Zobrazeno 1 - 10
of 655
pro vyhledávání: '"Summer, R."'
Autor:
Jackson, Summer R.1 (AUTHOR) sjackson@hbs.edu
Publikováno v:
Administrative Science Quarterly. Sep2023, Vol. 68 Issue 3, p824-866. 43p. 2 Diagrams, 5 Charts.
Autor:
Ballard-Kordeliski, Abigail, Lee, Robert H., O’Shaughnessy, Ellen C., Kim, Paul Y., Jones, Summer R., Pawlinski, Rafal, Flick, Matthew J., Paul, David S., Mackman, Nigel, Adalsteinsson, David A., Bergmeier, Wolfgang
Publikováno v:
In Blood 5 September 2024 144(10):1116-1126
Publikováno v:
PLoS ONE, Vol 19, Iss 1, p e0295899 (2024)
Despite considerable health consequences from preterm births, their incidence remains unchanged over recent decades, due partially to limited screening methods and limited use of extant methods. Wearable technology offers a novel, noninvasive, and ac
Externí odkaz:
https://doaj.org/article/cbf10c7c250a4749a77bb105ed0d474a
Publikováno v:
In The Journal of Pain December 2023 24(12):2153-2161
Autor:
Jasinski, Summer R.1 (AUTHOR), Rowan, Shon2 (AUTHOR), Presby, David M.1 (AUTHOR), Claydon, Elizabeth A.3 (AUTHOR), Capodilupo, Emily R.1 (AUTHOR) emily@whoop.com
Publikováno v:
PLoS ONE. 1/31/2024, Vol. 19 Issue 1, p1-9. 9p.
Publikováno v:
PLoS ONE, Vol 18, Iss 6, p e0285332 (2023)
Stress contributes to the progression of many diseases. Despite stress' contribution towards disease, few methods for continuously measuring stress exist. We investigated if continuously measured cardiovascular signals from a wearable device can be u
Externí odkaz:
https://doaj.org/article/4fb2c9df00c54e23828fbed7b8fbb1f0
Autor:
Presby, David M.1 (AUTHOR) David.Presby@whoop.com, Jasinski, Summer R.1 (AUTHOR), Capodilupo, Emily R.1 (AUTHOR)
Publikováno v:
PLoS ONE. 6/2/2023, Vol. 17 Issue 6, p1-11. 11p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Alecia Biel, Anthony S. Castanza, Ryan Rutherford, Summer R. Fair, Lincoln Chifamba, Jason C. Wester, Mark E. Hester, Robert F. Hevner
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 15 (2022)
AUTS2 syndrome is a genetic disorder that causes intellectual disability, microcephaly, and other phenotypes. Syndrome severity is worse when mutations involve 3’ regions (exons 9-19) of the AUTS2 gene. Human AUTS2 protein has two major isoforms, f
Externí odkaz:
https://doaj.org/article/b055d3ed8723439eb7145c9b8f026b2c
Autor:
Carrillo, Leah1, Wilmoth, Summer R.2, Mendoza, Raymundo3, Balarin, Ashton4, Pan, Meixia5, Martinez, Elena4, Sosa, Erica T.2, Zenong Yin2, Ullevig, Sarah6, Meizi He2 meizi.he@utsa.edu
Publikováno v:
Journal of Health Disparities Research & Practice. Spring2023, Vol. 16 Issue 1, p65-81. 17p.