Similar articles for PMID: 8426120

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1994	10
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1

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

Takahashi M, Takeda J, Hirose S, Hyman R, Inoue N, Miyata T, Ueda E, Kitani T, Medof ME, Kinoshita T. Takahashi M, et al. J Exp Med. 1993 Feb 1;177(2):517-21. doi: 10.1084/jem.177.2.517. J Exp Med. 1993. PMID: 8426120 Free PMC article.

2

Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuria.

Hillmen P, Bessler M, Mason PJ, Watkins WM, Luzzatto L. Hillmen P, et al. Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5272-6. doi: 10.1073/pnas.90.11.5272. Proc Natl Acad Sci U S A. 1993. PMID: 8389477 Free PMC article.

3

Glycosyl-phosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria: partial or complete defect in an early step.

Norris J, Hall S, Ware RE, Kamitani T, Chang HM, Yeh E, Rosse WF. Norris J, et al. Blood. 1994 Feb 1;83(3):816-21. Blood. 1994. PMID: 7507735 Free article.

4

[Mutations in the PIG-A gene lead to GPI-deficiency in paroxysmal nocturnal hemoglobinuria].

Ostendorf T, Schubert J, Schmidt RE. Ostendorf T, et al. Immun Infekt. 1994 Aug;22(4):154-5. Immun Infekt. 1994. PMID: 7927481 German.

5

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.

Armstrong C, Schubert J, Ueda E, Knez JJ, Gelperin D, Hirose S, Silber R, Hollan S, Schmidt RE, Medof ME. Armstrong C, et al. J Biol Chem. 1992 Dec 15;267(35):25347-51. J Biol Chem. 1992. PMID: 1460030 Free article.

6

Preferential expression of human Fc gamma RIIIPMN (CD16) in paroxysmal nocturnal hemoglobinuria. Discordant expression of glycosyl phosphatidylinositol-linked proteins.

Edberg JC, Salmon JE, Whitlow M, Kimberly RP. Edberg JC, et al. J Clin Invest. 1991 Jan;87(1):58-67. doi: 10.1172/JCI115001. J Clin Invest. 1991. PMID: 1702101 Free PMC article.

7

Paroxysmal nocturnal hemoglobinuria: the price for a chance.

Bessler M. Bessler M. Schweiz Med Wochenschr. 1996 Nov 9;126(45):1912-21. Schweiz Med Wochenschr. 1996. PMID: 8946596 Review.

8

Glycosyl phosphatidylinositol (GPI)-anchored molecules and the pathogenesis of paroxysmal nocturnal hemoglobinuria.

Boccuni P, Del Vecchio L, Di Noto R, Rotoli B. Boccuni P, et al. Crit Rev Oncol Hematol. 2000 Jan;33(1):25-43. doi: 10.1016/s1040-8428(99)00052-9. Crit Rev Oncol Hematol. 2000. PMID: 10714960 Review.

9

Assembly and deacetylation of N-acetylglucosaminyl-plasmanylinositol in normal and affected paroxysmal nocturnal hemoglobinuria cells.

Hirose S, Ravi L, Hazra SV, Medof ME. Hirose S, et al. Proc Natl Acad Sci U S A. 1991 May 1;88(9):3762-6. doi: 10.1073/pnas.88.9.3762. Proc Natl Acad Sci U S A. 1991. PMID: 1708886 Free PMC article.

10

Chromosomal assignment of genes involved in glycosylphosphatidylinositol anchor biosynthesis: implications for the pathogenesis of paroxysmal nocturnal hemoglobinuria.

Ware RE, Howard TA, Kamitani T, Chang H-M, Yeh ETH, Seldin MF. Ware RE, et al. Blood. 1994 Jun 15;83(12):3753-7. Blood. 1994. PMID: 8204896 Free article.

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