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Cellular and Molecular Life Sciences : CMLS|January 1, 2018
Tight co-twin similarity of monozygotic twins for hTERT protein level of T cell subsets, for telomere length and mitochondrial DNA copy number, but not for telomerase activityDóra Melicher, Anett Illés, Éva Pállinger, et al.Parkinson'S Disease|June 1, 2018
The rs13388259 Intergenic Polymorphism in the Genomic Context of the <i>BCYRN1</i> Gene Is Associated with Parkinson's Disease in the Hungarian PopulationSándor Márki, Anikó Göblös, Eszter Szlávicz, et al.American Journal of Medical Genetics. Part A|July 18, 2023
Compound heterozygous variants in MAPK8IP3 were detected in severe congenital hypotonia mimicking lethal spinal muscular atrophyJudit Kárteszi, Alban Ziegler, Mariann Tihanyi, et al.International Journal of Molecular Sciences|February 11, 2023
Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the <i>CCDC88C</i> GeneFanni Annamária Boros, László Szpisjak, Renáta Bozó, et al.Ideggyogyaszati Szemle|July 30, 2016
[DISEASE BURDEN OP DUCHENNE MUSCULAR DYSTROPHY PATIENTS AND THEIR CAREGIVERS]Márta Péntek, Ágnes Herczegfalvi, Mária Judit Molnár, et al.Cell Adhesion & Migration|December 10, 2015
Transmigration characteristics of breast cancer and melanoma cells through the brain endothelium: Role of Rac and PI3KJudit Molnár, Csilla Fazakas, János Haskó, et al.Plos One|June 16, 2011
Transmigration of melanoma cells through the blood-brain barrier: role of endothelial tight junctions and melanoma-released serine proteasesCsilla Fazakas, Imola Wilhelm, Péter Nagyoszi, et al.Schizophrenia Research|January 30, 2024
Probing the biological consequences of a previously undescribed de novo mutation of ZMYND11 in a schizophrenia patient by CRISPR genome editing and induced pluripotent stem cell based in vitro disease-modelingCsongor Tordai, Edit Hathy, Hella Gyergyák, et al.Stem Cell Research & Therapy|November 28, 2020
Investigation of de novo mutations in a schizophrenia case-parent trio by induced pluripotent stem cell-based in vitro disease modeling: convergence of schizophrenia- and autism-related cellular phenotypesEdit Hathy, Eszter Szabó, Nóra Varga, et al.Orphanet Journal of Rare Diseases|November 7, 2018
The European challenges of funding orphan medicinal productsMárta Szegedi, Tamás Zelei, Francis Arickx, et al.Pageof 11