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Cell|June 26, 2018
Immunomimetic Designer Cells Protect Mice from MRSA InfectionYing Liu, Peng Bai, Anne-Kathrin Woischnig, et al.
Ophthalmic Research|April 24, 2023
A Novel Intronic Deletion in PDE6B Causes Autosomal Recessive Retinitis Pigmentosa by Interfering with RNA SplicingMukhtar Ullah, Atta Ur Rehman, Marc Folcher, et al.
Nature Communications|November 12, 2014
Mind-controlled transgene expression by a wireless-powered optogenetic designer cell implantMarc Folcher, Sabine Oesterle, Katharina Zwicky, et al.
The Journal of Biological Chemistry|October 16, 2013
WhiB7, an Fe-S-dependent transcription factor that activates species-specific repertoires of drug resistance determinants in actinobacteriaSantiago Ramón-García, Carol Ng, Pernille R Jensen, et al.
Cornea|September 1, 2021
c.-61G>A in OVOL2 is a Pathogenic 5' Untranslated Region Variant Causing Posterior Polymorphous Corneal Dystrophy 1Lucas Janeschitz-Kriegl, Dhryata Kamdar, Mathieu Quinodoz, et al.
Human Molecular Genetics|January 9, 2022
Mutations in the ribosome biogenesis factor gene LTV1 are linked to LIPHAK syndrome, a novel poikiloderma-like disorderJi Hoon Han, Gavin Ryan, Alyson Guy, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|October 13, 2025
Encapsulated cells as an enzyme replacement therapy for metachromatic leukodystrophyEmilie Audouard, Florine Chereau, Camille Lupiet, et al.
American Journal of Human Genetics|September 3, 2024
Bi-allelic variants in COQ8B, a gene involved in the biosynthesis of coenzyme Q10, lead to non-syndromic retinitis pigmentosaAna Belén Iglesias-Romero, Karolina Kaminska, Mathieu Quinodoz, et al.
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