Hayashi K - Search Results

1

Precise estimation of allele frequencies of single-nucleotide polymorphisms by a quantitative SSCP analysis of pooled DNA.

Sasaki T, Tahira T, Suzuki A, Higasa K, Kukita Y, Baba S, Hayashi K. Sasaki T, et al. Among authors: hayashi k. Am J Hum Genet. 2001 Jan;68(1):214-8. doi: 10.1086/316928. Epub 2000 Nov 14. Am J Hum Genet. 2001. PMID: 11083945 Free PMC article.

2

Single-stranded conformational polymorphism analysis using automated capillary array electrophoresis apparatuses.

Baba S, Kukita Y, Higasa K, Tahira T, Hayashi K. Baba S, et al. Among authors: hayashi k. Biotechniques. 2003 Apr;34(4):746-50. doi: 10.2144/03344st03. Biotechniques. 2003. PMID: 12703299 Free article.

3

SSCP analysis of long DNA fragments in low pH gel.

Kukita Y, Tahira T, Sommer SS, Hayashi K. Kukita Y, et al. Among authors: hayashi k. Hum Mutat. 1997;10(5):400-7. doi: 10.1002/(SICI)1098-1004(1997)10:5<400::AID-HUMU11>3.0.CO;2-3. Hum Mutat. 1997. PMID: 9375857

4

Delineation of the critical interval for the familial exudative vitreoretinopathy gene by linkage and haplotype analysis.

Kondo H, Ohno K, Tahira T, Hayashi H, Oshima K, Hayashi K. Kondo H, et al. Among authors: hayashi k, hayashi h. Hum Genet. 2001 May;108(5):368-75. doi: 10.1007/s004390100503. Hum Genet. 2001. PMID: 11409862

5

SSCP analysis of point mutations by multicolor capillary electrophoresis.

Hayashi K, Wenz HM, Inazuka M, Tahira T, Sasaki T, Atha DH. Hayashi K, et al. Methods Mol Biol. 2001;163:109-26. doi: 10.1385/1-59259-116-7:109. Methods Mol Biol. 2001. PMID: 11242937 No abstract available.

6

One-tube post-PCR fluorescent labeling of DNA fragments.

Inazuka M, Tahira T, Hayashi K. Inazuka M, et al. Among authors: hayashi k. Genome Res. 1996 Jun;6(6):551-7. doi: 10.1101/gr.6.6.551. Genome Res. 1996. PMID: 8828044 Free article.

7

A streamlined mutation detection system: multicolor post-PCR fluorescence labeling and single-strand conformational polymorphism analysis by capillary electrophoresis.

Inazuka M, Wenz HM, Sakabe M, Tahira T, Hayashi K. Inazuka M, et al. Among authors: hayashi k. Genome Res. 1997 Nov;7(11):1094-103. doi: 10.1101/gr.7.11.1094. Genome Res. 1997. PMID: 9371745 Free PMC article.

8

ATM mutations in patients with ataxia telangiectasia screened by a hierarchical strategy.

Sasaki T, Tian H, Kukita Y, Inazuka M, Tahira T, Imai T, Yamauchi M, Saito T, Hori T, Hashimoto-Tamaoki T, Komatsu K, Nikaido O, Hayashi K. Sasaki T, et al. Among authors: hayashi k. Hum Mutat. 1998;12(3):186-95. doi: 10.1002/(SICI)1098-1004(1998)12:3<186::AID-HUMU6>3.0.CO;2-F. Hum Mutat. 1998. PMID: 9711876

9

[Methods for large-scale analyses of human genome diversity].

Kukita Y, Hayashi K. Kukita Y, et al. Among authors: hayashi k. Tanpakushitsu Kakusan Koso. 2001 Dec;46(16 Suppl):2283-8. Tanpakushitsu Kakusan Koso. 2001. PMID: 11802380 Review. Japanese. No abstract available.

10

Adult onset globoid cell leukodystrophy (Krabbe disease): analysis of galactosylceramidase cDNA from four Japanese patients.

Furuya H, Kukita Y, Nagano S, Sakai Y, Yamashita Y, Fukuyama H, Inatomi Y, Saito Y, Koike R, Tsuji S, Fukumaki Y, Hayashi K, Kobayashi T. Furuya H, et al. Among authors: hayashi k. Hum Genet. 1997 Sep;100(3-4):450-6. doi: 10.1007/s004390050532. Hum Genet. 1997. PMID: 9272171

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