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Plos Genetics
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January 25, 2019
Intronic CNVs and gene expression variation in human populations
Maria Rigau, David Juan, Alfonso Valencia, et al.
Current Opinion in Cell Biology
|
January 22, 2022
Emerging mechanisms and dynamics of three-dimensional genome organisation at zygotic genome activation
Elizabeth Ing-Simmons, Maria Rigau, Juan M Vaquerizas
Journal of Peptide Science : an Official Publication of the European Peptide Society
|
July 28, 2009
Solid-phase peptide synthesis using acetonitrile as a solvent in combination with PEG-based resins
Gerardo A Acosta, Montserrat del Fresno, Marta Paradis-Bas, et al.
Nucleic Acids Research
|
July 9, 2018
Loose ends: almost one in five human genes still have unresolved coding status
Federico Abascal, David Juan, Irwin Jungreis, et al.
Nature Structural & Molecular Biology
|
February 20, 2026
Global reorganization of genome architecture at the transition to gametogenesis
Tien-Chi Huang, Maria Rigau, Valeriya Malysheva, et al.
Macromolecular Bioscience
|
October 31, 2014
Degradable glycine-based photo-polymerizable polyphosphazenes for use as scaffolds for tissue regeneration
Sandra Rothemund, Tamara B Aigner, Aitziber Iturmendi, et al.
Scientific Data
|
January 16, 2021
A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration
Friederike Ehrhart, Annika Jacobsen, Maria Rigau, et al.
Molecular Autism
|
May 14, 2015
Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders
Marta Codina-Solà, Benjamín Rodríguez-Santiago, Aïda Homs, et al.
Nucleic Acids Research
|
December 1, 2022
3D chromatin connectivity underlies replication origin efficiency in mouse embryonic stem cells
Karolina Jodkowska, Vera Pancaldi, Maria Rigau, et al.
Nature Communications
|
February 28, 2024
Rare disease research workflow using multilayer networks elucidates the molecular determinants of severity in Congenital Myasthenic Syndromes
Iker Núñez-Carpintero, Maria Rigau, Mattia Bosio, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Plos Genetics
|
January 25, 2019
Intronic CNVs and gene expression variation in human populations
Maria Rigau, David Juan, Alfonso Valencia, et al.
Current Opinion in Cell Biology
|
January 22, 2022
Emerging mechanisms and dynamics of three-dimensional genome organisation at zygotic genome activation
Elizabeth Ing-Simmons, Maria Rigau, Juan M Vaquerizas
Journal of Peptide Science : an Official Publication of the European Peptide Society
|
July 28, 2009
Solid-phase peptide synthesis using acetonitrile as a solvent in combination with PEG-based resins
Gerardo A Acosta, Montserrat del Fresno, Marta Paradis-Bas, et al.
Nucleic Acids Research
|
July 9, 2018
Loose ends: almost one in five human genes still have unresolved coding status
Federico Abascal, David Juan, Irwin Jungreis, et al.
Nature Structural & Molecular Biology
|
February 20, 2026
Global reorganization of genome architecture at the transition to gametogenesis
Tien-Chi Huang, Maria Rigau, Valeriya Malysheva, et al.
Macromolecular Bioscience
|
October 31, 2014
Degradable glycine-based photo-polymerizable polyphosphazenes for use as scaffolds for tissue regeneration
Sandra Rothemund, Tamara B Aigner, Aitziber Iturmendi, et al.
Scientific Data
|
January 16, 2021
A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration
Friederike Ehrhart, Annika Jacobsen, Maria Rigau, et al.
Molecular Autism
|
May 14, 2015
Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders
Marta Codina-Solà, Benjamín Rodríguez-Santiago, Aïda Homs, et al.
Nucleic Acids Research
|
December 1, 2022
3D chromatin connectivity underlies replication origin efficiency in mouse embryonic stem cells
Karolina Jodkowska, Vera Pancaldi, Maria Rigau, et al.
Nature Communications
|
February 28, 2024
Rare disease research workflow using multilayer networks elucidates the molecular determinants of severity in Congenital Myasthenic Syndromes
Iker Núñez-Carpintero, Maria Rigau, Mattia Bosio, et al.
Page
of 2