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

Pablo Serrano

Showing results (71-80 of 141) with videos related to

Pageof 15
Sort By:
Genes|October 30, 2019
A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish PopulationVirginia Garcia-Solaesa, Pablo Serrano-Lorenzo, Maria Antonia Ramos-Arroyo, et al.
Methods of Information in Medicine|October 11, 2022
TransformEHRs: a flexible methodology for building transparent ETL processes for EHR reuseMiguel Pedrera-Jiménez, Noelia García-Barrio, Paula Rubio-Mayo, et al.
Breast Cancer Research and Treatment|November 26, 2008
Synergistic interaction of variants in CHEK2 and BRCA2 on breast cancer riskPablo Serrano-Fernández, Tadeusz Debniak, Bohdan Górski, et al.
BMC Research Notes|February 26, 2025
Identification of a novel transcript of mouse SdhaMaría J Esteban-Amo, Amaia Telleria, Dino Gobelli, et al.
Genes|July 30, 2020
Novel <i>NDUFA13</i> Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family ReportAdrián González-Quintana, Inés García-Consuegra, Amaya Belanger-Quintana, et al.
Computer Methods and Programs in Biomedicine Update|January 3, 2023
Predicting the evolution of COVID-19 mortality risk: A Recurrent Neural Network approachMarta Villegas, Aitor Gonzalez-Agirre, Asier Gutiérrez-Fandiño, et al.
The Journal of Molecular Diagnostics : JMD|December 17, 2009
Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patientsDagmara Dymerska, Pablo Serrano-Fernández, Janina Suchy, et al.
International Journal of Cancer|October 6, 2007
Germline mutations in the CHEK2 kinase gene are associated with an increased risk of bladder cancerElzbieta Złowocka, Cezary Cybulski, Bohdan Górski, et al.
Plos One|September 19, 2023
Development of a novel in vitro model to study the modulatory role of the respiratory complex I in macrophage effector functionsPablo Serrano-Lorenzo, Dino Gobelli, Rocío Garrido-Moraga, et al.
Artificial Organs|November 24, 2021
The role of extracorporeal membrane oxygenation in adult liver transplant patients: A qualitative systematic review of literatureTrista D Reid, Ian M Kratzke, Diana Dayal, et al.
Pageof 15

Showing results (71-80 of 141) with videos related to

Sort By:
Pageof 15
Genes|October 30, 2019
A Novel Missense Variant Associated with A Splicing Defect in A Myopathic Form of PGK1 Deficiency in The Spanish PopulationVirginia Garcia-Solaesa, Pablo Serrano-Lorenzo, Maria Antonia Ramos-Arroyo, et al.
Methods of Information in Medicine|October 11, 2022
TransformEHRs: a flexible methodology for building transparent ETL processes for EHR reuseMiguel Pedrera-Jiménez, Noelia García-Barrio, Paula Rubio-Mayo, et al.
Breast Cancer Research and Treatment|November 26, 2008
Synergistic interaction of variants in CHEK2 and BRCA2 on breast cancer riskPablo Serrano-Fernández, Tadeusz Debniak, Bohdan Górski, et al.
BMC Research Notes|February 26, 2025
Identification of a novel transcript of mouse SdhaMaría J Esteban-Amo, Amaia Telleria, Dino Gobelli, et al.
Genes|July 30, 2020
Novel <i>NDUFA13</i> Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family ReportAdrián González-Quintana, Inés García-Consuegra, Amaya Belanger-Quintana, et al.
Computer Methods and Programs in Biomedicine Update|January 3, 2023
Predicting the evolution of COVID-19 mortality risk: A Recurrent Neural Network approachMarta Villegas, Aitor Gonzalez-Agirre, Asier Gutiérrez-Fandiño, et al.
The Journal of Molecular Diagnostics : JMD|December 17, 2009
Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patientsDagmara Dymerska, Pablo Serrano-Fernández, Janina Suchy, et al.
International Journal of Cancer|October 6, 2007
Germline mutations in the CHEK2 kinase gene are associated with an increased risk of bladder cancerElzbieta Złowocka, Cezary Cybulski, Bohdan Górski, et al.
Plos One|September 19, 2023
Development of a novel in vitro model to study the modulatory role of the respiratory complex I in macrophage effector functionsPablo Serrano-Lorenzo, Dino Gobelli, Rocío Garrido-Moraga, et al.
Artificial Organs|November 24, 2021
The role of extracorporeal membrane oxygenation in adult liver transplant patients: A qualitative systematic review of literatureTrista D Reid, Ian M Kratzke, Diana Dayal, et al.
Pageof 15