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

Houria Daimi

Showing results (1-10 of 17) with videos related to

Pageof 2
Sort By:
International Journal of Molecular Sciences|August 14, 2020
Genetics and Epigenetics of Atrial FibrillationEstefanía Lozano-Velasco, Diego Franco, Amelia Aranega, et al.
International Journal of Molecular Sciences|February 15, 2022
Genomic and Non-Genomic Regulatory Mechanisms of the Cardiac Sodium Channel in Cardiac ArrhythmiasHouria Daimi, Estefanía Lozano-Velasco, Amelia Aranega, et al.
Frontiers in Genetics|January 25, 2024
The burden of cystic fibrosis in North AfricaNada El Makhzen, Houria Daimi, Laila Bouguenouch, et al.
Cardiovascular Research|March 24, 2011
Modulation of conductive elements by Pitx2 and their impact on atrial arrhythmogenesisDiego Franco, Ana Chinchilla, Houria Daimi, et al.
International Journal of Molecular Sciences|June 28, 2023
LncRNAs and CircRNAs in Endoplasmic Reticulum Stress: A Promising Target for Cardiovascular Disease?Francisco José Martinez-Amaro, Carlos Garcia-Padilla, Diego Franco, et al.
Cardiovascular Research|August 26, 2010
MicroRNA profiling during mouse ventricular maturation: a role for miR-27 modulating Mef2c expressionAna Chinchilla, Estefania Lozano, Houria Daimi, et al.
Pediatric Cardiology|March 12, 2015
Absence of family history and phenotype-genotype correlation in pediatric Brugada syndrome: more burden to bear in clinical and genetic diagnosisHouria Daimi, Amel Haj Khelil, Khaldoun Ben Hamda, et al.
Hemoglobin|February 2, 2010
Hemoglobinopathies in North Africa: a reviewAmel Haj Khelil, Sabri Denden, Nadia Leban, et al.
Disease Markers|July 8, 2011
Combined analysis of EPHX1, GSTP1, GSTM1 and GSTT1 gene polymorphisms in relation to chronic obstructive pulmonary disease risk and lung function impairmentRamzi Lakhdar, Sabri Denden, Jalel Knani, et al.
Biomedical Journal|October 20, 2019
Role of SCN5A coding and non-coding sequences in Brugada syndrome onset: What's behind the scenes?Houria Daimi, Amel Haj Khelil, Ali Neji, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
International Journal of Molecular Sciences|August 14, 2020
Genetics and Epigenetics of Atrial FibrillationEstefanía Lozano-Velasco, Diego Franco, Amelia Aranega, et al.
International Journal of Molecular Sciences|February 15, 2022
Genomic and Non-Genomic Regulatory Mechanisms of the Cardiac Sodium Channel in Cardiac ArrhythmiasHouria Daimi, Estefanía Lozano-Velasco, Amelia Aranega, et al.
Frontiers in Genetics|January 25, 2024
The burden of cystic fibrosis in North AfricaNada El Makhzen, Houria Daimi, Laila Bouguenouch, et al.
Cardiovascular Research|March 24, 2011
Modulation of conductive elements by Pitx2 and their impact on atrial arrhythmogenesisDiego Franco, Ana Chinchilla, Houria Daimi, et al.
International Journal of Molecular Sciences|June 28, 2023
LncRNAs and CircRNAs in Endoplasmic Reticulum Stress: A Promising Target for Cardiovascular Disease?Francisco José Martinez-Amaro, Carlos Garcia-Padilla, Diego Franco, et al.
Cardiovascular Research|August 26, 2010
MicroRNA profiling during mouse ventricular maturation: a role for miR-27 modulating Mef2c expressionAna Chinchilla, Estefania Lozano, Houria Daimi, et al.
Pediatric Cardiology|March 12, 2015
Absence of family history and phenotype-genotype correlation in pediatric Brugada syndrome: more burden to bear in clinical and genetic diagnosisHouria Daimi, Amel Haj Khelil, Khaldoun Ben Hamda, et al.
Hemoglobin|February 2, 2010
Hemoglobinopathies in North Africa: a reviewAmel Haj Khelil, Sabri Denden, Nadia Leban, et al.
Disease Markers|July 8, 2011
Combined analysis of EPHX1, GSTP1, GSTM1 and GSTT1 gene polymorphisms in relation to chronic obstructive pulmonary disease risk and lung function impairmentRamzi Lakhdar, Sabri Denden, Jalel Knani, et al.
Biomedical Journal|October 20, 2019
Role of SCN5A coding and non-coding sequences in Brugada syndrome onset: What's behind the scenes?Houria Daimi, Amel Haj Khelil, Ali Neji, et al.
Pageof 2