Feeder Layer Cell Actions and Applications

Tissue Engineering Part B-Reviews (p. 345-353) - 8/2015

https://doi.org/10.1089/ten.teb.2014.0547 Ver en origen

• EISSN 1937-3376
• ISSN 1937-3368

• UC3M

Early, Non-Invasive Sensing of Sustained Hyperglycemia in Mice Using Millimeter-Wave Spectroscopy

Sensors (p. 1-12) - 7/2019

https://doi.org/10.3390/s19153347 Ver en origen

• EISSN 1424-8220
• ISSN 1424-3210

• UC3M

Classification of skin phenotypes caused by diabetes mellitus using complex scattering parameters in the millimeter-wave frequency range

Scientific Reports (p. 1-8) - 7/2017

https://doi.org/10.1038/s41598-017-06034-0 Ver en origen

• ISSN 2045-2322

• UC3M

In-vivo, non-invasive detection of hyperglycemic states in animal models using mm-wave spectroscopy

Scientific Reports (p. 1-8) - 9/2016

https://doi.org/10.1038/srep34035 Ver en origen

• ISSN 2045-2322

• UC3M

The transition from linear to highly branched poly(beta-amino ester)s: Branching matters for gene delivery

Science Advances (p. 1-14) - 6/2016

https://doi.org/10.1126/sciadv.1600102 Ver en origen

• ISSN 2375-2548

• UC3M

Oxidative stress and mitochondrial dysfunction in Kindler syndrome

Orphanet journal of rare diseases (p. 1-10) - 12/2014

https://doi.org/10.1186/s13023-014-0211-8 Ver en origen

• EISSN 1750-1172

• UC3M

Deletion of a Pathogenic Mutation-Containing Exon of COL7A1 Allows Clonal Gene Editing Correction of RDEB Patient Epidermal Stem Cells

Molecular Therapy-Nucleic Acids (p. 68-78) - 6/2018

10.1016/j.omtn.2018.01.009 Ver en origen

• ISSN 2162-2531

• UC3M

Gene editing for the efficient correction of a recurrent COL7A1 mutation in recessive dystrophic epidermolysis bullosa keratinocytes

Molecular Therapy-Nucleic Acids (p. 1-13) - 1/2016

https://doi.org/10.1038/mtna.2016.19 Ver en origen

• ISSN 2162-2531

• UC3M

Preclinical model for phenotypic correction of dystrophic epidermolysis bullosa by in vivo CRISPR-Cas9 delivery using adenoviral vectors

Molecular Therapy - Methods and Clinical Development (p. 96-108) - 12/2022

https://doi.org/10.1016/j.omtm.2022.09.005 Ver en origen

• ISSN 2329-0501

• UC3M

Efficient CRISPR-Cas9-mediated gene ablation in human keratinocytes to recapitulate genodermatoses: modeling of Netherton syndrome

Molecular Therapy - Methods and Clinical Development (p. 280-290) - 9/2020

https://doi.org/10.1016/j.omtm.2020.05.031 Ver en origen

• ISSN 2329-0501

• UC3M

Current applications for bioengineered skin. In: Translating regenerative medicine to the clinic. Advances in translational medicine

Translating regenerative medicine to the clinic. Advances in translational medicine (p. 107-120) - 12/2016

Editor: Academic Press

10.1016/b978-0-12-800548-4.00008-5 Ver en origen

• UC3M

Organotypic and humanized animal models of genodermatoses. In: Skin tissue models

Skin tissue models (p. 77-102) - 11/2017

Editor: Academic Press

https://doi.org/10.1016/c2016-0-00093-1 Ver en origen

• ISBN 978-0-12-810545-0

• UC3M

Bioengineered Skin. In: Skin Biopsy: Perspectives

Skin Biopsy: Perspectives (p. 261-296) - 11/2011

Editor: INTECH

https://doi.org/10.5772/23587 Ver en origen

• ISBN 978-953-307-290-6

• UC3M

Bioresorbable nanoparticles for drug delivery and targeting. Preparation and application in wound healing

XXXVIII Congreso de la Sociedad Ibérica de Biomecánica y Biomateriales<br/><br/> (p. 29-29) - 2015

Editor: Sociedad Ibérica de Biomecánica y Biomateriales

• ISBN 978-84-608-3585-1

• UC3M

Gene editing-mediated excision of mutation-bearing exon 80 of COL7A1 gene for the efficient correction of recessive dystrophic epidermolysis bullosa patient derived-epidermalstem cells

XXV Anniversary Congress in Collaboration with the German Society for Gene Therapy (ESGCT 2017) - 2017

Editor: MARY ANN LIEBERT INC, PUBLISHERS

https://doi.org/10.1089/hum.2017.29055.abstracts Ver en origen

• UC3M

Síndrome de Netherton: de los modelos animales, al paciente. Ensayo clínico de terapia génica, para Síndrome de Netherton

XIV Jornadas de Convivencia de Afectados de Ictiosis - 2016

• UC3M

Identificación de nuevos mecanismos fisiopatológicos en el síndrome de Kindler

VII Reunión Científica Anual CIBERER - 2014

• UC3M

Generación de piel a partir de células madre epidérmicas: estudios preclínicos y extrapolaciones clínicas

VI Congreso de la Sociedad Española de Terapia Genética y Celular - 2011

• UC3M

Role of mitochondria in the pathogenesis of kindler syndrome

The European Society for Gene and Cell Therapy and the Spanish Society for Gene and Cell Therapy Collaborative Congress ((ESGCT and SETGyC Collaborative Congress) (p. 130-130) - 2013

Editor: Mary Anne Liebert

https://doi.org/10.1089/hum.2013.2513 Ver en origen

• ISBN 1043-0342

• UC3M

Novedades en el tratamiento de la Epidermolisis Bullosa distrófica /Advances in DEB treatment

International symposium Rare skin diseases: from clinic to gene and vice versa - 2016

• UC3M

Monitoring the evolution of hyperglycemia in mice using mm-wave spectroscopy

IRMMW-THz 2017 42 International Conference on Infrared, Millimeter, and Terahertz Waves - 2017

Editor: IEEE.THE INSTITUTE OF ELECTRICAL AND ELECTRONICS ENGINEERS, INC

https://doi.org/10.1109/irmmw-thz.2017.8066863 Ver en origen

• ISBN 978-1-5090-6051-1

• UC3M

Determination of hyperglycemic states in mice using millimeter-wave sensing

IEEE COMCAS 2017 International Conference on Microwaves, Antennas, Communications and Electronic Systems - 2017

Editor: IEEE.THE INSTITUTE OF ELECTRICAL AND ELECTRONICS ENGINEERS, INC

https://doi.org/10.1109/comcas.2017.8244712 Ver en origen

• ISBN 9781538631706

• UC3M

Non-invasive Detection and Monitoring of Sustained Glycemic Fluctuations using Mm-Wave Spectroscopy

EuMC 2018. 48th European Microwave Conference - 2018

Editor: IEEE.THE INSTITUTE OF ELECTRICAL AND ELECTRONICS ENGINEERS, INC

https://doi.org/10.23919/eumc.2018.8541413 Ver en origen

• ISBN 978-2-87487-051-4

• UC3M

Identification and functional characterization of mutation-independent disease-severity modulators in recessive dystrophic epidermolysis bullosa

Fecha de defensa: 18-03-2022

• UC3M

GENE EDITING-BASED PROTOCOLS FOR THE EX VIVO CORRECTION OF RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA

Fecha de defensa: 28-09-2020

• UC3M