Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sivaraj M. Sundaram"'
Autor:
Jiesi Chen, Eva Salveridou, Lutz Liebmann, Sivaraj M. Sundaram, Denica Doycheva, Boyka Markova, Christian A. Hübner, Anita Boelen, W. Edward Visser, Heike Heuer, Steffen Mayerl
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 4, p 3452 (2023)
Patients with inactive thyroid hormone (TH) transporter MCT8 display intellectual disability due to compromised central TH transport and action. As a therapeutic strategy, application of thyromimetic, MCT8-independent compounds Triac (3,5,3′-triiod
Externí odkaz:
https://doaj.org/article/b518b5239fc54f72b48ee7a8ed4a2a0e
Autor:
Mareike Böttcher, Helge Müller-Fielitz, Sivaraj M. Sundaram, Sarah Gallet, Vanessa Neve, Kiseko Shionoya, Adriano Zager, Ning Quan, Xiaoyu Liu, Ruth Schmidt-Ullrich, Ronny Haenold, Jan Wenzel, Anders Blomqvist, David Engblom, Vincent Prevot, Markus Schwaninger
Publikováno v:
Molecular Metabolism, Vol 39, Iss , Pp 101022- (2020)
Objectives: Infections, cancer, and systemic inflammation elicit anorexia. Despite the medical significance of this phenomenon, the question of how peripheral inflammatory mediators affect the central regulation of food intake is incompletely underst
Externí odkaz:
https://doaj.org/article/32bcc6908cdc4903aa299304edf1f1af
Publikováno v:
Mol Cell
The product of hexokinase (HK) enzymes, glucose-6-phosphate, can be metabolized through glycolysis or directed to alternative metabolic routes, such as the pentose phosphate pathway (PPP) to generate anabolic intermediates. HK1 contains an N-terminal
Autor:
Pretty Garg, Fabian Maass, Sivaraj M. Sundaram, Brit Mollenhauer, Sameehan Mahajani, Christoph van Riesen, Sebastian Kügler, Mathias Bähr
Publikováno v:
Molecular and cellular neurosciences. 121
Several studies have investigated if the levels of α-synuclein autoantibodies (α-syn AAb) differ in serum of Parkinson's disease (PD) patients and healthy subjects. Reproducible differences in their levels could serve as a biomarker for PD. The res
Autor:
Sivaraj M Sundaram, Adriana Arrulo Pereira, Helge Müller-Fielitz, Hannes Köpke, Meri De Angelis, Timo D Müller, Heike Heuer, Jakob Körbelin, Markus Krohn, Jens Mittag, Ruben Nogueiras, Vincent Prevot, Markus Schwaninger
Publikováno v:
Brain 145, 4264-4274 (2022)
A genetic deficiency of the solute carrier monocarboxylate transporter 8 (MCT8), termed Allan-Herndon-Dudley syndrome, is an important cause of X-linked intellectual and motor disability. MCT8 transports thyroid hormones across cell membranes. While
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b625c625d11d5d30c7fad13c5f1e896
https://www.ncbi.nlm.nih.gov/pubmed/35929549
https://www.ncbi.nlm.nih.gov/pubmed/35929549