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Roland Malli

Showing results (141-150 of 148) with videos related to

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American Journal of Human Genetics|May 1, 2012
Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disabilityMuzammil Ahmad Khan, Muhammad Arshad Rafiq, Abdul Noor, et al.
Nature Genetics|February 26, 2004
Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndromeChristian Windpassinger, Michaela Auer-Grumbach, Joy Irobi, et al.
Nature Communications|November 12, 2017
Novel genetically encoded fluorescent probes enable real-time detection of potassium in vitro and in vivoHelmut Bischof, Markus Rehberg, Sarah Stryeck, et al.
Elife|May 29, 2024
mitoBK<sub>Ca</sub> is functionally expressed in murine and human breast cancer cells and potentially contributes to metabolic reprogrammingHelmut Bischof, Selina Maier, Piotr Koprowski, et al.
Elife|March 14, 2020
Agonist-mediated switching of ion selectivity in TPC2 differentially promotes lysosomal functionSusanne Gerndt, Cheng-Chang Chen, Yu-Kai Chao, et al.
Science Advances|January 21, 2022
Fasting improves therapeutic response in hepatocellular carcinoma through p53-dependent metabolic synergismJelena Krstic, Isabel Reinisch, Katharina Schindlmaier, et al.
Communications Biology|July 1, 2026
Presenilin-1 controls glycolysis and identity of pancreatic beta cellsZhanat Koshenov, Sandra Postic, Gabriela Schoiswohl, et al.
Immunity|November 21, 2024
Acute suppression of mitochondrial ATP production prevents apoptosis and provides an essential signal for NLRP3 inflammasome activationBenedikt S Saller, Svenja Wöhrle, Larissa Fischer, et al.
Pageof 15

Showing results (141-150 of 148) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 148 results.
American Journal of Human Genetics|May 1, 2012
Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disabilityMuzammil Ahmad Khan, Muhammad Arshad Rafiq, Abdul Noor, et al.
Nature Genetics|February 26, 2004
Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndromeChristian Windpassinger, Michaela Auer-Grumbach, Joy Irobi, et al.
Nature Communications|November 12, 2017
Novel genetically encoded fluorescent probes enable real-time detection of potassium in vitro and in vivoHelmut Bischof, Markus Rehberg, Sarah Stryeck, et al.
Elife|May 29, 2024
mitoBK<sub>Ca</sub> is functionally expressed in murine and human breast cancer cells and potentially contributes to metabolic reprogrammingHelmut Bischof, Selina Maier, Piotr Koprowski, et al.
Elife|March 14, 2020
Agonist-mediated switching of ion selectivity in TPC2 differentially promotes lysosomal functionSusanne Gerndt, Cheng-Chang Chen, Yu-Kai Chao, et al.
Science Advances|January 21, 2022
Fasting improves therapeutic response in hepatocellular carcinoma through p53-dependent metabolic synergismJelena Krstic, Isabel Reinisch, Katharina Schindlmaier, et al.
Communications Biology|July 1, 2026
Presenilin-1 controls glycolysis and identity of pancreatic beta cellsZhanat Koshenov, Sandra Postic, Gabriela Schoiswohl, et al.
Immunity|November 21, 2024
Acute suppression of mitochondrial ATP production prevents apoptosis and provides an essential signal for NLRP3 inflammasome activationBenedikt S Saller, Svenja Wöhrle, Larissa Fischer, et al.
Pageof 15