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1-3 of 3
Keywords: Modifier
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Journal Articles
In collection:
Rare Disease Translational Research
Journal:
Disease Models & Mechanisms
Dis Model Mech (2021) 14 (4): dmm048231.
Published: 26 April 2021
... a genetic modifier screen to provide insight into the mechanisms contributing to Gould syndrome pathogenesis and identified a single locus [modifier of Gould syndrome 1 ( MoGS1 )] on Chromosome 1 that suppressed ASD. A separate screen showed that the same locus ameliorated myopathy. Interestingly, MoGS1 had...
Includes: Supplementary data
Journal Articles
In collection:
Zebrafish as a Disease Model
Journal:
Disease Models & Mechanisms
Dis Model Mech (2018) 11 (10): dmm035972.
Published: 18 October 2018
... in a CHD patient cohort, indicating that the PBX3 p.A136V variant could be a modifier allele for CHDs. Pbx genes encode three-amino-acid loop extension (TALE)-class homeodomain-containing DNA-binding proteins with diverse roles in development and disease, and are required for heart development in mouse...
Journal Articles
Dennis Y. Kim, Joanna Yu, Ryan K. Mui, Rieko Niibori, Hamza Bin Taufique, Rukhsana Aslam, John W. Semple, Sabine P. Cordes
Journal:
Disease Models & Mechanisms
Dis Model Mech (2017) 10 (5): 581–595.
Published: 1 May 2017
... revealed that the C19T Tyro3 mutation is present in a few other mouse strains, and hence is not the causative anx mutation, but rather an anx modifier. Our work shows that Tyro3 has prosurvival roles in the appetite regulatory circuitry and could also provide useful insights towards the development...
Includes: Supplementary data