Isomura M - Search Results

1

PTPN11, RAS and FLT3 mutations in childhood acute lymphoblastic leukemia.

Yamamoto T, Isomura M, Xu Y, Liang J, Yagasaki H, Kamachi Y, Kudo K, Kiyoi H, Naoe T, Kojma S. Yamamoto T, et al. Among authors: isomura m. Leuk Res. 2006 Sep;30(9):1085-9. doi: 10.1016/j.leukres.2006.02.004. Epub 2006 Mar 14. Leuk Res. 2006. PMID: 16533526

2

Expansion of human CMV-specific cytotoxic T lymphocytes to a clinical scale: a simple culture system using tetrameric HLA-peptide complexes.

Watanabe N, Kamachi Y, Koyama N, Hama A, Liang J, Nakamura Y, Yamamoto T, Isomura M, Kudo K, Kuzushima K, Kojima S. Watanabe N, et al. Among authors: isomura m. Cytotherapy. 2004;6(5):514-22. doi: 10.1080/14653240410005005. Cytotherapy. 2004. PMID: 15512918

3

Methylation status of the p15 and p16 genes in paediatric myelodysplastic syndrome and juvenile myelomonocytic leukaemia.

Hasegawa D, Manabe A, Kubota T, Kawasaki H, Hirose I, Ohtsuka Y, Tsuruta T, Ebihara Y, Goto Y, Zhao XY, Sakashita K, Koike K, Isomura M, Kojima S, Hoshika A, Tsuji K, Nakahata T. Hasegawa D, et al. Among authors: isomura m. Br J Haematol. 2005 Mar;128(6):805-12. doi: 10.1111/j.1365-2141.2005.05392.x. Br J Haematol. 2005. PMID: 15755284 Free article.

4

[Positional cloning of genes responsible for epilepsy and autism using a patient with chromosomal translocation].

Isomura M, Nakamura Y. Isomura M, et al. Tanpakushitsu Kakusan Koso. 1997 Dec;42(17 Suppl):2786-90. Tanpakushitsu Kakusan Koso. 1997. PMID: 9455194 Review. Japanese. No abstract available.

5

Allelic frequencies of twelve dinucleotide repeat marker loci on chromosome 13 in the normal Japanese population.

Yamane Y, Nakamura Y, Isomura M. Yamane Y, et al. Among authors: isomura m. Jpn J Hum Genet. 1997 Dec;42(4):533-7. doi: 10.1007/BF02767030. Jpn J Hum Genet. 1997. PMID: 9560953

6

Molecular cloning and characterization of two novel genes on chromosome 8p21.3.

Kinjo T, Isomura M, Iwamasa T, Nakamura Y. Kinjo T, et al. Among authors: isomura m. J Hum Genet. 2000;45(1):12-7. doi: 10.1007/s100380050003. J Hum Genet. 2000. PMID: 10697957

7

Isolation and mapping of RAB2L, a human cDNA that encodes a protein homologous to RalGDS.

Isomura M, Okui K, Fujiwara T, Shin S, Nakamura Y. Isomura M, et al. Cytogenet Cell Genet. 1996;74(4):263-5. doi: 10.1159/000134431. Cytogenet Cell Genet. 1996. PMID: 8976381

8

Cloning and mapping of a novel human cDNA homologous to DROER, the enhancer of the Drosophila melanogaster rudimentary gene.

Isomura M, Okui K, Fujiwara T, Shin S, Nakamura Y. Isomura M, et al. Genomics. 1996 Feb 15;32(1):125-7. doi: 10.1006/geno.1996.0086. Genomics. 1996. PMID: 8786099

9

Mutations of the fibroblast growth factor receptor-3 gene in one familial and six sporadic cases of achondroplasia in Japanese patients.

Ikegawa S, Fukushima Y, Isomura M, Takada F, Nakamura Y. Ikegawa S, et al. Among authors: isomura m. Hum Genet. 1995 Sep;96(3):309-11. doi: 10.1007/BF00210413. Hum Genet. 1995. PMID: 7649548

10

Cloning and characterization of human and mouse PROSC (proline synthetase co-transcribed) genes.

Ikegawa S, Isomura M, Koshizuka Y, Nakamura Y. Ikegawa S, et al. Among authors: isomura m. J Hum Genet. 1999;44(5):337-42. doi: 10.1007/s100380050172. J Hum Genet. 1999. PMID: 10496079

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