Tomoko Tahira

发表

GENESUS: a two-step sequence design program for DNA nanostructure self-assembly.

Kenshi Hayashi, Takao Okada, Takeshi Asakawa, 2014, BioTechniques.

3J0924 Design of self-assembling nanoscale DNAby "T-GUSP" : construction of an octahedron and its multimers(3J Bioengineering 1,The 49th Annual Meeting of the Biophysical Society of Japan)

Kenshi Hayashi, Takanobu Tsutsumi, Akemi Kanegami, 2011 .

2P336 Implosive addressing of space by self-assembled DNA(The 48th Annual Meeting of the Biophysical Society of Japan)

Kenshi Hayashi, Takanobu Tsutsumi, Akemi Kanegami, 2010 .

D-HaploDB: a database of definitive haplotypes determined by genotyping complete hydatidiform mole samples

Kenshi Hayashi, Tomoko Tahira, Koichiro Higasa, 2006, Nucleic Acids Res..

A single‐strand conformation polymorphism method for the large‐scale analysis of mutations/polymorphisms using capillary array electrophoresis

Kenshi Hayashi, Tomoko Tahira, Michihiro Nakamura, 2002, Electrophoresis.

ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature

Christian Gilissen, Alexander Hoischen, Tomoko Tahira, 2013, Proceedings of the National Academy of Sciences.

Outside-to-Inside Signal Through the Membrane TNF-α Induces E-Selectin (CD62E) Expression on Activated Human CD4+ T Cells1

Takahiko Horiuchi, Yoshiyuki Niho, Tomoko Tahira, 2001, The Journal of Immunology.

Characterization of the biological functions of a transcription factor, c-myc intron binding protein 1 (MIBP1).

Tomoko Tahira, Hiroaki Kawasaki, Shizuka Akieda, 2002, Journal of biochemistry.

Genome-wide definitive haplotypes determined using a collection of complete hydatidiform moles.

Tomoko Tahira, Takao Matsuda, Koichiro Higasa, 2005, Genome research.

Delineation of the critical interval for the familial exudative vitreoretinopathy gene by linkage and haplotype analysis

Kenshi Hayashi, Kenji Oshima, Tomoko Tahira, 2001, Human Genetics.