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Journal of Molecular Neuroscience : MN
|
January 22, 2018
Correction to: The Compassionate Side of Neuroscience: Tony Sermone's Undiagnosed Genetic Journey-ADNP Mutation
Illana Gozes, Celine Helsmoortel, Geert Vandeweyer, et al.
Calcified Tissue International
|
February 7, 2019
Genetic Variation in RIN3 in the Belgian Population Supports Its Involvement in the Pathogenesis of Paget's Disease of Bone and Modifies the Age of Onset
Raphaël De Ridder, Eveline Boudin, Geert Vandeweyer, et al.
Journal of Translational Medicine
|
March 3, 2024
CRISPR/Cas9-edited ROS1 + non-small cell lung cancer cell lines highlight differential drug sensitivity in 2D vs 3D cultures while reflecting established resistance profiles
Marc Terrones, Christophe Deben, Felicia Rodrigues-Fortes, et al.
Scientific Reports
|
January 29, 2021
Abundancy of polymorphic CGG repeats in the human genome suggest a broad involvement in neurological disease
Dale J Annear, Geert Vandeweyer, Ellen Elinck, et al.
Bioinformatics (Oxford, England)
|
February 17, 2018
pBRIT: gene prioritization by correlating functional and phenotypic annotations through integrative data fusion
Ajay Anand Kumar, Lut Van Laer, Maaike Alaerts, et al.
Epilepsy Research
|
January 17, 2012
A de novo balanced t(2;6)(p15;p22.3) in a patient with West Syndrome disrupts a lnc-RNA
Geert Vandeweyer, Nathalie Van der Aa, Berten Ceulemans, et al.
Journal of Biomolecular Structure & Dynamics
|
January 17, 2025
Exploring the conformational space of ROS1 kinase domain and the impact of allosteric mutations
Farhan Ul Haq, Juliana Fatima Vilachã, Ken Op de Beeck, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
June 13, 2012
Haploinsufficiency of CMIP in a girl with autism spectrum disorder and developmental delay due to a de novo deletion on chromosome 16q23.2
Nathalie Van der Aa, Geert Vandeweyer, Edwin Reyniers, et al.
Bioinformatics (Oxford, England)
|
November 28, 2022
varAmpliCNV: analyzing variance of amplicons to detect CNVs in targeted NGS data
Ajay Anand Kumar, Bart Loeys, Gerarda Van De Beek, et al.
Neurobiology of Aging
|
May 17, 2022
Protein interaction network analysis reveals genetic enrichment of immune system genes in frontotemporal dementia
Cemile Koçoğlu, Raffaele Ferrari, Maxime Roes, et al.
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Search research articles
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Showing results (21-30 of 77) with videos related to
Sort By:
Page
of 8
Journal of Molecular Neuroscience : MN
|
January 22, 2018
Correction to: The Compassionate Side of Neuroscience: Tony Sermone's Undiagnosed Genetic Journey-ADNP Mutation
Illana Gozes, Celine Helsmoortel, Geert Vandeweyer, et al.
Calcified Tissue International
|
February 7, 2019
Genetic Variation in RIN3 in the Belgian Population Supports Its Involvement in the Pathogenesis of Paget's Disease of Bone and Modifies the Age of Onset
Raphaël De Ridder, Eveline Boudin, Geert Vandeweyer, et al.
Journal of Translational Medicine
|
March 3, 2024
CRISPR/Cas9-edited ROS1 + non-small cell lung cancer cell lines highlight differential drug sensitivity in 2D vs 3D cultures while reflecting established resistance profiles
Marc Terrones, Christophe Deben, Felicia Rodrigues-Fortes, et al.
Scientific Reports
|
January 29, 2021
Abundancy of polymorphic CGG repeats in the human genome suggest a broad involvement in neurological disease
Dale J Annear, Geert Vandeweyer, Ellen Elinck, et al.
Bioinformatics (Oxford, England)
|
February 17, 2018
pBRIT: gene prioritization by correlating functional and phenotypic annotations through integrative data fusion
Ajay Anand Kumar, Lut Van Laer, Maaike Alaerts, et al.
Epilepsy Research
|
January 17, 2012
A de novo balanced t(2;6)(p15;p22.3) in a patient with West Syndrome disrupts a lnc-RNA
Geert Vandeweyer, Nathalie Van der Aa, Berten Ceulemans, et al.
Journal of Biomolecular Structure & Dynamics
|
January 17, 2025
Exploring the conformational space of ROS1 kinase domain and the impact of allosteric mutations
Farhan Ul Haq, Juliana Fatima Vilachã, Ken Op de Beeck, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
June 13, 2012
Haploinsufficiency of CMIP in a girl with autism spectrum disorder and developmental delay due to a de novo deletion on chromosome 16q23.2
Nathalie Van der Aa, Geert Vandeweyer, Edwin Reyniers, et al.
Bioinformatics (Oxford, England)
|
November 28, 2022
varAmpliCNV: analyzing variance of amplicons to detect CNVs in targeted NGS data
Ajay Anand Kumar, Bart Loeys, Gerarda Van De Beek, et al.
Neurobiology of Aging
|
May 17, 2022
Protein interaction network analysis reveals genetic enrichment of immune system genes in frontotemporal dementia
Cemile Koçoğlu, Raffaele Ferrari, Maxime Roes, et al.
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