Werner R - Search Results

1

Formin-mediated nuclear actin at androgen receptors promotes transcription.

Knerr J, Werner R, Schwan C, Wang H, Gebhardt P, Grötsch H, Caliebe A, Spielmann M, Holterhus PM, Grosse R, Hornig NC. Knerr J, et al. Among authors: werner r. Nature. 2023 May;617(7961):616-622. doi: 10.1038/s41586-023-05981-1. Epub 2023 Mar 27. Nature. 2023. PMID: 36972684

2

Homozygous disruption of P450 side-chain cleavage (CYP11A1) is associated with prematurity, complete 46,XY sex reversal, and severe adrenal failure.

Hiort O, Holterhus PM, Werner R, Marschke C, Hoppe U, Partsch CJ, Riepe FG, Achermann JC, Struve D. Hiort O, et al. Among authors: werner r. J Clin Endocrinol Metab. 2005 Jan;90(1):538-41. doi: 10.1210/jc.2004-1059. Epub 2004 Oct 26. J Clin Endocrinol Metab. 2005. PMID: 15507506

3

Transactivation properties of wild-type and mutant androgen receptors in transiently transfected primary human fibroblasts.

Holterhus PM, Salzburg J, Werner R, Hiort O. Holterhus PM, et al. Among authors: werner r. Horm Res. 2005;63(3):152-8. doi: 10.1159/000085005. Epub 2005 Apr 6. Horm Res. 2005. PMID: 15812177 Free article.

4

Molecular features and clinical phenotypes in androgen insensitivity syndrome in the absence and presence of androgen receptor gene mutations.

Holterhus PM, Werner R, Hoppe U, Bassler J, Korsch E, Ranke MB, Dörr HG, Hiort O. Holterhus PM, et al. Among authors: werner r. J Mol Med (Berl). 2005 Dec;83(12):1005-13. doi: 10.1007/s00109-005-0704-y. Epub 2005 Nov 11. J Mol Med (Berl). 2005. PMID: 16283146

5

The A645D mutation in the hinge region of the human androgen receptor (AR) gene modulates AR activity, depending on the context of the polymorphic glutamine and glycine repeats.

Werner R, Holterhus PM, Binder G, Schwarz HP, Morlot M, Struve D, Marschke C, Hiort O. Werner R, et al. J Clin Endocrinol Metab. 2006 Sep;91(9):3515-20. doi: 10.1210/jc.2006-0372. Epub 2006 Jun 27. J Clin Endocrinol Metab. 2006. PMID: 16804045

6

Androgen receptor gene mutations in androgen insensitivity syndrome cause distinct patterns of reduced activation of androgen-responsive promoter constructs.

Werner R, Schütt J, Hannema S, Röpke A, Wieacker P, Hiort O, Holterhus PM. Werner R, et al. J Steroid Biochem Mol Biol. 2006 Sep;101(1):1-10. doi: 10.1016/j.jsbmb.2006.06.016. Epub 2006 Aug 22. J Steroid Biochem Mol Biol. 2006. PMID: 16930995

7

Cell-line and tissue-specific signatures of androgen receptor-coregulator transcription.

Bebermeier JH, Brooks JD, DePrimo SE, Werner R, Deppe U, Demeter J, Hiort O, Holterhus PM. Bebermeier JH, et al. Among authors: werner r. J Mol Med (Berl). 2006 Nov;84(11):919-31. doi: 10.1007/s00109-006-0081-1. Epub 2006 Aug 24. J Mol Med (Berl). 2006. PMID: 16932916

8

Intrinsic androgen-dependent gene expression patterns revealed by comparison of genital fibroblasts from normal males and individuals with complete and partial androgen insensitivity syndrome.

Holterhus PM, Deppe U, Werner R, Richter-Unruh A, Bebermeier JH, Wünsch L, Krege S, Schweikert HU, Demeter J, Riepe F, Hiort O, Brooks JD. Holterhus PM, et al. Among authors: werner r. BMC Genomics. 2007 Oct 18;8:376. doi: 10.1186/1471-2164-8-376. BMC Genomics. 2007. PMID: 17945006 Free PMC article.

9

Mutation analysis of FOXF2 in patients with disorders of sex development (DSD) in combination with cleft palate.

Jochumsen U, Werner R, Miura N, Richter-Unruh A, Hiort O, Holterhus PM. Jochumsen U, et al. Among authors: werner r. Sex Dev. 2008;2(6):302-8. doi: 10.1159/000195679. Epub 2009 Mar 10. Sex Dev. 2008. PMID: 19276632 Free PMC article.

10

Apolipoprotein D (APOD) is a putative biomarker of androgen receptor function in androgen insensitivity syndrome.

Appari M, Werner R, Wünsch L, Cario G, Demeter J, Hiort O, Riepe F, Brooks JD, Holterhus PM. Appari M, et al. Among authors: werner r. J Mol Med (Berl). 2009 Jun;87(6):623-32. doi: 10.1007/s00109-009-0462-3. Epub 2009 Mar 30. J Mol Med (Berl). 2009. PMID: 19330472 Free PMC article.

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