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Blood
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March 2, 2026
Inflammatory cell death and monocyte dysfunction in VEXAS syndrome
Paul Breillat, Samuel J Magaziner, Stéphane M Camus, et al.
Neurogenetics
|
May 2, 2019
A pathogenic CtBP1 missense mutation causes altered cofactor binding and transcriptional activity
David B Beck, T Subramanian, S Vijayalingam, et al.
Kidney International Reports
|
February 23, 2023
Modeling of <i>ACTN4</i>-Based Podocytopathy Using <i>Drosophila</i> Nephrocytes
Johanna Odenthal, Sebastian Dittrich, Vivian Ludwig, et al.
The Journal of Experimental Medicine
|
February 27, 2025
The common HAQ STING allele prevents clinical penetrance of COPA syndrome
Noa Simchoni, Shogo Koide, Maryel Likhite, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 9, 2012
Federal seafood safety response to the Deepwater Horizon oil spill
Gina M Ylitalo, Margaret M Krahn, Walton W Dickhoff, et al.
European Journal of Human Genetics : EJHG
|
July 12, 2012
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies
Bodo B Beck, Anne Baasner, Anja Buescher, et al.
The EMBO Journal
|
February 15, 2024
Shared and distinct mechanisms of UBA1 inactivation across different diseases
Jason C Collins, Samuel J Magaziner, Maya English, et al.
Biorxiv : the Preprint Server for Biology
|
October 24, 2023
Shared and Distinct Mechanisms of UBA1 Inactivation Across Different Diseases
Jason C Collins, Samuel J Magaziner, Maya English, et al.
BMC Psychology
|
January 10, 2026
Study protocol for a comparative effectiveness randomized controlled trial comparing the emotion awareness and skills enhancement program to the unified protocol in autistic youth and young adults with emotion dysregulation
Carla A Mazefsky, Madison Bradley, Kara Duman, et al.
JAMA
|
January 24, 2023
Estimated Prevalence and Clinical Manifestations of UBA1 Variants Associated With VEXAS Syndrome in a Clinical Population
David B Beck, Dale L Bodian, Vandan Shah, et al.
Page
of 72
Search research articles
Search
Showing results (651-660 of 718) with videos related to
Sort By:
Page
of 72
Blood
|
March 2, 2026
Inflammatory cell death and monocyte dysfunction in VEXAS syndrome
Paul Breillat, Samuel J Magaziner, Stéphane M Camus, et al.
Neurogenetics
|
May 2, 2019
A pathogenic CtBP1 missense mutation causes altered cofactor binding and transcriptional activity
David B Beck, T Subramanian, S Vijayalingam, et al.
Kidney International Reports
|
February 23, 2023
Modeling of <i>ACTN4</i>-Based Podocytopathy Using <i>Drosophila</i> Nephrocytes
Johanna Odenthal, Sebastian Dittrich, Vivian Ludwig, et al.
The Journal of Experimental Medicine
|
February 27, 2025
The common HAQ STING allele prevents clinical penetrance of COPA syndrome
Noa Simchoni, Shogo Koide, Maryel Likhite, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 9, 2012
Federal seafood safety response to the Deepwater Horizon oil spill
Gina M Ylitalo, Margaret M Krahn, Walton W Dickhoff, et al.
European Journal of Human Genetics : EJHG
|
July 12, 2012
Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies
Bodo B Beck, Anne Baasner, Anja Buescher, et al.
The EMBO Journal
|
February 15, 2024
Shared and distinct mechanisms of UBA1 inactivation across different diseases
Jason C Collins, Samuel J Magaziner, Maya English, et al.
Biorxiv : the Preprint Server for Biology
|
October 24, 2023
Shared and Distinct Mechanisms of UBA1 Inactivation Across Different Diseases
Jason C Collins, Samuel J Magaziner, Maya English, et al.
BMC Psychology
|
January 10, 2026
Study protocol for a comparative effectiveness randomized controlled trial comparing the emotion awareness and skills enhancement program to the unified protocol in autistic youth and young adults with emotion dysregulation
Carla A Mazefsky, Madison Bradley, Kara Duman, et al.
JAMA
|
January 24, 2023
Estimated Prevalence and Clinical Manifestations of UBA1 Variants Associated With VEXAS Syndrome in a Clinical Population
David B Beck, Dale L Bodian, Vandan Shah, et al.
Page
of 72