Aydin A - Search Results

1

Mutant Phosphodiesterase 3A Protects From Hypertension-Induced Cardiac Damage.

Ercu M, Mücke MB, Pallien T, Markó L, Sholokh A, Schächterle C, Aydin A, Kidd A, Walter S, Esmati Y, McMurray BJ, Lato DF, Yumi Sunaga-Franze D, Dierks PH, Flores BIM, Walker-Gray R, Gong M, Merticariu C, Zühlke K, Russwurm M, Liu T, Batolomaeus TUP, Pautz S, Schelenz S, Taube M, Napieczynska H, Heuser A, Eichhorst J, Lehmann M, Miller DC, Diecke S, Qadri F, Popova E, Langanki R, Movsesian MA, Herberg FW, Forslund SK, Müller DN, Borodina T, Maass PG, Bähring S, Hübner N, Bader M, Klussmann E. Ercu M, et al. Among authors: aydin a. Circulation. 2022 Dec 6;146(23):1758-1778. doi: 10.1161/CIRCULATIONAHA.122.060210. Epub 2022 Oct 19. Circulation. 2022. PMID: 36259389

2

Oligonucleotide ligation assay (OLA) for the diagnosis of familial hypercholesterolemia.

Baron H, Fung S, Aydin A, Bähring S, Luft FC, Schuster H. Baron H, et al. Among authors: aydin a. Nat Biotechnol. 1996 Oct;14(10):1279-82. doi: 10.1038/nbt1096-1279. Nat Biotechnol. 1996. PMID: 9631093

3

Efficient and cost-effective single nucleotide polymorphism detection with different fluorescent applications.

Aydin A, Baron H, Bähring S, Schuster H, Luft FC. Aydin A, et al. Biotechniques. 2001 Oct;31(4):920-2, 924, 926-8. doi: 10.2144/01314rr03. Biotechniques. 2001. PMID: 11680723 Free article.

4

The study of gene polymorphisms. How complex is complex genetic disease?

Bähring S, Aydin A, Luft FC. Bähring S, et al. Among authors: aydin a. Methods Mol Med. 2003;86:221-35. doi: 10.1385/1-59259-392-5:221. Methods Mol Med. 2003. PMID: 12886772 No abstract available.

5

Validation of fluorescence-labeled artificial nonhuman sequences for single-strand conformation polymorphism mutation detection in familial hypercholesterolemia.

Aydin A, Luft FC, Bähring S. Aydin A, et al. Anal Biochem. 2004 Jan 1;324(1):16-21. doi: 10.1016/j.ab.2003.09.006. Anal Biochem. 2004. PMID: 14654040

6

Autosomal-dominant hypertension with type E brachydactyly is caused by rearrangement on the short arm of chromosome 12.

Bähring S, Rauch A, Toka O, Schroeder C, Hesse C, Siedler H, Fesüs G, Haefeli WE, Busjahn A, Aydin A, Neuenfeld Y, Mühl A, Toka HR, Gollasch M, Jordan J, Luft FC. Bähring S, et al. Among authors: aydin a. Hypertension. 2004 Feb;43(2):471-6. doi: 10.1161/01.HYP.0000111808.08715.ec. Epub 2004 Jan 5. Hypertension. 2004. PMID: 14707163

7

Single nucleotide polymorphism map of five long-QT genes.

Aydin A, Bähring S, Dahm S, Guenther UP, Uhlmann R, Busjahn A, Luft FC. Aydin A, et al. J Mol Med (Berl). 2005 Feb;83(2):159-65. doi: 10.1007/s00109-004-0595-3. Epub 2004 Dec 15. J Mol Med (Berl). 2005. PMID: 15599693

8

New universal primers facilitate Pyrosequencing.

Aydin A, Toliat MR, Bähring S, Becker C, Nürnberg P. Aydin A, et al. Electrophoresis. 2006 Feb;27(2):394-7. doi: 10.1002/elps.200500467. Electrophoresis. 2006. PMID: 16331584

9

Inversion region for hypertension and brachydactyly on chromosome 12p features multiple splicing and noncoding RNA.

Bähring S, Kann M, Neuenfeld Y, Gong M, Chitayat D, Toka HR, Toka O, Plessis G, Maass P, Rauch A, Aydin A, Luft FC. Bähring S, et al. Among authors: aydin a. Hypertension. 2008 Feb;51(2):426-31. doi: 10.1161/HYPERTENSIONAHA.107.101774. Epub 2007 Dec 17. Hypertension. 2008. PMID: 18086950

10

A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E.

Maass PG, Wirth J, Aydin A, Rump A, Stricker S, Tinschert S, Otero M, Tsuchimochi K, Goldring MB, Luft FC, Bähring S. Maass PG, et al. Among authors: aydin a. Hum Mol Genet. 2010 Mar 1;19(5):848-60. doi: 10.1093/hmg/ddp553. Epub 2009 Dec 16. Hum Mol Genet. 2010. PMID: 20015959 Free PMC article.

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