المؤلفون: Ebstein, Frédéric, Latypova, Xenia, Sharon Hung, Ka Ying, Prado, Miguel A., Lee, Byung-Hoon, Möller, Sophie, Wendlandt, Martin, Zieba, Barbara A., Florenceau, Laëtitia, Vignard, Virginie, Poirier, Léa, Toutain, Bérénice, Moroni, Isabella, Dubucs, Charlotte, Chassaing, Nicolas, Horvath, Judit, Prokisch, Holger, Küry, Sébastien, Bézieau, Stéphane, Paulo, Joao A., Finley, Daniel, Krüger, Elke, Ghezzi, Daniele, Isidor, Bertrand

المصدر: In Genetics in Medicine June 2024 26(6)

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المؤلفون: Coux, Olivier^Aff8, Zieba, Barbara A.^Aff9, Meiners, Silke^Aff10

المساهمون: Crusio, Wim E., Series Editor^Aff1, Lambris, John D., Series Editor^Aff2, Radeke, Heinfried H., Series Editor^Aff3, Rezaei, Nima, Series Editor^Aff4, Barrio, Rosa, editor^Aff5, Sutherland, James D., editor^Aff6, Rodriguez, Manuel S., editor^Aff7

المصدر: Proteostasis and Disease : From Basic Mechanisms to Clinics. 1233:55-100

المؤلفون: Śmiałowska, Maria, Zięba, Barbara, Domin, Helena

المصدر: In Neuropeptides August 2021 88

المؤلفون: Zieba, Barbara A., Henry, Laurent, Lacroix, Matthieu, Jemaà, Mohamed, Lavabre-Bertrand, Thierry, Meunier, Laurent, Coux, Olivier, Stoebner, Pierre-Emmanuel

المصدر: In Journal of Dermatological Science October 2017 88(1):10-19

المؤلفون: Domin, Helena ^*, Zięba, Barbara, Gołembiowska, Krystyna, Kowalska, Magdalena, Dziubina, Anna, Śmiałowska, Maria

المصدر: In Pharmacological Reports November-December 2010 62(6):1051-1061

المؤلفون: Wernicke, Catrin, Hellmann, Julian, Zięba, Barbara, Kuter, Katarzyna, Ossowska, Krystyna, Frenzel, Monika, Dencher, Norbert A., Rommelspacher, Hans

المصدر: In Pharmacological Reports January-February 2010 62(1):35-53

المؤلفون: Śmiałowska, Maria, Domin, Helena, Zięba, Barbara, Koźniewska, Ewa, Michalik, Radosław, Piotrowski, Piotr, Kajta, Małgorzata

المصدر: In Neuropeptides 2009 43(3):235-249

المؤلفون: Zięba, Barbara, Grzegorzewska, Małgorzata, Brański, Piotr, Domin, Helena, Wierońska, Joanna M., Hess, Grzegorz, Śmiałowska, Maria

المصدر: In Neuropeptides October-December 2008 42(5-6):513-523

المؤلفون: Kröll-Hermi, Ariane, Ebstein, Frédéric, Stoetzel, Corinne, Geoffroy, Véronique, Schaefer, Elise, Scheidecker, Sophie, Bär, Séverine, Takamiya, Masanari, Kawakami, Koichi, Zieba, Barbara, Studer, Fouzia, Pelletier, Valérie, Eyermann, Carine, Speeg‐schatz, Claude, Laugel, Vincent, Lipsker, Dan, Sandron, Florian, Mcginn, Steven, Boland, Anne, Deleuze, Jean‐françois, Kuhn, Lauriane, Chicher, Johana, Hammann, Philippe, Friant, Sylvie, Etard, Christelle, Krüger, Elke, Muller, Jean, Strähle, Uwe, Dollfus, Hélène

المساهمون: Friant, Sylvie, Laboratoire de Génétique Médicale (LGM), Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM), Karlsruher Institut für Technologie (KIT), Institut für Medizinische Biochemie und Molekularbiologie (IMBM), Génétique moléculaire, génomique, microbiologie (GMGM), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Institute for Toxicology and Genetics (ITG), Karlsruhe Institute of Technology (KIT), National Institute of Genetics (NIG), Centre de référence pour les affections ophtalmologiques héréditaires (CARGO), Hôpitaux Universitaires de Strasbourg, Les Hôptaux universitaires de Strasbourg (HUS), CHU Strasbourg, Centre National de Recherche en Génomique Humaine (CNRGH), Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Institut de biologie moléculaire et cellulaire (IBMC), Institute of Toxicology and Genetics [Karlsruhe] (ITG)

المصدر: EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 12, Iss 7, Pp n/a-n/a (2020)
EMBO Molecular Medicine, 2020, 12 (7), ⟨10.15252/emmm.201911861⟩
EMBO Molecular Medicine, Wiley Open Access, 2020, 12 (7), ⟨10.15252/emmm.201911861⟩

مصطلحات موضوعية: Male, Medicine (General), Proteasome Endopeptidase Complex, Adolescent, [SDV]Life Sciences [q-bio], Gene Therapy & Genetic Disease, QH426-470, Deafness, Article, Cataract, Consanguinity, R5-920, Stress, Physiological, Genetics, Animals, Humans, Child, Zebrafish, Nuclear Respiratory Factor 1, Ubiquitin, Infant, Articles, Syndrome, Zebrafish Proteins, PSMC3, Pedigree, [SDV] Life Sciences [q-bio], proteasome, Phenotype, Child, Preschool, Mutation, Proteolysis, ATPases Associated with Diverse Cellular Activities, Female, PSMC3 Subject Categories Genetics, Genetics, Gene Therapy & Genetic Disease, Proteasome Inhibitors, neurosensory disease, Neuroscience

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URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8fac6b75bc18e3b3050daecbe8edfef2
http://europepmc.org/articles/PMC7338805