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Morin, Matías
89
results:
Search for persons
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Format
Online (89)
Mediatypes
Articles (Online) (32)
OpenAccess-fulltext (57)
Languages
english (75)
spanish (3)
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1
Novel Cases of Non-Syndromic Hearing Impairment Caused by P..:
Domínguez-Ruiz, María
;
Olarte, Margarita
;
Onecha, Esther
...
Genes. 15 (2024) 7 - p. 951 , 2024
Link:
https://doi.org/10.3390/..
?
2
Specific correction of pyruvate kinase deficiency-causing p..:
Fañanas-Baquero, Sara
;
Morín, Matías
;
Fernández, Sergio
...
Frontiers in Genome Editing. 5 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
3
Evolution of CRISPR-associated endonucleases as inferred fr..:
Alonso-Lerma, Borja
;
Jabalera, Ylenia
;
Samperio, Sara
...
Nature Microbiology. 8 (2023) 1 - p. 77-90 , 2023
Link:
https://doi.org/10.1038/..
?
4
Insights into the pathophysiology of DFNA44 hearing loss as..:
Lachgar-Ruiz, María
;
Morín, Matías
;
Martelletti, Elisa
...
Disease Models & Mechanisms. 16 (2023) 8 - p. , 2023
Link:
https://doi.org/10.1242/..
?
5
Novel Pathogenic Variants in the Gene Encoding Stereocilin ..:
Domínguez-Ruiz, María
;
Ruiz-Palmero, Laura
;
Buonfiglio, Paula I.
...
Biomedicines. 11 (2023) 11 - p. 2943 , 2023
Link:
https://doi.org/10.3390/..
?
6
Cingulin regulates hair cell cuticular plate morphology and..:
Zhu, Guang‐Jie
;
Huang, Yuhang
;
Zhang, Linqing
...
EMBO Molecular Medicine. 15 (2023) 11 - p. , 2023
Link:
https://doi.org/10.15252..
?
7
Pathogenic variants of the coenzyme A biosynthesis‐associat..:
Bravo‐Alonso, Irene
;
Morin, Matías
;
Arribas‐Carreira, Laura
...
Journal of Inherited Metabolic Disease. 46 (2023) 2 - p. 261-272 , 2023
Link:
https://doi.org/10.1002/..
?
8
Selective miRNA inhibition in CD8+ cytotoxic T lymphocytes ..:
Madrid-Elena, Nadia
;
Serrano-Villar, Sergio
;
Gutiérrez, Carolina
...
Frontiers in Immunology. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
9
CRISPR/Cas9-Mediated Allele-Specific Disruption of a Domina..:
López-Márquez, Arístides
;
Morín, Matías
;
Fernández-Peñalver, Sergio
...
International Journal of Molecular Sciences. 23 (2022) 8 - p. 4410 , 2022
Link:
https://doi.org/10.3390/..
?
10
Genetic etiology of non-syndromic hearing loss in Europe:
del Castillo, Ignacio
;
Morín, Matías
;
Domínguez-Ruiz, María
.
Human Genetics. , 2022
Link:
https://doi.org/10.1007/..
?
11
Therapeutic Potential of EWSR1–FLI1 Inactivation by CRISPR/..:
Cervera, Saint T.
;
Rodríguez-Martín, Carlos
;
Fernández-Tabanera, Enrique
...
Cancers. 13 (2021) 15 - p. 3783 , 2021
Link:
https://doi.org/10.3390/..
?
12
A Novel Truncating Mutation in HOMER2 Causes Nonsyndromic P..:
Lachgar, María
;
Morín, Matías
;
Villamar, Manuela
..
Genes. 12 (2021) 3 - p. 411 , 2021
Link:
https://doi.org/10.3390/..
?
13
Simple Protocol for Generating and Genotyping Genome‐Edited..:
Fernández, Almudena
;
Morín, Matías
;
Muñoz‐Santos, Diego
...
Current Protocols in Mouse Biology. 10 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1002/..
?
14
Insights into the pathophysiology of DFNA10 hearing loss as..:
Morín, Matias
;
Borreguero, Lucía
;
Booth, Kevin T
...
Scientific Reports. 10 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/..
?
15
CSVS, a crowdsourcing database of the Spanish population ge..:
Peña-Chilet, María
;
Roldán, Gema
;
Perez-Florido, Javier
...
Nucleic Acids Research. 49 (2020) D1 - p. D1130-D1137 , 2020
Link:
https://doi.org/10.1093/..
1-15