Windl O - Search Results

1

Evidence of presynaptic location and function of the prion protein.

Herms J, Tings T, Gall S, Madlung A, Giese A, Siebert H, Schürmann P, Windl O, Brose N, Kretzschmar H. Herms J, et al. Among authors: windl o. J Neurosci. 1999 Oct 15;19(20):8866-75. doi: 10.1523/JNEUROSCI.19-20-08866.1999. J Neurosci. 1999. PMID: 10516306 Free PMC article.

2

Molecular genetics of human prion diseases in Germany.

Windl O, Giese A, Schulz-Schaeffer W, Zerr I, Skworc K, Arendt S, Oberdieck C, Bodemer M, Poser S, Kretzschmar HA. Windl O, et al. Hum Genet. 1999 Sep;105(3):244-52. doi: 10.1007/s004399900124. Hum Genet. 1999. PMID: 10987652

3

Prion protein binds copper within the physiological concentration range.

Kramer ML, Kratzin HD, Schmidt B, Römer A, Windl O, Liemann S, Hornemann S, Kretzschmar H. Kramer ML, et al. Among authors: windl o. J Biol Chem. 2001 May 18;276(20):16711-9. doi: 10.1074/jbc.M006554200. Epub 2001 Feb 27. J Biol Chem. 2001. PMID: 11278306 Free article.

4

Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease.

Schulz-Schaeffer WJ, Giese A, Windl O, Kretzschmar HA. Schulz-Schaeffer WJ, et al. Among authors: windl o. Clin Neuropathol. 1996 Nov-Dec;15(6):353-7. Clin Neuropathol. 1996. PMID: 8937783

5

The German FFI cases.

Kretzschmar H, Giese A, Zerr I, Windl O, Schulz-Schaeffer W, Skworc K, Poser S. Kretzschmar H, et al. Among authors: windl o. Brain Pathol. 1998 Jul;8(3):559-61. doi: 10.1111/j.1750-3639.1998.tb00181.x. Brain Pathol. 1998. PMID: 9669710 Free PMC article. No abstract available.

6

Cellular phenotyping of secretory and nuclear prion proteins associated with inherited prion diseases.

Lorenz H, Windl O, Kretzschmar HA. Lorenz H, et al. Among authors: windl o. J Biol Chem. 2002 Mar 8;277(10):8508-16. doi: 10.1074/jbc.M110197200. Epub 2001 Dec 27. J Biol Chem. 2002. PMID: 11756421 Free article.

7

Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease.

Zerr I, Bodemer M, Gefeller O, Otto M, Poser S, Wiltfang J, Windl O, Kretzschmar HA, Weber T. Zerr I, et al. Among authors: windl o. Ann Neurol. 1998 Jan;43(1):32-40. doi: 10.1002/ana.410430109. Ann Neurol. 1998. PMID: 9450766

8

Phenotypic variability in fatal familial insomnia (D178N-129M) genotype.

Zerr I, Giese A, Windl O, Kropp S, Schulz-Schaeffer W, Riedemann C, Skworc K, Bodemer M, Kretzschmar HA, Poser S. Zerr I, et al. Among authors: windl o. Neurology. 1998 Nov;51(5):1398-405. doi: 10.1212/wnl.51.5.1398. Neurology. 1998. PMID: 9818868

9

Breaking an absolute species barrier: transgenic mice expressing the mink PrP gene are susceptible to transmissible mink encephalopathy.

Windl O, Buchholz M, Neubauer A, Schulz-Schaeffer W, Groschup M, Walter S, Arendt S, Neumann M, Voss AK, Kretzschmar HA. Windl O, et al. J Virol. 2005 Dec;79(23):14971-5. doi: 10.1128/JVI.79.23.14971-14975.2005. J Virol. 2005. PMID: 16282497 Free PMC article.

10

Loss of glycosylation associated with the T183A mutation in human prion disease.

Grasbon-Frodl E, Lorenz H, Mann U, Nitsch RM, Windl O, Kretzschmar HA. Grasbon-Frodl E, et al. Among authors: windl o. Acta Neuropathol. 2004 Dec;108(6):476-84. doi: 10.1007/s00401-004-0913-4. Epub 2004 Oct 26. Acta Neuropathol. 2004. PMID: 15558291

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