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Showing results (671-680 of 719) with videos related to

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The Journal of Clinical Investigation|December 9, 2025
Age modifies the association between sex and the plasma inflammatory proteome in treated HIVRebecca A Abelman, Samuel R Schnittman, Natalia Faraj Murad, et al.
Blood Advances|August 24, 2021
Benign and malignant hematologic manifestations in patients with VEXAS syndrome due to somatic mutations in UBA1Ifeyinwa Emmanuela Obiorah, Bhavisha A Patel, Emma M Groarke, et al.
Open Forum Infectious Diseases|July 30, 2024
Opportunistic Infections, Mortality Risk, and Prevention Strategies in Patients With Vacuoles, E1 Enzyme, X-Linked, Autoinflammatory, Somatic (VEXAS) SyndromeMary Czech, Jennifer Cuellar-Rodriguez, Bhavisha A Patel, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|October 27, 2016
FutureTox III: Bridges for TranslationDaland R Juberg, Thomas B Knudsen, Miriam Sander, et al.
Kidney International|October 22, 2015
Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicityDaniela A Braun, Markus Schueler, Jan Halbritter, et al.
Journal of Internal Medicine|November 21, 2025
New cases of δ-aminolevulinic acid dehydratase deficiency: Functional insights into gene variants using an innovative mouse liver modelElena Di Pierro, Isabel Solares, Daniel Jericó, et al.
Human Mutation|December 11, 2019
The recurrent postzygotic pathogenic variant p.Glu47Lys in RHOA causes a novel recognizable neuroectodermal phenotypeGökhan Yigit, Ken Saida, Danielle DeMarzo, et al.
Journal of Clinical Immunology|July 9, 2020
Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual InheritanceOskar Schnappauf, Qing Zhou, Natalia Sampaio Moura, et al.
Kidney International|March 14, 2018
Single-nephron proteomes connect morphology and function in proteinuric kidney diseaseMartin Höhne, Christian K Frese, Florian Grahammer, et al.
Nature Metabolism|July 23, 2020
A molecular mechanism explaining albuminuria in kidney diseaseLinus Butt, David Unnersjö-Jess, Martin Höhne, et al.
Pageof 72

Showing results (671-680 of 719) with videos related to

Sort By:
Pageof 72
The Journal of Clinical Investigation|December 9, 2025
Age modifies the association between sex and the plasma inflammatory proteome in treated HIVRebecca A Abelman, Samuel R Schnittman, Natalia Faraj Murad, et al.
Blood Advances|August 24, 2021
Benign and malignant hematologic manifestations in patients with VEXAS syndrome due to somatic mutations in UBA1Ifeyinwa Emmanuela Obiorah, Bhavisha A Patel, Emma M Groarke, et al.
Open Forum Infectious Diseases|July 30, 2024
Opportunistic Infections, Mortality Risk, and Prevention Strategies in Patients With Vacuoles, E1 Enzyme, X-Linked, Autoinflammatory, Somatic (VEXAS) SyndromeMary Czech, Jennifer Cuellar-Rodriguez, Bhavisha A Patel, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|October 27, 2016
FutureTox III: Bridges for TranslationDaland R Juberg, Thomas B Knudsen, Miriam Sander, et al.
Kidney International|October 22, 2015
Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicityDaniela A Braun, Markus Schueler, Jan Halbritter, et al.
Journal of Internal Medicine|November 21, 2025
New cases of δ-aminolevulinic acid dehydratase deficiency: Functional insights into gene variants using an innovative mouse liver modelElena Di Pierro, Isabel Solares, Daniel Jericó, et al.
Human Mutation|December 11, 2019
The recurrent postzygotic pathogenic variant p.Glu47Lys in RHOA causes a novel recognizable neuroectodermal phenotypeGökhan Yigit, Ken Saida, Danielle DeMarzo, et al.
Journal of Clinical Immunology|July 9, 2020
Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual InheritanceOskar Schnappauf, Qing Zhou, Natalia Sampaio Moura, et al.
Kidney International|March 14, 2018
Single-nephron proteomes connect morphology and function in proteinuric kidney diseaseMartin Höhne, Christian K Frese, Florian Grahammer, et al.
Nature Metabolism|July 23, 2020
A molecular mechanism explaining albuminuria in kidney diseaseLinus Butt, David Unnersjö-Jess, Martin Höhne, et al.
Pageof 72