E. Nakajima

发表

A novel missense mutation and frameshift mutations in the type II receptor of transforming growth factor-beta gene in sporadic colon cancer with microsatellite instability.

M. Emi, T. Shimada, H. Orimo, 1998, Mutation research.

Identification of the protein components of mismatch binding complexes in human cells using a gel‐shift assay

T. Shimada, A. Watanabe, M. Ikejima, 1999, FEBS letters.

Frameshift Mutations and a Length Polymorphism in the hMSH3 Gene and the Spectrum of Microsatellite Instability in Sporadic Colon Cancer

M. Emi, T. Shimada, H. Orimo, 1999, Japanese journal of cancer research : Gann.

Loss of expression of the human MSH3 gene in hematological malignancies.

T. Shimada, A. Watanabe, H. Orimo, 1995, Biochemical and biophysical research communications.

hMutSβ, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA

J. Jiricny, I. Iaccarino, T. Shimada, 1996, Current Biology.

Close correlation between mutations of E2F4 and hMSH3 genes in colorectal cancers with microsatellite instability.

N. Matsubara, R. Mibu, N. Tanaka, 1998, Cancer research.

Association between single nucleotide polymorphisms in the hMSH3 gene and sporadic colon cancer with microsatellite instability

M. Emi, T. Shimada, H. Orimo, 2000, Journal of Human Genetics.

Nine-bp repeat polymorphism in exon 1 of the hMSH3 gene

T. Shimada, H. Orimo, M. Ikejima, 1995, Japanese Journal of Human Genetics.

Mutations in p53 cDNA sequence introduced by retroviral vector.

T. Shimada, K. Miyake, A. Watanabe, 2006, Biochemical and biophysical research communications.

FIRST‐TRIMESTER PRENATAL MOLECULAR DIAGNOSIS OF INFANTILE HYPOPHOSPHATASIA IN A JAPANESE FAMILY

T. Shimada, A. Watanabe, T. Araki, 1996, Prenatal diagnosis.