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

Plaja

Showing results (131-140 of 153) with videos related to

Pageof 16
Sort By:
Medicina Clinica|June 2, 2020
Effect of the application of the "Patient blood management" programme on the approach to elective hip and knee arthroplastiesSaioa Zalba Marcos, Inés Plaja Martí, María Luisa Antelo Caamaño, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 23, 2014
Generation of bright isolated attosecond soft X-ray pulses driven by multicycle midinfrared lasersMing-Chang Chen, Christopher Mancuso, Carlos Hernández-García, et al.
British Journal of Cancer|August 22, 2022
Natural immunity to SARS-CoV-2 and breakthrough infections in vaccinated and unvaccinated patients with cancerAlessio Cortellini, Juan Aguilar-Company, Ramon Salazar, et al.
American Journal of Medical Genetics. Part A|December 24, 2022
ZDHHC15 as a candidate gene for autism spectrum disorderDolors Casellas-Vidal, Irene Mademont-Soler, Joana Sánchez, et al.
Science (New York, N.Y.)|June 29, 2019
Generation of extreme-ultraviolet beams with time-varying orbital angular momentumLaura Rego, Kevin M Dorney, Nathan J Brooks, et al.
Clinical Immunology (Orlando, Fla.)|March 25, 2018
TNFAIP3 haploinsufficiency is the cause of autoinflammatory manifestations in a patient with a deletion of 13Mb on chromosome 6Clara Franco-Jarava, Hongying Wang, Andrea Martin-Nalda, et al.
Genes|August 26, 2022
A Novel Intragenic Duplication in the <i>HDAC8</i> Gene Underlying a Case of Cornelia de Lange SyndromeCristina Lucia-Campos, Irene Valenzuela, Ana Latorre-Pellicer, et al.
Human Genetics|October 7, 2011
Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosisLluís Armengol, Julián Nevado, Clara Serra-Juhé, et al.
Nature Photonics|October 26, 2020
Controlling the polarization and vortex charge of attosecond high-harmonic beams via simultaneous spin-orbit momentum conservationKevin M Dorney, Laura Rego, Nathan J Brooks, et al.
Journal of Medical Genetics|July 11, 2006
Tumour selection advantage of non-dominant negative P53 mutations in homozygotic MDM2-SNP309 colorectal cancer cellsHafid Alazzouzi, Gianpaolo Suriano, Angel Guerra, et al.
Pageof 16

Showing results (131-140 of 153) with videos related to

Sort By:
Pageof 16
Medicina Clinica|June 2, 2020
Effect of the application of the "Patient blood management" programme on the approach to elective hip and knee arthroplastiesSaioa Zalba Marcos, Inés Plaja Martí, María Luisa Antelo Caamaño, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 23, 2014
Generation of bright isolated attosecond soft X-ray pulses driven by multicycle midinfrared lasersMing-Chang Chen, Christopher Mancuso, Carlos Hernández-García, et al.
British Journal of Cancer|August 22, 2022
Natural immunity to SARS-CoV-2 and breakthrough infections in vaccinated and unvaccinated patients with cancerAlessio Cortellini, Juan Aguilar-Company, Ramon Salazar, et al.
American Journal of Medical Genetics. Part A|December 24, 2022
ZDHHC15 as a candidate gene for autism spectrum disorderDolors Casellas-Vidal, Irene Mademont-Soler, Joana Sánchez, et al.
Science (New York, N.Y.)|June 29, 2019
Generation of extreme-ultraviolet beams with time-varying orbital angular momentumLaura Rego, Kevin M Dorney, Nathan J Brooks, et al.
Clinical Immunology (Orlando, Fla.)|March 25, 2018
TNFAIP3 haploinsufficiency is the cause of autoinflammatory manifestations in a patient with a deletion of 13Mb on chromosome 6Clara Franco-Jarava, Hongying Wang, Andrea Martin-Nalda, et al.
Genes|August 26, 2022
A Novel Intragenic Duplication in the <i>HDAC8</i> Gene Underlying a Case of Cornelia de Lange SyndromeCristina Lucia-Campos, Irene Valenzuela, Ana Latorre-Pellicer, et al.
Human Genetics|October 7, 2011
Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosisLluís Armengol, Julián Nevado, Clara Serra-Juhé, et al.
Nature Photonics|October 26, 2020
Controlling the polarization and vortex charge of attosecond high-harmonic beams via simultaneous spin-orbit momentum conservationKevin M Dorney, Laura Rego, Nathan J Brooks, et al.
Journal of Medical Genetics|July 11, 2006
Tumour selection advantage of non-dominant negative P53 mutations in homozygotic MDM2-SNP309 colorectal cancer cellsHafid Alazzouzi, Gianpaolo Suriano, Angel Guerra, et al.
Pageof 16