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Simon Newstead

Showing results (91-100 of 95) with videos related to

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Nature Communications|May 16, 2024
Extracellular modulation of TREK-2 activity with nanobodies provides insight into the mechanisms of K2P channel regulationKarin E J Rödström, Alexander Cloake, Janina Sörmann, et al.
Bioelectricity|May 9, 2025
Lysosomal Ion Channels and Transporters: Recent Findings, Therapeutic Potential, and Technical ApproachesArtem Kondratskyi, Andre Bazzone, Markus Rapedius, et al.
Biorxiv : the Preprint Server for Biology|October 1, 2025
Identification of SLC45A4 as a pain gene encoding a neuronal polyamine transporterSteven J Middleton, Sigurbjörn Markússon, Mikael Åkerlund, et al.
Nature|August 20, 2025
SLC45A4 is a pain gene encoding a neuronal polyamine transporterSteven J Middleton, Sigurbjörn Markússon, Mikael Åkerlund, et al.
American Journal of Human Genetics|October 14, 2020
Interaction between KDELR2 and HSP47 as a Key Determinant in Osteogenesis Imperfecta Caused by Bi-allelic Variants in KDELR2Fleur S van Dijk, Oliver Semler, Julia Etich, et al.
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Showing results (91-100 of 95) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 95 results.
Nature Communications|May 16, 2024
Extracellular modulation of TREK-2 activity with nanobodies provides insight into the mechanisms of K2P channel regulationKarin E J Rödström, Alexander Cloake, Janina Sörmann, et al.
Bioelectricity|May 9, 2025
Lysosomal Ion Channels and Transporters: Recent Findings, Therapeutic Potential, and Technical ApproachesArtem Kondratskyi, Andre Bazzone, Markus Rapedius, et al.
Biorxiv : the Preprint Server for Biology|October 1, 2025
Identification of SLC45A4 as a pain gene encoding a neuronal polyamine transporterSteven J Middleton, Sigurbjörn Markússon, Mikael Åkerlund, et al.
Nature|August 20, 2025
SLC45A4 is a pain gene encoding a neuronal polyamine transporterSteven J Middleton, Sigurbjörn Markússon, Mikael Åkerlund, et al.
American Journal of Human Genetics|October 14, 2020
Interaction between KDELR2 and HSP47 as a Key Determinant in Osteogenesis Imperfecta Caused by Bi-allelic Variants in KDELR2Fleur S van Dijk, Oliver Semler, Julia Etich, et al.
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