Muckenthaler MU - Search Results

1

[Hereditary hyperferritinemia cataract syndrome--the first family in Germany].

Millonig G, Holzer MP, Tolle G, Auffarth GU, Muckenthaler MU, Seitz HK, Mueller S. Millonig G, et al. Among authors: muckenthaler mu. Z Gastroenterol. 2009 Dec;47(12):1211. doi: 10.1055/s-0028-1109523. Z Gastroenterol. 2009. PMID: 19994473 German.

2

Hyperferritinaemia-cataract syndrome: worldwide mutations and phenotype of an increasingly diagnosed genetic disorder.

Millonig G, Muckenthaler MU, Mueller S. Millonig G, et al. Among authors: muckenthaler mu. Hum Genomics. 2010 Apr;4(4):250-62. doi: 10.1186/1479-7364-4-4-250. Hum Genomics. 2010. PMID: 20511138 Free PMC article. Review.

3

Sustained submicromolar H2O2 levels induce hepcidin via signal transducer and activator of transcription 3 (STAT3).

Millonig G, Ganzleben I, Peccerella T, Casanovas G, Brodziak-Jarosz L, Breitkopf-Heinlein K, Dick TP, Seitz HK, Muckenthaler MU, Mueller S. Millonig G, et al. Among authors: muckenthaler mu. J Biol Chem. 2012 Oct 26;287(44):37472-82. doi: 10.1074/jbc.M112.358911. Epub 2012 Aug 29. J Biol Chem. 2012. PMID: 22932892 Free PMC article.

4

Novel mutations in the ferritin-L iron-responsive element that only mildly impair IRP binding cause hereditary hyperferritinaemia cataract syndrome.

Luscieti S, Tolle G, Aranda J, Campos CB, Risse F, Morán É, Muckenthaler MU, Sánchez M. Luscieti S, et al. Among authors: muckenthaler mu. Orphanet J Rare Dis. 2013 Feb 19;8:30. doi: 10.1186/1750-1172-8-30. Orphanet J Rare Dis. 2013. PMID: 23421845 Free PMC article.

5

Activating NOTCH1 mutations predict favorable early treatment response and long-term outcome in childhood precursor T-cell lymphoblastic leukemia.

Breit S, Stanulla M, Flohr T, Schrappe M, Ludwig WD, Tolle G, Happich M, Muckenthaler MU, Kulozik AE. Breit S, et al. Among authors: muckenthaler mu. Blood. 2006 Aug 15;108(4):1151-7. doi: 10.1182/blood-2005-12-4956. Epub 2006 Apr 13. Blood. 2006. PMID: 16614245 Free article. Clinical Trial.

6

The favorable effect of activating NOTCH1 receptor mutations on long-term outcome in T-ALL patients treated on the ALL-BFM 2000 protocol can be separated from FBXW7 loss of function.

Kox C, Zimmermann M, Stanulla M, Leible S, Schrappe M, Ludwig WD, Koehler R, Tolle G, Bandapalli OR, Breit S, Muckenthaler MU, Kulozik AE. Kox C, et al. Among authors: muckenthaler mu. Leukemia. 2010 Dec;24(12):2005-13. doi: 10.1038/leu.2010.203. Epub 2010 Oct 14. Leukemia. 2010. PMID: 20944675 Free PMC article.

7

Aqueous humor ferritin in hereditary hyperferritinemia cataract syndrome.

Lenzhofer M, Schroedl F, Trost A, Kaser-Eichberger A, Wiedemann H, Strohmaier C, Hohensinn M, Strasser M, Muckenthaler MU, Grabner G, Aigner E, Reitsamer HA. Lenzhofer M, et al. Among authors: muckenthaler mu. Optom Vis Sci. 2015 Apr;92(4 Suppl 1):S40-7. doi: 10.1097/OPX.0000000000000544. Optom Vis Sci. 2015. PMID: 25756341

8

Iron regulatory protein-1 and -2: transcriptome-wide definition of binding mRNAs and shaping of the cellular proteome by iron regulatory proteins.

Sanchez M, Galy B, Schwanhaeusser B, Blake J, Bähr-Ivacevic T, Benes V, Selbach M, Muckenthaler MU, Hentze MW. Sanchez M, et al. Among authors: muckenthaler mu. Blood. 2011 Nov 24;118(22):e168-79. doi: 10.1182/blood-2011-04-343541. Epub 2011 Sep 22. Blood. 2011. PMID: 21940823 Free article.

9

Iron-regulatory proteins limit hypoxia-inducible factor-2alpha expression in iron deficiency.

Sanchez M, Galy B, Muckenthaler MU, Hentze MW. Sanchez M, et al. Among authors: muckenthaler mu. Nat Struct Mol Biol. 2007 May;14(5):420-6. doi: 10.1038/nsmb1222. Epub 2007 Apr 8. Nat Struct Mol Biol. 2007. PMID: 17417656

10

Altered body iron distribution and microcytosis in mice deficient in iron regulatory protein 2 (IRP2).

Galy B, Ferring D, Minana B, Bell O, Janser HG, Muckenthaler M, Schümann K, Hentze MW. Galy B, et al. Blood. 2005 Oct 1;106(7):2580-9. doi: 10.1182/blood-2005-04-1365. Epub 2005 Jun 14. Blood. 2005. PMID: 15956281 Free article.

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