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Medientyp
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Autor/in
- Gal, Andreas
- Grob, Tobias J 3
- Kriegs, Malte 3
- Dikomey, Ekkehard 2
- Laban, Simon 2
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Sprache
11 Einträge gefunden
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OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67)
- Thoenes, Michaela
- Zimmermann, Ulrike
- Ebermann, Inga
- Ptok, Martin
- Lewis, Morag A
- Thiele, Holger
- Morlot, Susanne
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EGFRvIII does not affect radiosensitivity with or without gefitinib treatment in glioblastoma cells
- Struve, Nina
- Riedel, Matthias
- Schulte, Alexander
- Rieckmann, Thorsten
- Grob, Tobias J
- Gal, Andreas
- Rothkamm, Kai
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Ocular signs correlate well with disease severity and genotype in Fabry disease
- Pitz, Susanne
- Kalkum, Gisela
- Arash, Laila
- Karabul, Nesrin
- Sodi, Andrea
- Larroque, Sylvain
- Beck, Michael
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Dried Blood Spots Allow Targeted Screening to Diagnose Mucopolysaccharidosis and Mucolipidosis
2014 - Forschungsinformationssystem des UKE - frei zugänglich -
Sorafenib sensitizes head and neck squamous cell carcinoma cells to ionizing radiation
- Laban, Simon
- Steinmeister, Leonhard
- Gleißner, Lisa
- Grob, Tobias J
- Grénman, Reidar
- Petersen, Cordula
- Gal, Andreas
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Mucopolysaccharidosis type II in a female carrying a heterozygous stop mutation of the iduronate-2-sulfatase gene and showing a skewed X chromosome inactivation.
- Piña-Aguilar, Raul E
- Zaragoza-Arévalo, Gerardo R
- Rau, Isabella
- Gal, Andreas
- Alcántara-Ortigoza, Miguel A
- López-Martínez, Mónica S
- Santillán-Hernández, Yuritzi
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Ccdc66 null mutation causes retinal degeneration and dysfunction.
- Gerding, Wanda M
- Schreiber, Sabrina
- Schulte-Middelmann, Tobias
- de Castro Marques, Andreia
- Atorf, Jenny
- Akkad, Denis A
- Dekomien, Gabriele