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Showing results (821-830 of 1,165) with videos related to

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CA: a Cancer Journal for Clinicians|June 2, 2022
Oncologic emergencies and urgencies: A comprehensive reviewBonnie E Gould Rothberg, Tammie E Quest, Sai-Ching J Yeung, et al.
Nature Medicine|December 4, 2019
Prospective virome analyses in young children at increased genetic risk for type 1 diabetesKendra Vehik, Kristian F Lynch, Matthew C Wong, et al.
Pediatrics|December 9, 2024
Risk of Transmission of Vaccine-Strain Rotavirus in a Neonatal Intensive Care Unit That Routinely VaccinatesMorgan A Zalot, Margaret M Cortese, Kevin P O'Callaghan, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2026
Multi-Omics Characterization of Human Molecular Responses to Spaceflight Across Two Independent MissionsAbirami Santhanam, Zeineen Momin, Xiang Qin, et al.
Plos One|August 25, 2021
Oligonucleotide capture sequencing of the SARS-CoV-2 genome and subgenomic fragments from COVID-19 individualsHarsha Doddapaneni, Sara Javornik Cregeen, Richard Sucgang, et al.
Nature Communications|November 20, 2020
PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophreniaTanner O Monroe, Melanie E Garrett, Maria Kousi, et al.
Biorxiv : the Preprint Server for Biology|December 17, 2020
Oligonucleotide Capture Sequencing of the SARS-CoV-2 Genome and Subgenomic Fragments from COVID-19 IndividualsHarsha Doddapaneni, Sara Javornik Cregeen, Richard Sucgang, et al.
Biorxiv : the Preprint Server for Biology|August 9, 2020
Oligonucleotide capture sequencing of the SARS-CoV-2 genome and subgenomic fragments from COVID-19 individualsHarsha Doddapaneni, Sara Javornik Cregeen, Richard Sucgang, et al.
American Journal of Human Genetics|May 11, 2015
Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3Jessica X Chong, Lindsay C Burrage, Anita E Beck, et al.
Genome Medicine|March 29, 2022
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research ProgramEric Venner, Donna Muzny, Joshua D Smith, et al.
Pageof 117

Showing results (821-830 of 1,165) with videos related to

Sort By:
Pageof 117
CA: a Cancer Journal for Clinicians|June 2, 2022
Oncologic emergencies and urgencies: A comprehensive reviewBonnie E Gould Rothberg, Tammie E Quest, Sai-Ching J Yeung, et al.
Nature Medicine|December 4, 2019
Prospective virome analyses in young children at increased genetic risk for type 1 diabetesKendra Vehik, Kristian F Lynch, Matthew C Wong, et al.
Pediatrics|December 9, 2024
Risk of Transmission of Vaccine-Strain Rotavirus in a Neonatal Intensive Care Unit That Routinely VaccinatesMorgan A Zalot, Margaret M Cortese, Kevin P O'Callaghan, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2026
Multi-Omics Characterization of Human Molecular Responses to Spaceflight Across Two Independent MissionsAbirami Santhanam, Zeineen Momin, Xiang Qin, et al.
Plos One|August 25, 2021
Oligonucleotide capture sequencing of the SARS-CoV-2 genome and subgenomic fragments from COVID-19 individualsHarsha Doddapaneni, Sara Javornik Cregeen, Richard Sucgang, et al.
Nature Communications|November 20, 2020
PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophreniaTanner O Monroe, Melanie E Garrett, Maria Kousi, et al.
Biorxiv : the Preprint Server for Biology|December 17, 2020
Oligonucleotide Capture Sequencing of the SARS-CoV-2 Genome and Subgenomic Fragments from COVID-19 IndividualsHarsha Doddapaneni, Sara Javornik Cregeen, Richard Sucgang, et al.
Biorxiv : the Preprint Server for Biology|August 9, 2020
Oligonucleotide capture sequencing of the SARS-CoV-2 genome and subgenomic fragments from COVID-19 individualsHarsha Doddapaneni, Sara Javornik Cregeen, Richard Sucgang, et al.
American Journal of Human Genetics|May 11, 2015
Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3Jessica X Chong, Lindsay C Burrage, Anita E Beck, et al.
Genome Medicine|March 29, 2022
Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research ProgramEric Venner, Donna Muzny, Joshua D Smith, et al.
Pageof 117