E-LIB Suche - Ergebnisse für: Mencía, Angeles

1

Nonviral CRISPR/Cas9 mutagenesis for streamlined generation..:

Lara-Sáez, Irene ; Mencía, Ángeles ; Recuero, Enrique...
Proceedings of the National Academy of Sciences. 121 (2024) 28 - p. , 2024

Link: https://doi.org/10.1073/..

2

Preclinical model for phenotypic correction of dystrophic e..:

García, Marta ; Bonafont, Jose ; Martínez-Palacios, Jesús...
Molecular Therapy - Methods & Clinical Development. 27 (2022) - p. 96-108 , 2022

Link: https://doi.org/10.1016/..

3

Correction of recessive dystrophic epidermolysis bullosa by..:

Bonafont, Jose ; Mencía, Angeles ; Chacón-Solano, Esteban...
Molecular Therapy. 29 (2021) 6 - p. 2008-2018 , 2021

Link: https://doi.org/10.1016/..

4

Non-viral delivery of CRISPR–Cas9 complexes for targeted ge..:

O'Keeffe Ahern, Jonathan ; Lara-Sáez, Irene ; Zhou, Dezhong...
Gene Therapy. 29 (2021) 3-4 - p. 157-170 , 2021

Link: https://doi.org/10.1038/..

5

Efficient CRISPR-Cas9-Mediated Gene Ablation in Human Kerat..:

Gálvez, Victoria ; Chacón-Solano, Esteban ; Bonafont, Jose...
Molecular Therapy - Methods & Clinical Development. 18 (2020) - p. 280-290 , 2020

Link: https://doi.org/10.1016/..

6

Clinically Relevant Correction of Recessive Dystrophic Epid..:

Bonafont, Jose ; Mencía, Ángeles ; García, Marta...
Molecular Therapy. 27 (2019) 5 - p. 986-998 , 2019

Link: https://doi.org/10.1016/..

7

Deletion of a Pathogenic Mutation-Containing Exon of COL7A1..:

Mencía, Ángeles ; Chamorro, Cristina ; Bonafont, Jose...
Molecular Therapy - Nucleic Acids. 11 (2018) - p. 68-78 , 2018

Link: https://doi.org/10.1016/..

8

Identical COL71A1 heterozygous mutations resulting in diffe..:

Knöpfel, Nicole ; Noguera‐Morel, Lucero ; Hernández‐Martin, Angela...
Pediatric Dermatology. 35 (2017) 2 - p. , 2017

Link: https://doi.org/10.1111/..

9

Gene Editing for the Efficient Correction of a Recurrent CO..:

Chamorro, Cristina ; Mencía, Angeles ; Almarza, David...
Molecular Therapy - Nucleic Acids. 5 (2016) - p. e307 , 2016

Link: https://doi.org/10.1038/..

10

Identification of two rare and novel large deletions in ITG..:

Mencía, Ángeles ; García, Marta ; García, Eva...
Experimental Dermatology. 25 (2016) 4 - p. 269-274 , 2016

Link: https://doi.org/10.1111/..

11

Keratinocyte cell lines derived from severe generalized rec..:

Chamorro, Cristina ; Almarza, David ; Duarte, Blanca...
Experimental Dermatology. 22 (2013) 9 - p. 601-603 , 2013

Link: https://doi.org/10.1111/..

12

DFNA8/12 caused by TECTA mutations is the most identified s..:

Hildebrand, Michael S. ; Morín, Matías ; Meyer, Nicole C....
Human Mutation. 32 (2011) 7 - p. 825-834 , 2011

Link: https://doi.org/10.1002/..

13

Mutations in the seed region of human miR-96 are responsibl..:

Mencía, Ángeles ; Modamio-Høybjør, Silvia ; Redshaw, Nick...
Nature Genetics. 41 (2009) 5 - p. 609-613 , 2009

Link: https://doi.org/10.1038/..

14

In vivo and in vitro effects of two novel gamma-actin (ACTG..:

Morín, Matías ; Bryan, Keith E. ; Mayo-Merino, Fernando...
Human Molecular Genetics. 18 (2009) 16 - p. 3075-3089 , 2009

Link: https://doi.org/10.1093/..

15

Characterization of a Spontaneous, Recessive, Missense Muta..:

Moreno-Pelayo, Miguel Ángel ; Goodyear, Richard J. ; Mencía, Angeles...
Journal of the Association for Research in Otolaryngology. 9 (2008) 2 - p. 202-214 , 2008

Link: https://doi.org/10.1007/..