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Jennifer Müller

Showing results (41-50 of 50) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 10, 2013
Chorein sensitivity of cytoskeletal organization and degranulation of plateletsEva-Maria Schmidt, Evi Schmid, Patrick Münzer, et al.
Journal of Environmental Management|May 18, 2025
Towards transformative change for biodiversity: What can we learn from case studies in Germany?Vera Schreiner, Marion Mehring, Janina Kleemann, et al.
Gut Microbes|June 27, 2026
Early antibiotic exposure and vaccine immune responses in preterm infants: potential sex-specific differencesLaura Haag, Stefanie Dietz-Ziegler, Julian Schwarz, et al.
Immunology|March 26, 2025
Innate Immune Activation Is a Strong Suppressor of CCL22 and Impedes Regulatory T Cell-Dendritic Cell InteractionIgnazio Piseddu, Jan Gärtig, Stephan Eiber, et al.
The Lancet. Neurology|January 9, 2015
Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline dataKathrin Reetz, Imis Dogan, Ana S Costa, et al.
ACS ES&T Air|December 18, 2025
Characterization of German SF<sub>6</sub> EmissionsKatharina Meixner, Thomas Wagenhäuser, Tanja J Schuck, et al.
Disease Models & Mechanisms|September 3, 2021
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypesEva Lana-Elola, Heather Cater, Sheona Watson-Scales, et al.
Annals of Clinical and Translational Neurology|December 11, 2014
High prevalence of NMDA receptor IgA/IgM antibodies in different dementia typesSarah Doss, Klaus-Peter Wandinger, Bradley T Hyman, et al.
Human Mutation|November 1, 2012
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeatsJulie van der Zee, Ilse Gijselinck, Lubina Dillen, et al.
Acta Neuropathologica|June 6, 2014
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degenerationJulie van der Zee, Tim Van Langenhove, Gabor G Kovacs, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 10, 2013
Chorein sensitivity of cytoskeletal organization and degranulation of plateletsEva-Maria Schmidt, Evi Schmid, Patrick Münzer, et al.
Journal of Environmental Management|May 18, 2025
Towards transformative change for biodiversity: What can we learn from case studies in Germany?Vera Schreiner, Marion Mehring, Janina Kleemann, et al.
Gut Microbes|June 27, 2026
Early antibiotic exposure and vaccine immune responses in preterm infants: potential sex-specific differencesLaura Haag, Stefanie Dietz-Ziegler, Julian Schwarz, et al.
Immunology|March 26, 2025
Innate Immune Activation Is a Strong Suppressor of CCL22 and Impedes Regulatory T Cell-Dendritic Cell InteractionIgnazio Piseddu, Jan Gärtig, Stephan Eiber, et al.
The Lancet. Neurology|January 9, 2015
Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline dataKathrin Reetz, Imis Dogan, Ana S Costa, et al.
ACS ES&T Air|December 18, 2025
Characterization of German SF<sub>6</sub> EmissionsKatharina Meixner, Thomas Wagenhäuser, Tanja J Schuck, et al.
Disease Models & Mechanisms|September 3, 2021
Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypesEva Lana-Elola, Heather Cater, Sheona Watson-Scales, et al.
Annals of Clinical and Translational Neurology|December 11, 2014
High prevalence of NMDA receptor IgA/IgM antibodies in different dementia typesSarah Doss, Klaus-Peter Wandinger, Bradley T Hyman, et al.
Human Mutation|November 1, 2012
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeatsJulie van der Zee, Ilse Gijselinck, Lubina Dillen, et al.
Acta Neuropathologica|June 6, 2014
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degenerationJulie van der Zee, Tim Van Langenhove, Gabor G Kovacs, et al.
Pageof 5