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Frontiers in Cell and Developmental Biology
|
March 9, 2026
Integrative epigenetic and transcriptomic profiling of whole blood and fibroblasts in Hao-Fountain syndrome
Liselot van der Laan, Rob Zwart, Andrea Venema, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
May 3, 2011
Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy
A van den Wijngaard, P Volders, J P Van Tintelen, et al.
Frontiers in Immunology
|
May 10, 2021
Novel Insights Into Rheumatoid Arthritis Through Characterization of Concordant Changes in DNA Methylation and Gene Expression in Synovial Biopsies of Patients With Differing Numbers of Swollen Joints
Andrew Y F Li Yim, Enrico Ferrero, Klio Maratou, et al.
Clinical Epigenetics
|
September 27, 2017
An epigenome-wide association study in whole blood of measures of adiposity among Ghanaians: the RODAM study
Karlijn A C Meeks, Peter Henneman, Andrea Venema, et al.
International Journal of Epidemiology
|
August 15, 2018
Epigenome-wide association study in whole blood on type 2 diabetes among sub-Saharan African individuals: findings from the RODAM study
Karlijn A C Meeks, Peter Henneman, Andrea Venema, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 22, 2025
Discovery of a DNA methylation episignature as a molecular biomarker for fetal alcohol syndrome
Liselot van der Laan, Raissa Relator, Irene Valenzuela, et al.
Genes & Development
|
March 21, 2018
An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethality
Christina M Ferrer, Marielle Alders, Alex V Postma, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 19, 1995
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
J M Hoovers, L M Kalikin, L A Johnson, et al.
International Journal of Molecular Sciences
|
September 28, 2023
Functional Insight into and Refinement of the Genomic Boundaries of the <i>JARID2</i>-Neurodevelopmental Disorder Episignature
Liselot van der Laan, Kathleen Rooney, Sadegheh Haghshenas, et al.
Human Genetics
|
August 31, 2010
Intragenic deletions and a deep intronic mutation affecting pre-mRNA splicing in the dihydropyrimidine dehydrogenase gene as novel mechanisms causing 5-fluorouracil toxicity
André B P van Kuilenburg, Judith Meijer, Adri N P M Mul, et al.
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Search research articles
Search
Showing results (131-140 of 172) with videos related to
Sort By:
Page
of 18
Frontiers in Cell and Developmental Biology
|
March 9, 2026
Integrative epigenetic and transcriptomic profiling of whole blood and fibroblasts in Hao-Fountain syndrome
Liselot van der Laan, Rob Zwart, Andrea Venema, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
May 3, 2011
Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy
A van den Wijngaard, P Volders, J P Van Tintelen, et al.
Frontiers in Immunology
|
May 10, 2021
Novel Insights Into Rheumatoid Arthritis Through Characterization of Concordant Changes in DNA Methylation and Gene Expression in Synovial Biopsies of Patients With Differing Numbers of Swollen Joints
Andrew Y F Li Yim, Enrico Ferrero, Klio Maratou, et al.
Clinical Epigenetics
|
September 27, 2017
An epigenome-wide association study in whole blood of measures of adiposity among Ghanaians: the RODAM study
Karlijn A C Meeks, Peter Henneman, Andrea Venema, et al.
International Journal of Epidemiology
|
August 15, 2018
Epigenome-wide association study in whole blood on type 2 diabetes among sub-Saharan African individuals: findings from the RODAM study
Karlijn A C Meeks, Peter Henneman, Andrea Venema, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 22, 2025
Discovery of a DNA methylation episignature as a molecular biomarker for fetal alcohol syndrome
Liselot van der Laan, Raissa Relator, Irene Valenzuela, et al.
Genes & Development
|
March 21, 2018
An inactivating mutation in the histone deacetylase SIRT6 causes human perinatal lethality
Christina M Ferrer, Marielle Alders, Alex V Postma, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 19, 1995
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
J M Hoovers, L M Kalikin, L A Johnson, et al.
International Journal of Molecular Sciences
|
September 28, 2023
Functional Insight into and Refinement of the Genomic Boundaries of the <i>JARID2</i>-Neurodevelopmental Disorder Episignature
Liselot van der Laan, Kathleen Rooney, Sadegheh Haghshenas, et al.
Human Genetics
|
August 31, 2010
Intragenic deletions and a deep intronic mutation affecting pre-mRNA splicing in the dihydropyrimidine dehydrogenase gene as novel mechanisms causing 5-fluorouracil toxicity
André B P van Kuilenburg, Judith Meijer, Adri N P M Mul, et al.
Page
of 18