Publications by authors named "Evon DeBose-Scarlett"

Article Synopsis
  • Hereditary hemorrhagic telangiectasia (HHT) is a genetic disorder that leads to abnormal blood vessel formations, particularly in the skin and internal organs, due to mutations in one of three specific genes.
  • Research indicates that these vascular malformations result from a two-hit mutation mechanism, where a primary genetic mutation is compounded by additional events such as somatic mutations or loss of heterozygosity.
  • The study confirms that both skin and internal organ abnormalities share similar molecular processes, emphasizing that losing function in both copies of the HHT gene is essential for developing these vascular issues.
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Article Synopsis
  • Cerebral cavernous malformation (CCM) is a condition where abnormal blood vessels in the brain can bleed, linked to certain gene mutations.
  • Scientists tested a drug called rapamycin to see if it helps stop these blood vessel problems in mice without other mutations present.
  • While rapamycin seemed to prevent big lesions, it also caused some negative effects, like increasing the average size of smaller lesions and making some mice get worse, meaning more studies are needed to understand its impact fully.
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Obesity is considered a primary contributing factor in the development of many diseases, including cancer, diabetes, and cardiovascular illnesses. Phytochemical-rich foods, associated to healthy gastrointestinal microbiota, have been shown to reduce obesity and associated comorbidities. In the present article, we describe the effects of the probiotic N6.

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Centromeres are essential to genome inheritance, serving as the site of kinetochore assembly and coordinating chromosome segregation during cell division. Abnormal centromere function is associated with birth defects, infertility, and cancer. Normally, centromeres are assembled and maintained at the same chromosomal location.

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Mother's own milk provides personalized nutrition and immune protection to the developing infant. The presence of healthy microbes plays an important role in the infant's gut by programming the microbiota and excluding potential pathogens. This review describes the important components in mother's own milk that contribute to its superiority for infant nutrition and suggest potential strategies to replicate these factors in alternative feedings when sufficient milk is unavailable.

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Feeding preterm infants mother's own milk (MOM) lowers rates of sepsis, decreases necrotizing enterocolitis, and shortens hospital stay. In the absence of freshly expressed MOM, frozen MOM (FMOM) is provided. When MOM is unavailable, preterm infants are often fed pasteurized donor human milk (DHM), rendering it devoid of beneficial bacteria.

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Human milk could be considered an active and complex mixture of beneficial bacteria and bioactive compounds. Since pasteurization drastically reduces the microbial content, we recently demonstrated that pasteurized donor human milk (DHM) could be inoculated with different percentages (10% and 30%) of mother's own milk (MOM) to restore the unique live microbiota, resulting in personalized milk (RM10 and RM30, respectively). Pasteurization affects not only the survival of the microbiota but also the concentration of proteins and metabolites, in this study, we performed a comparative metabolomic analysis of the RM10, RM30, MOM and DHM samples to evaluate the impact of microbial restoration on metabolite profiles, where metabolite profiles clustered into four well-defined groups.

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Metabolic syndrome (MetS) is the underlying cause of some devastating diseases, including type 2 diabetes and cardiovascular disease. These diseases have been associated with over-activation of the mechanistic Target of Rapamycin (mTOR) pathway. This study utilizes a high fat diet (HFD) to induce MetS and to dissect the effects of a beneficial bacterium, N6.

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