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Tokuyuki Shinohara

Researcher at Tottori University

Publications -  12
Citations -  944

Tokuyuki Shinohara is an academic researcher from Tottori University. The author has contributed to research in topics: Chromosome 21 & Gene. The author has an hindex of 12, co-authored 12 publications receiving 929 citations.

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Double trans-chromosomic mice: Maintenance of two individual human chromosome fragments containing Ig heavy and κ loci and expression of fully human antibodies

TL;DR: These results represent a generation of mice with "humanized" loci by using the transmittable hCFs, which suggest that the Tc technology may allow for the humanization of over megabase-sized, complex loci in mice or other animals.
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Manipulation of human minichromosomes to carry greater than megabase-sized chromosome inserts.

TL;DR: The stable minichromosome vector allowed a 10 Mb-sized region of the mitotically unstable human chromosome 22 to be stably maintained in mouse embryonic stem (ES) cells, and in mice.
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Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down’s syndrome

TL;DR: These chimeric mice mimic a wide variety of phenotypic traits of DS, revealing the utility of mice containing Chr 21 as unique models for DS and for the identification of genes responsible for DS.
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Stability of transferred human chromosome fragments in cultured cells and in mice.

TL;DR: The present study shows that the stability of hCFs in Tc mice differs with tissue types and with genetic background used for successive breedings, and the hCF(SC20), which was relatively stable in both mouse and human cells, may be a promising candidate for development as a gene delivery vector.
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Efficient modification of a human chromosome by telomere-directed truncation in high homologous recombination-proficient chicken DT40 cells

TL;DR: An efficient method for targeted truncation in the chicken DT40 cells with a high homologous recombination rate is described and it is shown that the predicted truncation at the LIF locus occurred in all of the targeted clones.