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Simon G Gregory

Showing results (41-50 of 142) with videos related to

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Acta Neuropathologica Communications|March 25, 2023
Ganglioglioma deep transcriptomics reveals primitive neuroectoderm neural precursor-like populationJoshua A Regal, María E Guerra García, Vaibhav Jain, et al.
JID Innovations : Skin Science From Molecules to Population Health|June 10, 2025
Insights into Keratinocyte and Immunologic Landscape in Cutaneous Graft-Versus-Host Disease through Single-Cell TranscriptomicsAmy J Petty, Adela Rambi Cardones, Yingai Jane Jin, et al.
Development and Psychopathology|April 5, 2022
Adolescent peer struggles predict accelerated epigenetic aging in midlifeJoseph P Allen, Joshua S Danoff, Meghan A Costello, et al.
Molecular Vision|December 19, 2013
Genetic screen of African Americans with Fuchs endothelial corneal dystrophyMollie A Minear, Yi-Ju Li, Jacqueline Rimmler, et al.
BMC Medical Genomics|June 26, 2014
Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometricsChristina A Markunas, Eric Lock, Karen Soldano, et al.
Elife|January 27, 2021
Single-cell RNA-seq reveals transcriptomic heterogeneity mediated by host-pathogen dynamics in lymphoblastoid cell linesElliott D SoRelle, Joanne Dai, Emmanuela N Bonglack, et al.
Circulation. Cardiovascular Genetics|April 19, 2011
The S1103Y cardiac sodium channel variant is associated with implantable cardioverter-defibrillator events in blacks with heart failure and reduced ejection fractionAlbert Y Sun, Jason I Koontz, Svati H Shah, et al.
Birth Defects Research. Part B, Developmental and Reproductive Toxicology|December 11, 2013
Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotypeKaren L Soldano, Melanie E Garrett, Heidi L Cope, et al.
Biorxiv : the Preprint Server for Biology|January 31, 2024
Transcriptome Analysis Identifies An ASD-Like Phenotype In Oligodendrocytes And Microglia From C58/J Amygdala That Is Dependent On Sex and SociabilityGeorge D Dalton, Stephen K Siecinski, Viktoriya D Nikolova, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 19, 2012
Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE)Deidre R Krupp, Pu-Ting Xu, Sophie Thomas, et al.
Pageof 15

Showing results (41-50 of 142) with videos related to

Sort By:
Pageof 15
Acta Neuropathologica Communications|March 25, 2023
Ganglioglioma deep transcriptomics reveals primitive neuroectoderm neural precursor-like populationJoshua A Regal, María E Guerra García, Vaibhav Jain, et al.
JID Innovations : Skin Science From Molecules to Population Health|June 10, 2025
Insights into Keratinocyte and Immunologic Landscape in Cutaneous Graft-Versus-Host Disease through Single-Cell TranscriptomicsAmy J Petty, Adela Rambi Cardones, Yingai Jane Jin, et al.
Development and Psychopathology|April 5, 2022
Adolescent peer struggles predict accelerated epigenetic aging in midlifeJoseph P Allen, Joshua S Danoff, Meghan A Costello, et al.
Molecular Vision|December 19, 2013
Genetic screen of African Americans with Fuchs endothelial corneal dystrophyMollie A Minear, Yi-Ju Li, Jacqueline Rimmler, et al.
BMC Medical Genomics|June 26, 2014
Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometricsChristina A Markunas, Eric Lock, Karen Soldano, et al.
Elife|January 27, 2021
Single-cell RNA-seq reveals transcriptomic heterogeneity mediated by host-pathogen dynamics in lymphoblastoid cell linesElliott D SoRelle, Joanne Dai, Emmanuela N Bonglack, et al.
Circulation. Cardiovascular Genetics|April 19, 2011
The S1103Y cardiac sodium channel variant is associated with implantable cardioverter-defibrillator events in blacks with heart failure and reduced ejection fractionAlbert Y Sun, Jason I Koontz, Svati H Shah, et al.
Birth Defects Research. Part B, Developmental and Reproductive Toxicology|December 11, 2013
Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotypeKaren L Soldano, Melanie E Garrett, Heidi L Cope, et al.
Biorxiv : the Preprint Server for Biology|January 31, 2024
Transcriptome Analysis Identifies An ASD-Like Phenotype In Oligodendrocytes And Microglia From C58/J Amygdala That Is Dependent On Sex and SociabilityGeorge D Dalton, Stephen K Siecinski, Viktoriya D Nikolova, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 19, 2012
Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE)Deidre R Krupp, Pu-Ting Xu, Sophie Thomas, et al.
Pageof 15