Schell U - Search Results

1

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome.

Muenke M, Schell U, Hehr A, Robin NH, Losken HW, Schinzel A, Pulleyn LJ, Rutland P, Reardon W, Malcolm S, et al. Muenke M, et al. Among authors: schell u. Nat Genet. 1994 Nov;8(3):269-74. doi: 10.1038/ng1194-269. Nat Genet. 1994. PMID: 7874169

2

Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome.

Schell U, Hehr A, Feldman GJ, Robin NH, Zackai EH, de Die-Smulders C, Viskochil DH, Stewart JM, Wolff G, Ohashi H, et al. Schell U, et al. Hum Mol Genet. 1995 Mar;4(3):323-8. doi: 10.1093/hmg/4.3.323. Hum Mol Genet. 1995. PMID: 7795583

3

Fibroblast-growth-factor receptor mutations in human skeletal disorders.

Muenke M, Schell U. Muenke M, et al. Among authors: schell u. Trends Genet. 1995 Aug;11(8):308-13. doi: 10.1016/s0168-9525(00)89088-5. Trends Genet. 1995. PMID: 8585128 Free article. Review.

4

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.

Schell U, Wienberg J, Köhler A, Bray-Ward P, Ward DE, Wilson WG, Allen WP, Lebel RR, Sawyer JR, Campbell PL, Aughton DJ, Punnett HH, Lammer EJ, Kao FT, Ward DC, Muenke M. Schell U, et al. Hum Mol Genet. 1996 Feb;5(2):223-9. doi: 10.1093/hmg/5.2.223. Hum Mol Genet. 1996. PMID: 8824878

5

The importance of the alpha 2MR/LRP for human genetics. Investigations of the receptor expression in different human blood cells.

Gläser C, Handschug K, Ludvik S, Schell U, Hehr A, Küchenhoff A, Robenek H. Gläser C, et al. Among authors: schell u. Ann N Y Acad Sci. 1994 Sep 10;737:447-50. doi: 10.1111/j.1749-6632.1994.tb44336.x. Ann N Y Acad Sci. 1994. PMID: 7944149 No abstract available.

6

In vivo endomicroscopy improves detection of Barrett's esophagus-related neoplasia: a multicenter international randomized controlled trial (with video).

Canto MI, Anandasabapathy S, Brugge W, Falk GW, Dunbar KB, Zhang Z, Woods K, Almario JA, Schell U, Goldblum J, Maitra A, Montgomery E, Kiesslich R; Confocal Endomicroscopy for Barrett's Esophagus or Confocal Endomicroscopy for Barrett's Esophagus (CEBE) Trial Group. Canto MI, et al. Among authors: schell u. Gastrointest Endosc. 2014 Feb;79(2):211-21. doi: 10.1016/j.gie.2013.09.020. Epub 2013 Nov 9. Gastrointest Endosc. 2014. PMID: 24219822 Free PMC article. Clinical Trial.

7

Growth amplification in ultrahigh-throughput microdroplet screening increases sensitivity of clonal enzyme assays and minimizes phenotypic variation.

Zurek PJ, Hours R, Schell U, Pushpanath A, Hollfelder F. Zurek PJ, et al. Among authors: schell u. Lab Chip. 2021 Jan 5;21(1):163-173. doi: 10.1039/d0lc00830c. Lab Chip. 2021. PMID: 33242058

8

The pleiotropic Legionella transcription factor LvbR links the Lqs and c-di-GMP regulatory networks to control biofilm architecture and virulence.

Hochstrasser R, Kessler A, Sahr T, Simon S, Schell U, Gomez-Valero L, Buchrieser C, Hilbi H. Hochstrasser R, et al. Among authors: schell u. Environ Microbiol. 2019 Mar;21(3):1035-1053. doi: 10.1111/1462-2920.14523. Epub 2019 Feb 22. Environ Microbiol. 2019. PMID: 30623561

9

Legionella shows a diverse secondary metabolism dependent on a broad spectrum Sfp-type phosphopantetheinyl transferase.

Tobias NJ, Ahrendt T, Schell U, Miltenberger M, Hilbi H, Bode HB. Tobias NJ, et al. Among authors: schell u. PeerJ. 2016 Nov 24;4:e2720. doi: 10.7717/peerj.2720. eCollection 2016. PeerJ. 2016. PMID: 27904811 Free PMC article.

10

Ultrahigh-throughput-directed enzyme evolution by absorbance-activated droplet sorting (AADS).

Gielen F, Hours R, Emond S, Fischlechner M, Schell U, Hollfelder F. Gielen F, et al. Among authors: schell u. Proc Natl Acad Sci U S A. 2016 Nov 22;113(47):E7383-E7389. doi: 10.1073/pnas.1606927113. Epub 2016 Nov 7. Proc Natl Acad Sci U S A. 2016. PMID: 27821774 Free PMC article.

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