Results 231 to 240 of about 11,919,473 (381)

Expanding our thought horizons in systems biology and medicine

open access: yesFrontiers in Systems Biology
Jennifer C. Lovejoy   +2 more
doaj   +1 more source

Characterization of ribosome heterogeneity during endothelial to hematopoietic transition

open access: yesFEBS Open Bio, EarlyView.
The panorama of ribosome heterogeneity during embryonic hematopoiesis has not yet been portrayed. In this study, utilizing dual‐omics data, the heterogenous dynamic of ribosome during endothelial‐to‐hematopoietic transition has been systemically described. Moreover, stage‐specific upregulation and peripheral localization of RPL27 and RACK1 in hemogenic
Xitong Tian   +4 more
wiley   +1 more source

2009年度 環境デザイン工学科研究報告 [PDF]

open access: yes, 2010
Faculty of Environmental Science and Technology, Okayama University,
core  

「環境制御」投稿規定 [PDF]

open access: yes, 1990
Okayama University Administration Center for Environmental Science and Technology,
core   +3 more sources

Communicating environmental science to the general public

open access: yesIntegrated Environmental Assessment and Management, 2016
Thomas Backhaus, T. Seiler
semanticscholar   +1 more source

Polydatin ameliorates ovalbumin‐induced asthma in a rat model through NCOA4‐mediated ferroautophagy and ferroptosis pathway

open access: yesFEBS Open Bio, EarlyView.
In this research, a rat model of asthma was created using OVA, and polydatin served as an intervention. By inhibiting ferroautophagy mediated by NCOA4 and averting ferroptosis, polydatin has been demonstrated to reduce asthma. This work presents new ideas for investigating the mechanism of polydatin's ability to alleviate asthma, in addition to ...
Wei Li   +5 more
wiley   +1 more source

A Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra   +17 more
wiley   +1 more source

奥付 [PDF]

open access: yes, 2002
Okayama University Administration Center for Environmental Science and Technology,
core  

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