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

D Madsen

Showing results (241-250 of 246) with videos related to

Pageof 25
Sort By:
You have reached the last page of results.This site can display upto 246 results.
American Journal of Human Genetics|June 4, 2016
Mutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver DiseaseBinu Porath, Vladimir G Gainullin, Emilie Cornec-Le Gall, et al.
American Journal of Human Genetics|May 1, 2018
Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney DiseaseEmilie Cornec-Le Gall, Rory J Olson, Whitney Besse, et al.
Nature Materials|January 26, 2021
Basement membrane stiffness determines metastases formationRaphael Reuten, Sina Zendehroud, Monica Nicolau, et al.
American Journal of Human Genetics|December 10, 2021
Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotypeSarah R Senum, Ying Sabrina M Li, Katherine A Benson, et al.
Molecular Metabolism|January 9, 2018
The EndoC-βH1 cell line is a valid model of human beta cells and applicable for screenings to identify novel drug target candidatesVioleta Georgieva Tsonkova, Fredrik Wolfhagen Sand, Xenia Asbæk Wolf, et al.
Acta Anaesthesiologica Scandinavica|February 3, 2026
Intraoperative Hypotension and Vasoactive Treatment: An International Survey of AnaesthesiologistsEmilie S Bækgaard, Morten Vester-Andersen, Vera Crone, et al.
Pageof 25

Showing results (241-250 of 246) with videos related to

Sort By:
Pageof 25
You have reached the last page of results.This site can display upto 246 results.
American Journal of Human Genetics|June 4, 2016
Mutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver DiseaseBinu Porath, Vladimir G Gainullin, Emilie Cornec-Le Gall, et al.
American Journal of Human Genetics|May 1, 2018
Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney DiseaseEmilie Cornec-Le Gall, Rory J Olson, Whitney Besse, et al.
Nature Materials|January 26, 2021
Basement membrane stiffness determines metastases formationRaphael Reuten, Sina Zendehroud, Monica Nicolau, et al.
American Journal of Human Genetics|December 10, 2021
Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotypeSarah R Senum, Ying Sabrina M Li, Katherine A Benson, et al.
Molecular Metabolism|January 9, 2018
The EndoC-βH1 cell line is a valid model of human beta cells and applicable for screenings to identify novel drug target candidatesVioleta Georgieva Tsonkova, Fredrik Wolfhagen Sand, Xenia Asbæk Wolf, et al.
Acta Anaesthesiologica Scandinavica|February 3, 2026
Intraoperative Hypotension and Vasoactive Treatment: An International Survey of AnaesthesiologistsEmilie S Bækgaard, Morten Vester-Andersen, Vera Crone, et al.
Pageof 25