Blaschke RJ - Search Results

1

Expression of two novel eph-related receptor protein tyrosine kinases in mammary gland development and carcinogenesis.

Andres AC, Reid HH, Zürcher G, Blaschke RJ, Albrecht D, Ziemiecki A. Andres AC, et al. Among authors: blaschke rj. Oncogene. 1994 May;9(5):1461-7. Oncogene. 1994. PMID: 8152808

2

Characterization of a novel murine testis-specific serine/threonine kinase.

Bielke W, Blaschke RJ, Miescher GC, Zürcher G, Andres AC, Ziemiecki A. Bielke W, et al. Among authors: blaschke rj. Gene. 1994 Feb 25;139(2):235-9. doi: 10.1016/0378-1119(94)90762-5. Gene. 1994. PMID: 8112611

3

Tyrosine kinases: from viral oncogenes to developmental regulators.

Blaschke R, Andres AC, Reid HH, Zürcher G, Friis RR, Ziemiecki A. Blaschke R, et al. Behring Inst Mitt. 1991 Jul;(89):81-92. Behring Inst Mitt. 1991. PMID: 1930106 Review.

4

A novel murine PKA-related protein kinase involved in neuronal differentiation.

Blaschke RJ, Monaghan AP, Bock D, Rappold GA. Blaschke RJ, et al. Genomics. 2000 Mar 1;64(2):187-94. doi: 10.1006/geno.2000.6116. Genomics. 2000. PMID: 10729225

5

Targeted mutation reveals essential functions of the homeodomain transcription factor Shox2 in sinoatrial and pacemaking development.

Blaschke RJ, Hahurij ND, Kuijper S, Just S, Wisse LJ, Deissler K, Maxelon T, Anastassiadis K, Spitzer J, Hardt SE, Schöler H, Feitsma H, Rottbauer W, Blum M, Meijlink F, Rappold G, Gittenberger-de Groot AC. Blaschke RJ, et al. Circulation. 2007 Apr 10;115(14):1830-8. doi: 10.1161/CIRCULATIONAHA.106.637819. Epub 2007 Mar 19. Circulation. 2007. PMID: 17372176

6

Phosphorylation on Ser106 modulates the cellular functions of the SHOX homeodomain protein.

Marchini A, Daeffler L, Marttila T, Schneider KU, Blaschke RJ, Schnölzer M, Rommelaere J, Rappold G. Marchini A, et al. Among authors: blaschke rj. J Mol Biol. 2006 Jan 20;355(3):590-603. doi: 10.1016/j.jmb.2005.11.007. Epub 2005 Nov 21. J Mol Biol. 2006. PMID: 16325853

7

The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes.

Marchini A, Marttila T, Winter A, Caldeira S, Malanchi I, Blaschke RJ, Häcker B, Rao E, Karperien M, Wit JM, Richter W, Tommasino M, Rappold GA. Marchini A, et al. Among authors: blaschke rj. J Biol Chem. 2004 Aug 27;279(35):37103-14. doi: 10.1074/jbc.M307006200. Epub 2004 May 15. J Biol Chem. 2004. PMID: 15145945 Free article.

8

The pseudoautosomal regions, SHOX and disease.

Blaschke RJ, Rappold G. Blaschke RJ, et al. Curr Opin Genet Dev. 2006 Jun;16(3):233-9. doi: 10.1016/j.gde.2006.04.004. Epub 2006 May 2. Curr Opin Genet Dev. 2006. PMID: 16650979 Review.

9

A novel point mutation A170P in the SHOX gene defines impaired nuclear translocation as a molecular cause for Léri-Weill dyschondrosteosis and Langer dysplasia.

Sabherwal N, Blaschke RJ, Marchini A, Heine-Suner D, Rosell J, Ferragut J, Blum WF, Rappold G. Sabherwal N, et al. Among authors: blaschke rj. J Med Genet. 2004 Jun;41(6):e83. doi: 10.1136/jmg.2003.016402. J Med Genet. 2004. PMID: 15173249 Free PMC article. No abstract available.

10

The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator.

Rao E, Blaschke RJ, Marchini A, Niesler B, Burnett M, Rappold GA. Rao E, et al. Among authors: blaschke rj. Hum Mol Genet. 2001 Dec 15;10(26):3083-91. doi: 10.1093/hmg/10.26.3083. Hum Mol Genet. 2001. PMID: 11751690

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