Trülzsch B - Search Results

1

Ribozymes and siRNA for the treatment of diseases of the nervous system.

Wood MJ, Trülzsch B, Abdelgany A, Beeson D. Wood MJ, et al. Among authors: trulzsch b. Curr Opin Mol Ther. 2003 Aug;5(4):383-8. Curr Opin Mol Ther. 2003. PMID: 14513681 Review.

2

Therapeutic gene silencing in the nervous system.

Wood MJ, Trülzsch B, Abdelgany A, Beeson D. Wood MJ, et al. Among authors: trulzsch b. Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R279-84. doi: 10.1093/hmg/ddg275. Epub 2003 Aug 19. Hum Mol Genet. 2003. PMID: 12928477 Review.

3

Applications of nucleic acid technology in the CNS.

Trülzsch B, Wood M. Trülzsch B, et al. J Neurochem. 2004 Jan;88(2):257-65. doi: 10.1111/j.1471-4159.2004.02153.x. J Neurochem. 2004. PMID: 14690514 Free article. Review.

4

Survival of motor neuron gene downregulation by RNAi: towards a cell culture model of spinal muscular atrophy.

Trülzsch B, Davies K, Wood M. Trülzsch B, et al. Brain Res Mol Brain Res. 2004 Jan 5;120(2):145-50. doi: 10.1016/j.molbrainres.2003.10.015. Brain Res Mol Brain Res. 2004. PMID: 14741404

5

Knockdown of SMN by RNA interference induces apoptosis in differentiated P19 neural stem cells.

Trülzsch B, Garnett C, Davies K, Wood M. Trülzsch B, et al. Brain Res. 2007 Dec 5;1183:1-9. doi: 10.1016/j.brainres.2007.09.025. Epub 2007 Sep 21. Brain Res. 2007. PMID: 17976539

6

Neuromuscular defects in a Drosophila survival motor neuron gene mutant.

Chan YB, Miguel-Aliaga I, Franks C, Thomas N, Trülzsch B, Sattelle DB, Davies KE, van den Heuvel M. Chan YB, et al. Among authors: trulzsch b. Hum Mol Genet. 2003 Jun 15;12(12):1367-76. doi: 10.1093/hmg/ddg157. Hum Mol Genet. 2003. PMID: 12783845

7

Search for mitochondrial DNA mutation at position 3243 in German patients with a positive family history of maternal diabetes mellitus.

Klemm T, Neumann S, Trülzsch B, Pistrosch F, Hanefeld M, Paschke R. Klemm T, et al. Among authors: trulzsch b. Exp Clin Endocrinol Diabetes. 2001;109(5):283-7. doi: 10.1055/s-2001-16348. Exp Clin Endocrinol Diabetes. 2001. PMID: 11507652

8

Detection of thyroid-stimulating hormone receptor and Gsalpha mutations: in 75 toxic thyroid nodules by denaturing gradient gel electrophoresis.

Trülzsch B, Krohn K, Wonerow P, Chey S, Holzapfel HP, Ackermann F, Führer D, Paschke R. Trülzsch B, et al. J Mol Med (Berl). 2001;78(12):684-91. doi: 10.1007/s001090000170. J Mol Med (Berl). 2001. PMID: 11434721

9

DGGE is more sensitive for the detection of somatic point mutations than direct sequencing.

Trülzsch B, Krohn K, Wonerow P, Paschke R. Trülzsch B, et al. Biotechniques. 1999 Aug;27(2):266-8. doi: 10.2144/99272bm10. Biotechniques. 1999. PMID: 10457827 Free article. No abstract available.

10

The thyrotropin receptor mutation database.

Trülzsch B, Nebel T, Paschke R. Trülzsch B, et al. Thyroid. 1999 Jun;9(6):521-2. doi: 10.1089/thy.1999.9.521. Thyroid. 1999. PMID: 10411112 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

13 results

Search Page

Filters