نتائج البحث - "E. Ruiz-Del-Yerro"

1

Duchenne muscular dystrophy cell culture models created by CRISPR/Cas9 gene editing and their application in drug screening

المؤلفون: E. Ruiz-Del-Yerro, Aina Anton-Martinez, Javier Poyatos-Garcia, Edurne Albiasu-Arteta, Laura de la Puente-Ovejero, Gabriela Gonzalez-Iglesias, Patricia Soblechero-Martín, Virginia Arechavala-Gomeza, I. Garcia-Jimenez, Irene Larranaga-Aiestaran, Federico Gonzalez, Andrea López-Martínez

المصدر: Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Scientific Reports
SCIENTIFIC REPORTS
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname

مصطلحات موضوعية: Utrophin, Duchenne muscular dystrophy, PHENOTYPE, THERAPY, Dystrophin, Myoblasts, Dystrophin-associated glycoprotein complex, Exon, Genome editing, Drug Discovery, CRISPR, Dystroglycans, 3' Untranslated Regions, Cells, Cultured, Gene Editing, Multidisciplinary, Molecular medicine, MOUSE MODEL, MUSCLE, musculoskeletal system, Medicine, Myogenic Regulatory Factor 5, EXPRESSION, musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, Science, Primary Cell Culture, SARCOLEMMA, Biology, Article, Sarcoglycans, medicine, Humans, UTROPHIN UP-REGULATION, MUTATIONS, IN-VITRO, QUANTIFICATION, medicine.disease, Exon skipping, Muscular Dystrophy, Duchenne, Cytoskeletal Proteins, HEK293 Cells, Preclinical research, Cancer research, biology.protein, CRISPR-Cas Systems

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec490975a384fc3fca7b2fbba35f0d67
https://doi.org/10.1038/s41598-021-97730-5

Find this article in full text from Springer Verlag.

Find this article in full text from ProQuest

2

Duchenne Muscular Dystrophy Cell Culture Models Created By CRISPR/Cas 9 Gene Editing And Their Application To Drug Screening

المؤلفون: I. Garcia-Jimenez, E. Ruiz-Del-Yerro, Gabriela Gonzalez-Iglesias, Irene Larranaga-Aiestaran, Virginia Arechavala-Gomeza, Aina Anton-Martinez, L. de la Puente-Ovejero, Patricia Soblechero-Martín, Federico Gonzalez, Javier Poyatos-Garcia, Edurne Albiasu-Arteta, Andrea López-Martínez

مصطلحات موضوعية: Exon, Genome editing, Cas9, Duchenne muscular dystrophy, Utrophin, medicine, CRISPR, Computational biology, Biology, musculoskeletal system, medicine.disease, Gene, Exon skipping

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9d3e8f92330214727daaac60693e75ed
https://doi.org/10.1101/2020.02.24.962316

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A multicenter comparison of quantification methods for antisense oligonucleotideinduced DMD exon 51 skipping in Duchenne muscular dystrophy cell cultures

المؤلفون: Nicole A. Datson, Pietro Spitali, Kamel Mamchaoui, Karen Anthony, Monika Hiller, Alessandra Ferlini, E. Ruiz-Del-Yerro, H. Osman, Linda Popplewell, George Dickson, Maria Sofia Falzarano, Ruurd C. Verheul, Valentina Sardone, Jelle J. Goeman, I. Garcia-Jimenez, Francesco Muntoni, Annemieke Aartsma-Rus, Virginia Arechavala-Gomeza

المساهمون: Leiden University Medical Center (LUMC), Università degli Studi di Ferrara (UniFE), Biocruces Bizkaia Health Research Institute [Baracaldo], Great Ormond Street Institute of Child Health [London, UK] (UCL), University College of London [London] (UCL), Royal Holloway [University of London] (RHUL), University of Northampton, Centre de Recherche en Myologie, Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), Institut de Myologie, Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Association française contre les myopathies (AFM-Téléthon)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Centre de recherche en Myologie – U974 SU-INSERM, Centre National de la Recherche Scientifique (CNRS)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Association française contre les myopathies (AFM-Téléthon)-Sorbonne Université (SU)

المصدر: PLoS ONE
PLoS ONE, Public Library of Science, 2018, 13 (10), pp.e0204485. ⟨10.1371/journal.pone.0204485⟩
PLoS ONE, Vol 13, Iss 10, p e0204485 (2018)
PLoS ONE, 13(10)

مصطلحات موضوعية: 0301 basic medicine, Heredity, Genetic Linkage, Duchenne muscular dystrophy, lcsh:Medicine, cDNA synthesis, Artificial Gene Amplification and Extension, Biochemistry, Muscular Dystrophies, law.invention, Myoblasts, Dystrophin, Exon, 0302 clinical medicine, law, Medicine and Health Sciences, Computer software, Muscular dystrophy, lcsh:Science, Polymerase chain reaction, Multidisciplinary, biology, Exons, 3. Good health, Nucleic acids, Neurology, X-Linked Traits, Sex Linkage, RNA splicing, Nested polymerase chain reaction, Research Article, musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, RNA Splicing, Nucleic acid synthesis, Research and Analysis Methods, Transfection, NO, Cell Line, Electrophoretic Techniques, 03 medical and health sciences, Genetics, medicine, [SDV.MHEP.AHA]Life Sciences [q-bio]/Human health and pathology/Tissues and Organs [q-bio.TO], Humans, Chemical synthesis, RNA synthesis, Molecular Biology Techniques, Molecular Biology, Clinical Genetics, lcsh:R, Biology and Life Sciences, Proteins, Oligonucleotides, Antisense, medicine.disease, Gel electrophoresis, Molecular biology, Exon skipping, Muscular Dystrophy, Duchenne, Cytoskeletal Proteins, Biosynthetic techniques, 030104 developmental biology, biology.protein, RNA, lcsh:Q, 030217 neurology & neurosurgery