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Michael T Zimmermann

Showing results (71-80 of 146) with videos related to

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Case Reports in Genetics|February 7, 2017
Novel Pathogenic Variant in TGFBR2 Confirmed by Molecular Modeling Is a Rare Cause of Loeys-Dietz SyndromeMichael T Zimmermann, Raul A Urrutia, Patrick R Blackburn, et al.
Epigenomes|March 27, 2026
Mutant KRAS Heterogeneity Shapes Nuclear Architecture During Pancreatic Cancer InitiationGareth Pollin, Angela J Mathison, Elise N Leverence, et al.
Human Genetics|March 15, 2017
Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccineIana H Haralambieva, Inna G Ovsyannikova, Richard B Kennedy, et al.
Heliyon|July 22, 2016
Gene signatures related to HAI response following influenza A/H1N1 vaccine in older individualsInna G Ovsyannikova, Ann L Oberg, Richard B Kennedy, et al.
Circulation. Cardiovascular Genetics|June 19, 2015
Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection FractionJeanne L Theis, Michael T Zimmermann, Jared M Evans, et al.
Frontiers in Immunology|May 10, 2017
Integration of Immune Cell Populations, mRNA-Seq, and CpG Methylation to Better Predict Humoral Immunity to Influenza Vaccination: Dependence of mRNA-Seq/CpG Methylation on Immune Cell PopulationsMichael T Zimmermann, Richard B Kennedy, Diane E Grill, et al.
Biorxiv : the Preprint Server for Biology|October 3, 2023
A Multi-Layered Computational Structural Genomics Approach Enhances Domain-Specific Interpretation of Kleefstra Syndrome Variants in EHMT1Young-In Chi, Salomão D Jorge, Davin R Jensen, et al.
Computational and Structural Biotechnology Journal|November 13, 2023
A multi-layered computational structural genomics approach enhances domain-specific interpretation of Kleefstra syndrome variants in EHMT1Young-In Chi, Salomão D Jorge, Davin R Jensen, et al.
Journal of Proteome Research|March 22, 2014
Clinical proteome informatics workbench detects pathogenic mutations in hereditary amyloidosesSurendra Dasari, Jason D Theis, Julie A Vrana, et al.
Life (Basel, Switzerland)|March 28, 2024
Structural and Dynamic Analyses of Pathogenic Variants in <i>PIK3R1</i> Reveal a Shared Mechanism Associated among Cancer, Undergrowth, and Overgrowth SyndromesNikita R Dsouza, Catherine E Cottrell, Olivia M T Davies, et al.
Pageof 15

Showing results (71-80 of 146) with videos related to

Sort By:
Pageof 15
Case Reports in Genetics|February 7, 2017
Novel Pathogenic Variant in TGFBR2 Confirmed by Molecular Modeling Is a Rare Cause of Loeys-Dietz SyndromeMichael T Zimmermann, Raul A Urrutia, Patrick R Blackburn, et al.
Epigenomes|March 27, 2026
Mutant KRAS Heterogeneity Shapes Nuclear Architecture During Pancreatic Cancer InitiationGareth Pollin, Angela J Mathison, Elise N Leverence, et al.
Human Genetics|March 15, 2017
Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccineIana H Haralambieva, Inna G Ovsyannikova, Richard B Kennedy, et al.
Heliyon|July 22, 2016
Gene signatures related to HAI response following influenza A/H1N1 vaccine in older individualsInna G Ovsyannikova, Ann L Oberg, Richard B Kennedy, et al.
Circulation. Cardiovascular Genetics|June 19, 2015
Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection FractionJeanne L Theis, Michael T Zimmermann, Jared M Evans, et al.
Frontiers in Immunology|May 10, 2017
Integration of Immune Cell Populations, mRNA-Seq, and CpG Methylation to Better Predict Humoral Immunity to Influenza Vaccination: Dependence of mRNA-Seq/CpG Methylation on Immune Cell PopulationsMichael T Zimmermann, Richard B Kennedy, Diane E Grill, et al.
Biorxiv : the Preprint Server for Biology|October 3, 2023
A Multi-Layered Computational Structural Genomics Approach Enhances Domain-Specific Interpretation of Kleefstra Syndrome Variants in EHMT1Young-In Chi, Salomão D Jorge, Davin R Jensen, et al.
Computational and Structural Biotechnology Journal|November 13, 2023
A multi-layered computational structural genomics approach enhances domain-specific interpretation of Kleefstra syndrome variants in EHMT1Young-In Chi, Salomão D Jorge, Davin R Jensen, et al.
Journal of Proteome Research|March 22, 2014
Clinical proteome informatics workbench detects pathogenic mutations in hereditary amyloidosesSurendra Dasari, Jason D Theis, Julie A Vrana, et al.
Life (Basel, Switzerland)|March 28, 2024
Structural and Dynamic Analyses of Pathogenic Variants in <i>PIK3R1</i> Reveal a Shared Mechanism Associated among Cancer, Undergrowth, and Overgrowth SyndromesNikita R Dsouza, Catherine E Cottrell, Olivia M T Davies, et al.
Pageof 15