Results 181 to 190 of about 446,044 (333)

Higher structural connectivity and resistance against invasions of soil bioengineering over hard-engineering for riverbank stabilisation

, 2020
François-Marie Martin, Philippe Janssen, Laurent Bergès, Blandine Dupont, André Evette   +4 more
openalex   +2 more sources

C2α‐carbanion‐protonating glutamate discloses tradeoffs between substrate accommodation and reaction rate in actinobacterial 2‐hydroxyacyl‐CoA lyase

FEBS Open Bio, EarlyView.
Enzymes of the 2‐hydroxyacyl‐CoA lyase group catalyze the condensation of formyl‐CoA with aldehydes or ketones. Thus, by structural adaptation of active sites, practically any pharmaceutically and industrially important 2‐hydroxyacid could be biotechnologically synthesized. Combining crystal structure analysis, active site mutations and kinetic assays,
Michael Zahn, Barbara Seroka, Ryszard Lazny, Zenon Lotowski, Thore Rohwerder   +4 more
wiley   +1 more source

Correction: Ali et al. Real-Time Recognition of NZ Sign Language Alphabets by Optimal Use of Machine Learning. <i>Bioengineering</i> 2025, <i>12</i>, 1068. [PDF]

Bioengineering (Basel)
Ali M, Hosseini SE, Pervez S, Ahmad M.
europepmc   +1 more source

1P306 Computer Simulation of Actin Filament Movements Driven by Myosins in Microfabricated Patterns(Bioengineering, and new biophysical techniques and instrumentation,Oral Presentations)

, 2007
T. Nitta, Yu Obara, Akihito Tanahashi, Motohisa Hirano, Maria V. Razumova, Michael Regnier, Henry Hess   +6 more
openalex   +2 more sources

Erythropoietin modulates hepatic inflammation, glucose homeostasis, and soluble epoxide hydrolase and epoxides in high‐fat diet‐induced obese mice

FEBS Open Bio, EarlyView.
Erythropoietin administration suppresses hepatic soluble epoxide hydrolase (sEH) expression, leading to increased CYP‐derived epoxides. This is associated with a shift in hepatic macrophage polarization characterized by reduced M1 markers and increased M2 markers, along with reduced hepatic inflammation, suppressed hepatic lipogenesis, and attenuated ...
Takeshi Goda, Satoru Sugimoto, Chiharu Cho, Madoka Konishi, Nozomi Inoue, Satoshi Miyagaki, Yasuhiro Kawabe, Takuro Okamura, Masahide Hamaguchi, Hisakazu Nakajima, Michiaki Fukui, Masakazu Shinohara, Tomoko Iehara   +12 more
wiley   +1 more source

Correction: Hoang, P.; Guccione, J. Finite Element Modeling in Left Ventricular Cardiac Biomechanics: From Computational Tool to Clinical Practice. <i>Bioengineering</i> 2025, <i>12</i>, 913. [PDF]

Bioengineering (Basel)
Hoang P, Guccione J.
europepmc   +1 more source

Bioengineering: Genetic Logic Gates Enable Patterning of Amyloid Nanofibers (Adv. Mater. 39/2019) [PDF]

, 2019
Ebuzer Kalyoncu, Recep Erdem Ahan, Cemile Elif Özçelik, Urartu Özgür Şafak Şeker   +3 more
openalex   +1 more source

NR4A1 Exerts Pro‐Tumor Role in Glioblastoma via Inducing xCT/GPX4‐Regulated Ferroptosis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Purpose This study investigates NR4A1's paradoxical roles in glioblastoma (GBM) progression, focusing on its mechanistic link to ferroptosis regulation. We aimed to resolve conflicting reports of NR4A1 as both an oncogene and a tumor suppressor by defining its transcriptional control over xCT/GPX4‐mediated iron homeostasis and its clinical ...
Peng Tao, Shikuan Din, Zhengkang Fu, Qian Sun, Xiwei Zhu, Yuxin Wei, Huan Qu, Xinyi Zhang, Jiaxuan Liu, Chuhua Fu, Qianxue Chen   +10 more
wiley   +1 more source

Correction: Zhu et al. Injectable and Assembled Calcium Sulfate/Magnesium Silicate 3D Scaffold Promotes Bone Repair by In Situ Osteoinduction. <i>Bioengineering</i> 2025, <i>12</i>, 599. [PDF]

Bioengineering (Basel)
Zhu W, Zhao T, Wang H, Liu G, Bian Y, Wang Q, Xia W, Cai S, Weng X.   +8 more
europepmc   +1 more source

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas, Pablo Iruzubieta, Alberto Damborenea, Laura Pérez‐Fernández, Inmaculada Azorín, Juan Carlos Jiménez García, Ana Töpf, Pilar Martí, Lorena Fores‐Toribio, María Manterola, Rosana Blanco‐Mañez, Oihane Pikatza‐Menoio, Sonia Alonso‐Martín, Volker Straub, Aitziber L. Cortajarena, Adolfo López de Munain, David De Sancho, Lorea Blázquez, Juan J. Vilchez   +18 more
wiley   +1 more source