These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
176 related articles for article (PubMed ID: 25293775)
21. Immunophenotypic discrepancies between granulocytic and erythroid lineages in peripheral blood of patients with paroxysmal nocturnal haemoglobinuria. Pakdeesuwan K; Wanachiwanawin W; Siripanyaphinyo U; Pattanapanyasat K; Wilairat P; Issaragrisil S Eur J Haematol; 2000 Jul; 65(1):8-16. PubMed ID: 10914934 [TBL] [Abstract][Full Text] [Related]
22. Deficient surface expression of glycosylphosphatidylinositol-anchored proteins in B cell lines established from patients with paroxysmal nocturnal hemoglobinuria. Ueda E; Nishimura J; Kitani T; Nasu K; Kageyama T; Kim YU; Takeda J; Kinoshita T Int Immunol; 1992 Nov; 4(11):1263-71. PubMed ID: 1282030 [TBL] [Abstract][Full Text] [Related]
23. Role of Torres-Valdetano Á; Vallejo-Ruiz V; Milflores-Flores L; Martínez-Morales P Biomed Rep; 2024 Apr; 20(4):57. PubMed ID: 38414627 [TBL] [Abstract][Full Text] [Related]
24. Paroxysmal nocturnal hemoglobinuria as a molecular disease. Rosse WF Medicine (Baltimore); 1997 Mar; 76(2):63-93. PubMed ID: 9100736 [TBL] [Abstract][Full Text] [Related]
25. Regulation of transcription of the human erythropoietin receptor gene by proteins binding to GATA-1 and Sp1 motifs. Chin K; Oda N; Shen K; Noguchi CT Nucleic Acids Res; 1995 Aug; 23(15):3041-9. PubMed ID: 7659529 [TBL] [Abstract][Full Text] [Related]
26. [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]
27. A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGT. Kvarnung M; Nilsson D; Lindstrand A; Korenke GC; Chiang SC; Blennow E; Bergmann M; Stödberg T; Mäkitie O; Anderlid BM; Bryceson YT; Nordenskjöld M; Nordgren A J Med Genet; 2013 Aug; 50(8):521-8. PubMed ID: 23636107 [TBL] [Abstract][Full Text] [Related]
28. Paroxysmal nocturnal haemoglobinuria: a replacement of haematopoietic tissue? Schrezenmeier H; Hildebrand A; Rojewski M; Häcker H; Heimpel H; Raghavachar A Acta Haematol; 2000; 103(1):41-8. PubMed ID: 10705158 [TBL] [Abstract][Full Text] [Related]
29. The leukemia associated nuclear corepressor ETO homologue genes MTG16 and MTGR1 are regulated differently in hematopoietic cells. Ajore R; Kumar P; Dhanda RS; Gullberg U; Olsson I BMC Mol Biol; 2012 Mar; 13():11. PubMed ID: 22443175 [TBL] [Abstract][Full Text] [Related]
30. Roles of USF, Ikaros and Sp proteins in the transcriptional regulation of the human reduced folate carrier B promoter. Liu M; Whetstine JR; Payton SG; Ge Y; Flatley RM; Matherly LH Biochem J; 2004 Oct; 383(Pt 2):249-57. PubMed ID: 15214842 [TBL] [Abstract][Full Text] [Related]
31. Paroxysmal nocturnal hemoglobinuria: An acquired genetic disease. Nishimura J; Murakami Y; Kinoshita T Am J Hematol; 1999 Nov; 62(3):175-82. PubMed ID: 10539884 [TBL] [Abstract][Full Text] [Related]
32. Compound heterozygous mutations in the gene PIGP are associated with early infantile epileptic encephalopathy. Johnstone DL; Nguyen TT; Murakami Y; Kernohan KD; Tétreault M; Goldsmith C; Doja A; Wagner JD; Huang L; Hartley T; St-Denis A; le Deist F; Majewski J; Bulman DE; ; Kinoshita T; Dyment DA; Boycott KM; Campeau PM Hum Mol Genet; 2017 May; 26(9):1706-1715. PubMed ID: 28334793 [TBL] [Abstract][Full Text] [Related]
33. Phenotypic and functional analysis of lymphocytes in paroxysmal nocturnal hemoglobinuria. Tseng JE; Hall SE; Howard TA; Ware RE Am J Hematol; 1995 Dec; 50(4):244-53. PubMed ID: 7485098 [TBL] [Abstract][Full Text] [Related]
34. Recent advances in the diagnosis, monitoring, and management of patients with paroxysmal nocturnal hemoglobinuria. Richards SJ; Hill A; Hillmen P Cytometry B Clin Cytom; 2007 Sep; 72(5):291-8. PubMed ID: 17549742 [TBL] [Abstract][Full Text] [Related]
36. Immunophenotypic analysis of B cells in PNH: insights into the generation of circulating naive and memory B cells. Richards SJ; Morgan GJ; Hillmen P Blood; 2000 Nov; 96(10):3522-8. PubMed ID: 11071650 [TBL] [Abstract][Full Text] [Related]