Publications by authors named "M Krenn"

•FSHD1 may present with bilateral foot drop in adulthood.•Clinical examination, EMG and muscle MRI may additionally guide genetic testing.•Targeted genetic testing is crucial in atypical cases, particularly in light of new therapies.

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Quantum entanglement-correlations of particles that are stronger than any classical analog-is the basis for research on the foundations of quantum mechanics and for practical applications such as quantum networks. Traditionally, entanglement is achieved through local interactions or via entanglement swapping, where entanglement at a distance is generated through previously established entanglement and Bell-state measurements. However, the precise requirements enabling the generation of quantum entanglement without traditional local interactions remain less explored.

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The genus (Capparaceae) comprises 85 woody species distributed across the paleotropics, with some species used in traditional medicine. This study investigated the phylogenetic placement, genetic diversity, and phytochemical composition of , a species native to Indochina. Phylogenetic analyses using and markers confirmed the monophyly of the specimens collected from Thailand.

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Driven by human ingenuity and creativity, the discovery of super-resolution techniques, which circumvent the classical diffraction limit of light, represent a leap in optical microscopy. However, the vast space encompassing all possible experimental configurations suggests that some powerful concepts and techniques might have not been discovered yet, and might never be with a human-driven direct design approach. Thus, AI-based exploration techniques could provide enormous benefit, by exploring this space in a fast, unbiased way.

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Article Synopsis
  • Biallelic SUFU variants are linked to severe conditions like Joubert syndrome, while heterozygous truncating variants are associated with milder issues such as developmental delay and ocular motor apraxia, though limited cases have been studied. !* -
  • The study examined nine individuals across three families with truncating SUFU variants, detailing their neuroimaging and developmental assessments to explore the phenotypic expression of these variants. !* -
  • Findings revealed a wide range of symptoms including motor developmental delays and subtle neuroimaging abnormalities, indicating that SUFU haploinsufficiency presents with varying severity, even among family members. !*
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