5 Einträge gefunden

1. Mutations affecting the N-terminal domains of SHANK3 point to different pathomechanisms in neurodevelopmental disorders

   1. Woike, Daniel
   2. Wang, Emily
   3. Tibbe, Debora
   4. Hassani Nia, Fatemeh
   5. Failla, Antonio Virgilio
   6. Kibæk, Maria
   7. Overgård, Tinett Martesen

   2022 - Forschungsinformationssystem des UKE - frei zugänglich
2. Autism-associated SHANK3 missense point mutations impact conformational fluctuations and protein turnover at synapses

   1. Bucher, Michael
   2. Niebling, Stephan
   3. Han, Yuhao
   4. Molodenskiy, Dmitry
   5. Hassani Nia, Fatemeh
   6. Kreienkamp, Hans-Jürgen
   7. Svergun, Dmitri

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
3. Truncating mutations in SHANK3 associated with global developmental delay interfere with nuclear β-catenin signaling

   1. Hassani Nia, Fatemeh
   2. Woike, Daniel
   3. Kloth, Katja
   4. Kortüm, Fanny
   5. Kreienkamp, Hans-Jürgen

   2020 - Forschungsinformationssystem des UKE
4. Targeting of δ-catenin to postsynaptic sites through interaction with the Shank3 N-terminus

   1. Hassani Nia, Fatemeh
   2. Woike, Daniel
   3. Martens, Victoria
   4. Klüssendorf, Malte
   5. Hönck, Hans-Hinrich
   6. Harder, Sönke
   7. Kreienkamp, Hans-Jürgen

   2020 - Forschungsinformationssystem des UKE
5. Functional Relevance of Missense Mutations Affecting the N-Terminal Part of Shank3 Found in Autistic Patients

   1. Hassani Nia, Fatemeh
   2. Kreienkamp, Hans-Jürgen

   2018 - Forschungsinformationssystem des UKE - frei zugänglich