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Hirofumi Suemori

Researcher at Kyoto University

Publications -  118
Citations -  12129

Hirofumi Suemori is an academic researcher from Kyoto University. The author has contributed to research in topics: Embryonic stem cell & Stem cell. The author has an hindex of 47, co-authored 116 publications receiving 11489 citations. Previous affiliations of Hirofumi Suemori include Tokyo Medical and Dental University & Shimadzu Corp..

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Distinct and Essential Roles of Transcription Factors IRF-3 and IRF-7 in Response to Viruses for IFN-α/β Gene Induction

TL;DR: The results demonstrate the essential and distinct roles of the two factors, which together ensure the transcriptional efficiency and diversity of IFN-alpha/beta genes for the antiviral response.
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Characterization of human embryonic stem cell lines by the International Stem Cell Initiative

Oluseun Adewumi, +89 more
- 17 Jun 2007 - 
TL;DR: The International Stem Cell Initiative characterized 59 human embryonic stem cell lines from 17 laboratories worldwide and found that despite diverse genotypes and different techniques used for derivation and maintenance, all lines exhibited similar expression patterns for several markers ofhuman embryonic stem cells.
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Generation of dopaminergic neurons and pigmented epithelia from primate ES cells by stromal cell-derived inducing activity

TL;DR: It is reported here that SDIA induces efficient neural differentiation also in primate embryonic stem cells and provides an unlimited source of primate cells for the study of pathogenesis, drug development, and transplantation in degenerative diseases such as Parkinson's disease and retinitis pigmentosa.
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Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage

Katherine Amps, +124 more
- 27 Nov 2011 - 
TL;DR: Of these genes, BCL2L1 is a strong candidate for driving culture adaptation of ES cells, and single-nucleotide polymorphism analysis revealed that they included representatives of most major ethnic groups.
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Octamer and Sox elements are required for transcriptional cis regulation of Nanog gene expression.

TL;DR: Nanog transcription may be regulated through an interaction between Oct4 and Sox2 or a novel pluripotential cell-specific Sox element-binding factor which is prominent in ES cells.