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Anna Morgan

Showing results (41-50 of 86) with videos related to

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Frontiers in Genetics|March 14, 2019
Next Generation Sequencing and Animal Models Reveal <i>SLC9A3R1</i> as a New Gene Involved in Human Age-Related Hearing LossGiorgia Girotto, Anna Morgan, Navaneethakrishnan Krishnamoorthy, et al.
Human Molecular Genetics|January 29, 2015
The p.Cys169Tyr variant of connexin 26 is not a polymorphismFrancesco Zonta, Giorgia Girotto, Damiano Buratto, et al.
Journal of Urban Health : Bulletin of the New York Academy of Medicine|April 18, 2024
Cash Transfers and After-School Programs: A Randomized Controlled Trial for Young Men at Risk of Violence Exposure in Wilmington, DelawareChristina Plerhoples Stacy, Daniel Teles, Jorge González-Hermoso, et al.
American Journal of Medical Genetics. Part A|December 6, 2024
Does It Run in Your Family? Inherited Truncating PSMD12 Variants Broaden the Phenotypic Spectrum of Stankiewicz-Isidor SyndromeAgnese Feresin, Beatrice Spedicati, Stefania Zampieri, et al.
European Journal of Human Genetics : EJHG|March 17, 2021
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolatesBeatrice Spedicati, Massimiliano Cocca, Roberto Palmisano, et al.
American Journal of Medical Genetics. Part A|December 6, 2013
Next generation sequencing in nonsyndromic intellectual disability: from a negative molecular karyotype to a possible causative mutation detectionEmmanouil Athanasakis, Danilo Licastro, Flavio Faletra, et al.
Bioorganic & Medicinal Chemistry Letters|February 16, 2008
Adenosine analogues as inhibitors of P2Y12 receptor mediated platelet aggregationJames G Douglass, J Bryan deCamp, Emilee H Fulcher, et al.
Biomedicines|March 29, 2023
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian PopulationBeatrice Spedicati, Aurora Santin, Giuseppe Giovanni Nardone, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|March 25, 2014
Quantitative assessment of nanoparticle surface hydrophobicity and its influence on pulmonary biocompatibilityMarie-Christine Jones, Stuart A Jones, Yanira Riffo-Vasquez, et al.
Genes|February 25, 2023
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of <i>CSNK2B</i>-Associated DisordersMariateresa Di Stazio, Caterina Zanus, Flavio Faletra, et al.
Pageof 9

Showing results (41-50 of 86) with videos related to

Sort By:
Pageof 9
Frontiers in Genetics|March 14, 2019
Next Generation Sequencing and Animal Models Reveal <i>SLC9A3R1</i> as a New Gene Involved in Human Age-Related Hearing LossGiorgia Girotto, Anna Morgan, Navaneethakrishnan Krishnamoorthy, et al.
Human Molecular Genetics|January 29, 2015
The p.Cys169Tyr variant of connexin 26 is not a polymorphismFrancesco Zonta, Giorgia Girotto, Damiano Buratto, et al.
Journal of Urban Health : Bulletin of the New York Academy of Medicine|April 18, 2024
Cash Transfers and After-School Programs: A Randomized Controlled Trial for Young Men at Risk of Violence Exposure in Wilmington, DelawareChristina Plerhoples Stacy, Daniel Teles, Jorge González-Hermoso, et al.
American Journal of Medical Genetics. Part A|December 6, 2024
Does It Run in Your Family? Inherited Truncating PSMD12 Variants Broaden the Phenotypic Spectrum of Stankiewicz-Isidor SyndromeAgnese Feresin, Beatrice Spedicati, Stefania Zampieri, et al.
European Journal of Human Genetics : EJHG|March 17, 2021
Natural human knockouts and Mendelian disorders: deep phenotyping in Italian isolatesBeatrice Spedicati, Massimiliano Cocca, Roberto Palmisano, et al.
American Journal of Medical Genetics. Part A|December 6, 2013
Next generation sequencing in nonsyndromic intellectual disability: from a negative molecular karyotype to a possible causative mutation detectionEmmanouil Athanasakis, Danilo Licastro, Flavio Faletra, et al.
Bioorganic & Medicinal Chemistry Letters|February 16, 2008
Adenosine analogues as inhibitors of P2Y12 receptor mediated platelet aggregationJames G Douglass, J Bryan deCamp, Emilee H Fulcher, et al.
Biomedicines|March 29, 2023
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian PopulationBeatrice Spedicati, Aurora Santin, Giuseppe Giovanni Nardone, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|March 25, 2014
Quantitative assessment of nanoparticle surface hydrophobicity and its influence on pulmonary biocompatibilityMarie-Christine Jones, Stuart A Jones, Yanira Riffo-Vasquez, et al.
Genes|February 25, 2023
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of <i>CSNK2B</i>-Associated DisordersMariateresa Di Stazio, Caterina Zanus, Flavio Faletra, et al.
Pageof 9