scispace - formally typeset
M

Minoru S.H. Ko

Researcher at Keio University

Publications -  191
Citations -  16754

Minoru S.H. Ko is an academic researcher from Keio University. The author has contributed to research in topics: Embryonic stem cell & Gene. The author has an hindex of 62, co-authored 186 publications receiving 15543 citations. Previous affiliations of Minoru S.H. Ko include Johns Hopkins University & Government of the United States of America.

Papers
More filters
Journal ArticleDOI

Pluripotency governed by Sox2 via regulation of Oct3/4 expression in mouse embryonic stem cells

TL;DR: The results indicate that the essential function of Sox2 is to stabilize ES cells in a pluripotent state by maintaining the requisite level of Oct3/4 expression.
Journal ArticleDOI

Dynamics of Global Gene Expression Changes during Mouse Preimplantation Development

TL;DR: A cascade of gene activation from maternal RNA/protein sets to zygotic genome activation and thence to MGA gene sets is proposed, which is a first step toward analysis of the complex gene regulatory networks.
Journal ArticleDOI

The status, quality, and expansion of the NIH full-length cDNA project: The Mammalian Gene Collection (MGC)

Daniela S. Gerhard, +118 more
- 01 Oct 2004 - 
TL;DR: Comparison of the sequence of the MGC clones to reference genome sequences reveals that most cDNA clones are of very high sequence quality, although it is likely that some cDNAs may carry missense variants as a consequence of experimental artifact, such as PCR, cloning, or reverse transcriptase errors.
Journal ArticleDOI

Maps from two interspecific backcross DNA panels available as a community genetic mapping resource

TL;DR: Large quantities of DNA from most tissues of each animal are prepared to create a community resource of interspecific backcross DNA for use by laboratories interested in mapping loci in the mouse.
Journal ArticleDOI

Database for mRNA Half-Life of 19 977 Genes Obtained by DNA Microarray Analysis of Pluripotent and Differentiating Mouse Embryonic Stem Cells

TL;DR: The mRNA decay rates presented in this report are the largest data set for mammals and the first for ES cells and the stability of mRNAs correlated more significantly with the structural features of genes than the function of genes.