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Peter Proks

Showing results (51-60 of 55) with videos related to

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American Journal of Human Genetics|August 2, 2007
Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effectsSian Ellard, Sarah E Flanagan, Christophe A Girard, et al.
The Journal of Clinical Investigation|December 10, 2008
Expression of an activating mutation in the gene encoding the KATP channel subunit Kir6.2 in mouse pancreatic beta cells recapitulates neonatal diabetesChristophe A Girard, F Thomas Wunderlich, Kenju Shimomura, et al.
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.
The New England Journal of Medicine|April 30, 2004
Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetesAnna L Gloyn, Ewan R Pearson, Jennifer F Antcliff, et al.
Nature Genetics|October 4, 2022
Gain-of-function mutations in KCNK3 cause a developmental disorder with sleep apneaJanina Sörmann, Marcus Schewe, Peter Proks, et al.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
American Journal of Human Genetics|August 2, 2007
Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effectsSian Ellard, Sarah E Flanagan, Christophe A Girard, et al.
The Journal of Clinical Investigation|December 10, 2008
Expression of an activating mutation in the gene encoding the KATP channel subunit Kir6.2 in mouse pancreatic beta cells recapitulates neonatal diabetesChristophe A Girard, F Thomas Wunderlich, Kenju Shimomura, et al.
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.
The New England Journal of Medicine|April 30, 2004
Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetesAnna L Gloyn, Ewan R Pearson, Jennifer F Antcliff, et al.
Nature Genetics|October 4, 2022
Gain-of-function mutations in KCNK3 cause a developmental disorder with sleep apneaJanina Sörmann, Marcus Schewe, Peter Proks, et al.
Pageof 6