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B Beck

Showing results (471-480 of 717) with videos related to

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The Journal of Allergy and Clinical Immunology|September 28, 2020
The systemic autoinflammatory diseases: Coming of age with the human genomeDeborah L Stone, David B Beck, Kalpana Manthiram, et al.
Autism Research : Official Journal of the International Society for Autism Research|February 18, 2026
Integrating Dimensional Personality and Autistic Traits to Predict Suicidal Ideation, Suicide Attempts, and Nonsuicidal Self-Injury in Autistic AdultsAliona Tsypes, Timothy A Allen, Ligia Antezana, et al.
IARC Scientific Publications|January 1, 1990
A mortality study of a cohort of slate quarry workers in the German Democratic RepublicW H Mehnert, W Staneczek, M Möhner, et al.
Kidney International|July 3, 2014
Data from a large European study indicate that the outcome of primary hyperoxaluria type 1 correlates with the AGXT mutation typeGiorgia Mandrile, Christiaan S van Woerden, Paola Berchialla, et al.
Inorganic Chemistry|December 18, 2025
Investigation of Bimetallic Am(III) and Nd(III) Tetrazolate Complexes Under Ambient and High-Pressure ConditionsZhuanling Bai, Nicholas B Beck, Qiang Gao, et al.
Pediatric Nephrology (Berlin, Germany)|August 24, 2019
Subclinical myocardial disease in patients with primary hyperoxaluria and preserved left ventricular ejection fraction: a two-dimensional speckle-tracking imaging studyRuth Lagies, Floris E A Udink Ten Cate, Markus Feldkötter, et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]|August 27, 1998
Characterization of rat lung ICAM-1B Beck-Schimmer, R C Schimmer, H Schmal, et al.
Clinical and Experimental Immunology|July 6, 2005
Hypoxia aggravates lipopolysaccharide-induced lung injuryD Vuichard, M T Ganter, R C Schimmer, et al.
Kidney International|July 20, 2006
Oxalobacter formigenes: a potential tool for the treatment of primary hyperoxaluria type 1B Hoppe, B Beck, N Gatter, et al.
Pediatric Nephrology (Berlin, Germany)|October 11, 2008
Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)Matthias T F Wolf, Bethan E Hoskins, Bodo B Beck, et al.
Pageof 72

Showing results (471-480 of 717) with videos related to

Sort By:
Pageof 72
The Journal of Allergy and Clinical Immunology|September 28, 2020
The systemic autoinflammatory diseases: Coming of age with the human genomeDeborah L Stone, David B Beck, Kalpana Manthiram, et al.
Autism Research : Official Journal of the International Society for Autism Research|February 18, 2026
Integrating Dimensional Personality and Autistic Traits to Predict Suicidal Ideation, Suicide Attempts, and Nonsuicidal Self-Injury in Autistic AdultsAliona Tsypes, Timothy A Allen, Ligia Antezana, et al.
IARC Scientific Publications|January 1, 1990
A mortality study of a cohort of slate quarry workers in the German Democratic RepublicW H Mehnert, W Staneczek, M Möhner, et al.
Kidney International|July 3, 2014
Data from a large European study indicate that the outcome of primary hyperoxaluria type 1 correlates with the AGXT mutation typeGiorgia Mandrile, Christiaan S van Woerden, Paola Berchialla, et al.
Inorganic Chemistry|December 18, 2025
Investigation of Bimetallic Am(III) and Nd(III) Tetrazolate Complexes Under Ambient and High-Pressure ConditionsZhuanling Bai, Nicholas B Beck, Qiang Gao, et al.
Pediatric Nephrology (Berlin, Germany)|August 24, 2019
Subclinical myocardial disease in patients with primary hyperoxaluria and preserved left ventricular ejection fraction: a two-dimensional speckle-tracking imaging studyRuth Lagies, Floris E A Udink Ten Cate, Markus Feldkötter, et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]|August 27, 1998
Characterization of rat lung ICAM-1B Beck-Schimmer, R C Schimmer, H Schmal, et al.
Clinical and Experimental Immunology|July 6, 2005
Hypoxia aggravates lipopolysaccharide-induced lung injuryD Vuichard, M T Ganter, R C Schimmer, et al.
Kidney International|July 20, 2006
Oxalobacter formigenes: a potential tool for the treatment of primary hyperoxaluria type 1B Hoppe, B Beck, N Gatter, et al.
Pediatric Nephrology (Berlin, Germany)|October 11, 2008
Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT)Matthias T F Wolf, Bethan E Hoskins, Bodo B Beck, et al.
Pageof 72