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W Mueller

Showing results (471-480 of 671) with videos related to

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Global Change Biology|March 6, 2025
Smart Mixture Design Can Steer the Fate of Root-Derived Carbon Into Mineral-Associated and Particulate Organic Matter in Intensively Managed GrasslandsEsben Øster Mortensen, Diego Abalos, Tine Engedal, et al.
AIDS Care|December 22, 2009
The role of minor and adult children in the adjustment of women living with HIVCharles W Mueller, Lise D Martel, Yen-Chi L Le, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|September 13, 2020
Ribavirin and cellular ribavirin-triphosphate concentrations in blood and bronchoalveolar lavage fluid in two lung transplant patients with respiratory syncytial virusScott W Mueller, Tyree H Kiser, Taylor Morrisette, et al.
American Journal of Community Psychology|September 10, 2025
Facilitators and barriers to neighborhood social integrationJoelle Fuchs, Deena Shariq, Emily Yang, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|September 30, 2010
Concurrent TNFRSF1A R92Q and pyrin E230K mutations in a child with multiple sclerosisA Blaschek, P Lohse, K Huss, et al.
Environmental Science & Technology|September 29, 2017
Identification of Distinct Functional Microstructural Domains Controlling C Storage in SoilMarkus Steffens, Derek M Rogge, Carsten W Mueller, et al.
International Journal of Antimicrobial Agents|February 20, 2021
Combination ceftaroline and daptomycin salvage therapy for complicated methicillin-resistant Staphylococcus aureus bacteraemia compared with standard of careTanner M Johnson, Kyle C Molina, Matthew A Miller, et al.
Neuropathology and Applied Neurobiology|June 4, 2004
No evidence of hSNF5/INI1 point mutations in choroid plexus papillomaW Mueller, J-H David Eum, U Lass, et al.
Annals of the New York Academy of Sciences|September 7, 1994
Detection of paternally inherited mutations for beta-thalassemia in trophoblast isolated from peripheral maternal bloodC S Hawes, H A Suskin, B Kalionis, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Novel method to characterize CYP21A2 in Florida patients with congenital adrenal hyperplasia and commercially available cell linesChristopher N Greene, Suzanne K Cordovado, Daniel P Turner, et al.
Pageof 68

Showing results (471-480 of 671) with videos related to

Sort By:
Pageof 68
Global Change Biology|March 6, 2025
Smart Mixture Design Can Steer the Fate of Root-Derived Carbon Into Mineral-Associated and Particulate Organic Matter in Intensively Managed GrasslandsEsben Øster Mortensen, Diego Abalos, Tine Engedal, et al.
AIDS Care|December 22, 2009
The role of minor and adult children in the adjustment of women living with HIVCharles W Mueller, Lise D Martel, Yen-Chi L Le, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|September 13, 2020
Ribavirin and cellular ribavirin-triphosphate concentrations in blood and bronchoalveolar lavage fluid in two lung transplant patients with respiratory syncytial virusScott W Mueller, Tyree H Kiser, Taylor Morrisette, et al.
American Journal of Community Psychology|September 10, 2025
Facilitators and barriers to neighborhood social integrationJoelle Fuchs, Deena Shariq, Emily Yang, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|September 30, 2010
Concurrent TNFRSF1A R92Q and pyrin E230K mutations in a child with multiple sclerosisA Blaschek, P Lohse, K Huss, et al.
Environmental Science & Technology|September 29, 2017
Identification of Distinct Functional Microstructural Domains Controlling C Storage in SoilMarkus Steffens, Derek M Rogge, Carsten W Mueller, et al.
International Journal of Antimicrobial Agents|February 20, 2021
Combination ceftaroline and daptomycin salvage therapy for complicated methicillin-resistant Staphylococcus aureus bacteraemia compared with standard of careTanner M Johnson, Kyle C Molina, Matthew A Miller, et al.
Neuropathology and Applied Neurobiology|June 4, 2004
No evidence of hSNF5/INI1 point mutations in choroid plexus papillomaW Mueller, J-H David Eum, U Lass, et al.
Annals of the New York Academy of Sciences|September 7, 1994
Detection of paternally inherited mutations for beta-thalassemia in trophoblast isolated from peripheral maternal bloodC S Hawes, H A Suskin, B Kalionis, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Novel method to characterize CYP21A2 in Florida patients with congenital adrenal hyperplasia and commercially available cell linesChristopher N Greene, Suzanne K Cordovado, Daniel P Turner, et al.
Pageof 68