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Items: 7

1.

The Effect of Single Mismatches on Primer Extension.

Rejali NA, Moric E, Wittwer CT.

Clin Chem. 2018 May;64(5):801-809. doi: 10.1373/clinchem.2017.282285. Epub 2018 Feb 14.

2.

The implications of genetic mutations in the sodium channel gene (SCN5A).

Moric E, Herbert E, Trusz-Gluza M, Filipecki A, Mazurek U, Wilczok T.

Europace. 2003 Oct;5(4):325-34. Review.

PMID:
14753626
3.

Anti-inflammatory and antiproliferative actions of PPAR-gamma agonists on T lymphocytes derived from MS patients.

Schmidt S, Moric E, Schmidt M, Sastre M, Feinstein DL, Heneka MT.

J Leukoc Biol. 2004 Mar;75(3):478-85. Epub 2003 Dec 4.

PMID:
14657213
4.

Three novel mutations in exon 21 encoding beta-cardiac myosin heavy chain.

Moric E, Mazurek U, Połońska J, Domal-Kwiatkowska D, Smolik S, Kozakiewicz K, Tendera M, Wilczok T.

J Appl Genet. 2003;44(1):103-9.

PMID:
12590187
5.

KCNQ1 gene mutations and the respective genotype-phenotype correlations in the long QT syndrome.

Herbert E, Trusz-Gluza M, Moric E, Smiłowska-Dzielicka E, Mazurek U, Wilczok T.

Med Sci Monit. 2002 Oct;8(10):RA240-8. Review.

PMID:
12388934
6.

The KVLQT1 gene is not a common target for mutations in patients with various heart pathologies.

Moric E, Herbert E, Mazurek U, Samelska J, Cholewa K, Trusz-Gluza M, Wilczok T.

J Appl Genet. 2002;43(2):245-54.

PMID:
12080180
7.

[Genetic changes and clinical management in familial hypertrophic cardiomyopathy].

Domal-Kwiatkowska D, Smolik S, Mazurek U, Moric E, Polońska J, Nowalany-Kozielska E, Glanowska G, Wodniecki J, Szarek J, Wilczewski P, Kozakiewicz K, Tendera M, Wilczok T.

Wiad Lek. 2000;53(1-2):4-21. Review. Polish.

PMID:
10806915

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