Kretzschmar HA - Search Results

1

A pathogenic presenilin-1 deletion causes abberrant Abeta 42 production in the absence of congophilic amyloid plaques.

Steiner H, Revesz T, Neumann M, Romig H, Grim MG, Pesold B, Kretzschmar HA, Hardy J, Holton JL, Baumeister R, Houlden H, Haass C. Steiner H, et al. Among authors: kretzschmar ha. J Biol Chem. 2001 Mar 9;276(10):7233-9. doi: 10.1074/jbc.M007183200. Epub 2000 Nov 17. J Biol Chem. 2001. PMID: 11084029 Free article.

2

Elevation of beta-amyloid peptide 2-42 in sporadic and familial Alzheimer's disease and its generation in PS1 knockout cells.

Wiltfang J, Esselmann H, Cupers P, Neumann M, Kretzschmar H, Beyermann M, Schleuder D, Jahn H, Rüther E, Kornhuber J, Annaert W, De Strooper B, Saftig P. Wiltfang J, et al. J Biol Chem. 2001 Nov 16;276(46):42645-57. doi: 10.1074/jbc.M102790200. Epub 2001 Aug 28. J Biol Chem. 2001. PMID: 11526104 Free article.

3

[Molecular neuropathology of Non-Alzheimer dementia].

Neumann M, Kretzschmar HA. Neumann M, et al. Among authors: kretzschmar ha. Pathologe. 2008 Nov;29(6):434-41. doi: 10.1007/s00292-008-1063-6. Pathologe. 2008. PMID: 18773209 German.

4

Subcellular localization of wild-type and Parkinson's disease-associated mutant alpha -synuclein in human and transgenic mouse brain.

Kahle PJ, Neumann M, Ozmen L, Muller V, Jacobsen H, Schindzielorz A, Okochi M, Leimer U, van Der Putten H, Probst A, Kremmer E, Kretzschmar HA, Haass C. Kahle PJ, et al. Among authors: kretzschmar ha. J Neurosci. 2000 Sep 1;20(17):6365-73. doi: 10.1523/JNEUROSCI.20-17-06365.2000. J Neurosci. 2000. PMID: 10964942 Free PMC article.

5

Pick's disease associated with the novel Tau gene mutation K369I.

Neumann M, Schulz-Schaeffer W, Crowther RA, Smith MJ, Spillantini MG, Goedert M, Kretzschmar HA. Neumann M, et al. Among authors: kretzschmar ha. Ann Neurol. 2001 Oct;50(4):503-13. doi: 10.1002/ana.1223. Ann Neurol. 2001. PMID: 11601501

6

Selective insolubility of alpha-synuclein in human Lewy body diseases is recapitulated in a transgenic mouse model.

Kahle PJ, Neumann M, Ozmen L, Müller V, Odoy S, Okamoto N, Jacobsen H, Iwatsubo T, Trojanowski JQ, Takahashi H, Wakabayashi K, Bogdanovic N, Riederer P, Kretzschmar HA, Haass C. Kahle PJ, et al. Among authors: kretzschmar ha. Am J Pathol. 2001 Dec;159(6):2215-25. doi: 10.1016/s0002-9440(10)63072-6. Am J Pathol. 2001. PMID: 11733371 Free PMC article.

7

Mutant presenilins disturb neuronal calcium homeostasis in the brain of transgenic mice, decreasing the threshold for excitotoxicity and facilitating long-term potentiation.

Schneider I, Reverse D, Dewachter I, Ris L, Caluwaerts N, Kuiperi C, Gilis M, Geerts H, Kretzschmar H, Godaux E, Moechars D, Van Leuven F, Herms J. Schneider I, et al. J Biol Chem. 2001 Apr 13;276(15):11539-44. doi: 10.1074/jbc.M010977200. Epub 2001 Jan 23. J Biol Chem. 2001. PMID: 11278803 Free article.

8

Molecular cloning of a mink prion protein gene.

Kretzschmar HA, Neumann M, Riethmüller G, Prusiner SB. Kretzschmar HA, et al. J Gen Virol. 1992 Oct;73 ( Pt 10):2757-61. doi: 10.1099/0022-1317-73-10-2757. J Gen Virol. 1992. PMID: 1383401

9

Codon 178 mutation of the human prion protein gene in a German family (Backer family): sequencing data from 72-year-old celloidin-embedded brain tissue.

Kretzschmar HA, Neumann M, Stavrou D. Kretzschmar HA, et al. Acta Neuropathol. 1995;89(1):96-8. doi: 10.1007/BF00294264. Acta Neuropathol. 1995. PMID: 7709737

10

A new family with frontotemporal dementia with intronic 10+3 splice site mutation in the tau gene: neuropathology and molecular effects.

Neumann M, Mittelbronn M, Simon P, Vanmassenhove B, de Silva R, Lees A, Klapp J, Meyermann R, Kretzschmar HA. Neumann M, et al. Among authors: kretzschmar ha. Neuropathol Appl Neurobiol. 2005 Aug;31(4):362-73. doi: 10.1111/j.1365-2990.2005.00629.x. Neuropathol Appl Neurobiol. 2005. PMID: 16008820

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