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

Frederik H Aidt

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
Histopathology|April 11, 2013
Localization of A11-reactive oligomeric species in prion diseasesFrederik H Aidt, Lis F Hasholt, Michael Christiansen, et al.
Journal of Negative Results in Biomedicine|October 5, 2011
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene studyPaula L Hedley, Ole Haundrup, Paal S Andersen, et al.
Plos One|April 30, 2015
Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathyChristian M Hagen, Frederik H Aidt, Ole Havndrup, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|July 1, 2020
Evolutionary dissection of mtDNA hg H: a susceptibility factor for hypertrophic cardiomyopathyChristian M Hagen, Joanna L Elson, Paula L Hedley, et al.
Plos One|August 14, 2013
Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish populationChristian M Hagen, Frederik H Aidt, Paula L Hedley, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
MT-CYB mutations in hypertrophic cardiomyopathyChristian M Hagen, Frederik H Aidt, Ole Havndrup, et al.
Circulation. Cardiovascular Genetics|September 12, 2013
The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygotePaula L Hedley, Jørgen K Kanters, Maja Dembic, et al.
BMC Medical Genetics|March 11, 2014
Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2Michael Christiansen, Paula L Hedley, Juliane Theilade, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Histopathology|April 11, 2013
Localization of A11-reactive oligomeric species in prion diseasesFrederik H Aidt, Lis F Hasholt, Michael Christiansen, et al.
Journal of Negative Results in Biomedicine|October 5, 2011
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene studyPaula L Hedley, Ole Haundrup, Paal S Andersen, et al.
Plos One|April 30, 2015
Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathyChristian M Hagen, Frederik H Aidt, Ole Havndrup, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|July 1, 2020
Evolutionary dissection of mtDNA hg H: a susceptibility factor for hypertrophic cardiomyopathyChristian M Hagen, Joanna L Elson, Paula L Hedley, et al.
Plos One|August 14, 2013
Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish populationChristian M Hagen, Frederik H Aidt, Paula L Hedley, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
MT-CYB mutations in hypertrophic cardiomyopathyChristian M Hagen, Frederik H Aidt, Ole Havndrup, et al.
Circulation. Cardiovascular Genetics|September 12, 2013
The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygotePaula L Hedley, Jørgen K Kanters, Maja Dembic, et al.
BMC Medical Genetics|March 11, 2014
Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2Michael Christiansen, Paula L Hedley, Juliane Theilade, et al.
Pageof 1