Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 56

1.

A protein quality control pathway regulated by linear ubiquitination.

van Well EM, Bader V, Patra M, Sánchez-Vicente A, Meschede J, Furthmann N, Schnack C, Blusch A, Longworth J, Petrasch-Parwez E, Mori K, Arzberger T, Trümbach D, Angersbach L, Showkat C, Sehr DA, Berlemann LA, Goldmann P, Clement AM, Behl C, Woerner AC, Saft C, Wurst W, Haass C, Ellrichmann G, Gold R, Dittmar G, Hipp MS, Hartl FU, Tatzelt J, Winklhofer KF.

EMBO J. 2019 May 2;38(9). pii: e100730. doi: 10.15252/embj.2018100730. Epub 2019 Mar 18.

PMID:
30886048
2.

Neurodegeneration in the olfactory bulb and olfactory deficits in the Ccdc66 -/- mouse model for retinal degeneration.

Schreiber S, Petrasch-Parwez E, Porrmann-Kelterbaum E, Förster E, Epplen JT, Gerding WM.

IBRO Rep. 2018 Aug 24;5:43-53. doi: 10.1016/j.ibror.2018.08.004. eCollection 2018 Dec.

3.

Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families.

Kastner S, Thiemann IJ, Dekomien G, Petrasch-Parwez E, Schreiber S, Akkad DA, Gerding WM, Hoffjan S, Günes S, Günes S, Bagci H, Epplen JT.

Invest Ophthalmol Vis Sci. 2015 Dec;56(13):8045-53. doi: 10.1167/iovs.15-17473.

PMID:
26720455
4.

Association of variation in the LAMA3 gene, encoding the alpha-chain of laminin 5, with atopic dermatitis in a German case-control cohort.

Stemmler S, Parwez Q, Petrasch-Parwez E, Epplen JT, Hoffjan S.

BMC Dermatol. 2014 Nov 3;14:17. doi: 10.1186/1471-5945-14-17.

5.

SOX9 duplication linked to intersex in deer.

Kropatsch R, Dekomien G, Akkad DA, Gerding WM, Petrasch-Parwez E, Young ND, Altmüller J, Nürnberg P, Gasser RB, Epplen JT.

PLoS One. 2013 Sep 6;8(9):e73734. doi: 10.1371/journal.pone.0073734. eCollection 2013.

6.

Inactivation of ceramide synthase 6 in mice results in an altered sphingolipid metabolism and behavioral abnormalities.

Ebel P, Vom Dorp K, Petrasch-Parwez E, Zlomuzica A, Kinugawa K, Mariani J, Minich D, Ginkel C, Welcker J, Degen J, Eckhardt M, Dere E, Dörmann P, Willecke K.

J Biol Chem. 2013 Jul 19;288(29):21433-47. doi: 10.1074/jbc.M113.479907. Epub 2013 Jun 12.

7.

A novel transgenic rat model for spinocerebellar ataxia type 17 recapitulates neuropathological changes and supplies in vivo imaging biomarkers.

Kelp A, Koeppen AH, Petrasch-Parwez E, Calaminus C, Bauer C, Portal E, Yu-Taeger L, Pichler B, Bauer P, Riess O, Nguyen HP.

J Neurosci. 2013 May 22;33(21):9068-81. doi: 10.1523/JNEUROSCI.5622-12.2013.

8.

Postsynaptic NO/cGMP increases NMDA receptor currents via hyperpolarization-activated cyclic nucleotide-gated channels in the hippocampus.

Neitz A, Mergia E, Imbrosci B, Petrasch-Parwez E, Eysel UT, Koesling D, Mittmann T.

Cereb Cortex. 2014 Jul;24(7):1923-36. doi: 10.1093/cercor/bht048. Epub 2013 Feb 28.

PMID:
23448871
9.

Pannexin1 stabilizes synaptic plasticity and is needed for learning.

Prochnow N, Abdulazim A, Kurtenbach S, Wildförster V, Dvoriantchikova G, Hanske J, Petrasch-Parwez E, Shestopalov VI, Dermietzel R, Manahan-Vaughan D, Zoidl G.

PLoS One. 2012;7(12):e51767. doi: 10.1371/journal.pone.0051767. Epub 2012 Dec 20. Erratum in: PLoS One. 2013;8(1). doi:10.1371/annotation/d0972416-5fef-4f89-9c09-cb4cb0c6295d.

10.

A novel BACHD transgenic rat exhibits characteristic neuropathological features of Huntington disease.

Yu-Taeger L, Petrasch-Parwez E, Osmand AP, Redensek A, Metzger S, Clemens LE, Park L, Howland D, Calaminus C, Gu X, Pichler B, Yang XW, Riess O, Nguyen HP.

J Neurosci. 2012 Oct 31;32(44):15426-38. doi: 10.1523/JNEUROSCI.1148-12.2012.

11.

Selective hippocampal neurodegeneration in transgenic mice expressing small amounts of truncated Aβ is induced by pyroglutamate-Aβ formation.

Alexandru A, Jagla W, Graubner S, Becker A, Bäuscher C, Kohlmann S, Sedlmeier R, Raber KA, Cynis H, Rönicke R, Reymann KG, Petrasch-Parwez E, Hartlage-Rübsamen M, Waniek A, Rossner S, Schilling S, Osmand AP, Demuth HU, von Hörsten S.

J Neurosci. 2011 Sep 7;31(36):12790-801. doi: 10.1523/JNEUROSCI.1794-11.2011.

12.

Olfactory neuron-specific expression of A30P α-synuclein exacerbates dopamine deficiency and hyperactivity in a novel conditional model of early Parkinson's disease stages.

Nuber S, Petrasch-Parwez E, Arias-Carrión O, Koch L, Kohl Z, Schneider J, Calaminus C, Dermietzel R, Samarina A, Boy J, Nguyen HP, Teismann P, Velavan TP, Kahle PJ, von Hörsten S, Fendt M, Krüger R, Riess O.

Neurobiol Dis. 2011 Nov;44(2):192-204. doi: 10.1016/j.nbd.2011.06.017. Epub 2011 Jul 5.

PMID:
21767644
13.

Neuroanatomical correlates of suicide in psychosis: the possible role of von Economo neurons.

Brüne M, Schöbel A, Karau R, Faustmann PM, Dermietzel R, Juckel G, Petrasch-Parwez E.

PLoS One. 2011;6(6):e20936. doi: 10.1371/journal.pone.0020936. Epub 2011 Jun 22.

14.

Ccdc66 null mutation causes retinal degeneration and dysfunction.

Gerding WM, Schreiber S, Schulte-Middelmann T, de Castro Marques A, Atorf J, Akkad DA, Dekomien G, Kremers J, Dermietzel R, Gal A, Rülicke T, Ibrahim S, Epplen JT, Petrasch-Parwez E.

Hum Mol Genet. 2011 Sep 15;20(18):3620-31. doi: 10.1093/hmg/ddr282. Epub 2011 Jun 16.

PMID:
21680557
15.

Efficacy of fumaric acid esters in the R6/2 and YAC128 models of Huntington's disease.

Ellrichmann G, Petrasch-Parwez E, Lee DH, Reick C, Arning L, Saft C, Gold R, Linker RA.

PLoS One. 2011 Jan 31;6(1):e16172. doi: 10.1371/journal.pone.0016172.

16.

Theta-burst transcranial magnetic stimulation alters cortical inhibition.

Benali A, Trippe J, Weiler E, Mix A, Petrasch-Parwez E, Girzalsky W, Eysel UT, Erdmann R, Funke K.

J Neurosci. 2011 Jan 26;31(4):1193-203. doi: 10.1523/JNEUROSCI.1379-10.2011.

17.

Signal transducer and activator of transcription 3-mediated regulation of miR-199a-5p links cardiomyocyte and endothelial cell function in the heart: a key role for ubiquitin-conjugating enzymes.

Haghikia A, Missol-Kolka E, Tsikas D, Venturini L, Brundiers S, Castoldi M, Muckenthaler MU, Eder M, Stapel B, Thum T, Haghikia A, Petrasch-Parwez E, Drexler H, Hilfiker-Kleiner D, Scherr M.

Eur Heart J. 2011 May;32(10):1287-97. doi: 10.1093/eurheartj/ehq369. Epub 2010 Oct 21.

PMID:
20965886
18.

Generalized progressive retinal atrophy in the Irish Glen of Imaal Terrier is associated with a deletion in the ADAM9 gene.

Kropatsch R, Petrasch-Parwez E, Seelow D, Schlichting A, Gerding WM, Akkad DA, Epplen JT, Dekomien G.

Mol Cell Probes. 2010 Dec;24(6):357-63. doi: 10.1016/j.mcp.2010.07.007. Epub 2010 Aug 4.

PMID:
20691256
19.

Variation in the COL29A1 gene in German patients with atopic dermatitis, asthma and chronic obstructive pulmonary disease.

Harazin M, Parwez Q, Petrasch-Parwez E, Epplen JT, Arinir U, Hoffjan S, Stemmler S.

J Dermatol. 2010 Aug;37(8):740-2. doi: 10.1111/j.1346-8138.2010.00923.x. No abstract available.

PMID:
20649719
20.

First appraisal of brain pathology owing to A30P mutant alpha-synuclein.

Seidel K, Schöls L, Nuber S, Petrasch-Parwez E, Gierga K, Wszolek Z, Dickson D, Gai WP, Bornemann A, Riess O, Rami A, Den Dunnen WF, Deller T, Rüb U, Krüger R.

Ann Neurol. 2010 May;67(5):684-9. doi: 10.1002/ana.21966. Erratum in: Ann Neurol. 2010 Jun;67(6):841.

PMID:
20437567
21.

Von Economo neuron density in the anterior cingulate cortex is reduced in early onset schizophrenia.

Brüne M, Schöbel A, Karau R, Benali A, Faustmann PM, Juckel G, Petrasch-Parwez E.

Acta Neuropathol. 2010 Jun;119(6):771-8. doi: 10.1007/s00401-010-0673-2. Epub 2010 Mar 23.

PMID:
20309567
22.

Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene.

Dekomien G, Vollrath C, Petrasch-Parwez E, Boevé MH, Akkad DA, Gerding WM, Epplen JT.

Neurogenetics. 2010 May;11(2):163-74. doi: 10.1007/s10048-009-0223-z. Epub 2009 Sep 24.

PMID:
19777273
23.

Unintended spread of a biosafety level 2 recombinant retrovirus.

Stang A, Petrasch-Parwez E, Brandt S, Dermietzel R, Meyer HE, Stühler K, Liffers ST, Uberla K, Grunwald T.

Retrovirology. 2009 Sep 22;6:86. doi: 10.1186/1742-4690-6-86.

24.

Variation in genes of the epidermal differentiation complex in German atopic dermatitis patients.

Stemmler S, Nothnagel M, Parwez Q, Petrasch-Parwez E, Epplen JT, Hoffjan S.

Int J Immunogenet. 2009 Aug;36(4):217-22. doi: 10.1111/j.1744-313X.2009.00858.x.

PMID:
19601998
25.

Analysis of variation in the IL7RA and IL2RA genes in atopic dermatitis.

Hoffjan S, Beygo J, Akkad DA, Parwez Q, Petrasch-Parwez E, Epplen JT.

J Dermatol Sci. 2009 Aug;55(2):138-40. doi: 10.1016/j.jdermsci.2009.05.001. Epub 2009 Jun 11. No abstract available.

PMID:
19523791
26.

Variation in the IL7RA and IL2RA genes in German multiple sclerosis patients.

Akkad DA, Hoffjan S, Petrasch-Parwez E, Beygo J, Gold R, Epplen JT.

J Autoimmun. 2009 Mar;32(2):110-5. doi: 10.1016/j.jaut.2009.01.002. Epub 2009 Feb 23.

PMID:
19231135
27.

Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites.

Gierga K, Schelhaas HJ, Brunt ER, Seidel K, Scherzed W, Egensperger R, de Vos RA, den Dunnen W, Ippel PF, Petrasch-Parwez E, Deller T, Schöls L, Rüb U.

Neuropathol Appl Neurobiol. 2009 Oct;35(5):515-27. doi: 10.1111/j.1365-2990.2009.01015.x. Epub 2009 Jan 30.

PMID:
19207264
28.

Variation in the BDNF and NGFB genes in German atopic dermatitis patients.

Hoffjan S, Parwez Q, Petrasch-Parwez E, Stemmler S.

Mol Cell Probes. 2009 Feb;23(1):35-8. doi: 10.1016/j.mcp.2008.10.005. Epub 2008 Nov 11.

PMID:
19038326
29.

No evidence of an association between polymorphisms in the IRAK-M gene and atopic dermatitis in a German cohort.

Beygo J, Parwez Q, Petrasch-Parwez E, Epplen JT, Hoffjan S.

Mol Cell Probes. 2009 Feb;23(1):16-9. doi: 10.1016/j.mcp.2008.10.002. Epub 2008 Oct 26.

PMID:
19013233
30.

Neurodegeneration and motor dysfunction in a conditional model of Parkinson's disease.

Nuber S, Petrasch-Parwez E, Winner B, Winkler J, von Hörsten S, Schmidt T, Boy J, Kuhn M, Nguyen HP, Teismann P, Schulz JB, Neumann M, Pichler BJ, Reischl G, Holzmann C, Schmitt I, Bornemann A, Kuhn W, Zimmermann F, Servadio A, Riess O.

J Neurosci. 2008 Mar 5;28(10):2471-84. doi: 10.1523/JNEUROSCI.3040-07.2008.

31.

Characterization of connexin31.1-deficient mice reveals impaired placental development.

Zheng-Fischhöfer Q, Kibschull M, Schnichels M, Kretz M, Petrasch-Parwez E, Strotmann J, Reucher H, Lynn BD, Nagy JI, Lye SJ, Winterhager E, Willecke K.

Dev Biol. 2007 Dec 1;312(1):258-71. Epub 2007 Sep 26.

32.

Polymorphisms in NACHT-LRR (NLR) genes in atopic dermatitis.

Macaluso F, Nothnagel M, Parwez Q, Petrasch-Parwez E, Bechara FG, Epplen JT, Hoffjan S.

Exp Dermatol. 2007 Aug;16(8):692-8.

PMID:
17620097
33.

Localization of the pannexin1 protein at postsynaptic sites in the cerebral cortex and hippocampus.

Zoidl G, Petrasch-Parwez E, Ray A, Meier C, Bunse S, Habbes HW, Dahl G, Dermietzel R.

Neuroscience. 2007 Apr 25;146(1):9-16. Epub 2007 Mar 26.

PMID:
17379420
34.

Association of toll-interacting protein gene polymorphisms with atopic dermatitis.

Schimming TT, Parwez Q, Petrasch-Parwez E, Nothnagel M, Epplen JT, Hoffjan S.

BMC Dermatol. 2007 Mar 16;7:3.

35.

Haplotype-defined linkage region for gPRA in Schapendoes dogs.

Lippmann T, Jonkisz A, Dobosz T, Petrasch-Parwez E, Epplen JT, Dekomien G.

Mol Vis. 2007 Feb 7;13:174-80.

36.

Cellular and subcellular localization of Huntingtin [corrected] aggregates in the brain of a rat transgenic for Huntington disease.

Petrasch-Parwez E, Nguyen HP, Löbbecke-Schumacher M, Habbes HW, Wieczorek S, Riess O, Andres KH, Dermietzel R, Von Hörsten S.

J Comp Neurol. 2007 Apr 10;501(5):716-30. Erratum in: J Comp Neurol. 2007 May 20;502(3):483.

PMID:
17299753
37.

Association screen for atopic dermatitis candidate gene regions using microsatellite markers in pooled DNA samples.

Hoffjan S, Parwez Q, Petrasch-Parwez E, Falkenstein D, Nothnagel M, Epplen JT.

Int J Immunogenet. 2006 Dec;33(6):401-9.

PMID:
17117949
38.

Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7.

Rüb U, Brunt ER, Petrasch-Parwez E, Schöls L, Theegarten D, Auburger G, Seidel K, Schultz C, Gierga K, Paulson H, van Broeckhoven C, Deller T, de Vos RA.

Neuropathol Appl Neurobiol. 2006 Dec;32(6):635-49.

PMID:
17083478
39.

Two common loss-of-function mutations within the filaggrin gene predispose for early onset of atopic dermatitis.

Stemmler S, Parwez Q, Petrasch-Parwez E, Epplen JT, Hoffjan S.

J Invest Dermatol. 2007 Mar;127(3):722-4. Epub 2006 Sep 28. No abstract available.

40.

Behavioral abnormalities precede neuropathological markers in rats transgenic for Huntington's disease.

Nguyen HP, Kobbe P, Rahne H, Wörpel T, Jäger B, Stephan M, Pabst R, Holzmann C, Riess O, Korr H, Kántor O, Petrasch-Parwez E, Wetzel R, Osmand A, von Hörsten S.

Hum Mol Genet. 2006 Nov 1;15(21):3177-94. Epub 2006 Sep 19.

PMID:
16984963
41.

Cellular and subcellular localization of paralemmin-1, a protein involved in cell shape control, in the rat brain, adrenal gland and kidney.

Kutzleb C, Petrasch-Parwez E, Kilimann MW.

Histochem Cell Biol. 2007 Jan;127(1):13-30. Epub 2006 Jul 18.

PMID:
16847661
42.
43.

Is the retina affected in Huntington disease?

Petrasch-Parwez E, Saft C, Schlichting A, Andrich J, Napirei M, Arning L, Wieczorek S, Dermietzel R, Epplen JT.

Acta Neuropathol. 2005 Nov;110(5):523-5. Epub 2005 Oct 13. No abstract available.

PMID:
16222522
44.

Evaluation of the toll-like receptor 6 Ser249Pro polymorphism in patients with asthma, atopic dermatitis and chronic obstructive pulmonary disease.

Hoffjan S, Stemmler S, Parwez Q, Petrasch-Parwez E, Arinir U, Rohde G, Reinitz-Rademacher K, Schultze-Werninghaus G, Bufe A, Epplen JT.

BMC Med Genet. 2005 Sep 28;6:34.

45.

Loss of connexin36 increases retinal cell vulnerability to secondary cell loss.

Striedinger K, Petrasch-Parwez E, Zoidl G, Napirei M, Meier C, Eysel UT, Dermietzel R.

Eur J Neurosci. 2005 Aug;22(3):605-16.

PMID:
16101742
46.

Fine-structural analysis and connexin expression in the retina of a transgenic model of Huntington's disease.

Petrasch-Parwez E, Habbes HW, Weickert S, Löbbecke-Schumacher M, Striedinger K, Wieczorek S, Dermietzel R, Epplen JT.

J Comp Neurol. 2004 Nov 8;479(2):181-97.

PMID:
15452853
47.

Expression pattern of lacZ reporter gene representing connexin36 in transgenic mice.

Degen J, Meier C, Van Der Giessen RS, Söhl G, Petrasch-Parwez E, Urschel S, Dermietzel R, Schilling K, De Zeeuw CI, Willecke K.

J Comp Neurol. 2004 Jun 7;473(4):511-25.

PMID:
15116387
48.

Deformation of network connectivity in the inferior olive of connexin 36-deficient mice is compensated by morphological and electrophysiological changes at the single neuron level.

De Zeeuw CI, Chorev E, Devor A, Manor Y, Van Der Giessen RS, De Jeu MT, Hoogenraad CC, Bijman J, Ruigrok TJ, French P, Jaarsma D, Kistler WM, Meier C, Petrasch-Parwez E, Dermietzel R, Sohl G, Gueldenagel M, Willecke K, Yarom Y.

J Neurosci. 2003 Jun 1;23(11):4700-11.

49.

Evidence for a role of the N-terminal domain in subcellular localization of the neuronal connexin36 (Cx36).

Zoidl G, Meier C, Petrasch-Parwez E, Zoidl C, Habbes HW, Kremer M, Srinivas M, Spray DC, Dermietzel R.

J Neurosci Res. 2002 Aug 15;69(4):448-65.

PMID:
12210839
50.

Immunohistochemical detection of the neuronal connexin36 in the mouse central nervous system in comparison to connexin36-deficient tissues.

Meier C, Petrasch-Parwez E, Habbes HW, Teubner B, Güldenagel M, Degen J, Söhl G, Willecke K, Dermietzel R.

Histochem Cell Biol. 2002 Jun;117(6):461-71. Epub 2002 Jun 8.

PMID:
12107497

Supplemental Content

Loading ...
Support Center