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T J Corydon

Explore the profile of T J Corydon including associated specialties, affiliations and a list of published articles. Areas
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Articles 26
Citations 588
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Recent Articles
1.
Fernandez-Guerra P, Lund M, Corydon T, Cornelius N, Gregersen N, Palmfeldt J, et al.
JIMD Rep . 2015 Sep; 27:17-26. PMID: 26404456
Cellular phenotyping of human dermal fibroblasts (HDFs) from patients with inherited diseases provides invaluable information for diagnosis, disease aetiology, prognosis and assessing of treatment options. Here we present a cell...
2.
Magnoni R, Palmfeldt J, Hansen J, Christensen J, Corydon T, Bross P
Free Radic Res . 2013 Oct; 48(2):168-79. PMID: 24151936
Even though the deleterious effects of increased reactive oxygen species (ROS) levels have been implicated in a variety of neurodegenerative disorders, the triggering events that lead to the increased ROS...
3.
Lancaster C, Bruun G, Peer C, Mikkelsen T, Corydon T, Gibson A, et al.
Clin Pharmacol Ther . 2012 Sep; 92(5):642-50. PMID: 22990751
Previous studies have demonstrated that the pharmacokinetic profile of erythromycin, a probe for CYP3A4 activity, is affected by inhibitors or inducers of hepatic solute carriers. We hypothesized that these interactions...
4.
Christensen J, Kvistgaard H, Knudsen J, Shaikh G, Tolmie J, Cooke S, et al.
Clin Genet . 2011 Dec; 83(1):44-52. PMID: 22168581
Familial neurohypophyseal diabetes insipidus (FNDI) typically presents with age-dependent penetrance and autosomal dominant inheritance caused by missense variations in one allele of the AVP gene encoding the arginine vasopressin (AVP)...
5.
Schmidt S, Corydon T, Pedersen C, Bross P, Gregersen N
Mol Genet Metab . 2010 Apr; 100(2):155-62. PMID: 20371198
Short-chain acyl-CoA dehydrogenase deficiency (SCADD) is a rare inherited disorder of the mitochondrial beta-oxidation of fatty acids. Patients with SCADD present mainly with symptoms of neuromuscular character. In order to...
6.
Hansen J, Corydon T, Palmfeldt J, Durr A, Fontaine B, Nielsen M, et al.
Neuroscience . 2008 Apr; 153(2):474-82. PMID: 18378094
The mitochondrial chaperonin heat shock protein 60 (Hsp60) assists the folding of a subset of proteins localized in mitochondria and is an essential component of the mitochondrial protein quality control...
7.
Severinsen J, Bjarkam C, Kiaer-Larsen S, Olsen I, Nielsen M, Blechingberg J, et al.
Mol Psychiatry . 2006 Aug; 11(12):1126-38. PMID: 16924267
Linkage studies suggest that chromosome 22q12-13 may contain one or more shared susceptibility genes for schizophrenia (SZ) and bipolar affective disorder (BPD). In a Faeroese sample, we previously reported association...
8.
Kragh P, Du Y, Corydon T, Purup S, Bolund L, Vajta G
Theriogenology . 2005 Jun; 64(7):1536-45. PMID: 15935461
The purpose of our work was to establish an efficient protocol for activation of porcine cytoplast-fibroblast constructs produced by the handmade cloning technique. Firstly, we investigated a combined electrical and...
9.
Kragh P, Vajta G, Corydon T, Purup S, Bolund L, Callesen H
Reprod Fertil Dev . 2004 Aug; 16(3):315-8. PMID: 15304204
Recently, a zona-free technique for bovine somatic cell nuclear transfer (NT) with no requirement for micromanipulation (i.e. hand-made cloning (HMC)) has been described. The present study demonstrates the application of...
10.
Holst H, Dagnaes-Hansen F, Corydon T, Andreasen P, Jorgensen M, Kolvraa S, et al.
Eur J Hum Genet . 2002 Jan; 9(11):815-22. PMID: 11781697
The function of a series of LDL receptor GFP fusion proteins with different, flexible, unstructured spacer regions was analysed. An optimised version of the fusion protein was used to analyse...