Inazawa J - Search Results

1

Identification of target genes within an amplicon at 14q12-q13 in esophageal squamous cell carcinoma.

Yasui K, Imoto I, Fukuda Y, Pimkhaokham A, Yang ZQ, Naruto T, Shimada Y, Nakamura Y, Inazawa J. Yasui K, et al. Among authors: inazawa j. Genes Chromosomes Cancer. 2001 Oct;32(2):112-8. doi: 10.1002/gcc.1172. Genes Chromosomes Cancer. 2001. PMID: 11550278

2

Cloning and characterization of an interstitial deletion at chromosome 11p15 in a sporadic breast cancer.

Miyagi M, Inazawa J, Takita K, Nakamura Y. Miyagi M, et al. Among authors: inazawa j. Hum Mol Genet. 1992 Dec;1(9):705-8. doi: 10.1093/hmg/1.9.705. Hum Mol Genet. 1992. PMID: 1302607

3

Mapping of the 8q23 translocation breakpoint of t(8;13) observed in a patient with multiple exostoses.

Yoshiura K, Inazawa J, Koyama K, Nakamura Y, Niikawa N. Yoshiura K, et al. Among authors: inazawa j. Genes Chromosomes Cancer. 1994 Jan;9(1):57-61. doi: 10.1002/gcc.2870090110. Genes Chromosomes Cancer. 1994. PMID: 7507701

4

Detailed analysis of loss of heterozygosity on chromosome band 17p13 in breast carcinoma on the basis of a high-resolution physical map with 29 markers.

Isomura M, Tanigami A, Saito H, Harada Y, Katagiri T, Inazawa J, Ledbetter DH, Nakamura Y. Isomura M, et al. Among authors: inazawa j. Genes Chromosomes Cancer. 1994 Mar;9(3):173-9. doi: 10.1002/gcc.2870090305. Genes Chromosomes Cancer. 1994. PMID: 7515659

5

Mapping the breakpoint of a constitutional translocation on chromosome 22 in a patient with NF2.

Arai E, Tokino T, Imai T, Inazawa J, Ikeuchi T, Tonomura A, Nakamura Y. Arai E, et al. Among authors: inazawa j. Genes Chromosomes Cancer. 1993 Apr;6(4):235-8. doi: 10.1002/gcc.2870060408. Genes Chromosomes Cancer. 1993. PMID: 7685627

6

Precise ordering of 26 cosmid markers on chromosome region 3p23-->p21.3 by two-color FISH on human prophase chromosomes and stretched DNAs.

Ariyama T, Kimura T, Yamakawa K, Nakamura Y, Abe T, Inazawa J. Ariyama T, et al. Among authors: inazawa j. Cytogenet Cell Genet. 1995;70(1-2):129-33. doi: 10.1159/000134077. Cytogenet Cell Genet. 1995. PMID: 7736778

7

Clonal origin of Philadelphia chromosome negative cells with trisomy 8 appearing during the course of alpha-interferon therapy for Ph positive chronic myelocytic leukemia.

Ariyama T, Inazawa J, Uemura Y, Kakazu N, Maekawa T, Urase F, Irimajiri K, Horiuchi A, Nakamura Y, Abe T. Ariyama T, et al. Among authors: inazawa j. Cancer Genet Cytogenet. 1995 May;81(1):20-3. doi: 10.1016/0165-4608(94)00197-9. Cancer Genet Cytogenet. 1995. PMID: 7773954

8

High-resolution cytogenetic mapping of the short arm of chromosome 1 with newly isolated 411 cosmid markers by fluorescence in situ hybridization: the precise order of 18 markers on 1p36.1 on prophase chromosomes and "stretched" DNAs.

Ariyama T, Inazawa J, Ezaki T, Nakamura Y, Horii A, Abe T. Ariyama T, et al. Among authors: inazawa j. Genomics. 1995 Jan 1;25(1):114-23. doi: 10.1016/0888-7543(95)80116-4. Genomics. 1995. PMID: 7774908

9

Chromosome mapping of human (ZNF147) and mouse genes for estrogen-responsive finger protein (efp), a member of the RING finger family.

Inoue S, Orimo A, Matsuda Y, Inazawa J, Emi M, Nakamura Y, Hori T, Muramatsu M. Inoue S, et al. Among authors: inazawa j. Genomics. 1995 Jan 20;25(2):581-3. doi: 10.1016/0888-7543(95)80064-s. Genomics. 1995. PMID: 7789997

10

The human insulin receptor substrate-1 gene (IRS1) is localized on 2q36.

Nishiyama M, Inazawa J, Ariyama T, Nakamura Y, Matsufuji S, Furusaka A, Tanaka T, Hayashi S, Wands JR. Nishiyama M, et al. Among authors: inazawa j. Genomics. 1994 Mar 1;20(1):139-41. doi: 10.1006/geno.1994.1143. Genomics. 1994. PMID: 8020946 No abstract available.

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