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Items: 17

1.

Asymmetric Centriole Numbers at Spindle Poles Cause Chromosome Missegregation in Cancer.

Cosenza MR, Cazzola A, Rossberg A, Schieber NL, Konotop G, Bausch E, Slynko A, Holland-Letz T, Raab MS, Dubash T, Glimm H, Poppelreuther S, Herold-Mende C, Schwab Y, Krämer A.

Cell Rep. 2017 Aug 22;20(8):1906-1920. doi: 10.1016/j.celrep.2017.08.005.

2.

Pharmacological Inhibition of Centrosome Clustering by Slingshot-Mediated Cofilin Activation and Actin Cortex Destabilization.

Konotop G, Bausch E, Nagai T, Turchinovich A, Becker N, Benner A, Boutros M, Mizuno K, Krämer A, Raab MS.

Cancer Res. 2016 Nov 15;76(22):6690-6700. doi: 10.1158/0008-5472.CAN-16-1144. Epub 2016 Sep 13.

3.

MAP1S controls microtubule stability throughout the cell cycle in human cells.

Tegha-Dunghu J, Bausch E, Neumann B, Wuensche A, Walter T, Ellenberg J, Gruss OJ.

J Cell Sci. 2014 Dec 1;127(Pt 23):5007-13. doi: 10.1242/jcs.136457. Epub 2014 Oct 9.

4.

A novel microtubule inhibitor 4SC-207 with anti-proliferative activity in taxane-resistant cells.

Bausch E, Kohlhof H, Hamm S, Krauss R, Baumgartner R, Sironi L.

PLoS One. 2013 Nov 6;8(11):e79594. doi: 10.1371/journal.pone.0079594. eCollection 2013.

5.

A large TAT deletion in a tyrosinaemia type II patient.

Legarda M, Wlodarczyk K, Lage S, Andrade F, Kim GJ, Bausch E, Scherer G, Aldamiz-Echevarria LJ.

Mol Genet Metab. 2011 Nov;104(3):407-9. doi: 10.1016/j.ymgme.2011.05.009. Epub 2011 May 16.

PMID:
21636300
6.

A novel SOX9 nonsense mutation, q401x, in a case of campomelic dysplasia with XY sex reversal.

Stoeva R, Grozdanova L, Scherer G, Krasteva M, Bausch E, Krastev T, Linev A, Stefanova M.

Genet Couns. 2011;22(1):49-53.

PMID:
21614988
7.

Extended pedigree with multiple cases of XX sex reversal in the absence of SRY and of a mutation at the SOX9 locus.

Temel SG, Gulten T, Yakut T, Saglam H, Kilic N, Bausch E, Jin WJ, Leipoldt M, Scherer G.

Sex Dev. 2007;1(1):24-34. doi: 10.1159/000096236.

8.

Species-specific evolution of repeated DNA sequences in great apes.

Toder R, Grützner F, Haaf T, Bausch E.

Chromosome Res. 2001;9(6):431-5.

PMID:
11592477
10.

No association between the tyrosine hydroxylase microsatellite marker HUMTH01 and schizophrenia or bipolar I disorder.

Burgert E, Crocq MA, Bausch E, Macher JP, Morris-Rosendahl DJ.

Psychiatr Genet. 1998 Summer;8(2):45-8.

PMID:
9686421
11.

Novel and recurrent tyrosine aminotransferase gene mutations in tyrosinemia type II.

Hühn R, Stoermer H, Klingele B, Bausch E, Fois A, Farnetani M, Di Rocco M, Boué J, Kirk JM, Coleman R, Scherer G.

Hum Genet. 1998 Mar;102(3):305-13.

PMID:
9544843
12.

High-resolution mapping of a linkage group on mouse chromosome 8 conserved on human chromosome 16Q.

Becker-Follmann J, Gaa A, Baùsch E, Natt E, Scherer G, von Deimling O.

Mamm Genome. 1997 Mar;8(3):172-7.

PMID:
9069116
13.
14.

Analysis of two 47,XXX males reveals X-Y interchange and maternal or paternal nondisjunction.

Scherer G, Schempp W, Fraccaro M, Bausch E, Bigozzi V, Maraschio P, Montali E, Simoni G, Wolf U.

Hum Genet. 1989 Feb;81(3):247-51.

PMID:
2921034
15.

Laboratory requirements for the construction of subperiosteal Vitallium implants.

Bausch E.

J Oral Implant Transplant Surg. 1966;12:9-11. No abstract available.

PMID:
5227837
16.

PRESENTATION OF THE MICROSCOPE.

Bausch E.

Science. 1936 Aug 7;84(2171):124. No abstract available.

PMID:
17807998
17.

LETTERS TO THE EDITOR.

Bausch E.

Science. 1887 Dec 23;10(255):311. No abstract available.

PMID:
17751249

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