Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

L Andreu

Showing results (291-300 of 313) with videos related to

Pageof 32
Sort By:
Age (Dordrecht, Netherlands)|October 29, 2013
The rs1333049 polymorphism on locus 9p21.3 and extreme longevity in Spanish and Japanese cohortsTomàs Pinós, Noriyuki Fuku, Yolanda Cámara, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|August 24, 1999
The long isoform uncoupling protein-3 (UCP3L) in human energy homeostasisW K Chung, A Luke, R S Cooper, et al.
Frontiers in Molecular Biosciences|October 31, 2022
Tackling the translational challenges of multi-omics research in the realm of European personalised medicine: A workshop reportEmanuela Oldoni, Gary Saunders, Florence Bietrix, et al.
Respiratory Research|September 12, 2022
Lung function and radiological findings 1 year after COVID-19: a prospective follow-upJulia Tarraso, Belen Safont, Juan A Carbonell-Asins, et al.
BMC Genomics|November 17, 2017
Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 updateAlfredo Santalla, Gisela Nogales-Gadea, Alberto Blázquez Encinar, et al.
Plos One|May 7, 2014
Mitochondrial DAMPs induce endotoxin tolerance in human monocytes: an observation in patients with myocardial infarctionIrene Fernández-Ruiz, Francisco Arnalich, Carolina Cubillos-Zapata, et al.
Orphanet Journal of Rare Diseases|November 25, 2020
Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)Renata S Scalco, Alejandro Lucia, Alfredo Santalla, et al.
Diabetes|September 10, 1999
Genetic and physiologic analysis of the role of uncoupling protein 3 in human energy homeostasisW K Chung, A Luke, R S Cooper, et al.
Annals of Neurology|June 14, 2000
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutationsI Nishino, A Spinazzola, A Papadimitriou, et al.
Nature Reviews. Drug Discovery|January 29, 2022
A call to action for translational sciences in COVID-19 and future pandemicsKanny K Wan, Danielle Davis, Taylor N Lee, et al.
Pageof 32

Showing results (291-300 of 313) with videos related to

Sort By:
Pageof 32
Age (Dordrecht, Netherlands)|October 29, 2013
The rs1333049 polymorphism on locus 9p21.3 and extreme longevity in Spanish and Japanese cohortsTomàs Pinós, Noriyuki Fuku, Yolanda Cámara, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|August 24, 1999
The long isoform uncoupling protein-3 (UCP3L) in human energy homeostasisW K Chung, A Luke, R S Cooper, et al.
Frontiers in Molecular Biosciences|October 31, 2022
Tackling the translational challenges of multi-omics research in the realm of European personalised medicine: A workshop reportEmanuela Oldoni, Gary Saunders, Florence Bietrix, et al.
Respiratory Research|September 12, 2022
Lung function and radiological findings 1 year after COVID-19: a prospective follow-upJulia Tarraso, Belen Safont, Juan A Carbonell-Asins, et al.
BMC Genomics|November 17, 2017
Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 updateAlfredo Santalla, Gisela Nogales-Gadea, Alberto Blázquez Encinar, et al.
Plos One|May 7, 2014
Mitochondrial DAMPs induce endotoxin tolerance in human monocytes: an observation in patients with myocardial infarctionIrene Fernández-Ruiz, Francisco Arnalich, Carolina Cubillos-Zapata, et al.
Orphanet Journal of Rare Diseases|November 25, 2020
Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)Renata S Scalco, Alejandro Lucia, Alfredo Santalla, et al.
Diabetes|September 10, 1999
Genetic and physiologic analysis of the role of uncoupling protein 3 in human energy homeostasisW K Chung, A Luke, R S Cooper, et al.
Annals of Neurology|June 14, 2000
Mitochondrial neurogastrointestinal encephalomyopathy: an autosomal recessive disorder due to thymidine phosphorylase mutationsI Nishino, A Spinazzola, A Papadimitriou, et al.
Nature Reviews. Drug Discovery|January 29, 2022
A call to action for translational sciences in COVID-19 and future pandemicsKanny K Wan, Danielle Davis, Taylor N Lee, et al.
Pageof 32