Literature DB >> 7520848

The genetic defect of PNH.

T Kinoshita1.   

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Year:  1994        PMID: 7520848      PMCID: PMC1550361          DOI: 10.1111/j.1365-2249.1994.tb06253.x

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


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  12 in total

Review 1.  How to make a glycoinositol phospholipid anchor.

Authors:  A M Tartakoff; N Singh
Journal:  Trends Biochem Sci       Date:  1992-11       Impact factor: 13.807

2.  The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis.

Authors:  T Miyata; J Takeda; Y Iida; N Yamada; N Inoue; M Takahashi; K Maeda; T Kitani; T Kinoshita
Journal:  Science       Date:  1993-02-26       Impact factor: 47.728

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

Authors:  J Norris; S Hall; R E Ware; T Kamitani; H M Chang; E Yeh; W F Rosse
Journal:  Blood       Date:  1994-02-01       Impact factor: 22.113

4.  Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria.

Authors:  T Miyata; N Yamada; Y Iida; J Nishimura; J Takeda; T Kitani; T Kinoshita
Journal:  N Engl J Med       Date:  1994-01-27       Impact factor: 91.245

5.  Impaired glycosylation of glycosylphosphatidylinositol-anchor synthesis in paroxysmal nocturnal hemoglobinuria leucocytes.

Authors:  M Hidaka; S Nagakura; K Horikawa; T Kawaguchi; N Iwamoto; T Kagimoto; K Takatsuki; H Nakakuma
Journal:  Biochem Biophys Res Commun       Date:  1993-03-15       Impact factor: 3.575

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

Authors:  P Hillmen; M Bessler; P J Mason; W M Watkins; L Luzzatto
Journal:  Proc Natl Acad Sci U S A       Date:  1993-06-01       Impact factor: 11.205

7.  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.

Authors:  C Armstrong; J Schubert; E Ueda; J J Knez; D Gelperin; S Hirose; R Silber; S Hollan; R E Schmidt; M E Medof
Journal:  J Biol Chem       Date:  1992-12-15       Impact factor: 5.157

8.  Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria.

Authors:  J Takeda; T Miyata; K Kawagoe; Y Iida; Y Endo; T Fujita; M Takahashi; T Kitani; T Kinoshita
Journal:  Cell       Date:  1993-05-21       Impact factor: 41.582

9.  Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene.

Authors:  M Bessler; P J Mason; P Hillmen; T Miyata; N Yamada; J Takeda; L Luzzatto; T Kinoshita
Journal:  EMBO J       Date:  1994-01-01       Impact factor: 11.598

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

Authors:  M Takahashi; J Takeda; S Hirose; R Hyman; N Inoue; T Miyata; E Ueda; T Kitani; M E Medof; T Kinoshita
Journal:  J Exp Med       Date:  1993-02-01       Impact factor: 14.307

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