Rust S - Search Results

1

Genetic variants associated with Lp(a) lipoprotein level and coronary disease.

Clarke R, Peden JF, Hopewell JC, Kyriakou T, Goel A, Heath SC, Parish S, Barlera S, Franzosi MG, Rust S, Bennett D, Silveira A, Malarstig A, Green FR, Lathrop M, Gigante B, Leander K, de Faire U, Seedorf U, Hamsten A, Collins R, Watkins H, Farrall M; PROCARDIS Consortium. Clarke R, et al. Among authors: rust s. N Engl J Med. 2009 Dec 24;361(26):2518-28. doi: 10.1056/NEJMoa0902604. N Engl J Med. 2009. PMID: 20032323 Free article.

2

Impact of polymorphisms in the alpha- and beta-fibrinogen gene on plasma fibrinogen concentrations of coronary heart disease patients.

Heinrich J, Funke H, Rust S, Schulte H, Schönfeld R, Köhler E, Assmann G. Heinrich J, et al. Among authors: rust s. Thromb Res. 1995 Feb 1;77(3):209-15. doi: 10.1016/0049-3848(95)91608-n. Thromb Res. 1995. PMID: 7740513

3

Association of the GPIa C807T and GPIIIa PlA1/A2 polymorphisms with premature myocardial infarction in men.

Benze G, Heinrich J, Schulte H, Rust S, Nowak-Göttl U, Tataru MC, Köhler E, Assmann G, Junker R. Benze G, et al. Among authors: rust s. Eur Heart J. 2002 Feb;23(4):325-30. doi: 10.1053/euhj.2001.2776. Eur Heart J. 2002. PMID: 11812069

4

Detection of apolipoprotein E variants by an oligonucleotide "melting" procedure.

Funke H, Rust S, Assmann G. Funke H, et al. Among authors: rust s. Clin Chem. 1986 Jul;32(7):1285-9. Clin Chem. 1986. PMID: 3719940

5

Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrations.

Muntoni S, Wiebusch H, Jansen-Rust M, Rust S, Schulte H, Berger K, Pisciotta L, Bertolini S, Funke H, Seedorf U, Assmann G. Muntoni S, et al. Among authors: rust s. Nutr Metab Cardiovasc Dis. 2013 Aug;23(8):732-6. doi: 10.1016/j.numecd.2012.05.009. Epub 2012 Jul 12. Nutr Metab Cardiovasc Dis. 2013. PMID: 22795295

6

Mutagenically separated PCR (MS-PCR): a highly specific one step procedure for easy mutation detection.

Rust S, Funke H, Assmann G. Rust S, et al. Nucleic Acids Res. 1993 Aug 11;21(16):3623-9. doi: 10.1093/nar/21.16.3623. Nucleic Acids Res. 1993. PMID: 8367277 Free PMC article.

7

The transforming growth factor-beta1 gene polymorphism (G915C) is not associated with systemic lupus erythematosus.

Schotte H, Willeke P, Rust S, Assmann G, Domschke W, Gaubitz M, Schlüter B. Schotte H, et al. Among authors: rust s. Lupus. 2003;12(2):86-92. doi: 10.1191/0961203303lu336oa. Lupus. 2003. PMID: 12630751

8

The mutagenically separated polymerase chain reaction is a rapid and reliable method for genotyping of the tumour necrosis factor-alpha promoter polymorphism (-308 G/A).

Schlüter B, Erren M, Schotte H, Junker R, Rust S, Assmann G. Schlüter B, et al. Among authors: rust s. Clin Chim Acta. 2002 Jun;320(1-2):135-8. doi: 10.1016/s0009-8981(02)00054-2. Clin Chim Acta. 2002. PMID: 11983212

9

Mineral oil enhances the autoradiographic detection of 32P-labeled nucleic acids bound to nitrocellulose membranes.

Rust S, Funke H, Assmann G. Rust S, et al. Anal Biochem. 1987 May 15;163(1):196-9. doi: 10.1016/0003-2697(87)90112-6. Anal Biochem. 1987. PMID: 3619019

10

Impaired platelet activation in familial high density lipoprotein deficiency (Tangier disease).

Nofer JR, Herminghaus G, Brodde M, Morgenstern E, Rust S, Engel T, Seedorf U, Assmann G, Bluethmann H, Kehrel BE. Nofer JR, et al. Among authors: rust s. J Biol Chem. 2004 Aug 6;279(32):34032-7. doi: 10.1074/jbc.M405174200. Epub 2004 May 25. J Biol Chem. 2004. PMID: 15163665 Free article.

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