E Ueda

Inherited Complete Deficiency of 20-Kilodalton Homologous Restriction Factor (CD59) as a Cause of Paroxysmal Nocturnal Hemoglobinuria

Manabu Yamashina, E Ueda, Taroh Kinoshita et al. · New England Journal of Medicine · 1990 · 362 citations · Full text

Medicine, Genetics, Hematology +17

Deficient biosynthesis of N-acetylglucosaminyl-phosphatidylinositol, the first intermediate of glycosyl phosphatidylinositol anchor biosynthesis, in cell lines established from patients with paroxysmal nocturnal hemoglobinuria.

Minoru Takahashi, Junji Takeda, Shinichi Hirose et al. · The Journal of Experimental Medicine · 1993 · 190 citations · Full text

Life Sciences, Biochemistry, Cell Biology +13

Characterization of putative glycoinositol phospholipid anchor precursors in mammalian cells. Localization of phosphoethanolamine.

Shinichi Hirose, G. M. Shazzad Hossain Prince, Daniel Sevlever et al. · Journal of Biological Chemistry · 1992 · 134 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17

CT appearance of pulmonary tuberculosis in diabetic and immunocompromised patients: comparison with patients who had no underlying disease.

J Ikezoe, Naoko Takeuchi, Takeshi Johkoh et al. · American Journal of Roentgenology · 1992 · 120 citations · Full text

Medicine, Internal Medicine, Radiology +14

Affected paroxysmal nocturnal hemoglobinuria T lymphocytes harbor a common defect in assembly of N-acetyl-D-glucosamine inositol phospholipid corresponding to that in class A Thy-1- murine lymphoma mutants.

Claudia Armstrong, Jörg Schubert, E Ueda et al. · Journal of Biological Chemistry · 1992 · 114 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +13