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Plos Genetics
|
December 13, 2024
Integrin adhesome axis inhibits the RPM-1 ubiquitin ligase signaling hub to regulate growth cone and axon development
Jonathan Amezquita, Muriel Desbois, Karla J Opperman, et al.
Biorxiv : the Preprint Server for Biology
|
November 28, 2023
Axon development is regulated at genetic and proteomic interfaces between the integrin adhesome and the RPM-1 ubiquitin ligase signaling hub
Jonathan Amezquita, Muriel Desbois, Karla J Opperman, et al.
Cell Reports
|
April 27, 2017
The HECT Family Ubiquitin Ligase EEL-1 Regulates Neuronal Function and Development
Karla J Opperman, Ben Mulcahy, Andrew C Giles, et al.
Biorxiv : the Preprint Server for Biology
|
August 6, 2025
UBR-1 enzyme network regulates glutamate homeostasis to affect organismal behavior and developmental viability
Joseph S Pak, Seamus Morrone, Karla J Opperman, et al.
Elife
|
February 26, 2020
An alternatively spliced, non-signaling insulin receptor modulates insulin sensitivity via insulin peptide sequestration in <i>C. elegans</i>
Bryan A Martinez, Pedro Reis Rodrigues, Ricardo M Nuñez Medina, et al.
Cell Reports
|
February 3, 2021
Gαo is a major determinant of cAMP signaling in the pathophysiology of movement disorders
Brian S Muntean, Ikuo Masuho, Maria Dao, et al.
Science (New York, N.Y.)
|
August 17, 2019
Genetic behavioral screen identifies an orphan anti-opioid system
Dandan Wang, Hannah M Stoveken, Stefano Zucca, et al.
Current Biology : CB
|
May 8, 2025
Biased regulation of protein synthesis and hypoxic death by a conditional raptor mutation
Chun-Ling Sun, Cong Xu, Omar Itani, et al.
American Journal of Medical Genetics. Part A
|
April 14, 2026
35 Individuals With HUWE1-Related Neurodevelopmental Disorder and Suggested Clinical Evaluations
Mindy H Li, Deziree L Coleman, Kelsey Hogan, et al.
Brain : a Journal of Neurology
|
October 6, 2022
Loss-of-function variants in MYCBP2 cause neurobehavioural phenotypes and corpus callosum defects
Lama AlAbdi, Muriel Desbois, Domniţa-Valeria Rusnac, et al.
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of 5
Search research articles
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Showing results (41-50 of 50) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 50 results.
Plos Genetics
|
December 13, 2024
Integrin adhesome axis inhibits the RPM-1 ubiquitin ligase signaling hub to regulate growth cone and axon development
Jonathan Amezquita, Muriel Desbois, Karla J Opperman, et al.
Biorxiv : the Preprint Server for Biology
|
November 28, 2023
Axon development is regulated at genetic and proteomic interfaces between the integrin adhesome and the RPM-1 ubiquitin ligase signaling hub
Jonathan Amezquita, Muriel Desbois, Karla J Opperman, et al.
Cell Reports
|
April 27, 2017
The HECT Family Ubiquitin Ligase EEL-1 Regulates Neuronal Function and Development
Karla J Opperman, Ben Mulcahy, Andrew C Giles, et al.
Biorxiv : the Preprint Server for Biology
|
August 6, 2025
UBR-1 enzyme network regulates glutamate homeostasis to affect organismal behavior and developmental viability
Joseph S Pak, Seamus Morrone, Karla J Opperman, et al.
Elife
|
February 26, 2020
An alternatively spliced, non-signaling insulin receptor modulates insulin sensitivity via insulin peptide sequestration in <i>C. elegans</i>
Bryan A Martinez, Pedro Reis Rodrigues, Ricardo M Nuñez Medina, et al.
Cell Reports
|
February 3, 2021
Gαo is a major determinant of cAMP signaling in the pathophysiology of movement disorders
Brian S Muntean, Ikuo Masuho, Maria Dao, et al.
Science (New York, N.Y.)
|
August 17, 2019
Genetic behavioral screen identifies an orphan anti-opioid system
Dandan Wang, Hannah M Stoveken, Stefano Zucca, et al.
Current Biology : CB
|
May 8, 2025
Biased regulation of protein synthesis and hypoxic death by a conditional raptor mutation
Chun-Ling Sun, Cong Xu, Omar Itani, et al.
American Journal of Medical Genetics. Part A
|
April 14, 2026
35 Individuals With HUWE1-Related Neurodevelopmental Disorder and Suggested Clinical Evaluations
Mindy H Li, Deziree L Coleman, Kelsey Hogan, et al.
Brain : a Journal of Neurology
|
October 6, 2022
Loss-of-function variants in MYCBP2 cause neurobehavioural phenotypes and corpus callosum defects
Lama AlAbdi, Muriel Desbois, Domniţa-Valeria Rusnac, et al.
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of 5