Julia Weder
Overview
Explore the profile of Julia Weder including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
38
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0
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Recent Articles
1.
Lawong R, May F, Etang E, Vorrat P, George J, Weder J, et al.
Membranes (Basel)
. 2023 May;
13(5).
PMID: 37233590
The epithelial sodium channel (ENaC) is a key regulator of sodium homeostasis that contributes to blood pressure control. ENaC open probability is adjusted by extracellular sodium ions, a mechanism referred...
2.
Fan L, Kishore A, Jansen-Olliges L, Wang D, Stahl F, Psathaki O, et al.
ACS Omega
. 2022 Aug;
7(33):28932-28945.
PMID: 36033668
While many proteins are known clients of heat shock protein 90 (Hsp90), it is unclear whether the transcription factor, thyroid hormone receptor beta (TRb), interacts with Hsp90 to control hormonal...
3.
Fan L, Warnecke A, Weder J, Preller M, Zeilinger C
Int J Mol Sci
. 2022 Jul;
23(13).
PMID: 35806154
Microarray-based experiments revealed that thyroid hormone triiodothyronine (T3) enhanced the binding of Cy5-labeled ATP on heat shock protein 90 (Hsp90). By molecular docking experiments with T3 on Hsp90, we identified...
4.
Osmanovic A, Widjaja M, Forster A, Weder J, Wattjes M, Lange I, et al.
J Neurol
. 2020 May;
267(9):2732-2743.
PMID: 32447552
Amyotrophic lateral sclerosis (ALS) and hereditary spastic paraplegia (HSP) are motor neuron diseases sharing clinical, pathological, and genetic similarities. While biallelic SPG7 mutations are known to cause recessively inherited HSP,...
5.
In vivo efficacy of mutant IDH1 inhibitor HMS-101 and structural resolution of distinct binding site
Chaturvedi A, Goparaju R, Gupta C, Weder J, Klunemann T, Araujo Cruz M, et al.
Leukemia
. 2019 Oct;
34(2):416-426.
PMID: 31586149
Mutations in isocitrate dehydrogenase 1 (IDH1) are found in 6% of AML patients. Mutant IDH produces R-2-hydroxyglutarate (R-2HG), which induces histone- and DNA-hypermethylation through the inhibition of epigenetic regulators, thus...
6.
Beyer U, Brand F, Martens H, Weder J, Christians A, Elyan N, et al.
Acta Neuropathol
. 2017 Oct;
134(6):905-922.
PMID: 29030706
In search of novel germline alterations predisposing to tumors, in particular to gliomas, we studied a family with two brothers affected by anaplastic gliomas, and their father and paternal great-uncle...