Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F HOFFMANN

Showing results (341-350 of 1,073) with videos related to

Pageof 108
Sort By:
Bioengineered|March 13, 2013
A single point mutation in the listerial betL σ(A)-dependent promoter leads to improved osmo- and chill-tolerance and a morphological shift at elevated osmolarityRoland F Hoffmann, Susan McLernon, Audrey Feeney, et al.
International Journal for Parasitology. Drugs and Drug Resistance|November 21, 2018
Combining bioinformatics, cheminformatics, functional genomics and whole organism approaches for identifying epigenetic drug targets in Schistosoma mansoniGilda Padalino, Salvatore Ferla, Andrea Brancale, et al.
Scientific Reports|September 17, 2024
Transparency and adaptability aid in realigning the complexity of objectives, approaches, and systems in human-wildlife coexistence researchClaire F Hoffmann, Jacalyn M Beck, Roselyn W Kaihula, et al.
Scientific Reports|August 19, 2023
Rapid determination of levels of the main constituents in e-liquids by near infrared spectroscopyAnaïs R F Hoffmann, Jana Jeffery, Paul Dallin, et al.
Perfusion|October 1, 2021
Clinical monitoring of activated clotting time during cardiothoracic surgery: comparing the Hemochron<sup>®</sup> Response and Hemochron<sup>®</sup> Signature EliteRoland F Hoffmann, Sandra Horsten, Massimo A Mariani, et al.
Journal of Inherited Metabolic Disease|June 22, 2019
Ultra-orphan lysosomal storage diseases: A cross-sectional quantitative analysis of the natural history of alpha-mannosidosisMatthias Zielonka, Sven F Garbade, Stefan Kölker, et al.
Molecular Genetics and Metabolism|March 1, 2011
Natural course of glutamine synthetase deficiency in a 3 year old patientJohannes Häberle, Noora Shahbeck, Khalid Ibrahim, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|July 1, 1990
[Pre- and postnatal diagnosis of organoacidopathies]G F Hoffmann, C Jakobs, D Rating, et al.
The Journal of Pediatrics|March 1, 1996
Severe hyperchloriduria-hyperkaliuria: a new congenital renal tubular abnormality?J Meyburg, E Mayatepek, G F Hoffmann, et al.
Bone|August 6, 2017
Phantomless calibration of CT scans for measurement of BMD and bone strength-Inter-operator reanalysis precisionDavid C Lee, Paul F Hoffmann, David L Kopperdahl, et al.
Pageof 108

Showing results (341-350 of 1,073) with videos related to

Sort By:
Pageof 108
Bioengineered|March 13, 2013
A single point mutation in the listerial betL σ(A)-dependent promoter leads to improved osmo- and chill-tolerance and a morphological shift at elevated osmolarityRoland F Hoffmann, Susan McLernon, Audrey Feeney, et al.
International Journal for Parasitology. Drugs and Drug Resistance|November 21, 2018
Combining bioinformatics, cheminformatics, functional genomics and whole organism approaches for identifying epigenetic drug targets in Schistosoma mansoniGilda Padalino, Salvatore Ferla, Andrea Brancale, et al.
Scientific Reports|September 17, 2024
Transparency and adaptability aid in realigning the complexity of objectives, approaches, and systems in human-wildlife coexistence researchClaire F Hoffmann, Jacalyn M Beck, Roselyn W Kaihula, et al.
Scientific Reports|August 19, 2023
Rapid determination of levels of the main constituents in e-liquids by near infrared spectroscopyAnaïs R F Hoffmann, Jana Jeffery, Paul Dallin, et al.
Perfusion|October 1, 2021
Clinical monitoring of activated clotting time during cardiothoracic surgery: comparing the Hemochron<sup>®</sup> Response and Hemochron<sup>®</sup> Signature EliteRoland F Hoffmann, Sandra Horsten, Massimo A Mariani, et al.
Journal of Inherited Metabolic Disease|June 22, 2019
Ultra-orphan lysosomal storage diseases: A cross-sectional quantitative analysis of the natural history of alpha-mannosidosisMatthias Zielonka, Sven F Garbade, Stefan Kölker, et al.
Molecular Genetics and Metabolism|March 1, 2011
Natural course of glutamine synthetase deficiency in a 3 year old patientJohannes Häberle, Noora Shahbeck, Khalid Ibrahim, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|July 1, 1990
[Pre- and postnatal diagnosis of organoacidopathies]G F Hoffmann, C Jakobs, D Rating, et al.
The Journal of Pediatrics|March 1, 1996
Severe hyperchloriduria-hyperkaliuria: a new congenital renal tubular abnormality?J Meyburg, E Mayatepek, G F Hoffmann, et al.
Bone|August 6, 2017
Phantomless calibration of CT scans for measurement of BMD and bone strength-Inter-operator reanalysis precisionDavid C Lee, Paul F Hoffmann, David L Kopperdahl, et al.
Pageof 108