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P Levine

Showing results (631-640 of 646) with videos related to

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Infectious Diseases and Therapy|March 28, 2019
Open-Label Randomized Trial of Early Clinical Outcomes of Ceftaroline Fosamil Versus Vancomycin for the Treatment of Acute Bacterial Skin and Skin Structure Infections at Risk of Methicillin-Resistant Staphylococcus aureusKimberly C Claeys, Evan J Zasowski, Trang D Trinh, et al.
Cell|September 18, 2018
Aster Proteins Facilitate Nonvesicular Plasma Membrane to ER Cholesterol Transport in Mammalian CellsJaspreet Sandhu, Shiqian Li, Louise Fairall, et al.
Autism Research : Official Journal of the International Society for Autism Research|January 21, 2020
Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART StudyCarolyn E B McCormick, Brian C Kavanaugh, Danielle Sipsock, et al.
Nature|February 25, 2026
CLCC1 promotes hepatic neutral lipid flux and nuclear pore complex assemblyAlyssa J Mathiowetz, Emily S Meymand, Güneş Parlakgül, et al.
The New England Journal of Medicine|August 18, 2006
Daptomycin versus standard therapy for bacteremia and endocarditis caused by Staphylococcus aureusVance G Fowler, Helen W Boucher, G Ralph Corey, et al.
Optica|July 15, 2024
T staging esophageal tumors with x raysT Partridge, P Wolfson, J Jiang, et al.
Journal of the American Society of Nephrology : JASN|July 3, 2019
Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic SyndromeStephanie Dufek, Chris Cheshire, Adam P Levine, et al.
Nature Communications|April 20, 2023
Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patientsYiming Wu, Kyle Gettler, Meltem Ece Kars, et al.
Kidney International|December 14, 2023
Autosomal dominant ApoA4 mutations present as tubulointerstitial kidney disease with medullary amyloidosisTereza Kmochová, Kendrah O Kidd, Andrew Orr, et al.
Science Translational Medicine|January 12, 2018
Functional variants in the <i>LRRK2</i> gene confer shared effects on risk for Crohn's disease and Parkinson's diseaseKen Y Hui, Heriberto Fernandez-Hernandez, Jianzhong Hu, et al.
Pageof 65

Showing results (631-640 of 646) with videos related to

Sort By:
Pageof 65
Infectious Diseases and Therapy|March 28, 2019
Open-Label Randomized Trial of Early Clinical Outcomes of Ceftaroline Fosamil Versus Vancomycin for the Treatment of Acute Bacterial Skin and Skin Structure Infections at Risk of Methicillin-Resistant Staphylococcus aureusKimberly C Claeys, Evan J Zasowski, Trang D Trinh, et al.
Cell|September 18, 2018
Aster Proteins Facilitate Nonvesicular Plasma Membrane to ER Cholesterol Transport in Mammalian CellsJaspreet Sandhu, Shiqian Li, Louise Fairall, et al.
Autism Research : Official Journal of the International Society for Autism Research|January 21, 2020
Autism Heterogeneity in a Densely Sampled U.S. Population: Results From the First 1,000 Participants in the RI-CART StudyCarolyn E B McCormick, Brian C Kavanaugh, Danielle Sipsock, et al.
Nature|February 25, 2026
CLCC1 promotes hepatic neutral lipid flux and nuclear pore complex assemblyAlyssa J Mathiowetz, Emily S Meymand, Güneş Parlakgül, et al.
The New England Journal of Medicine|August 18, 2006
Daptomycin versus standard therapy for bacteremia and endocarditis caused by Staphylococcus aureusVance G Fowler, Helen W Boucher, G Ralph Corey, et al.
Optica|July 15, 2024
T staging esophageal tumors with x raysT Partridge, P Wolfson, J Jiang, et al.
Journal of the American Society of Nephrology : JASN|July 3, 2019
Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic SyndromeStephanie Dufek, Chris Cheshire, Adam P Levine, et al.
Nature Communications|April 20, 2023
Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patientsYiming Wu, Kyle Gettler, Meltem Ece Kars, et al.
Kidney International|December 14, 2023
Autosomal dominant ApoA4 mutations present as tubulointerstitial kidney disease with medullary amyloidosisTereza Kmochová, Kendrah O Kidd, Andrew Orr, et al.
Science Translational Medicine|January 12, 2018
Functional variants in the <i>LRRK2</i> gene confer shared effects on risk for Crohn's disease and Parkinson's diseaseKen Y Hui, Heriberto Fernandez-Hernandez, Jianzhong Hu, et al.
Pageof 65