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Relevant bibliographies by topics / Pantetheinase Assay

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Academic literature on the topic 'Pantetheinase Assay'

Author: Grafiati

Published: 4 June 2021

Last updated: 17 February 2022

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Journal articles on the topic "Pantetheinase Assay"

1

Rychlik and Roth-Maier. "Pantothenic Acid Quantification: Method Comparison of a Stable Isotope Dilution Assay and a Microbiological Assay." International Journal for Vitamin and Nutrition Research 75, no. 3 (2005): 218–23. http://dx.doi.org/10.1024/0300-9831.75.3.218.

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Different foods and feedstuffs were analyzed for pantothenic acid (PA) by the recently developed stable isotope dilution assay (SIDA) and by the standard method, a microbiological assay (MA). The SIDA involved the use of [13C3, 15N]-pantothenic acid as the internal standard and detection by liquid chromatography-tandem mass spectrometry. The analysis of identical extracts minimized systematic bias due to equal extraction yields and enabled an ideal comparison between both methods. For the samples derived from plants a good accordance between the MA and the SIDA of total PA was found, whereas f

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2

Bogdanov, Lachezar H., Margarita L. Alexandrova, Milena A. Atanasova, and Nikolay Tz Tzvetkov. "Original Article. Diagnostic and Prognostic Potential of Oxidative Stress Markers in Adults with Immune Thrombocytopenia." Journal of Biomedical and Clinical Research 9, no. 2 (2016): 121–25. http://dx.doi.org/10.1515/jbcr-2016-0017.

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Summary Immune thrombocytopenia (ІTP) is one of the most common causes of clinically overt hemorrhage. Despite the progress made in recent years in clarifying the pathogenesis of the disease, the exact unlockmechanisms still remain unclear. The aim of the study was to correlate the oxidative stress markers and the severity of immune thrombocytopenia in adults and to investigate their predictive value of transforming the acute formof ITPinto chronicІTP.We studiedatotal of 58 subjects (14 patients with newly diagnosedІTP, 13 patients with chronic form ofІTR, and 31 controls). The plasma levels o

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3

Wang, Zhongliang, Jianfeng Yu, Nan Hua та ін. "Regulation of chicken vanin1 gene expression by peroxisome proliferators activated receptor α and miRNA-181a-5p". Animal Bioscience 34, № 2 (2021): 172–84. http://dx.doi.org/10.5713/ajas.19.1000.

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Objective: Vanin1 (VNN1) is a pantetheinase that can catalyze the hydrolysis of pantetheine to produce pantothenic acid and cysteamine. Our previous studies showed that <i>VNN1</i> is specifically expressed in chicken liver. In this study, we aimed to investigate the roles of peroxisome proliferators activated receptor α (PPARα) and miRNA-181a-5p in regulating <i>VNN1</i> gene expression in chicken liver.Methods: 5′-RACE was performed to identify the transcription start site of chicken <i>VNN1</i>. JASPAR and TFSEARCH were used to analyze the potential trans

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4

Peat, Thomas, Ykelien Boersma, Janet Newman, Tim Adams, Guy Krippner, and Kiymet Bozaoglu. "Vanin-1- a human ectoenzyme involved in inflammation, metabolism and disease." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C829. http://dx.doi.org/10.1107/s2053273314091700.

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Inflammation is steadily gaining recognition as contributing to different disease states, e.g. cancer, immune dysfunction and cardiovascular disease. Vanin-1, a GPI-anchored, developmentally regulated member of the nitrilase family, sits at the intersection of many known pathways of inflammation. Three members of the vanin family of enzymes in humans have been described, with vanin-1 and vanin-2 having confirmed enzymatic activity. A known substrate is pantetheine which is hydrolyzed to give vitamin B5 and cysteamine. One function of these enzymes is in pantothenate recycling, and therefore th

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Dissertations / Theses on the topic "Pantetheinase Assay"

1

Davidson, Robert T. "Pantothenate-p-nitroanilide as a Substrate for Pantetheinase Assay." DigitalCommons@USU, 1994. https://digitalcommons.usu.edu/etd/5406.

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Pantothenate-p-nitroanilide has been synthesized for use as a substrate in a continuous spectrophotometric assay of pantetheinase activity monitoring absorbance at 41 0 nm. Pantothenate-p-nitroanilide is a crystalline compound with a molecular weight of 338.0 and a melting point of 146-149°C. Use of this substrate in the described assay is suitable for enzyme activity determination in high protein content media such as blood serum. Serum pantetheinase activity was determined for rats of varying pantothenate nutriture. Rats with mildly (but significantly, p

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