Jahresbericht 2001/2002 - Fritz Thyssen Stiftung

361
ANHANG
Walter, Claudia, et al.: Disorders of peroxisome biogenesis due to
mutations in PEX1. Phenotypes and PEX1 protein levels. – In: Am J
Hum Genet. 69. 2001. S. 35–48.
Winkler, David T., et al.: Spontaneous hemorrhagic stroke in a
mouse model of cerebral amyloid angiopathy. – In: The Journal of
Neuroscience. 21(5). 2001. S. 1619–1627.
Winkler, David T., et al.: Thrombolysis induces cerebral hemorrhage
in a mouse model of cerebral amyloid angiopathy. – In: Annals of
Neurology. 51. 2002. S. 790–793.
Wirths, Oliver, et al: Intraneuronal A� accumulation precedes plaque
formation in �-amyloid precursor protein and presenilin-1 doubletransgenic
mice. – In: Neuroscience Letters. 306. 2001. S. 116–120)
Wirths, Oliver, et al: Intraneuronal APP/A� trafficking and plaque
formation in �-amyloid precursor protein and presenilin-1 transgenic
mice. – In: Brain Pathol. 12. 2002. S. 275–286.
Wirths, Oliver, et al: Reelin in plaques of �-amyloid precursor protein
and presenilin-1 double-transgenic mice. – In: Neuroscience
Letters. 316. 2001. S. 145–148.
Yu, Fang, et al.: Methyl-CpG-binding protein 2 represses LINE-1
expression and retrotransposition but not Alu transcription. – In:
Nucleic Acids Research. 29. 2001. S. 4493–4501.
Zinn-Justin, Anne, et al.: Multipoint development of the weighted
pairwise correlation (WPC) linkage method for pedigrees of arbitrary
size and application to the analysis of breast cancer and alcoholism
familial data. – In: Genetic Epidemiology. 21. 2001. S. 40–52.
Zühlke, Christine, et al.: Different types of repeat expansion in the
TATA-binding protein gene are associated with a new form of inherited
ataxia. – In: European Journal of Human Genetics. 9. 2001.
S. 160–164.
Zühlke, Christine, et al.: Spinocerebellar ataxia type 1 (SCA1). Phenotype-genotype
correlation studies in intermediate alleles. – In:
European Journal of Human Genetics. 10. 2002. S. 204–209.