12 Einträge gefunden

1. RIT1 controls actin dynamics via complex formation with RAC1/CDC42 and PAK1

   1. Meyer Zum Büschenfelde, Uta
   2. Brandenstein, Laura Isabel
   3. von Elsner, Leonie
   4. Flato, Kristina
   5. Holling, Tess
   6. Zenker, Martin
   7. Rosenberger, Georg

   2018 - Forschungsinformationssystem des UKE - frei zugänglich
2. The role of the multidisciplinary health care team in the management of patients with Marfan syndrome

   1. von Kodolitsch, Yskert
   2. Rybczynski, Meike
   3. Vogler, Marina
   4. Mir, Thomas S
   5. Schüler, Helke
   6. Kutsche, Kerstin
   7. Rosenberger, Georg

   2016 - Forschungsinformationssystem des UKE - frei zugänglich
3. An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome

   1. Abdollahpour, Hengameh
   2. Alawi, Malik
   3. Kortüm, Fanny
   4. Beckstette, Michael
   5. Seemanova, Eva
   6. Komárek, Vladimír
   7. Rosenberger, Georg

   2015 - Forschungsinformationssystem des UKE
4. Exom-Sequenzierung zur Identifizierung von Krankheitsgenen für seltene Syndrome: Erfahrungen aus Hamburg

   1. Kortüm, Fanny
   2. Abdollahpour, Hengameh
   3. Alawi, Malik
   4. Korenke, Georg Christoph
   5. Seemanova, Eva
   6. Tinschert, Sigrid
   7. Zenker, Martin

   2014 - Forschungsinformationssystem des UKE
5. A 1-bp duplication in TGFB2 in three family members with a syndromic form of thoracic aortic aneurysm

   1. Leutermann, Ruth
   2. Sheikhzadeh, Sara
   3. Brockstädt, Lars
   4. Rybczynski, Meike
   5. van Rahden, Vanessa
   6. Kutsche, Kerstin
   7. Kodolitsch, Yskert

   2013 - Forschungsinformationssystem des UKE
6. Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies.

   1. Kortüm, Fanny
   2. Chyrek, Magdalena
   3. Fuchs, Sigrid
   4. Albrecht, B
   5. Gillessen-Kaesbach, G
   6. Mütze, U
   7. Seemanova, E

   2011 - Forschungsinformationssystem des UKE
7. Duplication of Glu37 in the switch I region of HRAS impairs effector/GAP binding and underlies Costello syndrome by promoting enhanced growth factor-dependent MAPK and AKT activation.

   1. Gremer, Lothar
   2. Alessandro, De Luca
   3. Merbitz-Zahradnik, Torsten
   4. Dallapiccola, Bruno
   5. Morlot, Susanne
   6. Tartaglia, Marco
   7. Kutsche, Kerstin

   2009 - Forschungsinformationssystem des UKE
8. Oncogenic HRAS mutations cause prolonged PI3K signaling in response to epidermal growth factor in fibroblasts of patients with Costello syndrome.

   1. Rosenberger, Georg
   2. Meien, Stefanie
   3. Kutsche, Kerstin

   2009 - Forschungsinformationssystem des UKE
9. Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome.

   1. Rau, Isabella
   2. Morleo, Manuela
   3. Rosenberger, Georg
   4. Iaconis, Daniela
   5. Orth, Ulrike
   6. Meinecke, Peter
   7. Lerer, Israela

   2006 - Forschungsinformationssystem des UKE
10. PAK4 and alphaPIX determine podosome size and number in macrophages through localized actin regulation.

    1. Gringel, Alexandra
    2. Walz, Daniel
    3. Rosenberger, Georg
    4. Minden, Audrey
    5. Kutsche, Kerstin
    6. Kopp, Petra
    7. Linder, Stefan

    2006 - Forschungsinformationssystem des UKE
11. AlphaPIX and betaPIX and their role in focal adhesion formation

    1. Rosenberger, Georg
    2. Kutsche, Kerstin

    2006 - Forschungsinformationssystem des UKE
12. AlphaPIX associates with calpain 4, the small subunit of calpain, and has a dual role in integrin-mediated cell spreading.

    1. Rosenberger, Georg
    2. Gal, Andreas
    3. Kutsche, Kerstin

    2005 - Forschungsinformationssystem des UKE