Nishiyama K - Search Results

1

Role of platelet-activating factor acetylhydrolase gene mutation in Japanese childhood IgA nephropathy.

Tanaka R, Iijima K, Xu H, Inoue Y, Murakami R, Shirakawa T, Nishiyama K, Miwa M, Shiozawa S, Nakamura H, Yoshikawa N. Tanaka R, et al. Among authors: nishiyama k. Am J Kidney Dis. 1999 Aug;34(2):289-95. doi: 10.1016/s0272-6386(99)70357-4. Am J Kidney Dis. 1999. PMID: 10430976

2

Platelet-activating factor acetylhydrolase gene mutation in Japanese nephrotic children.

Xu H, Iijima K, Shiozawa S, Tanaka SS, Inoue Y, Shirakawa T, Nishiyama K, Miwa M, Nakamura H, Yoshikawa N. Xu H, et al. Among authors: nishiyama k. Kidney Int. 1998 Dec;54(6):1867-71. doi: 10.1046/j.1523-1755.1998.00215.x. Kidney Int. 1998. PMID: 9853251 Free article.

3

Detection of mutations in the COL4A5 gene in over 90% of male patients with X-linked Alport's syndrome by RT-PCR and direct sequencing.

Inoue Y, Nishio H, Shirakawa T, Nakanishi K, Nakamura H, Sumino K, Nishiyama K, Iijima K, Yoshikawa N. Inoue Y, et al. Among authors: nishiyama k. Am J Kidney Dis. 1999 Nov;34(5):854-62. doi: 10.1016/S0272-6386(99)70042-9. Am J Kidney Dis. 1999. PMID: 10561141

4

Molecular basis of glucose-6-phosphate dehydrogenase deficiency among Filipinos.

Silao CL, Shirakawa T, Nishiyama K, Padilla C, Matsuo M. Silao CL, et al. Among authors: nishiyama k. Pediatr Int. 1999 Apr;41(2):138-41. doi: 10.1046/j.1442-200x.1999.4121035.x. Pediatr Int. 1999. PMID: 10221015

5

A comprehensive method to scan for point mutations of the glucose 6 phosphate dehydrogenase gene.

Shirakawa T, Nishiyama K, Lai PS, Matsuo M. Shirakawa T, et al. Among authors: nishiyama k. Jpn J Hum Genet. 1997 Sep;42(3):417-23. doi: 10.1007/BF02766942. Jpn J Hum Genet. 1997. PMID: 12503188

6

Comparison of insertion rate of L1 retroposon into intron 30 of the neurofibromatosis type 1 gene in seven Asian and Pacific populations.

Shirakawa T, Nishiyama K, Poh-San L, Ishida T, Matsuo M. Shirakawa T, et al. Among authors: nishiyama k. Jpn J Hum Genet. 1996 Mar;41(1):209-14. doi: 10.1007/BF01892629. Jpn J Hum Genet. 1996. PMID: 8914637

7

[Mutation detection by PCR-TGGE].

Shirakawa T, Nishiyama K, Matsuo M. Shirakawa T, et al. Among authors: nishiyama k. Rinsho Byori. 1995 Jul;43(7):679-85. Rinsho Byori. 1995. PMID: 7674540 Japanese.

8

Two new variants of G6PD deficiencies in Singapore.

Hamada M, Shirakawa T, Poh-San L, Nishiyama K, Uga S, Matsuo M. Hamada M, et al. Among authors: nishiyama k. Nepal Med Coll J. 2010 Sep;12(3):137-41. Nepal Med Coll J. 2010. PMID: 21446359

9

Introducing a point mutation identified in a patient with pituitary resistance to thyroid hormone (Arg 338 to Trp) into other mutant thyroid hormone receptors weakens their dominant negative activities.

Ando S, Nakamura H, Sasaki S, Nishiyama K, Kitahara A, Nagasawa S, Mikami T, Natsume H, Genma R, Yoshimi T. Ando S, et al. Among authors: nishiyama k. J Endocrinol. 1996 Nov;151(2):293-300. doi: 10.1677/joe.0.1510293. J Endocrinol. 1996. PMID: 8958790

10

Difference in dominant negative activities between mutant thyroid hormone receptors alpha1 and beta1 with an identical truncation in the extreme carboxyl-terminal tau4 domain.

Nishiyama K, Andoh S, Kitahara A, Natsume H, Mikami T, Genma R, Nakamura H. Nishiyama K, et al. Mol Cell Endocrinol. 1998 Mar 16;138(1-2):95-104. doi: 10.1016/s0303-7207(98)00014-8. Mol Cell Endocrinol. 1998. PMID: 9685218

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