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Peter Frommolt

Showing results (21-30 of 64) with videos related to

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European Heart Journal|June 3, 2008
Decreased number of circulating progenitor cells in obesity: beneficial effects of weight reductionJochen Müller-Ehmsen, Daniela Braun, Thorsten Schneider, et al.
Nature Communications|July 27, 2019
KLF-1 orchestrates a xenobiotic detoxification program essential for longevity of mitochondrial mutantsMarija Herholz, Estela Cepeda, Linda Baumann, et al.
Human Mutation|February 1, 2012
Assessing the enrichment performance in targeted resequencing experimentsPeter Frommolt, Ali T Abdallah, Janine Altmüller, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|November 14, 2009
Methyl-L-11C-methionine PET as a diagnostic marker for malignant progression in patients with gliomaRoland T Ullrich, Lutz Kracht, Anna Brunn, et al.
Aging Cell|April 10, 2013
Loss of the Birt-Hogg-Dubé gene product folliculin induces longevity in a hypoxia-inducible factor-dependent mannerHakam Gharbi, Francesca Fabretti, Puneet Bharill, et al.
Plos Pathogens|September 23, 2021
Salmonella Typhimurium impairs glycolysis-mediated acidification of phagosomes to evade macrophage defenseSaray Gutiérrez, Julia Fischer, Raja Ganesan, et al.
Translational Oncology|October 15, 2018
Genomic Characterization of TP53-Wild-Type Esophageal CarcinomaAlexander Quaas, Carina Heydt, Florian Gebauer, et al.
The Lancet. Neurology|August 2, 2012
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification studyHendrik Rosewich, Holger Thiele, Andreas Ohlenbusch, et al.
The Journal of Cell Biology|October 29, 2014
CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteinsJie Gao, Désirée Schatton, Paola Martinelli, et al.
Human Molecular Genetics|October 27, 2022
A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2Shashank Chepurwar, Sarah M von Loh, Daniela C Wigger, et al.
Pageof 7

Showing results (21-30 of 64) with videos related to

Sort By:
Pageof 7
European Heart Journal|June 3, 2008
Decreased number of circulating progenitor cells in obesity: beneficial effects of weight reductionJochen Müller-Ehmsen, Daniela Braun, Thorsten Schneider, et al.
Nature Communications|July 27, 2019
KLF-1 orchestrates a xenobiotic detoxification program essential for longevity of mitochondrial mutantsMarija Herholz, Estela Cepeda, Linda Baumann, et al.
Human Mutation|February 1, 2012
Assessing the enrichment performance in targeted resequencing experimentsPeter Frommolt, Ali T Abdallah, Janine Altmüller, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|November 14, 2009
Methyl-L-11C-methionine PET as a diagnostic marker for malignant progression in patients with gliomaRoland T Ullrich, Lutz Kracht, Anna Brunn, et al.
Aging Cell|April 10, 2013
Loss of the Birt-Hogg-Dubé gene product folliculin induces longevity in a hypoxia-inducible factor-dependent mannerHakam Gharbi, Francesca Fabretti, Puneet Bharill, et al.
Plos Pathogens|September 23, 2021
Salmonella Typhimurium impairs glycolysis-mediated acidification of phagosomes to evade macrophage defenseSaray Gutiérrez, Julia Fischer, Raja Ganesan, et al.
Translational Oncology|October 15, 2018
Genomic Characterization of TP53-Wild-Type Esophageal CarcinomaAlexander Quaas, Carina Heydt, Florian Gebauer, et al.
The Lancet. Neurology|August 2, 2012
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification studyHendrik Rosewich, Holger Thiele, Andreas Ohlenbusch, et al.
The Journal of Cell Biology|October 29, 2014
CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteinsJie Gao, Désirée Schatton, Paola Martinelli, et al.
Human Molecular Genetics|October 27, 2022
A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2Shashank Chepurwar, Sarah M von Loh, Daniela C Wigger, et al.
Pageof 7