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Maja Dembic

Showing results (11-20 of 21) with videos related to

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Biochimica Et Biophysica Acta|October 9, 2007
Cystatin B and its EPM1 mutants are polymeric and aggregate prone in vivoElena Cipollini, Massimo Riccio, Rossella Di Giaimo, et al.
Cancer Letters|December 17, 2005
Establishment and characterization of murine small cell lung carcinoma cell lines derived from HPV-16 E6/E7 transgenic miceLaura Carraresi, Rosanna Martinelli, Alessandro Vannoni, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|September 26, 2015
Combined gating and trafficking defect in Kv11.1 manifests as a malignant long QT syndrome phenotype in a large Danish p.F29L founder familyJørgen K Kanters, Lasse Skibsbye, Paula L Hedley, et al.
Frontiers in Genetics|November 7, 2022
Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencingAlexander Varzari, Igor V Deyneko, Gitte Hoffmann Bruun, et al.
Molecular Genetics and Metabolism|November 18, 2018
Next generation sequencing of RNA reveals novel targets of resveratrol with possible implications for Canavan diseaseMaja Dembic, Henriette S Andersen, Jean Bastin, et al.
Nucleic Acids Research|August 26, 2016
RNA-sequencing of a mouse-model of spinal muscular atrophy reveals tissue-wide changes in splicing of U12-dependent intronsThomas Koed Doktor, Yimin Hua, Henriette Skovgaard Andersen, et al.
Molecular Genetics and Metabolism|November 11, 2017
An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiencySigne Mosegaard, Gitte Hoffmann Bruun, Karen Freund Flyvbjerg, 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.
Molecular Therapy. Nucleic Acids|January 11, 2024
Regulating <i>PCCA</i> gene expression by modulation of pseudoexon splicing patterns to rescue enzyme activity in propionic acidemiaUlrika Simone Spangsberg Petersen, Maja Dembic, Ainhoa Martínez-Pizarro, et al.
JCI Insight|April 8, 2025
Mutational landscape of atherosclerotic plaques reveals large clonal cell populationsLasse Bach Steffensen, Stephanie Kavan, Pia Søndergaard Jensen, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Biochimica Et Biophysica Acta|October 9, 2007
Cystatin B and its EPM1 mutants are polymeric and aggregate prone in vivoElena Cipollini, Massimo Riccio, Rossella Di Giaimo, et al.
Cancer Letters|December 17, 2005
Establishment and characterization of murine small cell lung carcinoma cell lines derived from HPV-16 E6/E7 transgenic miceLaura Carraresi, Rosanna Martinelli, Alessandro Vannoni, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|September 26, 2015
Combined gating and trafficking defect in Kv11.1 manifests as a malignant long QT syndrome phenotype in a large Danish p.F29L founder familyJørgen K Kanters, Lasse Skibsbye, Paula L Hedley, et al.
Frontiers in Genetics|November 7, 2022
Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencingAlexander Varzari, Igor V Deyneko, Gitte Hoffmann Bruun, et al.
Molecular Genetics and Metabolism|November 18, 2018
Next generation sequencing of RNA reveals novel targets of resveratrol with possible implications for Canavan diseaseMaja Dembic, Henriette S Andersen, Jean Bastin, et al.
Nucleic Acids Research|August 26, 2016
RNA-sequencing of a mouse-model of spinal muscular atrophy reveals tissue-wide changes in splicing of U12-dependent intronsThomas Koed Doktor, Yimin Hua, Henriette Skovgaard Andersen, et al.
Molecular Genetics and Metabolism|November 11, 2017
An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiencySigne Mosegaard, Gitte Hoffmann Bruun, Karen Freund Flyvbjerg, 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.
Molecular Therapy. Nucleic Acids|January 11, 2024
Regulating <i>PCCA</i> gene expression by modulation of pseudoexon splicing patterns to rescue enzyme activity in propionic acidemiaUlrika Simone Spangsberg Petersen, Maja Dembic, Ainhoa Martínez-Pizarro, et al.
JCI Insight|April 8, 2025
Mutational landscape of atherosclerotic plaques reveals large clonal cell populationsLasse Bach Steffensen, Stephanie Kavan, Pia Søndergaard Jensen, et al.
Pageof 3