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Showing results (641-650 of 921) with videos related to

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Acta Dermato-Venereologica|March 28, 2009
Lack of association between neuropeptide S receptor 1 gene (NPSR1) and eczema in five European populationsElisabeth Ekelund, Maria Bradley, Stephan Weidinger, et al.
Biological Psychiatry|July 12, 2005
Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depressionJohannes Schumacher, Rami Abou Jamra, Tim Becker, et al.
Inhalation Toxicology|October 4, 2007
Air pollution and inflammatory response in myocardial infarction survivors: gene-environment interactions in a high-risk groupAnnette Peters, Alexandra Schneider, Sonja Greven, et al.
Frontiers in Immunology|February 16, 2026
Disturbed regulation of immunothrombosis in cerebral ischemia associated with SARS-CoV-2 infectionRichard Plem, Nicole de Buhr, Rabea Imker, et al.
Leukemia|September 29, 2012
ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcomeS Schnittger, C Eder, S Jeromin, et al.
Allergy|June 17, 2014
Fine-mapping of IgE-associated loci 1q23, 5q31, and 12q13 using 1000 Genomes Project dataV Sharma, S Michel, V Gaertner, et al.
The Journal of Clinical Endocrinology and Metabolism|February 24, 2006
Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from GermanyAnke Hinney, Thomas Bettecken, Patrick Tarnow, et al.
Plos One|April 28, 2016
The Pharmacogenetic Footprint of ACE Inhibition: A Population-Based Metabolomics StudyElisabeth Altmaier, Cristina Menni, Margit Heier, et al.
Cancers|November 27, 2021
Transcriptional and Mutational Profiling of B-Other Acute Lymphoblastic Leukemia for Improved DiagnosticsPhilippe Chouvarine, Željko Antić, Jana Lentes, et al.
Hormone Research in Paediatrics|June 13, 2012
Do common variants separate between obese melanocortin-4 receptor gene mutation carriers and non-carriers? The impact of cryptic relatednessJessica Mühlhaus, Carolin Pütter, Harald Brumm, et al.
Pageof 93

Showing results (641-650 of 921) with videos related to

Sort By:
Pageof 93
Acta Dermato-Venereologica|March 28, 2009
Lack of association between neuropeptide S receptor 1 gene (NPSR1) and eczema in five European populationsElisabeth Ekelund, Maria Bradley, Stephan Weidinger, et al.
Biological Psychiatry|July 12, 2005
Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depressionJohannes Schumacher, Rami Abou Jamra, Tim Becker, et al.
Inhalation Toxicology|October 4, 2007
Air pollution and inflammatory response in myocardial infarction survivors: gene-environment interactions in a high-risk groupAnnette Peters, Alexandra Schneider, Sonja Greven, et al.
Frontiers in Immunology|February 16, 2026
Disturbed regulation of immunothrombosis in cerebral ischemia associated with SARS-CoV-2 infectionRichard Plem, Nicole de Buhr, Rabea Imker, et al.
Leukemia|September 29, 2012
ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcomeS Schnittger, C Eder, S Jeromin, et al.
Allergy|June 17, 2014
Fine-mapping of IgE-associated loci 1q23, 5q31, and 12q13 using 1000 Genomes Project dataV Sharma, S Michel, V Gaertner, et al.
The Journal of Clinical Endocrinology and Metabolism|February 24, 2006
Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from GermanyAnke Hinney, Thomas Bettecken, Patrick Tarnow, et al.
Plos One|April 28, 2016
The Pharmacogenetic Footprint of ACE Inhibition: A Population-Based Metabolomics StudyElisabeth Altmaier, Cristina Menni, Margit Heier, et al.
Cancers|November 27, 2021
Transcriptional and Mutational Profiling of B-Other Acute Lymphoblastic Leukemia for Improved DiagnosticsPhilippe Chouvarine, Željko Antić, Jana Lentes, et al.
Hormone Research in Paediatrics|June 13, 2012
Do common variants separate between obese melanocortin-4 receptor gene mutation carriers and non-carriers? The impact of cryptic relatednessJessica Mühlhaus, Carolin Pütter, Harald Brumm, et al.
Pageof 93