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Alexandra Götz

Showing results (21-30 of 26) with videos related to

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Studies in Health Technology and Informatics|May 25, 2022
An Image Based Object Recognition System for Wound Detection and Classification of Diabetic Foot and Venous Leg UlcersJens Hüsers, Maurice Moelleken, Mats L Richter, et al.
American Journal of Human Genetics|May 10, 2011
Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathyAlexandra Götz, Henna Tyynismaa, Liliya Euro, et al.
Human Molecular Genetics|July 27, 2012
Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathyJenni M Elo, Srujana S Yadavalli, Liliya Euro, et al.
Hepatology (Baltimore, Md.)|September 3, 2022
A shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantationMikal Jacob Hole, Kristin Kaasen Jørgensen, Kristian Holm, et al.
Cell Metabolism|January 10, 2012
Somatic progenitor cell vulnerability to mitochondrial DNA mutagenesis underlies progeroid phenotypes in Polg mutator miceKati J Ahlqvist, Riikka H Hämäläinen, Shuichi Yatsuga, et al.
Ebiomedicine|July 30, 2021
Rifaximin or Saccharomyces boulardii in heart failure with reduced ejection fraction: Results from the randomized GutHeart trialAyodeji Awoyemi, Cristiane Mayerhofer, Alex S Felix, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Studies in Health Technology and Informatics|May 25, 2022
An Image Based Object Recognition System for Wound Detection and Classification of Diabetic Foot and Venous Leg UlcersJens Hüsers, Maurice Moelleken, Mats L Richter, et al.
American Journal of Human Genetics|May 10, 2011
Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathyAlexandra Götz, Henna Tyynismaa, Liliya Euro, et al.
Human Molecular Genetics|July 27, 2012
Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathyJenni M Elo, Srujana S Yadavalli, Liliya Euro, et al.
Hepatology (Baltimore, Md.)|September 3, 2022
A shared mucosal gut microbiota signature in primary sclerosing cholangitis before and after liver transplantationMikal Jacob Hole, Kristin Kaasen Jørgensen, Kristian Holm, et al.
Cell Metabolism|January 10, 2012
Somatic progenitor cell vulnerability to mitochondrial DNA mutagenesis underlies progeroid phenotypes in Polg mutator miceKati J Ahlqvist, Riikka H Hämäläinen, Shuichi Yatsuga, et al.
Ebiomedicine|July 30, 2021
Rifaximin or Saccharomyces boulardii in heart failure with reduced ejection fraction: Results from the randomized GutHeart trialAyodeji Awoyemi, Cristiane Mayerhofer, Alex S Felix, et al.
Pageof 3