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

Klaver

Showing results (761-770 of 1,112) with videos related to

Pageof 112
Sort By:
Investigative Ophthalmology & Visual Science|February 5, 2010
A novel nonsense mutation in CEP290 induces exon skipping and leads to a relatively mild retinal phenotypeKarin W Littink, Jan-Willem R Pott, Rob W J Collin, et al.
Gut|April 15, 2019
Personalised surveillance for serrated polyposis syndrome: results from a prospective 5-year international cohort studyArne Gc Bleijenberg, Joep Eg IJspeert, Yasmijn J van Herwaarden, et al.
Ophthalmology|August 11, 2024
The Clinical Usefulness of a Glaucoma Polygenic Risk Score in 4 Population-Based European Ancestry CohortsVictor A de Vries, Akiko Hanyuda, Joëlle E Vergroesen, et al.
The Lancet. Oncology|February 12, 2024
The multitarget faecal immunochemical test for improving stool-based colorectal cancer screening programmes: a Dutch population-based, paired-design, intervention studyPieter H A Wisse, Willemijn de Klaver, Francine van Wifferen, et al.
Retina (Philadelphia, Pa.)|February 8, 2020
LONGITUDINAL STUDY OF RPE65-ASSOCIATED INHERITED RETINAL DEGENERATIONSLaurence H M Pierrache, Babak Ghafaryasl, Muhammad I Khan, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|June 7, 2018
The Amsterdam ReBus progressor cohort: identification of 165 Barrett's surveillance patients who progressed to early neoplasia and 723 nonprogressor patientsL C Duits, E Klaver, A Bureo Gonzalez, et al.
NPJ Genomic Medicine|November 19, 2021
Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseasesZeinab Fadaie, Laura Whelan, Tamar Ben-Yosef, et al.
Ophthalmic Genetics|February 5, 2003
A pooled case-control study of the apolipoprotein E (APOE) gene in age-related maculopathySilke Schmidt, Caroline Klaver, Ann Saunders, et al.
European Journal of Endocrinology|August 3, 2021
Estradiol-driven metabolism in transwomen associates with reduced circulating extracellular vesicle microRNA-224/452Barend W Florijn, Jacques M G J Duijs, Maartje Klaver, et al.
BJU International|May 10, 2022
NeuroSAFE in radical prostatectomy increases the rate of nerve-sparing surgery without affecting oncological outcomeMargaretha A van der Slot, Michael A den Bakker, Tamara S C Tan, et al.
Pageof 112

Showing results (761-770 of 1,112) with videos related to

Sort By:
Pageof 112
Investigative Ophthalmology & Visual Science|February 5, 2010
A novel nonsense mutation in CEP290 induces exon skipping and leads to a relatively mild retinal phenotypeKarin W Littink, Jan-Willem R Pott, Rob W J Collin, et al.
Gut|April 15, 2019
Personalised surveillance for serrated polyposis syndrome: results from a prospective 5-year international cohort studyArne Gc Bleijenberg, Joep Eg IJspeert, Yasmijn J van Herwaarden, et al.
Ophthalmology|August 11, 2024
The Clinical Usefulness of a Glaucoma Polygenic Risk Score in 4 Population-Based European Ancestry CohortsVictor A de Vries, Akiko Hanyuda, Joëlle E Vergroesen, et al.
The Lancet. Oncology|February 12, 2024
The multitarget faecal immunochemical test for improving stool-based colorectal cancer screening programmes: a Dutch population-based, paired-design, intervention studyPieter H A Wisse, Willemijn de Klaver, Francine van Wifferen, et al.
Retina (Philadelphia, Pa.)|February 8, 2020
LONGITUDINAL STUDY OF RPE65-ASSOCIATED INHERITED RETINAL DEGENERATIONSLaurence H M Pierrache, Babak Ghafaryasl, Muhammad I Khan, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|June 7, 2018
The Amsterdam ReBus progressor cohort: identification of 165 Barrett's surveillance patients who progressed to early neoplasia and 723 nonprogressor patientsL C Duits, E Klaver, A Bureo Gonzalez, et al.
NPJ Genomic Medicine|November 19, 2021
Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseasesZeinab Fadaie, Laura Whelan, Tamar Ben-Yosef, et al.
Ophthalmic Genetics|February 5, 2003
A pooled case-control study of the apolipoprotein E (APOE) gene in age-related maculopathySilke Schmidt, Caroline Klaver, Ann Saunders, et al.
European Journal of Endocrinology|August 3, 2021
Estradiol-driven metabolism in transwomen associates with reduced circulating extracellular vesicle microRNA-224/452Barend W Florijn, Jacques M G J Duijs, Maartje Klaver, et al.
BJU International|May 10, 2022
NeuroSAFE in radical prostatectomy increases the rate of nerve-sparing surgery without affecting oncological outcomeMargaretha A van der Slot, Michael A den Bakker, Tamara S C Tan, et al.
Pageof 112