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Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|May 29, 2020
Finding Suitable Clinical Endpoints for a Potential Treatment of a Rare Genetic Disease: the Case of ARID1BMatthijs D Kruizinga, Rob G J A Zuiker, Elif Sali, et al.
BMC Medical Genetics|May 20, 2018
The conserved p.Arg108 residue in S1PR2 (DFNB68) is fundamental for proper hearing: evidence from a consanguineous Iranian familyMichaela A H Hofrichter, Majid Mojarad, Julia Doll, et al.
International Journal of Molecular Sciences|January 11, 2022
Concomitant Activation of OSM and LIF Receptor by a Dual-Specific hlOSM Variant Confers Cardioprotection after Myocardial Infarction in MiceHolger Lörchner, Juan M Adrian-Segarra, Christian Waechter, et al.
Cancers|January 21, 2022
Predictors for Adherence to Treatment Strategies in Elderly HNSCC PatientsRaphaela Graessle, Carmen Stromberger, Max Heiland, et al.
Frontiers in Bioengineering and Biotechnology|October 6, 2025
Current clinical and translational challenges in temporomandibular joint reconstructionHelena Baecher, Bhagvat Maheta, Lisa-Marie Lottner, et al.
Genetics in Medicine Open|July 21, 2025
Educational videos in genetic counseling: Meeting patients where they are?Julia Mahal, Carlotta J Mayer, Sebastian Sailer, et al.
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