Results 131 to 140 of about 10,563,202 (308)

Getting Participatory Design Done: From Methods and Choices to Translation Work across Constituent Domains

open access: yes, 2020
Collaborative arrangements between users and designers today are enacted in a broadening array of circumstances. These include extended, even years-long projects within corporations, the public and third sectors, as well as open-ended, peer-to-peer open ...
Hyysalo, Sampsa   +3 more
core  

Developmental programmes drive cellular plasticity, disease progression and therapy resistance in lung adenocarcinoma

open access: yesMolecular Oncology, EarlyView.
This study shows that lung adenocarcinomas exploit developmental branching morphogenesis to acquire a therapy resistant basal‐like tumour cell state. This process was found to be regulated by combined TP53 loss‐of‐function and type‐I interferon signalling, identifying a novel axis for biomarker and therapeutic target discovery.
Kamila J Bienkowska   +13 more
wiley   +1 more source

Design Annual (2016-2017) [PDF]

open access: yes, 2017
Design Annual is the yearly compilation of the activities and works by students and faculty at University of Central Oklahoma's Department of Design. UCO Library's Digital Initiatives Working Group has provided 2 copies of each issue: one file is the ...
University of Central Oklahoma. Department of Design.
core  

Ferrocene- and Fullerene[60]- Containing Liquid-Crystalline Materials

open access: yesCHIMIA, 1998
This paper shows the versatility of ferrocene and fullerene for the design of thermotropic liquid-crystalline materials: i) the electrochemical properties of the ferrocene-ferrocenium system were exploited to design redox-active metallomesogens (
Thierry Chuard, Robert Deschenaux
doaj  

USP29‐regulated noncanonical stabilization of the hypoxia‐inducible factor‐α in aggressive prostate cancer

open access: yesMolecular Oncology, EarlyView.
We identify USP29 as the only DUB mirroring CA9 expression, a marker of hypoxia and HIF pathway activation associated with PCA aggressiveness. USP29 stabilizes HIF‐1α and HIF‐2α via a noncanonical mechanism that is independent of PHD/pVHL activity yet relies on proteasomal regulation, establishing USP29 as a previously unrecognized regulator of hypoxic
Amelie S Schober   +16 more
wiley   +1 more source

Design Annual (2015-2016) [PDF]

open access: yes, 2016
Design Annual is the yearly compilation of the activities and works by students and faculty at University of Central Oklahoma's Department of Design. UCO Library's Digital Initiatives Working Group has provided 2 copies of each issue: one file is the ...
University of Central Oklahoma. Department of Design.
core  

Finding novel vulnerabilities of hypomorphic BRCA1 alleles

open access: yesMolecular Oncology, EarlyView.
Synthetic lethality screens performed to identify novel vulnerabilities often model complete gene loss, thereby overlooking patient‐derived hypomorphic mutations. In this study, we have performed genome‐wide CRISPR screens on BRCA1 hypomorphic mutations, showing BRCA1I26A behaves like wild‐type, while BRCA1R1699Q mimics deficiency. Furthermore, we have
Anne Schreuder   +10 more
wiley   +1 more source

Mindfulness and resource-sensitive design : a literature overview and an agenda for research

open access: yes
21st International Conference on Engineering Design (ICED 17), Vancouver, Canada, 21-25 August 2017202403 bckwVersion of RecordSelf-fundedPublishedVoR ...
de Bont, C, Chan, WMH
core  

A novel quinazolinone insulin receptor inhibitor and its synergy with an EGFR inhibitor in glucose‐driven glioblastoma

open access: yesMolecular Oncology, EarlyView.
The novel styrylquinazolinone‐based molecule W1B effectively suppresses glioblastoma by inhibiting IGF1R and EGFR. In high‐glucose microenvironments driving tumor resistance, W1B acts synergistically with the EGFR inhibitor dacomitinib. This combination safely blocks compensatory survival signaling in zebrafish xenograft models. Showcasing promising in
Patryk Rurka   +9 more
wiley   +1 more source

Synthesis, molecular docking study and biological evaluation of new pyrrole scaffolds as potential antitubercular agents for dual targeting of enoyl ACP reductase and dihydrofolate reductase.

open access: yesPLoS ONE
In this study, new series of N'-(2-(substitutedphenoxy)acetyl)-4-(1H-pyrrol-1-yl)benzohydrazides (3a-j) 4-(2,5-dimethyl-1H-pyrrol-1-yl)-N'-(2-(substitutedphenoxy)acetyl)benzohydrazides (5a-j) were synthesized, characterized and assessed as inhibitors of ...
Mater H Mahnashi   +11 more
doaj   +1 more source

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