Miyata T - Search Results

1

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

Miyata T, Takeda J, Iida Y, Yamada N, Inoue N, Takahashi M, Maeda K, Kitani T, Kinoshita T. Miyata T, et al. Science. 1993 Feb 26;259(5099):1318-20. doi: 10.1126/science.7680492. Science. 1993. PMID: 7680492

2

Expression cloning of genes for GPI-anchor biosynthesis.

Kinoshita T, Takahashi M, Inoue N, Miyata T, Takeda J. Kinoshita T, et al. Among authors: miyata t. Braz J Med Biol Res. 1994 Feb;27(2):127-32. Braz J Med Biol Res. 1994. PMID: 8081220

3

Characterization of genomic PIG-A gene: a gene for glycosylphosphatidylinositol-anchor biosynthesis and paroxysmal nocturnal hemoglobinuria.

Iida Y, Takeda J, Miyata T, Inoue N, Nishimura J, Kitani T, Maeda K, Kinoshita T. Iida Y, et al. Among authors: miyata t. Blood. 1994 Jun 1;83(11):3126-31. Blood. 1994. PMID: 8193350 Free article.

4

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

Miyata T, Yamada N, Iida Y, Nishimura J, Takeda J, Kitani T, Kinoshita T. Miyata T, et al. N Engl J Med. 1994 Jan 27;330(4):249-55. doi: 10.1056/NEJM199401273300404. N Engl J Med. 1994. PMID: 8272086 Free article.

5

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. Among authors: miyata t. 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.

6

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

Takeda J, Miyata T, Kawagoe K, Iida Y, Endo Y, Fujita T, Takahashi M, Kitani T, Kinoshita T. Takeda J, et al. Among authors: miyata t. Cell. 1993 May 21;73(4):703-11. doi: 10.1016/0092-8674(93)90250-t. Cell. 1993. PMID: 8500164

7

Somatic mutations of the PIG-A gene found in Japanese patients with paroxysmal nocturnal hemoglobinuria.

Yamada N, Miyata T, Maeda K, Kitani T, Takeda J, Kinoshita T. Yamada N, et al. Among authors: miyata t. Blood. 1995 Feb 15;85(4):885-92. Blood. 1995. PMID: 7531514 Free article.

8

Expression cloning strategies for glycosylphosphatidylinositol-anchor biosynthesis enzymes and regulators.

Kinoshita T, Miyata T, Inoue N, Takeda J. Kinoshita T, et al. Among authors: miyata t. Methods Enzymol. 1995;250:547-60. doi: 10.1016/0076-6879(95)50096-0. Methods Enzymol. 1995. PMID: 7651177 No abstract available.

9

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

Bessler M, Mason PJ, Hillmen P, Miyata T, Yamada N, Takeda J, Luzzatto L, Kinoshita T. Bessler M, et al. Among authors: miyata t. EMBO J. 1994 Jan 1;13(1):110-7. doi: 10.1002/j.1460-2075.1994.tb06240.x. EMBO J. 1994. PMID: 8306954 Free PMC article.

10

beta 2-Microglobulin modified with advanced glycation end products is a major component of hemodialysis-associated amyloidosis.

Miyata T, Oda O, Inagi R, Iida Y, Araki N, Yamada N, Horiuchi S, Taniguchi N, Maeda K, Kinoshita T. Miyata T, et al. J Clin Invest. 1993 Sep;92(3):1243-52. doi: 10.1172/JCI116696. J Clin Invest. 1993. PMID: 8376584 Free PMC article.

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