11 Einträge gefunden

1. OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67)

   1. Thoenes, Michaela
   2. Zimmermann, Ulrike
   3. Ebermann, Inga
   4. Ptok, Martin
   5. Lewis, Morag A
   6. Thiele, Holger
   7. Morlot, Susanne

   2015 - Forschungsinformationssystem des UKE - frei zugänglich
2. Ocular signs correlate well with disease severity and genotype in Fabry disease

   1. Pitz, Susanne
   2. Kalkum, Gisela
   3. Arash, Laila
   4. Karabul, Nesrin
   5. Sodi, Andrea
   6. Larroque, Sylvain
   7. Beck, Michael

   2015 - Forschungsinformationssystem des UKE - frei zugänglich
3. Radiosensitization of NSCLC cells by EGFR inhibition is the result of an enhanced p53-dependent G1 arrest

   1. Kriegs, Malte
   2. Gurtner, Kristin
   3. Can, Yildiz
   4. Brammer, Ingo
   5. Rieckmann, Thorsten
   6. Oertel, Reinhard
   7. Wysocki, Marek

   2015 - Forschungsinformationssystem des UKE
4. EGFRvIII does not affect radiosensitivity with or without gefitinib treatment in glioblastoma cells

   1. Struve, Nina
   2. Riedel, Matthias
   3. Schulte, Alexander
   4. Rieckmann, Thorsten
   5. Grob, Tobias J
   6. Gal, Andreas
   7. Rothkamm, Kai

   2015 - Forschungsinformationssystem des UKE
5. Dried Blood Spots Allow Targeted Screening to Diagnose Mucopolysaccharidosis and Mucolipidosis

   1. Cobos, Paulina Nieves
   2. Steglich, Cordula
   3. Santer, René
   4. Lukacs, Zoltan
   5. Gal, Andreas

   2014 - Forschungsinformationssystem des UKE - frei zugänglich
6. Mucopolysaccharidosis type II in a female carrying a heterozygous stop mutation of the iduronate-2-sulfatase gene and showing a skewed X chromosome inactivation.

   1. Piña-Aguilar, Raul E
   2. Zaragoza-Arévalo, Gerardo R
   3. Rau, Isabella
   4. Gal, Andreas
   5. Alcántara-Ortigoza, Miguel A
   6. López-Martínez, Mónica S
   7. Santillán-Hernández, Yuritzi

   2013 - Forschungsinformationssystem des UKE
7. Sorafenib sensitizes head and neck squamous cell carcinoma cells to ionizing radiation

   1. Laban, Simon
   2. Steinmeister, Leonhard
   3. Gleißner, Lisa
   4. Grob, Tobias J
   5. Grénman, Reidar
   6. Petersen, Cordula
   7. Gal, Andreas

   2013 - Forschungsinformationssystem des UKE
8. Toward a consensus in the laboratory diagnostics of Fabry disease - recommendations of a European expert group.

   1. Gal, Andreas
   2. Hughes, Derralynn A
   3. Winchester, Bryan

   2011 - Forschungsinformationssystem des UKE
9. Ccdc66 null mutation causes retinal degeneration and dysfunction.

   1. Gerding, Wanda M
   2. Schreiber, Sabrina
   3. Schulte-Middelmann, Tobias
   4. de Castro Marques, Andreia
   5. Atorf, Jenny
   6. Akkad, Denis A
   7. Dekomien, Gabriele

   2011 - Forschungsinformationssystem des UKE
10. Residual activity and proteasomal degradation of p.Ser298Pro sulfamidase identified in patients with a mild clinical phenotype of Sanfilippo A syndrome

    1. Muschol, Nicole
    2. Pohl, Sandra
    3. Meyer, Ann
    4. Gal, Andreas
    5. Ullrich, Kurt
    6. Braulke, Thomas

    2011 - Forschungsinformationssystem des UKE
11. Autosomal-recessive posterior microphthalmos is caused by mutations in PRSS56, a gene encoding a trypsin-like serine protease.

    1. Gal, Andreas
    2. Rau, Isabella
    3. Leila, El Matri
    4. Kreienkamp, Hans-Jürgen
    5. Fehr, Susanne
    6. Baklouti, Karim
    7. Chouchane, Ibtissem

    2011 - Forschungsinformationssystem des UKE