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Aminoglycoside-driven biosynthesis of selenium-deficient Selenoprotein P.
Sci Rep. 2017 Jun 29;7(1):4391. doi: 10.1038/s41598-017-04586-9.
Sci Rep. 2017.
PMID: 28663583
Free PMC article.
Gene-specific regulation of hepatic selenoprotein expression by interleukin-6.
Martitz J, Becker NP, Renko K, Stoedter M, Hybsier S, Schomburg L.
Martitz J, et al.
Metallomics. 2015 Nov;7(11):1515-21. doi: 10.1039/c5mt00211g. Epub 2015 Sep 23.
Metallomics. 2015.
PMID: 26399395
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Hypoxia reduces and redirects selenoprotein biosynthesis.
Becker NP, Martitz J, Renko K, Stoedter M, Hybsier S, Cramer T, Schomburg L.
Becker NP, et al. Among authors: martitz j.
Metallomics. 2014 May;6(5):1079-86. doi: 10.1039/c4mt00004h.
Metallomics. 2014.
PMID: 24700164
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Factors impacting the aminoglycoside-induced UGA stop codon readthrough in selenoprotein translation.
Martitz J, Hofmann PJ, Johannes J, Köhrle J, Schomburg L, Renko K.
Martitz J, et al.
J Trace Elem Med Biol. 2016 Sep;37:104-110. doi: 10.1016/j.jtemb.2016.04.010. Epub 2016 Apr 26.
J Trace Elem Med Biol. 2016.
PMID: 27157664
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Selenium status in neonates with connatal infection.
Wiehe L, Cremer M, Wisniewska M, Becker NP, Rijntjes E, Martitz J, Hybsier S, Renko K, Bührer C, Schomburg L.
Wiehe L, et al. Among authors: martitz j.
Br J Nutr. 2016 Aug;116(3):504-13. doi: 10.1017/S0007114516002208. Epub 2016 Jun 8.
Br J Nutr. 2016.
PMID: 27267586
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Strong induction of iodothyronine deiodinases by chemotherapeutic selenocompounds.
Stoedter M, Renko K, Ibáñez E, Plano D, Becker NP, Martitz J, Palop JA, Calvo A, Sanmartín C, Schomburg L.
Stoedter M, et al. Among authors: martitz j.
Metallomics. 2015 Feb;7(2):347-54. doi: 10.1039/c4mt00273c.
Metallomics. 2015.
PMID: 25579002
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Copper to Zinc Ratio as Disease Biomarker in Neonates with Early-Onset Congenital Infections.
Wisniewska M, Cremer M, Wiehe L, Becker NP, Rijntjes E, Martitz J, Renko K, Bührer C, Schomburg L.
Wisniewska M, et al. Among authors: martitz j.
Nutrients. 2017 Mar 30;9(4):343. doi: 10.3390/nu9040343.
Nutrients. 2017.
PMID: 28358335
Free PMC article.
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Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.
Arndt AK, Schafer S, Drenckhahn JD, Sabeh MK, Plovie ER, Caliebe A, Klopocki E, Musso G, Werdich AA, Kalwa H, Heinig M, Padera RF, Wassilew K, Bluhm J, Harnack C, Martitz J, Barton PJ, Greutmann M, Berger F, Hubner N, Siebert R, Kramer HH, Cook SA, MacRae CA, Klaassen S.
Arndt AK, et al. Among authors: martitz j.
Am J Hum Genet. 2013 Jul 11;93(1):67-77. doi: 10.1016/j.ajhg.2013.05.015. Epub 2013 Jun 13.
Am J Hum Genet. 2013.
PMID: 23768516
Free PMC article.
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