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Gene|September 8, 2020
Hair dysmorphology in the R6/1 and R6/2 mouse models of Huntington's diseaseKarolina Pierzynowska, Magdalena Podlacha, Dorota Łuszczek, et al.
Metabolic Brain Disease|December 20, 2021
Impaired ion homeostasis as a possible associate factor in mucopolysaccharidosis pathogenesis: transcriptomic, cellular and animal studiesLidia Gaffke, Zuzanna Szczudło, Magdalena Podlacha, et al.
International Journal of Molecular Sciences|January 8, 2023
Mucopolysaccharidoses: Cellular Consequences of Glycosaminoglycans Accumulation and Potential TargetsAndrés Felipe Leal, Eliana Benincore-Flórez, Estera Rintz, et al.
Metabolic Brain Disease|March 16, 2018
Autophagy stimulation as a promising approach in treatment of neurodegenerative diseasesKarolina Pierzynowska, Lidia Gaffke, Zuzanna Cyske, et al.
International Journal of Molecular Sciences|August 28, 2025
Integrative Approaches to Myopathies and Muscular Dystrophies: Molecular Mechanisms, Diagnostics, and Future TherapiesMaja Ziemian, Joanna Szmydtka, Wojciech Snoch, et al.
Diagnostics (Basel, Switzerland)|September 28, 2021
Glycosaminoglycans as Biomarkers for Mucopolysaccharidoses and Other DisordersPaige C Amendum, Shaukat Khan, Seiji Yamaguchi, et al.
Genes|April 25, 2020
The Role of Metabolites in the Link between DNA Replication and Central Carbon Metabolism in Escherichia coliKlaudyna Krause, Monika Maciąg-Dorszyńska, Anna Wosinski, et al.
Biochemical and Biophysical Research Communications|April 2, 2026
Extensive transcriptomic changes in cellular and animal models of Huntington's disease depending on the length of CAG repeats in the exon 1 of the HTT geneAneta Szulc, Beata M Walter, Lidia Gaffke, et al.
Molecular Genetics and Metabolism|August 20, 2023
Molecular Trojan Horses for treating lysosomal storage diseasesAndrés Felipe Leal, Orhan Kerim Inci, Volkan Seyrantepe, et al.
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