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Showing results (41-50 of 45) with videos related to

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Plos Biology|May 22, 2018
Endoplasmic reticulum-plasma membrane contact sites integrate sterol and phospholipid regulationEvan Quon, Yves Y Sere, Neha Chauhan, et al.
Nature Communications|August 5, 2025
Two successive oligomeric Munc13 assemblies scaffold vesicle docking and SNARE assembly to support neurotransmitter releaseManindra Bera, Kirill Grushin, R Venkat Kalyana Sundaram, et al.
Nature Communications|October 4, 2016
Dimerization deficiency of enigmatic retinitis pigmentosa-linked rhodopsin mutantsBirgit Ploier, Lydia N Caro, Takefumi Morizumi, et al.
The Journal of Clinical Investigation|February 14, 2017
Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorderNoa Lipstein, Nanda M Verhoeven-Duif, Francesco E Michelassi, et al.
Nature Genetics|October 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic functionReza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, et al.
Pageof 5

Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Plos Biology|May 22, 2018
Endoplasmic reticulum-plasma membrane contact sites integrate sterol and phospholipid regulationEvan Quon, Yves Y Sere, Neha Chauhan, et al.
Nature Communications|August 5, 2025
Two successive oligomeric Munc13 assemblies scaffold vesicle docking and SNARE assembly to support neurotransmitter releaseManindra Bera, Kirill Grushin, R Venkat Kalyana Sundaram, et al.
Nature Communications|October 4, 2016
Dimerization deficiency of enigmatic retinitis pigmentosa-linked rhodopsin mutantsBirgit Ploier, Lydia N Caro, Takefumi Morizumi, et al.
The Journal of Clinical Investigation|February 14, 2017
Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorderNoa Lipstein, Nanda M Verhoeven-Duif, Francesco E Michelassi, et al.
Nature Genetics|October 22, 2025
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic functionReza Asadollahi, Aisha Ahmad, Paranchai Boonsawat, et al.
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