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European Journal of Medical Genetics|March 18, 2008
A 15Mb duplication of 6q24.1-q25.3 associated with typical but milder features of the duplication 6q syndromeChristiane Zweier, Udo Trautmann, Arif Ekici, et al.
Ophthalmic Genetics|September 28, 2018
Novel truncating mutation in CACNA1F in a young male patient diagnosed with optic atrophyFrancesca Pasutto, Arif Ekici, André Reis, et al.
Biomolecular Engineering|June 29, 2007
Heterologous expression of wildtype and mutant myocilin in High Five insect cells shows comparable effects to cultivated trabecular meshwork cellsSevinc Oezbey, Corinna Stengel, Ursula Schlötzer-Schrehardt, et al.
Human Genetics|October 18, 2002
Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneityGerald Stöber, Dominik Seelow, Franz Rüschendorf, et al.
Brain Sciences|April 21, 2022
Nimodipine Exerts Beneficial Effects on the Rat Oligodendrocyte Cell Line OLN-93Felix Boltz, Michael Enders, Andreas Feigenspan, et al.
Frontiers in Immunology|August 23, 2018
Effects of Anti-Integrin Treatment With Vedolizumab on Immune Pathways and Cytokines in Inflammatory Bowel DiseasesTimo Rath, Ulrike Billmeier, Fulvia Ferrazzi, et al.
International Journal of Molecular Sciences|November 26, 2022
Impact of Siponimod on Enteric and Central Nervous System Pathology in Late-Stage Experimental Autoimmune EncephalomyelitisAlicia Weier, Michael Enders, Philipp Kirchner, et al.
Biochemical Genetics|September 10, 2025
Exploring Differentially Expressed Genes and Understanding the Underlying Mechanisms in GlioblastomaDidem Seven, Arif Ekici, Steffen Uebe, et al.
JIMD Reports|January 29, 2017
A Homozygous Mutation in GPT2 Associated with Nonsyndromic Intellectual Disability in a Consanguineous Family from Costa RicaTanya Lobo-Prada, Heinrich Sticht, Sixto Bogantes-Ledezma, et al.
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