Antonius Plagge
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Explore the profile of Antonius Plagge including associated specialties, affiliations and a list of published articles.
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Articles
31
Citations
692
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0
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Recent Articles
1.
Aljuraysi S, Platt M, Pulix M, Poptani H, Plagge A
Neurobiol Dis
. 2024 Feb;
192:106431.
PMID: 38331351
Mutations of the human TRAFFICKING PROTEIN PARTICLE COMPLEX SUBUNIT 9 (TRAPPC9) cause a neurodevelopmental disorder characterised by microcephaly and intellectual disability. Trappc9 constitutes a subunit specific to the intracellular membrane-associated...
2.
Rengifo Rojas C, Cercy J, Perillous S, Gonthier-Gueret C, Montibus B, Maupetit-Mehouas S, et al.
HGG Adv
. 2024 Feb;
5(2):100271.
PMID: 38297831
It is only partially understood how constitutive allelic methylation at imprinting control regions (ICRs) interacts with other regulation levels to drive timely parental allele-specific expression along large imprinted domains. The...
3.
Claxton M, Pulix M, Seah M, Bernardo R, Zhou P, Aljuraysi S, et al.
Front Cell Dev Biol
. 2022 Oct;
10:1022422.
PMID: 36313557
Genomic imprinting is an epigenetic process through which genes are expressed in a parent-of-origin specific manner resulting in mono-allelic or strongly biased expression of one allele. For some genes, imprinted...
4.
Amadeo F, Plagge A, Chacko A, Wilm B, Hanson V, Liptrott N, et al.
Eur J Nucl Med Mol Imaging
. 2021 Jul;
49(3):796-808.
PMID: 34313817
Introduction: A novel, red-shifted bioluminescence imaging (BLI) system called AkaBLI has been recently developed for cell tracking in preclinical models and to date, limited data is available on how it...
5.
Cui Q, Aksu C, Ay B, Remillard C, Plagge A, Gardezi M, et al.
Front Genet
. 2021 Jul;
12:680537.
PMID: 34220953
encodes the stimulatory G protein alpha-subunit (Gsα) and its large variant XLαs. Studies have suggested that XLαs is expressed exclusively paternally. Thus, XLαs deficiency is considered to be responsible for...
6.
Matthias J, Cui Q, Shumate L, Plagge A, He Q, Bastepe M
Endocrinology
. 2019 Nov;
161(1).
PMID: 31758181
Fibroblast growth factor-23 (FGF23) is critical for phosphate and vitamin D homeostasis. Cellular and molecular mechanisms underlying FGF23 production remain poorly defined. The extra-large Gα subunit (XLαs) is a variant...
7.
Hughes J, Liu K, Plagge A, Wilson P, Sutherland H, Norman B, et al.
Hum Mol Genet
. 2019 Oct;
28(23):3928-3939.
PMID: 31600782
Alkaptonuria is an inherited disease caused by homogentisate 1,2-dioxygenase (HGD) deficiency. Circulating homogentisic acid (HGA) is elevated and deposits in connective tissues as ochronotic pigment. In this study, we aimed...
8.
He Q, Shumate L, Matthias J, Aydin C, Wein M, Spatz J, et al.
JCI Insight
. 2019 Sep;
4(17).
PMID: 31484825
Dysregulated actions of bone-derived phosphaturic hormone fibroblast growth factor 23 (FGF23) result in several inherited diseases, such as X-linked hypophosphatemia (XLH), and contribute substantially to the mortality in kidney failure....
9.
Taylor A, Sharkey J, Plagge A, Wilm B, Murray P
Contrast Media Mol Imaging
. 2019 Jan;
2018:2514796.
PMID: 30627058
The ability to track the biodistribution and fate of multiple cell populations administered to rodents has the potential to facilitate the understanding of biological processes in a range of fields...
10.
Comenge J, Sharkey J, Fragueiro O, Wilm B, Brust M, Murray P, et al.
Elife
. 2018 Jun;
7.
PMID: 29949503
Understanding the fate of exogenous cells after implantation is important for clinical applications. Preclinical studies allow imaging of cell location and survival. Labelling with nanoparticles enables high sensitivity detection, but...