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Jennifer Morrison

Showing results (1-10 of 19) with videos related to

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Australian Family Physician|July 12, 2011
Persistent hoarseness - a case studyJennifer Morrison
Fetal Diagnosis and Therapy|August 13, 2003
Effect of alpha-fetoprotein and derived peptides on insulin- and estrogen-induced fetotoxicityGeorge Butterstein, Jennifer Morrison, G J Mizejewski
Clinical Pediatrics|November 14, 2019
Is There Benefit in Identifying Asthma Triggers During an Exacerbation?Pushpom James, Anna Cornish, Kaylan Brady, et al.
Journal of the American Board of Family Medicine : JABFM|May 13, 2024
The Role of Telehealth in Improving Care Connections and Outcomes for Community Health Center Patients with DiabetesJodi Simon, Alice Eggleston, Dana Bright, et al.
Journal of Nutrition Education and Behavior|April 17, 2026
Attributes of Thriving School Gardens in the USJennifer Morrison Daspin, Mariela Jiménez-Rivero, Bonnie Martin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2021
Missense NAA20 variants impairing the NatB protein N-terminal acetyltransferase cause autosomal recessive developmental delay, intellectual disability, and microcephalyJennifer Morrison, Norah K Altuwaijri, Kirsten Brønstad, et al.
Archives of Virology|September 7, 2023
First detection and complete genome sequence of a new potexvirus naturally infecting Adenium obesumMarie-Emilie A Gauthier, Shamila W Abeynayake, Ruvini V Lelwala, et al.
HGG Advances|April 11, 2026
Heterozygous CECR2 Variants Support a Distinct Neurodevelopmental Syndrome with Features Overlapping Cat Eye SyndromeAnushree Acharya, Irma Järvelä, Andrea Hernandez, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 18, 2006
A polymorphism within a conserved beta(1)-adrenergic receptor motif alters cardiac function and beta-blocker response in human heart failureStephen B Liggett, Jeanne Mialet-Perez, Surai Thaneemit-Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2024
The characterization of new de novo CACNA1G variants affecting the intracellular gate of Cav3.1 channel broadens the spectrum of neurodevelopmental phenotypes in SCA42NDLeila Qebibo, Amaël Davakan, Mathilde Nesson-Dauphin, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Australian Family Physician|July 12, 2011
Persistent hoarseness - a case studyJennifer Morrison
Fetal Diagnosis and Therapy|August 13, 2003
Effect of alpha-fetoprotein and derived peptides on insulin- and estrogen-induced fetotoxicityGeorge Butterstein, Jennifer Morrison, G J Mizejewski
Clinical Pediatrics|November 14, 2019
Is There Benefit in Identifying Asthma Triggers During an Exacerbation?Pushpom James, Anna Cornish, Kaylan Brady, et al.
Journal of the American Board of Family Medicine : JABFM|May 13, 2024
The Role of Telehealth in Improving Care Connections and Outcomes for Community Health Center Patients with DiabetesJodi Simon, Alice Eggleston, Dana Bright, et al.
Journal of Nutrition Education and Behavior|April 17, 2026
Attributes of Thriving School Gardens in the USJennifer Morrison Daspin, Mariela Jiménez-Rivero, Bonnie Martin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2021
Missense NAA20 variants impairing the NatB protein N-terminal acetyltransferase cause autosomal recessive developmental delay, intellectual disability, and microcephalyJennifer Morrison, Norah K Altuwaijri, Kirsten Brønstad, et al.
Archives of Virology|September 7, 2023
First detection and complete genome sequence of a new potexvirus naturally infecting Adenium obesumMarie-Emilie A Gauthier, Shamila W Abeynayake, Ruvini V Lelwala, et al.
HGG Advances|April 11, 2026
Heterozygous CECR2 Variants Support a Distinct Neurodevelopmental Syndrome with Features Overlapping Cat Eye SyndromeAnushree Acharya, Irma Järvelä, Andrea Hernandez, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 18, 2006
A polymorphism within a conserved beta(1)-adrenergic receptor motif alters cardiac function and beta-blocker response in human heart failureStephen B Liggett, Jeanne Mialet-Perez, Surai Thaneemit-Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2024
The characterization of new de novo CACNA1G variants affecting the intracellular gate of Cav3.1 channel broadens the spectrum of neurodevelopmental phenotypes in SCA42NDLeila Qebibo, Amaël Davakan, Mathilde Nesson-Dauphin, et al.
Pageof 2