Zobrazeno 1 - 10
of 256
pro vyhledávání: '"Sharon F Terry"'
Web-Based Mindfulness-Based Interventions for Well-being: Randomized Comparative Effectiveness Trial
Autor:
Louisa G Sylvia, Mitchell R Lunn, Juno Obedin-Maliver, Robert N McBurney, W Benjamin Nowell, Rachel L Nosheny, Richard A Mularski, Millie D Long, Peter A Merkel, Mark J Pletcher, Roberta E Tovey, Christopher Scalchunes, Rebecca Sutphen, Ann S Martin, Elizabeth J Horn, Megan O'Boyle, Lisa Pitch, Michael Seid, Susan Redline, Sophie Greenebaum, Nevita George, Noah J French, Caylin M Faria, Nicha Puvanich, Dustin J Rabideau, Caitlin A Selvaggi, Chu Yu, Stephen V Faraone, Shilpa Venkatachalam, Debbe McCall, Sharon F Terry, Thilo Deckersbach, Andrew A Nierenberg
Publikováno v:
Journal of Medical Internet Research, Vol 24, Iss 9, p e35620 (2022)
BackgroundMindfulness can improve overall well-being by training individuals to focus on the present moment without judging their thoughts. However, it is unknown how much mindfulness practice and training are necessary to improve well-being. Object
Externí odkaz:
https://doaj.org/article/77ab1de8c9d845ecbbea1911bace79a9
Autor:
Douglas Ralph, Yvonne Nitschke, Michael A Levine, Matthew Caffet, Tamara Wurst, Amir Hossein Saeidian, Leila Youssefian, Hassan Vahidnezhad, Sharon F Terry, Frank Rutsch, Jouni Uitto, Qiaoli Li
Publikováno v:
PLoS Genetics, Vol 18, Iss 4, p e1010192 (2022)
Pseudoxanthoma elasticum (PXE) and generalized arterial calcification of infancy (GACI) are clinically distinct genetic entities of ectopic calcification associated with differentially reduced circulating levels of inorganic pyrophosphate (PPi), a po
Externí odkaz:
https://doaj.org/article/33be5d418ebc4c14bc28e34b680fc2b8
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
IntroductionPseudoxanthoma elasticum (PXE) is an autosomal recessive ectopic calcification disorder clinically affecting the skin, eyes, and vascular system. Most cases of PXE are caused by inactivating pathogenic variants in the ABCC6 gene encoding
Externí odkaz:
https://doaj.org/article/1c7cd63b56ed4d839a2c08508a7a5642
Publikováno v:
International Journal of Dermatology and Venerology, Vol 3, Iss 4, Pp 198-204 (2020)
Abstract. Objective:. Pseudoxanthoma elasticum (PXE) is a rare genetic disorder caused by loss-of-function mutations in the ABCC6 gene. While PXE is characterized by ectopic mineralization of connective tissues clinically affecting the skin, eyes, an
Externí odkaz:
https://doaj.org/article/a38ed1a3e16641f1ba0c54ef4c94ec6d
Autor:
Sharon F. Terry
Publikováno v:
Genetic Testing and Molecular Biomarkers. 27:131-132
Autor:
Sharon F. Terry
Publikováno v:
Genetic Testing and Molecular Biomarkers. 27:121-122
Autor:
Da-Young (Diane) Kang, Sharon F. Terry
Publikováno v:
Genetic testing and molecular biomarkers. 26(11)
Autor:
Kealy T. Korte, Sharon F. Terry
Publikováno v:
Genetic Testing and Molecular Biomarkers. 27:34-35
Publikováno v:
Therapeutic Innovation & Regulatory Science. 55:1250-1257
The 21st Century Cures Act allows the US Food and Drug Administration (FDA) to utilize real-world data (RWD) to create real-world evidence (RWE) for new indications or post approval study requirements. We compared central adjudication with two insura
Autor:
Flora Szeri, Agnes Miko, Nastassia Navasiolava, Ambrus Kaposi, Shana Verschuere, Beatrix Molnar, Qiaoli Li, Sharon F. Terry, Federica Boraldi, Jouni Uitto, Koen van de Wetering, Ludovic Martin, Daniela Quaglino, Olivier M. Vanakker, Kalman Tory, Tamas Aranyi
Publikováno v:
HUMAN MUTATION
ABCC6 promotes ATP efflux from hepatocytes to bloodstream. ATP is metabolized to pyrophosphate, an inhibitor of ectopic calcification. Pathogenic variants of ABCC6 cause pseudoxanthoma elasticum, a highly variable recessive ectopic calcification diso