Molecular Transducers of Physical Activity Consortium (MoTrPAC): Mapping the Dynamic Responses to Exercise

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203 Scopus citations

Abstract

The Molecular Transducers of Physical Activity Consortium aims to create a comprehensive, integrative multi-omic map of the effects of exercise across tissues in rodents and healthy people.

Original languageEnglish
Pages (from-to)1464-1474
Number of pages11
JournalCell
Volume181
Issue number7
DOIs
StatePublished - Jun 25 2020

Bibliographical note

Publisher Copyright:
© 2020 Elsevier Inc.

Funding

The authors would like to gratefully acknowledge Jill K. Gregory, CMI, FAMI (Certified Medical Illustrator) of the Icahn School of Medicine at Mount Sinai for working with the writing group to generate the figures enclosed within this article. Additionally, the authors would like to gratefully acknowledge the expert administrative functions by Heather Kiesel of the University of Florida for help organizing efforts by the MoTrPAC Writing Group to better enable the completion of this article. The MoTrPAC Study is supported by NIH grants U24OD026629 (Bioinformatics Center), U24DK112349 , U24DK112342 , U24DK112340 , U24DK112341 , U24DK112326 , U24DK112331 , U24DK112348 (Chemical Analysis Sites), U01AR071133 , U01AR071130 , U01AR071124-01 , U01AR071128 , U01AR071150 , U01AR071160 , U01AR071158 (Clinical Centers), U24AR071113 (Consortium Coordinating Center), U01AG055133 , U01AG055137 , and U01AG055135 (PASS/Animal Sites). The views expressed are those of the authors and do not necessarily reflect those of the NIH or the Department of Health and Human Services of the United States. The authors would like to gratefully acknowledge Jill K. Gregory, CMI, FAMI (Certified Medical Illustrator) of the Icahn School of Medicine at Mount Sinai for working with the writing group to generate the figures enclosed within this article. Additionally, the authors would like to gratefully acknowledge the expert administrative functions by Heather Kiesel of the University of Florida for help organizing efforts by the MoTrPAC Writing Group to better enable the completion of this article. The MoTrPAC Study is supported by NIH grants U24OD026629 (Bioinformatics Center), U24DK112349, U24DK112342, U24DK112340, U24DK112341, U24DK112326, U24DK112331, U24DK112348 (Chemical Analysis Sites), U01AR071133, U01AR071130, U01AR071124-01, U01AR071128, U01AR071150, U01AR071160, U01AR071158 (Clinical Centers), U24AR071113 (Consortium Coordinating Center), U01AG055133, U01AG055137, and U01AG055135 (PASS/Animal Sites). The views expressed are those of the authors and do not necessarily reflect those of the NIH or the Department of Health and Human Services of the United States.

FundersFunder number
FAMI
National Institutes of Health (NIH)U24OD026629, U01AG055137, U24DK112340, U24DK112341, U24DK112331, U24DK112342, U01AR071128, U01AR071158, U01AR071133, U24AR071113, U01AR071124-01, U01AR071130, U01AR071150, U24DK112326, U24DK112348, U24DK112349, U01AG055133, U01AG055135
National Institutes of Health (NIH)
National Institute of Arthritis and Musculoskeletal and Skin DiseasesU01AR071160
National Institute of Arthritis and Musculoskeletal and Skin Diseases
Icahn School of Medicine at Mount Sinai
Cambridge-MIT Institute

    ASJC Scopus subject areas

    • General Biochemistry, Genetics and Molecular Biology

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