يعرض 1 - 11 نتائج من 11 نتيجة بحث عن '"Benetó, Noelia"', وقت الاستعلام: 0.43s تنقيح النتائج
  1. 1
    Neuronal and Astrocytic Differentiation from Sanfilippo C Syndrome iPSCs for Disease Modeling and Drug Development

    المؤلفون: Benetó, Noelia, Cozar, Monica, Castilla-Vallmanya, Laura, Zetterdahl, Oskar G, Sacultanu, Madalina, Segur-Bailach, Eulalia, García-Morant, María, Ribes, Antonia, Ahlenius, Henrik, Grinberg, Daniel, Vilageliu, Lluïsa, Canals, Isaac

    المصدر: Journal of Clinical Medicine StemTherapy: National Initiative on Stem Cells for Regenerative Therapy. 9(3)

    مصطلحات موضوعية: Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Neurovetenskaper, Medical and Health Sciences, Basic Medicine, Neurosciences, Cell- och molekylärbiologi, Cell and Molecular Biology

    URL الوصول: https://lup.lub.lu.se/record/5f5e43f1-9efd-4252-b9f7-aaab1e785bd2
    http://dx.doi.org/10.3390/jcm9030644

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  2. 2
    Generation of two NAGLU-mutated homozygous cell lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo B syndrome

    المؤلفون: Benetó, Noelia, Cozar, Monica, Gort, Laura, Pacheco, Laura, Vilageliu, Lluïsa, Grinberg, Daniel, Canals, Isaac

    المصدر: Stem Cell Research StemTherapy: National Initiative on Stem Cells for Regenerative Therapy. 42

    مصطلحات موضوعية: Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Cell- och molekylärbiologi, Medical and Health Sciences, Basic Medicine, Cell and Molecular Biology

    URL الوصول: https://lup.lub.lu.se/record/c9838557-5ff1-461c-a1f2-a59c28c4cb9f
    http://dx.doi.org/10.1016/j.scr.2019.101668

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  3. 3
    Sanfilippo syndrome : Molecular basis, disease models and therapeutic approaches

    المؤلفون: Benetó, Noelia, Vilageliu, Lluïsa, Grinberg, Daniel, Canals, Isaac

    المصدر: International Journal of Molecular Sciences StemTherapy: National Initiative on Stem Cells for Regenerative Therapy. 21(21)

    مصطلحات موضوعية: Animal models, Cellular models, Heparan sulfate, Induced pluripotent stem cells, Lysosomal storage disorders, Mucopolysaccharidosis III, Sanfilippo syndrome, Therapeutic approaches, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Cell- och molekylärbiologi, Medical and Health Sciences, Basic Medicine, Cell and Molecular Biology

    URL الوصول: https://lup.lub.lu.se/record/e586bbad-f01e-4bb3-9c99-a544084ac325
    http://dx.doi.org/10.3390/ijms21217819

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  4. 4
    Genome Editing Using Cas9-gRNA Ribonucleoprotein in Human Pluripotent Stem Cells for Disease Modeling

    المؤلفون: Benetó, Noelia, Grinberg, Daniel, Vilageliu, Lluïsa, Canals, Isaac

    المصدر: Methods in Molecular Biology MultiPark: Multidisciplinary research focused on Parkinson´s disease StemTherapy: National Initiative on Stem Cells for Regenerative Therapy. 2549:409-425

    مصطلحات موضوعية: CRISPR/Cas9, Disease modeling, Genome editing, Human pluripotent stem cells, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics

    URL الوصول: https://lup.lub.lu.se/record/b1ae57d9-c2cb-4e54-b063-7d354e9551d7
    http://dx.doi.org/10.1007/7651_2021_374


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  5. 5
    Generation of two compound heterozygous HGSNAT-mutated lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo C syndrome

    المؤلفون: Benetó, Noelia, Cozar, Monica, García-Morant, María, Creus-Bachiller, Edgar, Vilageliu, Lluïsa, Grinberg, Daniel, Canals, Isaac

    المصدر: Stem Cell Research StemTherapy: National Initiative on Stem Cells for Regenerative Therapy MultiPark: Multidisciplinary research focused on Parkinson´s disease. 41

    مصطلحات موضوعية: Acetyltransferases/genetics, Base Sequence, CRISPR-Cas Systems/genetics, Cell Culture Techniques/methods, Heterozygote, Humans, Induced Pluripotent Stem Cells/cytology, Male, Models, Biological, Mucopolysaccharidosis III/pathology, Mutation/genetics, Reproducibility of Results, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics

    URL الوصول: https://lup.lub.lu.se/record/82fe1b2f-2196-4cdb-b9a9-b5bb46250b22
    http://dx.doi.org/10.1016/j.scr.2019.101616

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  6. 6
    Academic Journal
    EXTL2 and EXTL3 inhibition with siRNAs as a promising substrate reduction therapy for Sanfilippo C syndrome

    المؤلفون: Canals Montferrer, Isaac, Benetó, Noelia, Cozar, Mónica, Vilageliu i Arqués, Lluïsa, Grinberg Vaisman, Daniel Raúl

    المصدر: Articles publicats en revistes (Genètica, Microbiologia i Estadística)

    مصطلحات موضوعية: Malalties hereditàries, Mutació (Biologia), Genètica molecular humana, Malalties neurodegeneratives, Terapèutica, Genetic diseases, Mutation (Biology), Human molecular genetics, Neurodegenerative Diseases, Therapeutics

    وصف الملف: 5 p.; application/pdf

    Relation: Reproducció del document publicat a: http://dx.doi.org/10.1038/srep13654; Scientific Reports, 2015, vol. 5, p. 13654; http://dx.doi.org/10.1038/srep13654; http://hdl.handle.net/2445/95835; 654647

    الاتاحة: http://hdl.handle.net/2445/95835

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  7. 7
    Academic Journal
    EXTL2 and EXTL3 inhibition with siRNAs as a promising substrate reduction therapy for Sanfilippo C syndrome

    المؤلفون: Canals, Isaac, Benetó, Noelia, Cozar, Mónica, Vilageliu, Lluïsa, Grinberg, Daniel

    المصدر: Scientific Reports ; volume 5, issue 1 ; ISSN 2045-2322

    الاتاحة: http://dx.doi.org/10.1038/srep13654
    https://www.nature.com/articles/srep13654
    https://www.nature.com/articles/srep13654.pdf

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  8. 8
    Academic Journal
    Role of Adenosine Receptors in Rare Neurodegenerative Diseases with Motor Symptoms

    المؤلفون: Beltran-Beltran, Vicent, Benetó, Noelia, Lapeña-Luzón, Tamara, Rodríguez, Laura R., Pallardó, Federico V., Gonzalez-Cabo, Pilar

    المساهمون: Instituto de Salud Carlos III (ISCIII)-Subdirección General de Evaluación, Generalitat Valenciana

    المصدر: Current Protein & Peptide Science ; volume 22, issue 9, page 675-694 ; ISSN 1389-2037

    الاتاحة: http://dx.doi.org/10.2174/1389203722666210910110126
    https://www.eurekaselect.com/article/download/196355
    https://www.eurekaselect.com/196355/article

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  9. 9
    Academic Journal
    DDC expression is not regulated by NFAT5 (TonEBP) in dopaminergic neural cell lines

    المؤلفون: Pineda-Cirera, Laura, Cabana-Domínguez, Judit, Benetó, Noelia, Diez, Hector, Arenas, Concepció, Cormand, Bru, Fernàndez-Castillo, Noèlia

    المساهمون: Spanish 'Ministerio de Economía y Competitividad', AGAUR, 'Generalitat de Catalunya', European Union H2020 Program, CIBERER

    المصدر: Gene ; volume 742, page 144569 ; ISSN 0378-1119

    الاتاحة: http://dx.doi.org/10.1016/j.gene.2020.144569
    https://api.elsevier.com/content/article/PII:S0378111920302389?httpAccept=text/xml
    https://api.elsevier.com/content/article/PII:S0378111920302389?httpAccept=text/plain

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  10. 10
    Academic Journal
    Cofilin and Neurodegeneration: New Functions for an Old but Gold Protein.

    المؤلفون: Lapeña-Luzón, Tamara, Rodríguez, Laura R., Beltran-Beltran, Vicent, Benetó, Noelia, Pallardó, Federico V., Gonzalez-Cabo, Pilar

    المصدر: Brain Sciences (2076-3425); Jul2021, Vol. 11 Issue 7, p954, 1p

    مصطلحات موضوعية: MICROFILAMENT proteins, NEURODEGENERATION, CYTOLOGY, CELL physiology, DENDRITIC spines

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  11. 11
    EXTL2 and EXTL3 inhibition with siRNAs as a promising substrate reduction therapy for Sanfilippo C syndrome

    المؤلفون: Canals Montferrer, Isaac, Benetó, Noelia, Cozar, Mónica, Vilageliu i Arqués, Lluïsa, Grinberg Vaisman, Daniel Raúl

    المساهمون: Universitat de Barcelona

    المصدر: Recercat. Dipósit de la Recerca de Catalunya
    instname
    Scientific Reports
    Dipòsit Digital de la UB
    Universidad de Barcelona

    مصطلحات موضوعية: Human molecular genetics, Mutació (Biologia), Malalties neurodegeneratives, Neurodegenerative diseases, Gene Expression, Membrane Proteins, Therapeutics, Fibroblasts, Mutation (Biology), N-Acetylglucosaminyltransferases, Transfection, Terapèutica, Immunohistochemistry, Article, Mucopolysaccharidosis III, Malalties hereditàries, Humans, RNA Interference, Genètica molecular humana, Heparitin Sulfate, RNA, Messenger, RNA, Small Interfering, Glycosaminoglycans, Genetic diseases

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::14292226568f0fee784188a0e9f61eb9
    http://hdl.handle.net/2445/95835

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