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Meg Potter

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Articles 8
Citations 58
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Recent Articles
1.
Thillainadesan S, Lambert A, Cooke K, Stockli J, Yau B, Masson S, et al.
Int J Obes (Lond) . 2024 Jul; 48(8):1170-1179. PMID: 38961153
Background: Weight loss can improve the metabolic complications of obesity. However, it is unclear whether insulin resistance persists despite weight loss and whether any protective benefits are preserved following weight...
2.
Diaz-Vegas A, Cooke K, Cutler H, Yau B, Masson S, Harney D, et al.
Mol Metab . 2024 Jul; 86:101983. PMID: 38960128
Objective: To determine the role of miPEP in insulin resistance. Methods: To experimentally test this observation, we generated adipocyte-specific miPEP knockout mice to interrogate its role in the aetiology of...
3.
van Gerwen J, Masson S, Cutler H, Vegas A, Potter M, Stockli J, et al.
Elife . 2024 Feb; 12. PMID: 38329473
Metabolic disease is caused by a combination of genetic and environmental factors, yet few studies have examined how these factors influence signal transduction, a key mediator of metabolism. Using mass...
4.
Cutler H, Madsen S, Masson S, Cooke K, Potter M, Burchfield J, et al.
Diabetes . 2023 Sep; 73(3):359-373. PMID: 37699358
Article Highlights:
5.
Masson S, Madsen S, Cooke K, Potter M, Vegas A, Carroll L, et al.
Elife . 2023 Jul; 12. PMID: 37494090
Systems genetics has begun to tackle the complexity of insulin resistance by capitalising on computational advances to study high-diversity populations. 'Diversity Outbred in Australia (DOz)' is a population of genetically...
6.
Diaz-Vegas A, Norris D, Jall-Rogg S, Cooke K, Conway O, Shun-Shion A, et al.
Life Sci Alliance . 2022 Oct; 6(1). PMID: 36283703
Insulin-induced GLUT4 translocation to the plasma membrane in muscle and adipocytes is crucial for whole-body glucose homeostasis. Currently, GLUT4 trafficking assays rely on overexpression of tagged GLUT4. Here we describe...
7.
Zheng Y, Ding L, Meng X, Potter M, Kearney A, Zhang J, et al.
Proc Natl Acad Sci U S A . 2022 May; 119(19):e2119990119. PMID: 35522713
Over the years it has been established that SIN1, a key component of mTORC2, could interact with Ras family small GTPases through its Ras-binding domain (RBD). The physical association of...
8.
Nelson M, Madsen S, Cooke K, Fritzen A, Thorius I, Masson S, et al.
Cell Metab . 2022 Jan; 34(2):227-239.e6. PMID: 35021042
Skeletal muscle and adipose tissue insulin resistance are major drivers of metabolic disease. To uncover pathways involved in insulin resistance, specifically in these tissues, we leveraged the metabolic diversity of...