Ikeda H - Search Results

1

Molecular analysis of dihydropteridine reductase deficiency: identification of two novel mutations in Japanese patients.

Ikeda H, Matsubara Y, Mikami H, Kure S, Owada M, Gough T, Smooker PM, Dobbs M, Dahl HH, Cotton RG, Narisawa K. Ikeda H, et al. Hum Genet. 1997 Oct;100(5-6):637-42. doi: 10.1007/s004390050566. Hum Genet. 1997. PMID: 9341885

2

Prevalence of K329E mutation in the medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards.

Matsubara Y, Narisawa K, Tada K, Ikeda H, Yeqi Y, Danks DM, Green A, McCabe ER. Matsubara Y, et al. Among authors: ikeda h. Prog Clin Biol Res. 1992;375:453-62. Prog Clin Biol Res. 1992. PMID: 1359564 No abstract available.

3

Dried blood spot on filter paper as a source of mRNA.

Matsubara Y, Ikeda H, Endo H, Narisawa K. Matsubara Y, et al. Among authors: ikeda h. Nucleic Acids Res. 1992 Apr 25;20(8):1998. doi: 10.1093/nar/20.8.1998. Nucleic Acids Res. 1992. PMID: 1579508 Free PMC article.

4

Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards.

Matsubara Y, Narisawa K, Tada K, Ikeda H, Yao YQ, Danks DM, Green A, McCabe ER. Matsubara Y, et al. Among authors: ikeda h. Lancet. 1991 Aug 31;338(8766):552-3. doi: 10.1016/0140-6736(91)91110-g. Lancet. 1991. PMID: 1678810

5

The molecular defect in propionic acidemia: exon skipping caused by an 8-bp deletion from an intron in the PCCB allele.

Ohura T, Ogasawara M, Ikeda H, Narisawa K, Tada K. Ohura T, et al. Among authors: ikeda h. Hum Genet. 1993 Oct;92(4):397-402. doi: 10.1007/BF01247343. Hum Genet. 1993. PMID: 8225321

6

Novel mutations of the peripheral myelin protein 22 gene in two pedigrees with Dejerine-Sottas disease.

Ikegami T, Ikeda H, Aoyama M, Matsuki T, Imota T, Fukuuchi Y, Amano T, Toyoshima I, Ishihara Y, Endoh H, Hayasaka K. Ikegami T, et al. Among authors: ikeda h. Hum Genet. 1998 Mar;102(3):294-8. doi: 10.1007/s004390050694. Hum Genet. 1998. PMID: 9544841

7

Novel mutations of the glutaryl-CoA dehydrogenase gene in two Japanese patients with glutaric aciduria type I.

Ikeda H, Kimura T, Ikegami T, Kato M, Matsunaga A, Yokoyama S, Yamaguchi S, Ohura T, Hayasaka K. Ikeda H, et al. Am J Med Genet. 1998 Dec 4;80(4):327-9. Am J Med Genet. 1998. PMID: 9856558

8

Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26.

Ikeda H, Sasaki T, Yoshimoto T, Fukui M, Arinami T. Ikeda H, et al. Am J Hum Genet. 1999 Feb;64(2):533-7. doi: 10.1086/302243. Am J Hum Genet. 1999. PMID: 9973290 Free PMC article.

9

Molecular analysis of lambda bio transducing phage produced by oxolinic acid-induced illegitimate recombination in vivo.

Shimizu H, Yamaguchi H, Ikeda H. Shimizu H, et al. Among authors: ikeda h. Genetics. 1995 Jul;140(3):889-96. doi: 10.1093/genetics/140.3.889. Genetics. 1995. PMID: 7672589 Free PMC article.

10

Effects of uvsX, uvsY and DNA topoisomerase on the formation of tandem duplications of the rII gene in bacteriophage T4.

Kumagai M, Yamashita T, Honda M, Ikeda H. Kumagai M, et al. Among authors: ikeda h. Genetics. 1993 Oct;135(2):255-64. doi: 10.1093/genetics/135.2.255. Genetics. 1993. PMID: 7916730 Free PMC article.

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