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Items: 17

1.

New technologies for DNA analysis - a review of the READNA Project.

McGinn S, Bauer D, Brefort T, Dong L, El-Sagheer A, Elsharawy A, Evans G, Falk-Sörqvist E, Forster M, Fredriksson S, Freeman P, Freitag C, Fritzsche J, Gibson S, Gullberg M, Gut M, Heath S, Heath-Brun I, Heron AJ, Hohlbein J, Ke R, Lancaster O, Le Reste L, Maglia G, Marie R, Mauger F, Mertes F, Mignardi M, Moens L, Oostmeijer J, Out R, Pedersen JN, Persson F, Picaud V, Rotem D, Schracke N, Sengenes J, Stähler PF, Stade B, Stoddart D, Teng X, Veal CD, Zahra N, Bayley H, Beier M, Brown T, Dekker C, Ekström B, Flyvbjerg H, Franke A, Guenther S, Kapanidis AN, Kaye J, Kristensen A, Lehrach H, Mangion J, Sauer S, Schyns E, Tost J, van Helvoort JM, van der Zaag PJ, Tegenfeldt JO, Brookes AJ, Mir K, Nilsson M, Willcocks JP, Gut IG.

N Biotechnol. 2016 May 25;33(3):311-30. doi: 10.1016/j.nbt.2015.10.003. Epub 2015 Oct 26. Review.

PMID:
26514324
2.

Honoring patients' organ donation decisions when family conflict is present: Experience from a single organ procurement organization.

Stahler PA, Weese SE, Nygaard RM, Hill MJ, Richardson CJ, Larson SM, Gunderson S, Quickel RR.

J Trauma Acute Care Surg. 2014 Oct;77(4):555-8. doi: 10.1097/TA.0000000000000417.

PMID:
25250593
3.

Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing.

Elsharawy A, Forster M, Schracke N, Keller A, Thomsen I, Petersen BS, Stade B, Stähler P, Schreiber S, Rosenstiel P, Franke A.

BMC Genomics. 2012 Aug 22;13:417. doi: 10.1186/1471-2164-13-417.

4.

Targeted next-generation sequencing for the molecular genetic diagnostics of cardiomyopathies.

Meder B, Haas J, Keller A, Heid C, Just S, Borries A, Boisguerin V, Scharfenberger-Schmeer M, Stähler P, Beier M, Weichenhan D, Strom TM, Pfeufer A, Korn B, Katus HA, Rottbauer W.

Circ Cardiovasc Genet. 2011 Apr;4(2):110-22. doi: 10.1161/CIRCGENETICS.110.958322. Epub 2011 Jan 20.

5.

High-fidelity gene synthesis by retrieval of sequence-verified DNA identified using high-throughput pyrosequencing.

Matzas M, Stähler PF, Kefer N, Siebelt N, Boisguérin V, Leonard JT, Keller A, Stähler CF, Häberle P, Gharizadeh B, Babrzadeh F, Church GM.

Nat Biotechnol. 2010 Dec;28(12):1291-4. doi: 10.1038/nbt.1710. Epub 2010 Nov 28.

6.

Deciphering the porcine intestinal microRNA transcriptome.

Sharbati S, Friedländer MR, Sharbati J, Hoeke L, Chen W, Keller A, Stähler PF, Rajewsky N, Einspanier R.

BMC Genomics. 2010 Apr 30;11:275. doi: 10.1186/1471-2164-11-275.

7.

A flexible and fully integrated system for amplification, detection and genotyping of genomic DNA targets based on microfluidic oligonucleotide arrays.

Summerer D, Hevroni D, Jain A, Oldenburger O, Parker J, Caruso A, Stähler CF, Stähler PF, Beier M.

N Biotechnol. 2010 May 31;27(2):149-55. doi: 10.1016/j.nbt.2010.03.005. Epub 2010 Mar 30.

PMID:
20359559
8.

Targeted high throughput sequencing of a cancer-related exome subset by specific sequence capture with a fully automated microarray platform.

Summerer D, Schracke N, Wu H, Cheng Y, Bau S, Stähler CF, Stähler PF, Beier M.

Genomics. 2010 Apr;95(4):241-6. doi: 10.1016/j.ygeno.2010.01.006. Epub 2010 Feb 6.

9.

Specific sequence selection and next generation resequencing of 68 E. coli genes using HybSelect.

Schracke N, Kornmeyer T, Kränzle M, Stähler PF, Summerer D, Beier M.

N Biotechnol. 2009 Nov 30;26(5):229-33. doi: 10.1016/j.nbt.2009.08.013. Epub 2009 Sep 6.

PMID:
19735750
10.

Microarray-based multicycle-enrichment of genomic subsets for targeted next-generation sequencing.

Summerer D, Wu H, Haase B, Cheng Y, Schracke N, Stähler CF, Chee MS, Stähler PF, Beier M.

Genome Res. 2009 Sep;19(9):1616-21. doi: 10.1101/gr.091942.109. Epub 2009 Jul 28.

11.

Targeted next-generation sequencing by specific capture of multiple genomic loci using low-volume microfluidic DNA arrays.

Bau S, Schracke N, Kränzle M, Wu H, Stähler PF, Hoheisel JD, Beier M, Summerer D.

Anal Bioanal Chem. 2009 Jan;393(1):171-5. doi: 10.1007/s00216-008-2460-7. Epub 2008 Oct 29.

PMID:
18958448
12.

Microfluidic-based enzymatic on-chip labeling of miRNAs.

Vorwerk S, Ganter K, Cheng Y, Hoheisel J, Stähler PF, Beier M.

N Biotechnol. 2008 Oct-Dec;25(2-3):142-9. doi: 10.1016/j.nbt.2008.08.005. Epub 2008 Aug 20.

PMID:
18786664
13.

Another side of genomics: synthetic biology as a means for the exploitation of whole-genome sequence information.

Stähler P, Beier M, Gao X, Hoheisel JD.

J Biotechnol. 2006 Jun 25;124(1):206-12. Epub 2006 Jan 24. Review.

PMID:
16436303
14.

Validation of a novel, fully integrated and flexible microarray benchtop facility for gene expression profiling.

Baum M, Bielau S, Rittner N, Schmid K, Eggelbusch K, Dahms M, Schlauersbach A, Tahedl H, Beier M, Güimil R, Scheffler M, Hermann C, Funk JM, Wixmerten A, Rebscher H, Hönig M, Andreae C, Büchner D, Moschel E, Glathe A, Jäger E, Thom M, Greil A, Bestvater F, Obermeier F, Burgmaier J, Thome K, Weichert S, Hein S, Binnewies T, Foitzik V, Müller M, Stähler CF, Stähler PF.

Nucleic Acids Res. 2003 Dec 1;31(23):e151.

15.

Geniom technology--the benchtop array facility.

Güimil R, Beier M, Scheffler M, Rebscher H, Funk J, Wixmerten A, Baum M, Hermann C, Tahedl H, Moschel E, Obermeier F, Sommer I, Büchner D, Viehweger R, Burgmaier J, Stähler CF, Müller M, Stähler PF.

Nucleosides Nucleotides Nucleic Acids. 2003 May-Aug;22(5-8):1721-3.

PMID:
14565504
16.

Exploring nature's plasticity with a flexible probing tool, and finding new ways for its electronic distribution.

Beier M, Baum M, Rebscher H, Mauritz R, Wixmerten A, Stähler CF, Müller M, Stähler PF.

Biochem Soc Trans. 2002 Apr;30(2):78-82.

PMID:
12023829
17.

Enhanced suicide gene effect by adenoviral transduction of a VP22-cytosine deaminase (CD) fusion gene.

Wybranietz WA, Gross CD, Phelan A, O'Hare P, Spiegel M, Graepler F, Bitzer M, Stähler P, Gregor M, Lauer UM.

Gene Ther. 2001 Nov;8(21):1654-64.

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