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1 - 25 of 48 results for author:"Weissmann C." in Literature citations

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The frontotemporal dementia mutation R406W blocks tau's interaction with the membrane in an annexin A2-dependent manner.

Gauthier-Kemper A., Weissmann C., Golovyashkina N., Sebo-Lemke Z., Drewes G., Gerke V., Heinisch J.J., Brandt R.

J. Cell Biol. 192:647-661(2011) · Mapped (8)

Spontaneous generation of mammalian prions.

Edgeworth J.A., Gros N., Alden J., Joiner S., Wadsworth J.D., Linehan J., Brandner S., Jackson G.S., Weissmann C., Collinge J.

Proc. Natl. Acad. Sci. U.S.A. 107:14402-14406(2010) · Mapped (6)

Chronic lymphocytic inflammation specifies the organ tropism of prions.

Heikenwalder M., Zeller N., Seeger H., Prinz M., Klohn P.C., Schwarz P., Ruddle N.H., Weissmann C., Aguzzi A.

Science 307:1107-1110(2005) · Mapped (13)

A mouse to remember.

Weissmann C., Bueler H.

Cell 116:S111-3, 2 p following 2004:S113-S113(2004) · Mapped (8)

Transgene-driven expression of the Doppel protein in Purkinje cells causes Purkinje cell degeneration and motor impairment.

Anderson L., Rossi D., Linehan J., Brandner S., Weissmann C.

Proc. Natl. Acad. Sci. U.S.A. 101:3644-3649(2004) · Mapped (4)

Expression of truncated PrP targeted to Purkinje cells of PrP knockout mice causes Purkinje cell death and ataxia.

Flechsig E., Hegyi I., Leimeroth R., Zuniga A., Rossi D., Cozzio A., Schwarz P., Rulicke T., Gotz J., Aguzzi A. et al.

EMBO J. 22:3095-3101(2003) · Mapped (8)

B lymphocyte-restricted expression of prion protein does not enable prion replication in prion protein knockout mice.

Montrasio F., Cozzio A., Flechsig E., Rossi D., Klein M.A., Rulicke T., Raeber A.J., Vosshenrich C.A., Proft J., Aguzzi A. et al.

Proc. Natl. Acad. Sci. U.S.A. 98:4034-4037(2001) · Mapped (6)

Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain.

Rossi D., Cozzio A., Flechsig E., Klein M.A., Rulicke T., Aguzzi A., Weissmann C.

EMBO J. 20:694-702(2001) · Mapped (9)

Prion protein devoid of the octapeptide repeat region restores susceptibility to scrapie in PrP knockout mice.

Flechsig E., Shmerling D., Hegyi I., Raeber A.J., Fischer M., Cozzio A., von Mering C., Aguzzi A., Weissmann C.

Neuron 27:399-408(2000) · Mapped (6)

Genetic background changes the pattern of forebrain commissure defects in transgenic mice underexpressing the beta-amyloid-precursor protein.

Magara F., Muller U., Li Z.W., Lipp H.P., Weissmann C., Stagljar M., Wolfer D.P.

Proc. Natl. Acad. Sci. U.S.A. 96:4656-4661(1999) · Mapped (8)

Molecular genetics of transmissible spongiform encephalopathies.

Weissmann C.

J. Biol. Chem. 274:3-6(1999) · Mapped (6)

Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions.

Shmerling D., Hegyi I., Fischer M., Blattler T., Brandner S., Gotz J., Rulicke T., Flechsig E., Cozzio A., von Mering C. et al.

Cell 93:203-214(1998) · Mapped (6)

Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie.

Raeber A.J., Race R.E., Brandner S., Priola S.A., Sailer A., Bessen R.A., Mucke L., Manson J., Aguzzi A., Oldstone M.B. et al.

EMBO J. 16:6057-6065(1997) · Mapped (6)

Deficient cytokine signaling in mouse embryo fibroblasts with a targeted deletion in the PKR gene: role of IRF-1 and NF-kappaB.

Kumar A., Yang Y.L., Flati V., Der S., Kadereit S., Deb A., Haque J., Reis L., Weissmann C., Williams B.R.

EMBO J. 16:406-416(1997) · Mapped (3)

Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system.

Brandner S., Raeber A., Sailer A., Blattler T., Fischer M., Weissmann C., Aguzzi A.

Proc. Natl. Acad. Sci. U.S.A. 93:13148-13151(1996) · Mapped (6)

High prion and PrPSc levels but delayed onset of disease in scrapie-inoculated mice heterozygous for a disrupted PrP gene.

Bueler H., Raeber A., Sailer A., Fischer M., Aguzzi A., Weissmann C.

Mol. Med. 1:19-30(1994) · Mapped (6)

Generation of mice with a 200-kb amyloid precursor protein gene deletion by Cre recombinase-mediated site-specific recombination in embryonic stem cells.

Li Z.W., Stark G., Gotz J., Rulicke T., Gschwind M., Huber G., Muller U., Weissmann C.

Proc. Natl. Acad. Sci. U.S.A. 93:6158-6162(1996) · Mapped (8)

Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie.

Fischer M., Rulicke T., Raeber A., Sailer A., Moser M., Oesch B., Brandner S., Aguzzi A., Weissmann C.

EMBO J. 15:1255-1264(1996) · Mapped (6)

Deficient signaling in mice devoid of double-stranded RNA-dependent protein kinase.

Yang Y.L., Reis L.F., Pavlovic J., Aguzzi A., Schafer R., Kumar A., Williams B.R., Aguet M., Weissmann C.

EMBO J. 14:6095-6106(1995) · Mapped (3)

Normal host prion protein necessary for scrapie-induced neurotoxicity.

Brandner S., Isenmann S., Raeber A., Fischer M., Sailer A., Kobayashi Y., Marino S., Weissmann C., Aguzzi A.

Nature 379:339-343(1996) · Mapped (6)

Role of the PrP gene in transmissible spongiform encephalopathies.

Weissmann C., Bueler H., Fischer M., Aguet M.

Intervirology 35:164-175(1993) · Mapped (6)

Induction of type I interferon genes and interferon-inducible genes in embryonal stem cells devoid of interferon regulatory factor 1.

Ruffner H., Reis L.F., Naf D., Weissmann C.

Proc. Natl. Acad. Sci. U.S.A. 90:11503-11507(1993) · Mapped (9)

Mice devoid of PrP are resistant to scrapie.

Bueler H., Aguzzi A., Sailer A., Greiner R.A., Autenried P., Aguet M., Weissmann C.

Cell 73:1339-1347(1993) · Mapped (6)

PrP-deficient mice are resistant to scrapie.

Weissmann C., Bueler H., Fischer M., Sailer A., Aguzzi A., Aguet M.

Ann. N. Y. Acad. Sci. 724:235-240(1994) · Mapped (6)

Behavioral and anatomical deficits in mice homozygous for a modified beta-amyloid precursor protein gene.

Muller U., Cristina N., Li Z.W., Wolfer D.P., Lipp H.P., Rulicke T., Brandner S., Aguzzi A., Weissmann C.

Cell 79:755-765(1994) · Mapped (8)

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