Publications by authors named "J Sulc"

Article Synopsis
  • Biological aging involves a gradual loss of homeostasis in molecular and cellular functions, particularly in the brain, which contains diverse cell types that differ in their aging resilience.
  • This study offers an extensive single-cell RNA sequencing dataset of approximately 1.2 million transcriptomes from brain cells in young and aged mice, identifying 847 cell clusters and 14 age-biased clusters predominantly involving glial types.
  • Key findings reveal specific gene expression changes with aging, including decreased neuronal function genes and increased immune-related genes, particularly in cells around the third ventricle of the hypothalamus, suggesting its critical role in the aging process of the mouse brain.
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Lifespan is influenced by complex interactions between genetic and environmental factors. Studying those factors in model organisms of a single genetic background limits their translational value for humans. Here, we mapped lifespan determinants in 85 C.

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We report on the first, to our knowledge, room-temperature continuous-wave laser operation of Tm,Ho-codoped barium and strontium fluoride crystals at ∼2.1 µm. The 3 at.

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Background & Aims: Recent findings reveal the importance of tryptophan-initiated de novo nicotinamide adenine dinucleotide (NAD) synthesis in the liver, a process previously considered secondary to biosynthesis from nicotinamide. The enzyme α-amino-β-carboxymuconate-ε-semialdehyde decarboxylase (ACMSD), primarily expressed in the liver and kidney, acts as a modulator of de novo NAD synthesis. Boosting NAD levels has previously demonstrated remarkable metabolic benefits in mouse models.

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Article Synopsis
  • The susceptibility to metabolic syndrome (MetS) is influenced by genetic and environmental factors, complicating the study of its mechanisms.
  • A new metabolic health score (MHS) was developed to assess metabolic health based on clinical parameters, which shows an association with MetS and predicts future disease risk.
  • The research identified two genetic loci linked to MHS in mice and suggested TNKS and MCPH1 as potential regulators, enhancing understanding of metabolic health across different species.
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