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David Sant

Showing results (1-10 of 16) with videos related to

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Molecular Neurobiology|January 13, 2018
Phenotypic and Functional Characteristics of Human Schwann Cells as Revealed by Cell-Based Assays and RNA-SEQPaula V Monje, David Sant, Gaofeng Wang
Immunity, Inflammation and Disease|February 23, 2026
LSTM-Based Recurrent Neural Network Predicts Influenza-Like-Illness in Variable Climate ZonesAlfred Amendolara, Christopher Gowans, Joshua Barton, et al.
BMC Public Health|September 14, 2023
LSTM-based recurrent neural network provides effective short term flu forecastingAlfred B Amendolara, David Sant, Horacio G Rotstein, et al.
Frontiers in Medicine|October 21, 2024
Effectiveness of osteopathic craniosacral techniques: a meta-analysisAlfred Amendolara, Alexander Sheppert, Ryan Powers, et al.
Frontiers in Neurology|May 2, 2022
Long-Term Health Outcomes of Infantile Spasms Following Prednisolone vs. Adrenocorticotropic Hormone Treatment Characterized Using Phenome-Wide Association StudyMonika Baker, Clint C Mason, Jacob Wilkes, et al.
Cureus|March 29, 2024
Chronic Migraine May Be Associated With Postprandial Hypoglycemia in Adult Men: A Case SeriesAlfred Amendolara, Wyatt D Magoffin, Aparna U Naik, et al.
Nucleic Acids Research|May 27, 2015
Identifying high-affinity aptamer ligands with defined cross-reactivity using high-throughput guided systematic evolution of ligands by exponential enrichmentAgata Levay, Randall Brenneman, Jan Hoinka, et al.
Biology|July 15, 2026
Glucose Dysregulation as a Driver of Autoimmune Mimicry, Inflammation, and Psychiatric Symptoms: A Narrative ReviewJacob Warner-Palacio, Hannah Hunsaker, Amanda McKenna, et al.
JAMA Ophthalmology|November 10, 2017
Molecular Characteristics of Conjunctival Melanoma Using Whole-Exome SequencingSwarup S Swaminathan, Matthew G Field, David Sant, et al.
The Journal of Molecular Diagnostics : JMD|April 24, 2017
Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial PseudarthrosisRebecca L Margraf, Chad VanSant-Webb, David Sant, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Molecular Neurobiology|January 13, 2018
Phenotypic and Functional Characteristics of Human Schwann Cells as Revealed by Cell-Based Assays and RNA-SEQPaula V Monje, David Sant, Gaofeng Wang
Immunity, Inflammation and Disease|February 23, 2026
LSTM-Based Recurrent Neural Network Predicts Influenza-Like-Illness in Variable Climate ZonesAlfred Amendolara, Christopher Gowans, Joshua Barton, et al.
BMC Public Health|September 14, 2023
LSTM-based recurrent neural network provides effective short term flu forecastingAlfred B Amendolara, David Sant, Horacio G Rotstein, et al.
Frontiers in Medicine|October 21, 2024
Effectiveness of osteopathic craniosacral techniques: a meta-analysisAlfred Amendolara, Alexander Sheppert, Ryan Powers, et al.
Frontiers in Neurology|May 2, 2022
Long-Term Health Outcomes of Infantile Spasms Following Prednisolone vs. Adrenocorticotropic Hormone Treatment Characterized Using Phenome-Wide Association StudyMonika Baker, Clint C Mason, Jacob Wilkes, et al.
Cureus|March 29, 2024
Chronic Migraine May Be Associated With Postprandial Hypoglycemia in Adult Men: A Case SeriesAlfred Amendolara, Wyatt D Magoffin, Aparna U Naik, et al.
Nucleic Acids Research|May 27, 2015
Identifying high-affinity aptamer ligands with defined cross-reactivity using high-throughput guided systematic evolution of ligands by exponential enrichmentAgata Levay, Randall Brenneman, Jan Hoinka, et al.
Biology|July 15, 2026
Glucose Dysregulation as a Driver of Autoimmune Mimicry, Inflammation, and Psychiatric Symptoms: A Narrative ReviewJacob Warner-Palacio, Hannah Hunsaker, Amanda McKenna, et al.
JAMA Ophthalmology|November 10, 2017
Molecular Characteristics of Conjunctival Melanoma Using Whole-Exome SequencingSwarup S Swaminathan, Matthew G Field, David Sant, et al.
The Journal of Molecular Diagnostics : JMD|April 24, 2017
Utilization of Whole-Exome Next-Generation Sequencing Variant Read Frequency for Detection of Lesion-Specific, Somatic Loss of Heterozygosity in a Neurofibromatosis Type 1 Cohort with Tibial PseudarthrosisRebecca L Margraf, Chad VanSant-Webb, David Sant, et al.
Pageof 2