Møller LB - Search Results

1

Normalization of Fetal Cerebral and Hepatic Iron by Parental Iron Therapy to Pregnant Rats with Systemic Iron Deficiency without Anemia.

Burkhart A, Johnsen KB, Skjørringe T, Nielsen AH, Routhe LJ, Hertz S, Møller LB, Thomsen LL, Moos T. Burkhart A, et al. Among authors: moller lb. Nutrients. 2024 Sep 27;16(19):3264. doi: 10.3390/nu16193264. Nutrients. 2024. PMID: 39408231 Free PMC article.

2

Impairment of interrelated iron- and copper homeostatic mechanisms in brain contributes to the pathogenesis of neurodegenerative disorders.

Skjørringe T, Møller LB, Moos T. Skjørringe T, et al. Among authors: moller lb. Front Pharmacol. 2012 Sep 25;3:169. doi: 10.3389/fphar.2012.00169. eCollection 2012. Front Pharmacol. 2012. PMID: 23055972 Free PMC article.

3

Editorial: The Neurodietetics and Genetics of Copper and Iron.

Moos T, Møller LB. Moos T, et al. Among authors: moller lb. Front Mol Neurosci. 2021 Jul 23;14:722234. doi: 10.3389/fnmol.2021.722234. eCollection 2021. Front Mol Neurosci. 2021. PMID: 34366787 Free PMC article. No abstract available.

4

Splice site mutations in the ATP7A gene.

Skjørringe T, Tümer Z, Møller LB. Skjørringe T, et al. Among authors: moller lb. PLoS One. 2011 Apr 11;6(4):e18599. doi: 10.1371/journal.pone.0018599. PLoS One. 2011. PMID: 21494555 Free PMC article.

5

Exon duplications in the ATP7A gene: frequency and transcriptional behaviour.

Mogensen M, Skjørringe T, Kodama H, Silver K, Horn N, Møller LB. Mogensen M, et al. Among authors: moller lb. Orphanet J Rare Dis. 2011 Nov 10;6:73. doi: 10.1186/1750-1172-6-73. Orphanet J Rare Dis. 2011. PMID: 22074552 Free PMC article.

6

Metal-Dependent Regulation of ATP7A and ATP7B in Fibroblast Cultures.

Lenartowicz M, Moos T, Ogórek M, Jensen TG, Møller LB. Lenartowicz M, et al. Among authors: moller lb. Front Mol Neurosci. 2016 Aug 18;9:68. doi: 10.3389/fnmol.2016.00068. eCollection 2016. Front Mol Neurosci. 2016. PMID: 27587995 Free PMC article.

7

A silent nucleotide substitution in the ATP7A gene in a child with Menkes disease.

Møller LB, Rea G, Yasmeen S, Skjørringe T, Thorborg SS, Morrison PJ, Donnelly DE. Møller LB, et al. Mol Genet Metab. 2013 Dec;110(4):490-2. doi: 10.1016/j.ymgme.2013.09.012. Epub 2013 Sep 24. Mol Genet Metab. 2013. PMID: 24100245

8

Occipital horn syndrome and classical Menkes Syndrome caused by deep intronic mutations, leading to the activation of ATP7A pseudo-exon.

Yasmeen S, Lund K, De Paepe A, De Bie S, Heiberg A, Silva J, Martins M, Skjørringe T, Møller LB. Yasmeen S, et al. Among authors: moller lb. Eur J Hum Genet. 2014 Apr;22(4):517-21. doi: 10.1038/ejhg.2013.191. Epub 2013 Sep 4. Eur J Hum Genet. 2014. PMID: 24002164 Free PMC article.

9

Crystal structure of a copper-transporting PIB-type ATPase.

Gourdon P, Liu XY, Skjørringe T, Morth JP, Møller LB, Pedersen BP, Nissen P. Gourdon P, et al. Among authors: moller lb. Nature. 2011 Jun 29;475(7354):59-64. doi: 10.1038/nature10191. Nature. 2011. PMID: 21716286

10

Missense dopamine transporter mutations associate with adult parkinsonism and ADHD.

Hansen FH, Skjørringe T, Yasmeen S, Arends NV, Sahai MA, Erreger K, Andreassen TF, Holy M, Hamilton PJ, Neergheen V, Karlsborg M, Newman AH, Pope S, Heales SJ, Friberg L, Law I, Pinborg LH, Sitte HH, Loland C, Shi L, Weinstein H, Galli A, Hjermind LE, Møller LB, Gether U. Hansen FH, et al. Among authors: moller lb. J Clin Invest. 2014 Jul;124(7):3107-20. doi: 10.1172/JCI73778. Epub 2014 Jun 9. J Clin Invest. 2014. PMID: 24911152 Free PMC article.

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