Original language | English |
---|---|
Pages (from-to) | 3977-3981 |
Number of pages | 5 |
Journal | Blood Advances |
Volume | 3 |
Issue number | 23 |
DOIs | |
Publication status | Published - 2019 |
Externally published | Yes |
ASJC Scopus subject areas
- Hematology
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Computational analysis of continuous body temperature provides early discrimination of graft-versus-host disease in mice. / He, Kuang; Wu, Zhenke; Fujiwara, Hideaki et al.
In: Blood Advances, Vol. 3, No. 23, 2019, p. 3977-3981.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Computational analysis of continuous body temperature provides early discrimination of graft-versus-host disease in mice
AU - He, Kuang
AU - Wu, Zhenke
AU - Fujiwara, Hideaki
AU - Whitesall, Steven
AU - Zajac, Cynthia K.
AU - Choi, Sung Won
AU - Reddy, Pavan
AU - Tewari, Muneesh
N1 - Funding Information: K.H. was supported by a Clinical and Translational Science Award from the National Center for Advancing Translational Sciences of the National Institutes of Health (NIH). Z.W. was supported in part by NIH grant CA046592 (National Cancer Institute) through the Cancer Center Support Grant Development Funds from the Rogel Cancer Center and an investigator award from Michigan Precision Health Initiative. H.F. was supported by a Postdoctoral Fellowship for Research Abroad from Japan Society for the Promotion of Science and YASUDA Medical Foundation Grants for Research Abroad. M.T. and S.W.C. acknowledge support from an A. Alfred Taubman Medical Research Institute Grand Challenge Award. P.R. acknowledges support from NIH grants CA203542 (National Cancer Institute), CA217156 (National Cancer Institute), and HL128046 (National Heart, Lung, and Blood Institute). M.T. acknowledges support from Mary Petrovich through the University of Michigan Fast Forward Gastrointestinal Innovation Fund. The Physiology Phenotyping Core at the University of Michigan was supported in part by the Frankel Cardiovascular Center. Funding Information: The authors thank Ryan Spengler, Erin Sandford, Nicholas W. Lukacs, and Erin G. Janowicz for helpful discussions and the Physiology Phenotyping Core at the University of Michigan for technical assistance. K.H. was supported by a Clinical and Translational Science Award from the National Center for Advancing Translational Sciences of the National Institutes of Health (NIH). Z.W. was supported in part by NIH grant CA046592 (National Cancer Institute) through the Cancer Center Support Grant Development Funds from the Rogel Cancer Center and an investigator award from Michigan Precision Health Initiative. H.F. was supported by a Postdoctoral Fellowship for Research Abroad from Japan Society for the Promotion of Science and YASUDA Medical Foundation Grants for Research Abroad. M.T. and S.W.C. acknowledge support from an A. Alfred Taubman Medical Research Institute Grand Challenge Award. P.R. acknowledges support from NIH grants CA203542 (National Cancer Institute), CA217156 (National Cancer Institute), and HL128046 (National Heart, Lung, and Blood Institute). M.T. acknowledges support from Mary Petrovich through the University of Michigan Fast Forward Gastrointestinal Innovation Fund. The Physiology Phenotyping Core at the University of Michigan was supported in part by the Frankel Cardiovascular Center.
PY - 2019
Y1 - 2019
UR - http://www.scopus.com/inward/record.url?scp=85076358101&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85076358101&partnerID=8YFLogxK
U2 - 10.1182/bloodadvances.2019000613
DO - 10.1182/bloodadvances.2019000613
M3 - Article
C2 - 31809535
AN - SCOPUS:85076358101
VL - 3
SP - 3977
EP - 3981
JO - Blood advances
JF - Blood advances
SN - 2473-9529
IS - 23
ER -