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Maria Rigau

Showing results (1-10 of 11) with videos related to

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Plos Genetics|January 25, 2019
Intronic CNVs and gene expression variation in human populationsMaria 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 activationElizabeth 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 resinsGerardo 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 statusFederico Abascal, David Juan, Irwin Jungreis, et al.
Nature Structural & Molecular Biology|February 20, 2026
Global reorganization of genome architecture at the transition to gametogenesisTien-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 regenerationSandra 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 integrationFriederike 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 disordersMarta 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 cellsKarolina 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 SyndromesIker Núñez-Carpintero, Maria Rigau, Mattia Bosio, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Plos Genetics|January 25, 2019
Intronic CNVs and gene expression variation in human populationsMaria 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 activationElizabeth 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 resinsGerardo 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 statusFederico Abascal, David Juan, Irwin Jungreis, et al.
Nature Structural & Molecular Biology|February 20, 2026
Global reorganization of genome architecture at the transition to gametogenesisTien-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 regenerationSandra 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 integrationFriederike 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 disordersMarta 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 cellsKarolina 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 SyndromesIker Núñez-Carpintero, Maria Rigau, Mattia Bosio, et al.
Pageof 2