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

Wienker

Showing results (211-220 of 282) with videos related to

Pageof 29
Sort By:
International Journal of Psychophysiology : Official Journal of the International Organization of Psychophysiology|June 12, 2010
The P300 event-related potential and smoking--a population-based case-control studyA Mobascher, J Brinkmeyer, T Warbrick, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
European Radiology Experimental|December 5, 2024
Fully automatic quantification of pulmonary fat attenuation volume by CT: an exploratory pilot studyLuca Salhöfer, Mathias Holtkamp, Francesco Bonella, et al.
Plos One|April 8, 2016
Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based SampleA Mobascher, A Diaz-Lacava, M Wagner, et al.
Addiction Biology|August 24, 2012
Impaired sleep quality and sleep duration in smokers-results from the German Multicenter Study on Nicotine DependenceStefan Cohrs, Andrea Rodenbeck, Dieter Riemann, et al.
American Journal of Human Genetics|February 11, 1999
Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27H van Bokhoven, M Jung, A P Smits, et al.
American Journal of Medical Genetics. Part A|August 16, 2014
NDST1 missense mutations in autosomal recessive intellectual disabilityMiriam S Reuter, Luciana Musante, Hao Hu, et al.
Biological Psychiatry|July 1, 2008
The opioid peptides enkephalin and beta-endorphin in alcohol dependenceIldiko Racz, Britta Schürmann, Anna Karpushova, et al.
The European Respiratory Journal|February 6, 2025
First assessment of photon-counting CT for virtual bronchoscopic navigationMarcel Opitz, Faustina Funke, Kaid Darwiche, et al.
American Journal of Human Genetics|May 4, 2000
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3R C Betz, Y A Lee, A Bygum, et al.
Pageof 29

Showing results (211-220 of 282) with videos related to

Sort By:
Pageof 29
International Journal of Psychophysiology : Official Journal of the International Organization of Psychophysiology|June 12, 2010
The P300 event-related potential and smoking--a population-based case-control studyA Mobascher, J Brinkmeyer, T Warbrick, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
European Radiology Experimental|December 5, 2024
Fully automatic quantification of pulmonary fat attenuation volume by CT: an exploratory pilot studyLuca Salhöfer, Mathias Holtkamp, Francesco Bonella, et al.
Plos One|April 8, 2016
Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based SampleA Mobascher, A Diaz-Lacava, M Wagner, et al.
Addiction Biology|August 24, 2012
Impaired sleep quality and sleep duration in smokers-results from the German Multicenter Study on Nicotine DependenceStefan Cohrs, Andrea Rodenbeck, Dieter Riemann, et al.
American Journal of Human Genetics|February 11, 1999
Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27H van Bokhoven, M Jung, A P Smits, et al.
American Journal of Medical Genetics. Part A|August 16, 2014
NDST1 missense mutations in autosomal recessive intellectual disabilityMiriam S Reuter, Luciana Musante, Hao Hu, et al.
Biological Psychiatry|July 1, 2008
The opioid peptides enkephalin and beta-endorphin in alcohol dependenceIldiko Racz, Britta Schürmann, Anna Karpushova, et al.
The European Respiratory Journal|February 6, 2025
First assessment of photon-counting CT for virtual bronchoscopic navigationMarcel Opitz, Faustina Funke, Kaid Darwiche, et al.
American Journal of Human Genetics|May 4, 2000
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3R C Betz, Y A Lee, A Bygum, et al.
Pageof 29