Egashira M - Search Results

1

Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.

Coêlho KE, Egashira M, Kato R, Fujimoto M, Matsumoto N, Rerkamnuaychoke B, Abe K, Harada N, Ohashi H, Fukushima Y, Niikawa N. Coêlho KE, et al. Among authors: egashira m. Am J Med Genet. 1996 Jun 14;63(3):468-71. doi: 10.1002/(SICI)1096-8628(19960614)63:3<468::AID-AJMG10>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8737654

2

The human HCLS1 gene maps to chromosome 3q13 by fluorescence in situ hybridization.

Egashira M, Kitamura D, Watanabe T, Niikawa N. Egashira M, et al. Cytogenet Cell Genet. 1996;72(2-3):175-6. doi: 10.1159/000134179. Cytogenet Cell Genet. 1996. PMID: 8978766

3

Visible integration of the adenosine deaminase (ADA) gene into the recipient genome after gene therapy.

Egashira M, Ariga T, Kawamura N, Miyoshi O, Niikawa N, Sakiyama Y. Egashira M, et al. Am J Med Genet. 1998 Jan 23;75(3):314-7. Am J Med Genet. 1998. PMID: 9475605

4

The human gene encoding the heavy chain of the major histocompatibility complex class I-like Fc receptor (FCGRT) maps to 19q13.3.

Kandil E, Egashira M, Miyoshi O, Niikawa N, Ishibashi T, Kasahara M. Kandil E, et al. Among authors: egashira m. Cytogenet Cell Genet. 1996;73(1-2):97-8. doi: 10.1159/000134316. Cytogenet Cell Genet. 1996. PMID: 8646894

5

Mapping of the alpha-1,6-fucosyltransferase gene, FUT8, to human chromosome 14q24.3.

Yamaguchi Y, Fujii J, Inoue S, Uozumi N, Yanagidani S, Ikeda Y, Egashira M, Miyoshi O, Niikawa N, Taniguchi N. Yamaguchi Y, et al. Among authors: egashira m. Cytogenet Cell Genet. 1999;84(1-2):58-60. doi: 10.1159/000015215. Cytogenet Cell Genet. 1999. PMID: 10343104

6

Breakpoint analysis of a familial balanced translocation t(2;8)(q31;p21) associated with mesomelic dysplasia.

Sugawara H, Egashira M, Harada N, Jakobs TC, Yoshiura K, Kishino T, Ohta T, Niikawa N, Matsumoto N. Sugawara H, et al. Among authors: egashira m. J Med Genet. 2002 Jul;39(7):E34. doi: 10.1136/jmg.39.7.e34. J Med Genet. 2002. PMID: 12114491 Free PMC article. No abstract available.

7

The structural organization of the human aldehyde reductase gene, AKR1A1, and mapping to chromosome 1p33-->p32.

Fujii J, Hamaoka R, Matsumoto A, Fujii T, Yamaguchi Y, Egashira M, Miyoshi O, Niikawa N, Taniguchi N. Fujii J, et al. Among authors: egashira m. Cytogenet Cell Genet. 1999;84(3-4):230-2. doi: 10.1159/000015265. Cytogenet Cell Genet. 1999. PMID: 10393438

8

Cancer-associated alternative usage of multiple promoters of human GalCer sulfotransferase gene.

Tsuda M, Egashira M, Niikawa N, Wada Y, Honke K. Tsuda M, et al. Among authors: egashira m. Eur J Biochem. 2000 May;267(9):2672-9. doi: 10.1046/j.1432-1327.2000.01281.x. Eur J Biochem. 2000. PMID: 10785389 Free article.

9

Two nonsense mutations of PAX6 in two Japanese aniridia families: case report and review of the literature.

Kondo-Saitoh A, Matsumoto N, Sasaki T, Egashira M, Saitoh A, Yamada K, Niikawa N, Amemiya T. Kondo-Saitoh A, et al. Among authors: egashira m. Eur J Ophthalmol. 2000 Apr-Jun;10(2):167-72. doi: 10.1177/112067210001000213. Eur J Ophthalmol. 2000. PMID: 10887930 Review.

10

Human ESP1/CRP2, a member of the LIM domain protein family: characterization of the cDNA and assignment of the gene locus to chromosome 14q32.3.

Karim MA, Ohta K, Egashira M, Jinno Y, Niikawa N, Matsuda I, Indo Y. Karim MA, et al. Among authors: egashira m. Genomics. 1996 Jan 15;31(2):167-76. doi: 10.1006/geno.1996.0028. Genomics. 1996. PMID: 8824798

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