5 Einträge gefunden

1. A rare ancestral HLA-DRB1∗15:01~DQB1∗02:01 haplotype and its reversion in the same Western European family

   1. Binder, Thomas M C
   2. Kelsch, Reinhard
   3. Wikner, Julia M
   4. Aly, Lilian
   5. Brendel, Cornelia
   6. Alster, Ina
   7. Kühnl, Peter

   2015 - Forschungsinformationssystem des UKE
2. A novel presenilin 1 mutation (Ala275Val) as cause of early-onset familial Alzheimer disease

   1. Lüdecke, Daniel
   2. Becktepe, Jos S
   3. Lehmbeck, Jan T
   4. Finckh, Ulrich
   5. Yamamoto, Raina
   6. Jahn, Holger
   7. Boelmans, Kai

   2014 - Forschungsinformationssystem des UKE
3. Plexin B3 is genetically associated with verbal performance and white matter volume in human brain.

   1. Rujescu, D
   2. Meisenzahl, E M
   3. Krejcova, S
   4. Giegling, I
   5. Zetzsche, T
   6. Reiser, M
   7. Born, C M

   2007 - Forschungsinformationssystem des UKE
4. Elevated phenylalanine levels interfere with neurite outgrowth stimulated by the neuronal cell adhesion molecule L1 in vitro.

   1. Hartwig, Christine
   2. Gal, Andreas
   3. Santer, René
   4. Ullrich, Kurt
   5. Finckh, Ulrich
   6. Kreienkamp, Hans-Jürgen

   2006 - Forschungsinformationssystem des UKE
5. Novel mutations and repeated findings of mutations in familial Alzheimer disease.

   1. Finckh, Ulrich
   2. Kuschel, Christian
   3. Anagnostouli, Maria
   4. Patsouris, Efstratios
   5. Pantes, George V
   6. Gatzonis, Stylianos
   7. Kapaki, Elisabeth

   2005 - Forschungsinformationssystem des UKE