Jahresbericht 2001/2002 - Fritz Thyssen Stiftung

Ethnologie
Mallebrein, Cornelia: Living gods on earth. Exhibition: Indian folk
and tribal traditions. – In: German News. 43, Febr. 2002. S. 17/18.
Mallebrein, Cornelia: Living gods on earth. Indian folk and tribal
traditions. Exhibition of photographs. – New Delhi: Archana, 2002.
22 S.
Medizin und Naturwissenschaften
ANHANG 356
Abicht, Angela, et al.: A newly identified chromosomal microdeletion
and an N-box mutation of the AChRε gene cause a congenital
myasthenic syndrome. In: Brain. 125. 2002. S. 1005–1013.
Ahrens, Wilhelm: Scherz und Ernst in der Mathematik. Geflügelte
und ungeflügelte Worte. Nachdr. der Ausg. Leipzig 1904. Mit einer
Einl. hrsg. von Jochen Brüning. – Hildesheim usw.: Olms-Weidmann,
2002. X, 522 S. (Historia Scientiarum: Fachgebiet Mathematik
und Astronomie)
Aigner, Ludwig, et al.: Isolated lissencephaly sequence and doublecortex
syndrome in a German family with a novel doublecortin
mutation. – In: Neuropediatrics. 31. 2000. S. 195–198.
Bayer, Thomas A., et al.: Key factors in Alzheimer’s disease. �-amyloid
precursor protein processing, metabolism and intraneuronal
transport. – In: Brain Pathology. 11. 2001. S. 1–11.
Becker, Lore, et al.: Disease-specific human glycine receptor α 1 subunit
causes hyperekplexia phenotype and impaired glycine- and
GABA A-receptor transmission in transgenic mice. – In: The Journal
of Neuroscience. 22. 2002. S. 2505–2512.
Biniszkiewicz, Detlev, et al.: Dnmt1 overexpression causes genomic
hypermethylation, loss of imprinting, and embryonic lethality. – In:
Molecular and Cellular Biology. 22. 2002. S. 2124–2135.
Brandt, Thomas: Modelling brain function: the vestibulo-ocular
reflex. – In: Current Opinion in Neurology. 14. 2001. S. 1–4.
Brocke, Katja S., et al.: The human intronless melanocortin 4-receptor
gene is NMD insensitive. – In: Human Molecular Genetics. 11.
2002. S. 331–335.
Cahana, A., et al.: LIS1 homodimerization and brain development. –
In: Proc Natl Acad Sci USA. 98. 2001. S. 6429–6434.
Couillard-Despres, S. et al.: Molecular mechanisms of neuronal
migration disorder, quo vadis? – In: Current Molecular Medicine. 1.
2001. S. 677–688.