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Evon Debose-Scarlett

Showing results (1-10 of 11) with videos related to

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Journal of Clinical Medicine|July 12, 2025
The Role of Somatic Mutation in Hereditary Hemorrhagic Telangiectasia PathogenesisEvon DeBose-Scarlett, Douglas A Marchuk
Seminars in Perinatology|July 16, 2021
Human milk microbes: Strategies to improve delivery to the infantEvon DeBose-Scarlett, Marion M Bendixen, Graciela L Lorca, et al.
Molecules (Basel, Switzerland)|December 11, 2020
Metabolomic Profile of Personalized Donor Human MilkMonica F Torrez Lamberti, Evon DeBose-Scarlett, Timothy Garret, et al.
Journal of Medical Genetics|February 12, 2025
Arteriovenous malformation from a patient with JP-HHT harbours two second-hit somatic DNA alterations in <i>SMAD4</i>Evon DeBose-Scarlett, Andrew K Ressler, Cassi Friday, et al.
Biorxiv : the Preprint Server for Biology|August 6, 2025
Multi-region spatial transcriptomics reveals region specific differences in response to amyloid beta (Aβ) plaque induced changes in Alzheimer's Disease (AD)Odmaa Bayaraa, Michael Aksu, Evon DeBose-Scarlett, et al.
Human Genomics|November 29, 2025
Multi-region spatial transcriptomics reveals region specific differences in response to amyloid beta (Aβ) plaque induced changes in Alzheimer's disease (AD)Odmaa Bayaraa, Michael Aksu, Evon DeBose-Scarlett, et al.
JACC. Case Reports|January 21, 2026
Somatic PIK3CA Activating Mutation in a Plexiform Lesion of a Patient With HHT and PAHKatharina Schimmel, Tucker Hallmark, Evon DeBose-Scarlett, et al.
Frontiers in Nutrition|November 1, 2021
<i>Lactobacillus johnsonii</i> N6.2 and Blueberry Phytophenols Affect Lipidome and Gut Microbiota Composition of Rats Under High-Fat DietLeandro Dias Teixeira, Monica F Torrez Lamberti, Evon DeBose-Scarlett, et al.
Human Genomics|December 10, 2025
Recurrent somatic copy number alterations in resected cerebral cavernous malformationsAndrew K Ressler, Evon Debose-Scarlett, Amanda Fuenzalida, et al.
American Journal of Human Genetics|September 19, 2024
Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesisEvon DeBose-Scarlett, Andrew K Ressler, Carol J Gallione, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Journal of Clinical Medicine|July 12, 2025
The Role of Somatic Mutation in Hereditary Hemorrhagic Telangiectasia PathogenesisEvon DeBose-Scarlett, Douglas A Marchuk
Seminars in Perinatology|July 16, 2021
Human milk microbes: Strategies to improve delivery to the infantEvon DeBose-Scarlett, Marion M Bendixen, Graciela L Lorca, et al.
Molecules (Basel, Switzerland)|December 11, 2020
Metabolomic Profile of Personalized Donor Human MilkMonica F Torrez Lamberti, Evon DeBose-Scarlett, Timothy Garret, et al.
Journal of Medical Genetics|February 12, 2025
Arteriovenous malformation from a patient with JP-HHT harbours two second-hit somatic DNA alterations in <i>SMAD4</i>Evon DeBose-Scarlett, Andrew K Ressler, Cassi Friday, et al.
Biorxiv : the Preprint Server for Biology|August 6, 2025
Multi-region spatial transcriptomics reveals region specific differences in response to amyloid beta (Aβ) plaque induced changes in Alzheimer's Disease (AD)Odmaa Bayaraa, Michael Aksu, Evon DeBose-Scarlett, et al.
Human Genomics|November 29, 2025
Multi-region spatial transcriptomics reveals region specific differences in response to amyloid beta (Aβ) plaque induced changes in Alzheimer's disease (AD)Odmaa Bayaraa, Michael Aksu, Evon DeBose-Scarlett, et al.
JACC. Case Reports|January 21, 2026
Somatic PIK3CA Activating Mutation in a Plexiform Lesion of a Patient With HHT and PAHKatharina Schimmel, Tucker Hallmark, Evon DeBose-Scarlett, et al.
Frontiers in Nutrition|November 1, 2021
<i>Lactobacillus johnsonii</i> N6.2 and Blueberry Phytophenols Affect Lipidome and Gut Microbiota Composition of Rats Under High-Fat DietLeandro Dias Teixeira, Monica F Torrez Lamberti, Evon DeBose-Scarlett, et al.
Human Genomics|December 10, 2025
Recurrent somatic copy number alterations in resected cerebral cavernous malformationsAndrew K Ressler, Evon Debose-Scarlett, Amanda Fuenzalida, et al.
American Journal of Human Genetics|September 19, 2024
Somatic mutations in arteriovenous malformations in hereditary hemorrhagic telangiectasia support a bi-allelic two-hit mutation mechanism of pathogenesisEvon DeBose-Scarlett, Andrew K Ressler, Carol J Gallione, et al.
Pageof 2