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Showing results (781-790 of 1,165) with videos related to

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Biorxiv : the Preprint Server for Biology|November 18, 2024
VizCNV: An integrated platform for concurrent phased BAF and CNV analysis with trio genome sequencing dataHaowei Du, Ming Yin Lun, Lidiia Gagarina, et al.
Biorxiv : the Preprint Server for Biology|September 16, 2024
INTRA- AND INTER-HOST EVOLUTION OF HUMAN NOROVIRUS IN HEALTHY ADULTSSasirekha Ramani, Sara J Javornik Cregeen, Anil Surathu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2021
Neptune: an environment for the delivery of genomic medicineVenner Eric, Victoria Yi, David Murdock, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|February 28, 2013
Next-generation sequencing for disorders of low and high bone mineral densityG Sule, P M Campeau, V W Zhang, et al.
Scientific Reports|January 4, 2017
Insensitivity to pain induced by a potent selective closed-state Nav1.7 inhibitorM Flinspach, Q Xu, A D Piekarz, et al.
Annals of Clinical and Translational Neurology|September 15, 2021
Deep clinicopathological phenotyping identifies a previously unrecognized pathogenic EMD splice variantDaniel G Calame, Jawid M Fatih, Isabella Herman, et al.
Pediatric Pulmonology|December 17, 2025
Associations of Early Life Ambient PM<sub>2.5</sub> Exposure With Asthma Risk in a Cohort of Preterm Infants With Bronchopulmonary DysplasiaLizbeth F Gomez, Jonathan J Szeto, Joshua K Radack, et al.
American Journal of Human Genetics|March 1, 2016
DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow SyndromeJanson J White, Juliana F Mazzeu, Alexander Hoischen, et al.
NPJ Genomic Medicine|August 28, 2019
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genesPamela Feliciano, Xueya Zhou, Irina Astrovskaya, et al.
JAMA Neurology|October 16, 2013
Mutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephalyClaudia Gonzaga-Jauregui, Timothy Lotze, Leila Jamal, et al.
Pageof 117

Showing results (781-790 of 1,165) with videos related to

Sort By:
Pageof 117
Biorxiv : the Preprint Server for Biology|November 18, 2024
VizCNV: An integrated platform for concurrent phased BAF and CNV analysis with trio genome sequencing dataHaowei Du, Ming Yin Lun, Lidiia Gagarina, et al.
Biorxiv : the Preprint Server for Biology|September 16, 2024
INTRA- AND INTER-HOST EVOLUTION OF HUMAN NOROVIRUS IN HEALTHY ADULTSSasirekha Ramani, Sara J Javornik Cregeen, Anil Surathu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 14, 2021
Neptune: an environment for the delivery of genomic medicineVenner Eric, Victoria Yi, David Murdock, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|February 28, 2013
Next-generation sequencing for disorders of low and high bone mineral densityG Sule, P M Campeau, V W Zhang, et al.
Scientific Reports|January 4, 2017
Insensitivity to pain induced by a potent selective closed-state Nav1.7 inhibitorM Flinspach, Q Xu, A D Piekarz, et al.
Annals of Clinical and Translational Neurology|September 15, 2021
Deep clinicopathological phenotyping identifies a previously unrecognized pathogenic EMD splice variantDaniel G Calame, Jawid M Fatih, Isabella Herman, et al.
Pediatric Pulmonology|December 17, 2025
Associations of Early Life Ambient PM<sub>2.5</sub> Exposure With Asthma Risk in a Cohort of Preterm Infants With Bronchopulmonary DysplasiaLizbeth F Gomez, Jonathan J Szeto, Joshua K Radack, et al.
American Journal of Human Genetics|March 1, 2016
DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow SyndromeJanson J White, Juliana F Mazzeu, Alexander Hoischen, et al.
NPJ Genomic Medicine|August 28, 2019
Exome sequencing of 457 autism families recruited online provides evidence for autism risk genesPamela Feliciano, Xueya Zhou, Irina Astrovskaya, et al.
JAMA Neurology|October 16, 2013
Mutations in VRK1 associated with complex motor and sensory axonal neuropathy plus microcephalyClaudia Gonzaga-Jauregui, Timothy Lotze, Leila Jamal, et al.
Pageof 117