Scherzinger E - Search Results

1

HIP-I: a huntingtin interacting protein isolated by the yeast two-hybrid system.

Wanker EE, Rovira C, Scherzinger E, Hasenbank R, Wälter S, Tait D, Colicelli J, Lehrach H. Wanker EE, et al. Among authors: scherzinger e. Hum Mol Genet. 1997 Mar;6(3):487-95. doi: 10.1093/hmg/6.3.487. Hum Mol Genet. 1997. PMID: 9147654

2

A protein interaction network links GIT1, an enhancer of huntingtin aggregation, to Huntington's disease.

Goehler H, Lalowski M, Stelzl U, Waelter S, Stroedicke M, Worm U, Droege A, Lindenberg KS, Knoblich M, Haenig C, Herbst M, Suopanki J, Scherzinger E, Abraham C, Bauer B, Hasenbank R, Fritzsche A, Ludewig AH, Büssow K, Coleman SH, Gutekunst CA, Landwehrmeyer BG, Lehrach H, Wanker EE. Goehler H, et al. Among authors: scherzinger e. Mol Cell. 2004 Sep 24;15(6):853-65. doi: 10.1016/j.molcel.2004.09.016. Mol Cell. 2004. PMID: 15383276 Free article.

3

Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vitro and in vivo.

Scherzinger E, Lurz R, Turmaine M, Mangiarini L, Hollenbach B, Hasenbank R, Bates GP, Davies SW, Lehrach H, Wanker EE. Scherzinger E, et al. Cell. 1997 Aug 8;90(3):549-58. doi: 10.1016/s0092-8674(00)80514-0. Cell. 1997. PMID: 9267034 Free article.

4

Ataxin-3 is transported into the nucleus and associates with the nuclear matrix.

Tait D, Riccio M, Sittler A, Scherzinger E, Santi S, Ognibene A, Maraldi NM, Lehrach H, Wanker EE. Tait D, et al. Among authors: scherzinger e. Hum Mol Genet. 1998 Jun;7(6):991-7. doi: 10.1093/hmg/7.6.991. Hum Mol Genet. 1998. PMID: 9580663

5

SH3GL3 associates with the Huntingtin exon 1 protein and promotes the formation of polygln-containing protein aggregates.

Sittler A, Wälter S, Wedemeyer N, Hasenbank R, Scherzinger E, Eickhoff H, Bates GP, Lehrach H, Wanker EE. Sittler A, et al. Among authors: scherzinger e. Mol Cell. 1998 Oct;2(4):427-36. doi: 10.1016/s1097-2765(00)80142-2. Mol Cell. 1998. PMID: 9809064 Free article.

6

Self-assembly of polyglutamine-containing huntingtin fragments into amyloid-like fibrils: implications for Huntington's disease pathology.

Scherzinger E, Sittler A, Schweiger K, Heiser V, Lurz R, Hasenbank R, Bates GP, Lehrach H, Wanker EE. Scherzinger E, et al. Proc Natl Acad Sci U S A. 1999 Apr 13;96(8):4604-9. doi: 10.1073/pnas.96.8.4604. Proc Natl Acad Sci U S A. 1999. PMID: 10200309 Free PMC article.

7

Accumulation of mutant huntingtin fragments in aggresome-like inclusion bodies as a result of insufficient protein degradation.

Waelter S, Boeddrich A, Lurz R, Scherzinger E, Lueder G, Lehrach H, Wanker EE. Waelter S, et al. Among authors: scherzinger e. Mol Biol Cell. 2001 May;12(5):1393-407. doi: 10.1091/mbc.12.5.1393. Mol Biol Cell. 2001. PMID: 11359930 Free PMC article.

8

The huntingtin interacting protein HIP1 is a clathrin and alpha-adaptin-binding protein involved in receptor-mediated endocytosis.

Waelter S, Scherzinger E, Hasenbank R, Nordhoff E, Lurz R, Goehler H, Gauss C, Sathasivam K, Bates GP, Lehrach H, Wanker EE. Waelter S, et al. Among authors: scherzinger e. Hum Mol Genet. 2001 Aug 15;10(17):1807-17. doi: 10.1093/hmg/10.17.1807. Hum Mol Genet. 2001. PMID: 11532990

9

Huntingtin aggregation monitored by dynamic light scattering.

Georgalis Y, Starikov EB, Hollenbach B, Lurz R, Scherzinger E, Saenger W, Lehrach H, Wanker EE. Georgalis Y, et al. Among authors: scherzinger e. Proc Natl Acad Sci U S A. 1998 May 26;95(11):6118-21. doi: 10.1073/pnas.95.11.6118. Proc Natl Acad Sci U S A. 1998. PMID: 9600927 Free PMC article.

10

Aggregation of truncated GST-HD exon 1 fusion proteins containing normal range and expanded glutamine repeats.

Hollenbach B, Scherzinger E, Schweiger K, Lurz R, Lehrach H, Wanker EE. Hollenbach B, et al. Among authors: scherzinger e. Philos Trans R Soc Lond B Biol Sci. 1999 Jun 29;354(1386):991-4. doi: 10.1098/rstb.1999.0450. Philos Trans R Soc Lond B Biol Sci. 1999. PMID: 10434297 Free PMC article.

We have shown previously by electron microscopy that the purified glutathione S-transferase (GST)-Huntington's disease (HD) exon 1 fusion protein with 51 glutamine residues (GST-HD51) is an oligomer, and that site-specific proteolytic cleavage of this fusion protein results in th …

We have shown previously by electron microscopy that the purified glutathione S-transferase (GST)-Huntington's disease (HD) exon 1 fusion pr …

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