hubs of nuclear function. Gene. 2001; 277: 63-81
PubMed CrossRef
医中誌リンクサービス
43) Schoenmakers EF, Wanschura S, Mols R, et al. Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours. Nat Genet. 1995; 10: 436-44
PubMed CrossRef
医中誌リンクサービス
44) Fedele M, Battista S, Manfioletti G, et al. Role of the high mobility group A proteins in human lipomas. Carcinogenesis. 2001; 22: 1583-91
PubMed CrossRef
医中誌リンクサービス
45) Fedele M, Battista S, Kenyon L, et al. Overexpression of the HMGA2 gene in transgenic mice leads to the onset of pituitary adenomas. Oncogene. 2002; 21: 3190-8
PubMed CrossRef
医中誌リンクサービス
46) Ligon AH, Moore SD, Parisi MA, et al. Constitutional rearrangement of the architectural factor HMGA2: a novel human phenotype including overgrowth and lipomas. Am J Hum Genet. 2005; 76: 340-8
PubMed CrossRef
医中誌リンクサービス
47) Andrieux J, Demory JL, Dupriez B, et al. Dysregulation and overexpression of HMGA2 in myelofibrosis with myeloid metaplasia. Genes Chromosomes Cancer. 2004; 39: 82-7
PubMed CrossRef
医中誌リンクサービス
48) Odero MD, Grand FH, Iqbal S, et al. Disruption and aberrant expression of HMGA2 as a consequence of diverse chromosomal translocations in myeloid malignancies. Leukemia. 2005; 19: 245-52
PubMed CrossRef
医中誌リンクサービス
49) Ikeda K, Shichishima T, Yasukawa M, et al. The role of Wilms' tumor gene peptide-specific cytotoxic T lymphocytes in immunologic selection of a paroxysmal nocturnal hemoglobinuria clone. Exp Hematol. 2007; 35: 618-26
PubMed CrossRef
医中誌リンクサービス
50) Li L, He S, Sun JM, et al. Gene regulation by Sp1 and Sp3. Biochem Cell Biol. 2004; 82: 460-71
PubMed CrossRef
医中誌リンクサービス
51) Bouwman P, Philipsen S. Regulation of the activity of Sp1-related transcription factors. Mol Cell Endocrinol. 2002; 195: 27-38
PubMed CrossRef
医中誌リンクサービス
52) Davie JR. Inhibition of histone deacetylase activity by butyrate. J Nutr. 2003; 133: 2485S-93S
医中誌リンクサービス
53) Almeida AM, Murakami Y, Baker A, et al. Targeted therapy for inherited GPI deficiency. N Engl J Med. 2007; 356: 1641-7
PubMed CrossRef
医中誌リンクサービス
54) Hillmen P, Young NS, Schubert J, et al. The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria. N Engl J Med. 2006; 355: 1233-43
PubMed CrossRef
医中誌リンクサービス


NPO医学中央雑誌刊行会
https://www.jamas.or.jp/
info@jamas.or.jp