W. Schulz-Schaeffer

Publication List Details

Period

2000 - 2006

Number

12

Co-Authors

LPS receptor (CD14): a receptor for phagocytosis of Alzheimer’s amyloid peptide (2005)

Liu, Y., Walter, S., Stagi, M., Cherny, D. I., Letiembre, M., Schulz-Schaeffer, W., ...

The amyloid β peptide 42 (Aβ₄₂) plays a key role in neurotoxicity in Alzheimer’s disease. Mononuclear phagocytes, i.e. microglia, have the potential to clear Aβ by phagocytosis. Recently,...

Ultrasensitive detection of pathological prion protein aggregates by dual-color scanning for intensely fluorescent targets

Bieschke, J., Giese, A., Schulz-Schaeffer, W., Zerr, I., Poser, S., Eigen, M., ...

A definite diagnosis of prion diseases such as Creutzfeldt–Jakob disease (CJD) relies on the detection of pathological prion protein (PrPSc). However, no test for PrPSc in cerebrospinal fluid (CSF)...

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., ...

Transmissible mink encephalopathy (TME) is a rare disease of the North American mink, which has never been successfully transmitted to laboratory mice. We generated transgenic mice expressing the...

Ultrasensitive detection of pathological prion protein aggregates by dual-color scanning for intensely fluorescent targets

Bieschke, J., Giese, A., Schulz-Schaeffer, W., Zerr, I., Poser, S., Eigen, M., ...

A definite diagnosis of prion diseases such as Creutzfeldt–Jakob disease (CJD) relies on the detection of pathological prion protein (PrPSc). However, no test for PrPSc in cerebrospinal fluid (CSF)...

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., ...

Transmissible mink encephalopathy (TME) is a rare disease of the North American mink, which has never been successfully transmitted to laboratory mice. We generated transgenic mice expressing the...

Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2

Samman, I., Schulz-Schaeffer, W, Wohrle, J, Sommer, A, Kretzschmar, H, Hennerici, M

A 68 year old woman with sporadic Creutzfeldt-Jakob disease is described, who neither showed characteristic EEG abnormalities nor a positive test of the neuronal protein 14-3-3 or neuron specific...

Patients with Alzheimer's disease and dementia with Lewy bodies mistaken for Creutzfeldt-Jakob disease

Tschampa, H, Neumann, M, Zerr, I, Henkel, K, Schroter, A, Schulz-Schaeffer, W, ...

OBJECTIVES—To describe the clinical presentation of patients with Alzheimer's disease (AD) or dementia with Lewy bodies (DLB) who were suspected of having Creutzfeldt-Jakob disease (CJD) and to...