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Items: 9

1.

Iron Metabolism, Hepcidin, and Mortality (the Ludwigshafen Risk and Cardiovascular Health Study).

Grammer TB, Scharnagl H, Dressel A, Kleber ME, Silbernagel G, Pilz S, Tomaschitz A, Koenig W, Mueller-Myhsok B, März W, Strnad P.

Clin Chem. 2019 Jul;65(7):849-861. doi: 10.1373/clinchem.2018.297242. Epub 2019 Mar 27.

PMID:
30917972
2.

From Epigenetic Associations to Biological and Psychosocial Explanations in Mental Health.

Renzi C, Provencal N, Bassil KC, Evers K, Kihlbom U, Radford EJ, Koupil I, Mueller-Myhsok B, Hansson MG, Rutten BPF.

Prog Mol Biol Transl Sci. 2018;158:299-323. doi: 10.1016/bs.pmbts.2018.04.011. Epub 2018 Jun 8. Review.

PMID:
30072059
3.

MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene.

Nischwitz S, Wolf C, Andlauer TF, Czamara D, Zettl UK, Rieckmann P, Buck D, Ising M, Bettecken T, Mueller-Myhsok B, Weber F.

J Neuroimmunol. 2015 Feb 15;279:46-9. doi: 10.1016/j.jneuroim.2015.01.008. Epub 2015 Jan 23.

PMID:
25670000
4.

The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders.

Thoeringer CK, Ripke S, Unschuld PG, Lucae S, Ising M, Bettecken T, Uhr M, Keck ME, Mueller-Myhsok B, Holsboer F, Binder EB, Erhardt A.

J Neural Transm (Vienna). 2009 Jun;116(6):649-57. doi: 10.1007/s00702-008-0075-y. Epub 2008 Jul 8.

5.

Association of a Met88Val diazepam binding inhibitor (DBI) gene polymorphism and anxiety disorders with panic attacks.

Thoeringer CK, Binder EB, Salyakina D, Erhardt A, Ising M, Unschuld PG, Kern N, Lucae S, Brueckl TM, Mueller MB, Fuchs B, Puetz B, Lieb R, Uhr M, Holsboer F, Mueller-Myhsok B, Keck ME.

J Psychiatr Res. 2007 Oct;41(7):579-84. Epub 2006 Aug 14.

PMID:
16904689
6.

The variant Arg110Gln of human IL-13 is associated with an immunologically hyper-reactive form of onchocerciasis (sowda).

Hoerauf A, Kruse S, Brattig NW, Heinzmann A, Mueller-Myhsok B, Deichmann KA.

Microbes Infect. 2002 Jan;4(1):37-42.

PMID:
11825773
7.

Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2).

Kress W, Mueller-Myhsok B, Ricker K, Schneider C, Koch MC, Toyka KV, Mueller CR, Grimm T.

Neuromuscul Disord. 2000 Oct;10(7):478-80.

PMID:
10996776
8.

Linkage of proximal myotonic myopathy to chromosome 3q.

Ricker K, Grimm T, Koch MC, Schneider C, Kress W, Reimers CD, Schulte-Mattler W, Mueller-Myhsok B, Toyka KV, Mueller CR.

Neurology. 1999 Jan 1;52(1):170-1.

PMID:
9921867
9.

A xanthomatosis-susceptibility gene may exist in a Syrian family with familial hypercholesterolemia.

Vergopoulos A, Bajari T, Jouma M, Knoblauch H, Aydin A, Bähring S, Mueller-Myhsok B, Dresel A, Joubran R, Luft FC, Schuster H.

Eur J Hum Genet. 1997 Sep-Oct;5(5):315-23.

PMID:
9412789

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