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Safety Assessment of Vitamin D and Its Photo-Isomers in UV-Irradiated Baker’s YeastSchümmer, Tobias, Stangl, Gabriele I., Wätjen, Wim 04 May 2023 (has links)
Vitamin D deficiency due to, e.g., nutritional and life style reasons is a health concern that is gaining increasing attention over the last two decades. Vitamin D3, the most common isoform of vitamin D, is only available in food derived from animal sources. However, mushrooms and yeast are rich in ergosterol. This compound can be converted into vitamin D2 by UV-light, and therefore act as a precursor for vitamin D. Vitamin D2 from UV-irradiated mushrooms has become an alternative source of vitamin D, especially for persons pursuing a vegan diet. UV-irradiated baker’s yeast (Saccharomyces cerevisiae) for the production of fortified yeast-leavened bread and baked goods was approved as a Novel Food Ingredient in the European Union, according to Regulation (EC) No. 258/97. The Scientific Opinion provided by the European Food Safety Authority Panel on Dietetic Products, Nutrition, and Allergies has assessed this Novel Food Ingredient as safe under the intended nutritional use. However, recent findings on the formation of side products during UV-irradiation, e.g., the photoproducts tachysterol and lumisterol which are compounds with no adequate risk assessment performed, have only been marginally considered for this EFSA opinion. Furthermore, proceedings in analytics can provide additional insights, which might open up new perspectives, also regarding the bioavailability and potential health benefits of vitamin D-fortified mushrooms and yeast. Therefore, this review is intended to give an overview on the current status of UV irradiation in mushrooms and yeast in general and provide a detailed assessment on the potential health effects of UV-irradiated baker’s yeast.
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Vitamin D Metabolites Inhibit Adipocyte Differentiation in 3t3-l1 PreadipocytesNatarajan, Radhika 01 January 2008 (has links) (PDF)
No description available.
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Real-World Evidence Studies on the Association of Serum 25-Hydroxyvitamin D Levels with Pain Intensity and Opioid UseChoong, Casey Kar-chan 12 1900 (has links)
Indiana University-Purdue University Indianapolis (IUPUI) / Vitamin D deficiency has been linked to chronic pain and increased opioid use. Realworld
data such as electronic medical records and administrative claim data contain large
amounts of clinical data and present an opportunity to study the relationship of serum 25-
hydroxyvitamin D [25(OH)D] with pain intensity and opioid use. The first study assessed
the association between serum 25(OH)D) levels and pain intensity. Compared to patients
with normal 25(OH)D levels, those who had insufficient or deficient levels were more
likely to experience moderate or severe pain, with multivariable-adjusted odds ratios
(95% confidence intervals) of 1.19 (1.05-1.36) and 1.51 (1.28-1.79), respectively. Similar
findings were obtained using propensity scores in the matched analyses. In the second
study, we investigated the association between serum 25(OH.)D levels and opioid use
among opioid-naïve patients. We revealed that those who had insufficient or deficient
levels of 25(OH)D were more likely to receive an opioid prescription, with multivariableadjusted
odds ratios of 1.10 (1.02-1.17) and 1.18 (1.09-1.28), respectively, compared to
patients with normal 25(OH)D levels. Vitamin D deficiency was also associated with a
longer duration of opioid use. In the third study, we performed machine learning to
identify patient characteristics associated with persistent moderate-to-severe pain
(PMSP), explicitly investigating if low serum 25(OH)D levels were a risk factor for
heightened pain intensity among obese patients. Low levels of 25(OH)D were
consistently identified as a key predictor from a large number of candidate variables in
the machine learning models. We detected a significant positive association between serum 25(OH)D levels and PMSP in the logistic regression analysis. Compared to
patients with normal levels of 25(OH)D, those who had insufficient or deficient levels of
25(OH)D were more likely to report PMSP, with multivariable-adjusted OR (95% CIs) of
1.15 (1.10-1.21) and 1.28 (1.21-1.35) respectively. We replicated the findings in the first
study in a different cohort that showed that low serum 25(OH)D levels might play a role
in pain perception. This research contributes to an improved understanding of the role of
vitamin D on pain, and opioid use. Individuals who experience pain and need opioid
therapy may benefit from optimizing their serum 25(OH)D levels.
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USE OF A TRANSGENIC MOUSE MODEL OF OVARIAN HYPERSTIUMLUATION TO IDENTIFY THERAPEUTIC TARGETS AND MECHANISMS IN HORMONE-INDUCED MAMMARY CANCERMilliken, Erin L. 13 July 2005 (has links)
No description available.
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The vitamin D endocrine system in skin: Uncoupling the actions of the vitamin D receptor and its ligand in keratinocytesEllison, Tara Ingrid 21 July 2008 (has links)
No description available.
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DESCRIPTIVE STUDY OF VITAMIN D STATUS AND CYSTIC FIBROSIS RELATED DIABETESFeinglass, Erica A. 21 May 2015 (has links)
No description available.
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Serum Vitamin D Status and Breast Cancer Risk by Receptor Status: A Systematic ReviewTommie, Jessica January 2017 (has links)
No description available.
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Hypovitaminosis D and Associated Mortality Within the Hamann-Todd Human Osteological CollectionBrahler, Emily A. 24 April 2018 (has links)
No description available.
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DIFFERENTIAL REGULATION OF VITAMIN D RECEPTOR (VDR) BY p53, p63 AND p73Kommagani, Ramakrishna 14 May 2009 (has links)
No description available.
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Molecular Studies of Host-pathogen Interactions in Human Cytomegalovirus-infected Myeloid CellsWu, Shu-en 11 September 2015 (has links)
No description available.
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