Yamauchi M - Search Results

1

Haplotype analysis at the FRAXA locus in the Japanese population.

Richards RI, Kondo I, Holman K, Yamauchi M, Seki N, Kishi K, Staples A, Sutherland GR, Hori T. Richards RI, et al. Among authors: yamauchi m. Am J Med Genet. 1994 Jul 15;51(4):412-6. doi: 10.1002/ajmg.1320510422. Am J Med Genet. 1994. PMID: 7943009

2

Heritable unstable DNA sequences and hypermethylation associated with fragile X syndrome in Japanese families.

Hori T, Yamauchi M, Seki N, Tsuji S, Kondo I. Hori T, et al. Among authors: yamauchi m. Clin Genet. 1993 Jan;43(1):34-8. doi: 10.1111/j.1399-0004.1993.tb04423.x. Clin Genet. 1993. PMID: 8462194

3

Prenatal diagnosis of a hypermethylated full fragile X mutation in chorionic villi of a male fetus.

Suzumori K, Yamauchi M, Seki N, Kondo I, Hori T. Suzumori K, et al. Among authors: yamauchi m. J Med Genet. 1993 Sep;30(9):785-7. doi: 10.1136/jmg.30.9.785. J Med Genet. 1993. PMID: 8411077 Free PMC article.

4

Induction of a BrdU-enhanceable fragile site-like lesion and sister chromatid exchanges at 11q23.1 in EBV-transformed lymphoblastoid cell lines.

Seki N, Tsuji H, Takahashi E, Yamauchi M, Saito T, Hashimoto T, Yamamoto K, Hori T. Seki N, et al. Among authors: yamauchi m. Cytogenet Cell Genet. 1992;61(2):95-8. doi: 10.1159/000133379. Cytogenet Cell Genet. 1992. PMID: 1327661

5

Rapid preparation of diagnostic probes for the fragile X syndrome by direct PCR amplification of human chromosomal DNA.

Yamauchi M, Seki N, Hori T. Yamauchi M, et al. Jpn J Hum Genet. 1992 Sep;37(3):195-203. doi: 10.1007/BF01900713. Jpn J Hum Genet. 1992. PMID: 1472701

6

Cytogenetic and molecular analysis of dynamic mutation associated with fragile X syndrome.

Seki N, Ishikiriyama S, Yamauchi M, Hori T. Seki N, et al. Among authors: yamauchi m. Jpn J Genet. 1994 Jun;69(3):259-67. doi: 10.1266/jjg.69.259. Jpn J Genet. 1994. PMID: 8080657 Free article.

7

Prenatal diagnosis of fragile X syndrome by direct detection of the dynamic mutation due to an unstable DNA sequence.

Yamauchi M, Nagata S, Seki N, Toyama Y, Harada N, Niikawa N, Masuno I, Kajii T, Hori T. Yamauchi M, et al. Clin Genet. 1993 Oct;44(4):169-72. doi: 10.1111/j.1399-0004.1993.tb03873.x. Clin Genet. 1993. PMID: 8261644

8

Sequence tagged sites of microclones obtained by microdissection of a human chromosomal region 11q23 and isolation of yeast artificial chromosomes.

Seki N, Yamauchi M, Saito T, Harada Y, Hori T. Seki N, et al. Among authors: yamauchi m. Jpn J Hum Genet. 1994 Jun;39(2):249-54. doi: 10.1007/BF01876845. Jpn J Hum Genet. 1994. PMID: 8086642

9

[Dynamic mutation and its molecular cytogenetics].

Hori T, Tsuji S, Yamauchi M. Hori T, et al. Among authors: yamauchi m. Nihon Rinsho. 1999 Apr;57(4):771-7. Nihon Rinsho. 1999. PMID: 10222764 Review. Japanese.

10

A distamycin A-inducible fragile site, FRA8E, located in the region of the hereditary multiple exostoses gene, is not involved in HPV16 DNA integration and amplification.

Hori T, Seki N, Ohira M, Saito T, Yamauchi M, Sagara M, Hayashi A, Tsuji S, Ito H, Imai T. Hori T, et al. Among authors: yamauchi m. Cancer Genet Cytogenet. 1998 Feb;101(1):24-34. doi: 10.1016/s0165-4608(97)00222-7. Cancer Genet Cytogenet. 1998. PMID: 9460496

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