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Journal of Biomedical Science
|
November 4, 2024
The molecular consequences of FOXF1 missense mutations associated with alveolar capillary dysplasia with misalignment of pulmonary veins
G G Edel, M van Kempen, A Boerema-de Munck, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 7, 2018
PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disability
Demy J S Kuipers, Jonathan Carr, Soraya Bardien, et al.
Nature Communications
|
June 12, 2026
Tunable magnons in a dual-gated 2D antiferromagnet
Nele Stetzuhn, Abhijeet M Kumar, Sviatoslav Kovalchuk, et al.
RNA Biology
|
April 1, 2015
Deciphering the RNA landscape by RNAome sequencing
Kasper W J Derks, Branislav Misovic, Mirjam C G N van den Hout, et al.
Frontiers in Immunology
|
October 5, 2020
Validation of a Combined Transcriptome and T Cell Receptor Alpha/Beta (TRA/TRB) Repertoire Assay at the Single Cell Level for Paucicellular Samples
Nicolle H R Litjens, Anton W Langerak, Amy C J van der List, et al.
International Journal of Molecular Sciences
|
January 25, 2025
Non-Invasive Determination of the Paternal Inheritance in Pregnancies at Risk for β-Thalassaemia by Analyzing Cell-Free Fetal DNA Using Targeted Next-Generation Sequencing
Stefania Byrou, Rutger W W Brouwer, Marios Tomazou, et al.
Human Molecular Genetics
|
July 7, 2020
Targeted chromatin conformation analysis identifies novel distal neural enhancers of ZEB2 in pluripotent stem cell differentiation
Judith C Birkhoff, Rutger W W Brouwer, Petros Kolovos, et al.
Frontiers in Genetics
|
October 26, 2018
Whole-Genome Linkage Scan Combined With Exome Sequencing Identifies Novel Candidate Genes for Carotid Intima-Media Thickness
Dina Vojinovic, Maryam Kavousi, Mohsen Ghanbari, et al.
Scientific Reports
|
January 11, 2022
Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts
Steven Heshusius, Laura Grech, Nynke Gillemans, et al.
Nature Protocols
|
February 9, 2018
Investigation of the spatial structure and interactions of the genome at sub-kilobase-pair resolution using T2C
Petros Kolovos, Rutger W W Brouwer, Christel E M Kockx, et al.
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of 23
Search research articles
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Showing results (181-190 of 227) with videos related to
Sort By:
Page
of 23
Journal of Biomedical Science
|
November 4, 2024
The molecular consequences of FOXF1 missense mutations associated with alveolar capillary dysplasia with misalignment of pulmonary veins
G G Edel, M van Kempen, A Boerema-de Munck, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 7, 2018
PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disability
Demy J S Kuipers, Jonathan Carr, Soraya Bardien, et al.
Nature Communications
|
June 12, 2026
Tunable magnons in a dual-gated 2D antiferromagnet
Nele Stetzuhn, Abhijeet M Kumar, Sviatoslav Kovalchuk, et al.
RNA Biology
|
April 1, 2015
Deciphering the RNA landscape by RNAome sequencing
Kasper W J Derks, Branislav Misovic, Mirjam C G N van den Hout, et al.
Frontiers in Immunology
|
October 5, 2020
Validation of a Combined Transcriptome and T Cell Receptor Alpha/Beta (TRA/TRB) Repertoire Assay at the Single Cell Level for Paucicellular Samples
Nicolle H R Litjens, Anton W Langerak, Amy C J van der List, et al.
International Journal of Molecular Sciences
|
January 25, 2025
Non-Invasive Determination of the Paternal Inheritance in Pregnancies at Risk for β-Thalassaemia by Analyzing Cell-Free Fetal DNA Using Targeted Next-Generation Sequencing
Stefania Byrou, Rutger W W Brouwer, Marios Tomazou, et al.
Human Molecular Genetics
|
July 7, 2020
Targeted chromatin conformation analysis identifies novel distal neural enhancers of ZEB2 in pluripotent stem cell differentiation
Judith C Birkhoff, Rutger W W Brouwer, Petros Kolovos, et al.
Frontiers in Genetics
|
October 26, 2018
Whole-Genome Linkage Scan Combined With Exome Sequencing Identifies Novel Candidate Genes for Carotid Intima-Media Thickness
Dina Vojinovic, Maryam Kavousi, Mohsen Ghanbari, et al.
Scientific Reports
|
January 11, 2022
Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts
Steven Heshusius, Laura Grech, Nynke Gillemans, et al.
Nature Protocols
|
February 9, 2018
Investigation of the spatial structure and interactions of the genome at sub-kilobase-pair resolution using T2C
Petros Kolovos, Rutger W W Brouwer, Christel E M Kockx, et al.
Page
of 23