Results 251 to 260 of about 1,670,847 (343)

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

Input to the European strategy for particle physics: strong-field quantum electrodynamics. [PDF]

Eur Phys J Plus
Sarri G, King B, Blackburn T, Ilderton A, Boogert S, Bulanov SS, Bulanov SV, Di Piazza A, Ji L, Karbstein F, Keitel CH, Krajewska K, Malka V, Mangles SPD, Mathieu F, McKenna P, Meuren S, Mirzaie M, Ridgers C, Seipt D, Thomas AGR, Uggerhøj U, Vranic M, Wing M.   +23 more
europepmc   +1 more source

Dimension-8 SMEFT contact-terms for vector-pair production via on-shell Higgsing [PDF]

J. Goldberg, Hongkai Liu, Yael Shadmi
openalex   +1 more source

Systemic T Cell Receptor Profiling Reveals Adaptive Immune Activation and Potential Immune Signatures of Diagnosis and Brain Atrophy in Epilepsy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Epilepsy is increasingly associated with immune dysregulation and inflammation. The T cell receptor (TCR), a key mediator of adaptive immunity, shows repertoire alterations in various immune‐mediated diseases. The unique TCR sequence serves as a molecular barcode for T cells, and clonal expansion accompanied by reduced overall TCR ...
Yong‐Won Shin, Sang Bin Hong, Yong Woo Shin, Inpyeong Hwang, Jaeseong Oh, Jihyeon Choi, Narae Kim, Jangsup Moon, Keun‐Hwa Jung, Kyung‐Il Park, Ki‐Young Jung, Kon Chu, Sang Kun Lee   +12 more
wiley   +1 more source

Proteome profiling indicates a link between mitochondrial pathways and the host-microbial sensor ELMO1 following <i>Salmonella</i> infection. [PDF]

Gut Microbes
Achi SC, McGrosso D, Tocci S, Amao I, Saha B, Ibeawuchi SR, Sayed IM, Gonzalez DJ, Das S.   +8 more
europepmc   +1 more source

A Search for Top Quark Pair Production in the Dilepton Decay Mode

, 1995
James C. Romano
openalex   +2 more sources

Interleukin‐6 as a Key Biomarker in Facioscapulohumeral Dystrophy: Evidence From Longitudinal Analyses

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini, Emanuela Martinuzzi, Sandra Dhifallah, Abderhmane Slioui, Angela Puma, Luisa Villa, Michele Cavalli, Andra Ezaru, Jérémy Garcia, Manuela Gambella, Federico Torre, Luca Jacopo Pavan, Nicolas Glaichenhaus, Sabrina Sacconi   +13 more
wiley   +1 more source

Primer-Dependent Insights into Rumen Microbiota and Methanogen Shifts Induced by Orange Peel Secondary Feed in Dairy Sheep. [PDF]

Animals (Basel)
Karatzia MA, Basdagianni Z, Termatzidou SA, Kotsampasi B, Kasapidou E, Mai S, Barampouti EM, Alvanou MV, Loukovitis D.   +8 more
europepmc   +1 more source

Novel Trigger-Capable Modules for the Future CMS Tracking Detector and Inclusive Top Quark Pair Production Cross Section at √s = 13TeV

, 2017
A. Harb
openalex   +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