Results 151 to 160 of about 984,137 (343)

Keap1-Nrf2システムにおける2つの部位基質認識モデル : 酸化ストレス応答の蝶番と掛け金メカニズム [PDF]

open access: yes, 2007
筑波大学University of Tsukuba博士(医学)Doctor of Philosophy in Medical Sciences2006【要旨 ...
51506, Tong, Kit Leng
core  

The study of philosophy as a method of forming the spiritual guidelines of modern student youth in a medical university

open access: diamond, 2022
N.F. Loman   +4 more
openalex   +1 more source

On the Prospects for African Philosophy in Australia

open access: yesAustralian Journal of Social Issues, EarlyView.
ABSTRACT This paper grapples with the situation of people of African descent in Australia by working through the constitution of the body of academic philosophy in the country. It contends with the parochialism of the Australian philosophical community and the prospects for the cultivation of greater pluralism. Taking African philosophy as one possible
Bryan Mukandi
wiley   +1 more source

モンゴルにおいて社会経済学的格差が5歳未満の小児の栄養状態に与える影響 [PDF]

open access: yes, 2011
筑波大学University of Tsukuba博士(医学)Doctor of Philosophy in Medical Sciences2010【要旨 ...
88968, Ganzorig, Dorjdagva
core  

Back Again to the Future: A New Era for Cerebroprotection

open access: yesAnnals of Neurology, EarlyView.
Cerebroprotection is a fresh framework for designing neurological therapy that targets glia and vascular cells, in addition to neurons. In the future, successful cerebroprotection will involve targeting all elements of the neurovascular unit. Preclinical trials must include functional outcomes, as well as lesion morphometry.
Patrick Lyden
wiley   +1 more source

Signal-averaged ECGの開心術への応用 [PDF]

open access: yes, 1993
筑波大学University of Tsukuba博士(医学)Doctor of Philosophy in Medical Sciences1992付:参考論文doctoral ...
50719   +2 more
core  

Non‐Synaptic Function and Localization of Syntaxin‐Binding Protein 1 in a Mouse Model of STXBP1‐Related Epileptic Encephalopathy

open access: yesAnnals of Neurology, EarlyView.
Objective De novo mutations in the syntaxin‐binding protein 1 (STXBP1), encoded by STXBP1, are among the most prevalent causes of variable neurodevelopmental disorders, including epileptic encephalopathy, developmental delay, and movement disorders.
Tao Yang   +7 more
wiley   +1 more source

Reduced gene dosage of GATA factors induces deafness in mice due to the degeneration of spiral ganglion cells [PDF]

open access: yes, 2004
筑波大学University of Tsukuba博士(医学)Doctor of Philosophy in Medical Sciences2003【要旨】Joint authors: Masatsugu Ema ...
49632, Terunuma, Tsumoru, 照沼, 積
core  

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