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David B Beck

Showing results (41-50 of 83) with videos related to

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JAMA Dermatology|June 12, 2024
Skin Manifestations of VEXAS Syndrome and Associated GenotypesIsabella J Tan, Marcela A Ferrada, Serene Ahmad, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|September 21, 2025
Clinical Manifestations of VEXAS Syndrome Across a Broad Spectrum of UBA1 Mutation BurdenMeghan Anderson, Defne Ercelen, Ashley Richardson, et al.
Journal of Clinical Medicine|February 27, 2026
PAXIS: A Randomized, Double-Blind, Placebo-Controlled, Dose-Finding Phase 2 Study (Part 1) Followed by an Open-Label Period (Part 2) to Assess the Efficacy and Safety of Pacritinib in Patients with VEXAS SyndromeDavid B Beck, Maël Heiblig, Sinisa Savic, et al.
Rheumatology (Oxford, England)|March 29, 2024
Description of a novel splice site variant in UBA1 gene causing VEXAS syndromeDaniela Ospina Cardona, Ignasi Rodriguez-Pinto, Sonia Iosim, et al.
Frontiers in Neuroscience|November 16, 2020
Human iPSC-Derived Neuronal Cells From <i>CTBP1</i>-Mutated Patients Reveal Altered Expression of Neurodevelopmental Gene NetworksS Vijayalingam, Uthayashanker R Ezekiel, Fenglian Xu, et al.
Blood|March 10, 2021
Novel somatic mutations in UBA1 as a cause of VEXAS syndromeJames A Poulter, Jason C Collins, Catherine Cargo, et al.
Genes & Development|March 8, 2013
The tumor suppressor SirT2 regulates cell cycle progression and genome stability by modulating the mitotic deposition of H4K20 methylationLourdes Serrano, Paloma Martínez-Redondo, Anna Marazuela-Duque, et al.
Annals of Internal Medicine|January 20, 2025
Germline <i>UBA1</i> Variant With Somatic Amplification in a Woman With Inflammatory Diseases and Myelodysplastic SyndromeMaria Creignou, Maria Sirenko, Pedro L Moura, et al.
Neurogenetics|April 21, 2016
A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defectsDavid B Beck, Megan T Cho, Francisca Millan, et al.
European Journal of Haematology|February 15, 2023
VEXAS syndrome: A review of bone marrow aspirate and biopsies reporting myeloid and erythroid precursor vacuolationHannah Cherniawsky, Jordan Friedmann, Hamish Nicolson, et al.
Pageof 9

Showing results (41-50 of 83) with videos related to

Sort By:
Pageof 9
JAMA Dermatology|June 12, 2024
Skin Manifestations of VEXAS Syndrome and Associated GenotypesIsabella J Tan, Marcela A Ferrada, Serene Ahmad, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|September 21, 2025
Clinical Manifestations of VEXAS Syndrome Across a Broad Spectrum of UBA1 Mutation BurdenMeghan Anderson, Defne Ercelen, Ashley Richardson, et al.
Journal of Clinical Medicine|February 27, 2026
PAXIS: A Randomized, Double-Blind, Placebo-Controlled, Dose-Finding Phase 2 Study (Part 1) Followed by an Open-Label Period (Part 2) to Assess the Efficacy and Safety of Pacritinib in Patients with VEXAS SyndromeDavid B Beck, Maël Heiblig, Sinisa Savic, et al.
Rheumatology (Oxford, England)|March 29, 2024
Description of a novel splice site variant in UBA1 gene causing VEXAS syndromeDaniela Ospina Cardona, Ignasi Rodriguez-Pinto, Sonia Iosim, et al.
Frontiers in Neuroscience|November 16, 2020
Human iPSC-Derived Neuronal Cells From <i>CTBP1</i>-Mutated Patients Reveal Altered Expression of Neurodevelopmental Gene NetworksS Vijayalingam, Uthayashanker R Ezekiel, Fenglian Xu, et al.
Blood|March 10, 2021
Novel somatic mutations in UBA1 as a cause of VEXAS syndromeJames A Poulter, Jason C Collins, Catherine Cargo, et al.
Genes & Development|March 8, 2013
The tumor suppressor SirT2 regulates cell cycle progression and genome stability by modulating the mitotic deposition of H4K20 methylationLourdes Serrano, Paloma Martínez-Redondo, Anna Marazuela-Duque, et al.
Annals of Internal Medicine|January 20, 2025
Germline <i>UBA1</i> Variant With Somatic Amplification in a Woman With Inflammatory Diseases and Myelodysplastic SyndromeMaria Creignou, Maria Sirenko, Pedro L Moura, et al.
Neurogenetics|April 21, 2016
A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defectsDavid B Beck, Megan T Cho, Francisca Millan, et al.
European Journal of Haematology|February 15, 2023
VEXAS syndrome: A review of bone marrow aspirate and biopsies reporting myeloid and erythroid precursor vacuolationHannah Cherniawsky, Jordan Friedmann, Hamish Nicolson, et al.
Pageof 9