欧文原著(2012)

2012年2月22日

 

欧文原著

 

2012

 

Kinoshita M, Numata S, Tajima A, Ohi K, Hashimoto R, Shimodera S, Imoto I, Itakura M, Takeda M, Ohmori T.

 

Meta-analysis of association studies between DISK1 missense variants and schizophrenia in Japanese population.

 

Schizophr Res 2012;141(2-3):271-3.

 

 

 

Matsumura S, Imoto I, Kozaki K, Matsui T, Muramatsu T, Furuta M, Tanaka S, Sakamoto M, Arii S, Inazawa J.

 

Integrative array-based approach identifies MZB1 as a frequently methylated putative tumor-suppressor in hepatocellular carcinoma.

 

Clin Cancer Res 2012;18(13):3541-51.

 

 

 

Miyawaki Y, Kawauchi H, Ooi A, Eishi Y, Kawamoto T, Inazawa J, Imoto I.

 

Genomic copy-number alterations of MYC and FHIT genes are associated with survival in esophageal squamous-cell carcinoma.

 

Cancer Sci 2012;103(8):1558-66.

 

 

 

Okamoto N, Hayashi S, Masui A, Kosaki R, Oguri I, Hasegawa T, Imoto I, Makita Y, Hata A, Moriyama K, Inazawa J.

 

Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion.

 

J Hum Genet 2012;57:191-6.

 

 

 

Ono H, Imoto I, Kozaki K, Tsuda H, Matsui T, Kurasawa Y, Muramatsu T, Sugihara K, Inazawa J.

 

SIX1 promotes epithelial-mesenchymal transition in colorectal cancer through ZEB1 actibation.

 

Oncogene 2012;31(47):4923-34.

 

 

 

Honda S, Satomura S, Hayashi S, Imoto I, Nakagawa E, Goto Y, Inazawa J.

 

Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation.

 

J Hum Genet 2012;57:73-77.

 

 

 

Hayashi S, Okamoto N, Chinen Y, Takanashi JI, Makita Y, Hata A, Imoto I, Inazawa J.

 

Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH).

 

Hum Genet 2012;131:99-110.

 

 

 

Honda S, Hayashi S, Nakane T, Imoto I, Kurosawa K, Mizuno S, Okamoto N, Kato M, Yoshihashi H, Kubota T, Nakagawa E, Goto Y, Inazawa J.

 

The Incidence of hypoplasia Corpus Callosum in patients with dup (X) (q28) involving MECP2 is associated with the location of distal breakpoints.

 

Am J Med Genet Part A. 2012;158A(6):1292-303.

 

 

 

Yamamoto S, Tsuda H, Honda K, Takano M, Tamai S, Imoto I, Inazawa J, Yamada T, Matsubara O.

 

ACTN4 gene amplification and actinin-4 protein overexpression drive tumour development and histological progression in a high-grade subset of ovarian clear-cell adenocarcinomas.

 

Histopathology 2012;60(7):1073-1083.

 

 

 

Murata C, Yamada F, Kawauchi N, Matsuda Y, Kuroiwa A.

 

The Y chromosome of the Okinawa spiny rat, tokudaia muenninki, was rescued through fusion with an autosome.

 

Chromosome Res 2012;20(1):111-25.

 

 

 

Kurasawa Y, Kozaki K, Pimkhaokham A, Muramatsu T, Ono H, Ishihara T, Uzawa N, Imoto I, Amagasa T, Inazawa J.

 

Stabilization of phenotypic plasticity through mesenchymal-specific DNA hypermethylation in cancer cells.

 

Oncogene 2012;31:1963-74.

 

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