Machine‐learning potentials are increasingly taking on the exploratory tasks of homogeneous catalysis, enabling rapid conformer sampling and reaction‐space mapping. However, when selectivity depends on subtle electronic effects, electronic‐structure methods remain essential.
Maxime Ferrer +3 more
wiley +1 more source
A forest is more than its trees: haplotypes and ancestral recombination graphs. [PDF]
Fritze H, Pope N, Kelleher J, Ralph P.
europepmc +1 more source
ABSTRACT Sustainability assessment advances corporate social responsibility toward inclusive development. Widely recognized approaches prove inadequate for micro, small, and medium enterprises (MSMEs), resulting in fragmented proliferation that hinders cumulative knowledge.
Luísa Couto Gonçalves de Souza +2 more
wiley +1 more source
Ten tips for ordering, interpreting, and communicating genetic test results in nephrology. [PDF]
Selvathesan N +3 more
europepmc +1 more source
Stability Bounds for the Generalized Kadanoff‐Baym Ansatz in the Holstein Dimer
ABSTRACT Predicting real‐time dynamics in correlated systems is demanding: exact two‐time Green's function methods are accurate but often too costly, while the Generalized Kadanoff‐Baym Ansatz (GKBA) offers time‐linear propagation at the risk of uncontrolled behavior. We examine when and why GKBA fails in a minimal yet informative setting, the Holstein
Oscar Moreno Segura +2 more
wiley +1 more source
Proposed differential diagnosis and classification of non-syndromic and syndromic supernumerary teeth. [PDF]
Zhang C +5 more
europepmc +1 more source
KCNJ4 variants disrupt inward‐rectifier potassium channel function and cause refractory epilepsy
Abstract Objective Epilepsy is a common neurological disorder with a strong genetic basis, most frequently arising from ion channel dysfunction. Although multiple inwardly rectifying potassium (Kir) channels have been implicated in epileptogenesis, the contribution of KCNJ4, which encodes the Kir2.3 channel, has not previously been established in human
Hu Pan +20 more
wiley +1 more source
Case Report: Severe protein S deficiency unmasks a cryptic <i>PROC</i> mutation with normal activity, triggering life-threatening pulmonary thromboembolism. [PDF]
Liu Y, Zhou B, Xue J, Zhang W, Liu J.
europepmc +1 more source
Inherited metabolic epilepsies–established diseases, new approaches
Abstract Inherited metabolic epilepsies (IMEs) represent the inherited metabolic disorders (IMDs) in which epilepsy is a prevailing component, often determining other neurodevelopmental outcomes associated with the disorder. The different metabolic pathways affected by individual IMEs are the basis of their rarity and heterogeneity.
Itay Tokatly Latzer, Phillip L. Pearl
wiley +1 more source
Estimating recombination fraction via Pearson correlation. [PDF]
Teng CS, Xu S.
europepmc +1 more source

