Search research articles
Contact Us
Filters
Showing results (1-10 of 13) with videos related to
Page
of 2
Sort By:
Bio-Protocol
|
March 3, 2021
Detection of Heteroplasmic Variants in the Mitochondrial Genome through Massive Parallel Sequencing
Joke Mertens, Filippo Zambelli, Dorien Daneels, et al.
Ecology and Evolution
|
October 8, 2015
Signatures of selection in the three-spined stickleback along a small-scale brackish water - freshwater transition zone
Nellie Konijnendijk, Takahito Shikano, Dorien Daneels, et al.
Nucleic Acids Research
|
September 16, 2017
Understanding mutational effects in digenic diseases
Andrea Gazzo, Daniele Raimondi, Dorien Daneels, et al.
BMC Bioinformatics
|
October 21, 2016
Convert your favorite protein modeling program into a mutation predictor: "MODICT"
Ibrahim Tanyalcin, Katrien Stouffs, Dorien Daneels, et al.
Nucleic Acids Research
|
October 21, 2015
DIDA: A curated and annotated digenic diseases database
Andrea M Gazzo, Dorien Daneels, Elisa Cilia, et al.
F&S Reports
|
July 5, 2021
Novel inactivating follicle-stimulating hormone receptor mutations in a patient with premature ovarian insufficiency identified by next-generation sequencing gene panel analysis
Asma Sassi, Julie Désir, Véronique Janssens, et al.
European Journal of Human Genetics : EJHG
|
August 24, 2017
Accurate and comprehensive analysis of single nucleotide variants and large deletions of the human mitochondrial genome in DNA and single cells
Filippo Zambelli, Kim Vancampenhout, Dorien Daneels, et al.
European Journal of Human Genetics : EJHG
|
June 4, 2015
SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap between cardiac and skeletal muscle sodium channelopathies
Véronique Bissay, Sophie C H Van Malderen, Kathelijn Keymolen, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
August 8, 2017
Prolonged Right Ventricular Ejection Delay in Brugada Syndrome Depends on the Type of SCN5A Variant - Electromechanical Coupling Through Tissue Velocity Imaging as a Bridge Between Genotyping and Phenotyping
Sophie C H Van Malderen, Dorien Daneels, Dirk Kerkhove, et al.
International Journal of Cardiology
|
May 13, 2015
Prolonged right ventricular ejection delay identifies high risk patients and gender differences in Brugada syndrome
Sophie C H Van Malderen, Dirk Kerkhove, Dominic A M J Theuns, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
Bio-Protocol
|
March 3, 2021
Detection of Heteroplasmic Variants in the Mitochondrial Genome through Massive Parallel Sequencing
Joke Mertens, Filippo Zambelli, Dorien Daneels, et al.
Ecology and Evolution
|
October 8, 2015
Signatures of selection in the three-spined stickleback along a small-scale brackish water - freshwater transition zone
Nellie Konijnendijk, Takahito Shikano, Dorien Daneels, et al.
Nucleic Acids Research
|
September 16, 2017
Understanding mutational effects in digenic diseases
Andrea Gazzo, Daniele Raimondi, Dorien Daneels, et al.
BMC Bioinformatics
|
October 21, 2016
Convert your favorite protein modeling program into a mutation predictor: "MODICT"
Ibrahim Tanyalcin, Katrien Stouffs, Dorien Daneels, et al.
Nucleic Acids Research
|
October 21, 2015
DIDA: A curated and annotated digenic diseases database
Andrea M Gazzo, Dorien Daneels, Elisa Cilia, et al.
F&S Reports
|
July 5, 2021
Novel inactivating follicle-stimulating hormone receptor mutations in a patient with premature ovarian insufficiency identified by next-generation sequencing gene panel analysis
Asma Sassi, Julie Désir, Véronique Janssens, et al.
European Journal of Human Genetics : EJHG
|
August 24, 2017
Accurate and comprehensive analysis of single nucleotide variants and large deletions of the human mitochondrial genome in DNA and single cells
Filippo Zambelli, Kim Vancampenhout, Dorien Daneels, et al.
European Journal of Human Genetics : EJHG
|
June 4, 2015
SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap between cardiac and skeletal muscle sodium channelopathies
Véronique Bissay, Sophie C H Van Malderen, Kathelijn Keymolen, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
August 8, 2017
Prolonged Right Ventricular Ejection Delay in Brugada Syndrome Depends on the Type of SCN5A Variant - Electromechanical Coupling Through Tissue Velocity Imaging as a Bridge Between Genotyping and Phenotyping
Sophie C H Van Malderen, Dorien Daneels, Dirk Kerkhove, et al.
International Journal of Cardiology
|
May 13, 2015
Prolonged right ventricular ejection delay identifies high risk patients and gender differences in Brugada syndrome
Sophie C H Van Malderen, Dirk Kerkhove, Dominic A M J Theuns, et al.
Page
of 2