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- Gal, Andreas
- Beck, Michael 8
- Hübner, Christian 5
- Kampmann, Christoph 5
- Kurth, Ingo 5
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60 Einträge gefunden
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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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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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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
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Incontinetia pigmenti-related myopathy or unsolved "double trouble"?
2010 - Forschungsinformationssystem des UKE -
Clinical, radiological and genetic aspects of leukodystrophies.
2010 - Forschungsinformationssystem des UKE -
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RDH12 Activity and Effects on Retinoid Processing in the Murine Retina.
- Chrispell, Jared D
- Feathers, Kecia L
- Kane, Maureen A
- Kim, Chul Y
- Brooks, Matthew
- Khanna, Ritu
- Kurth, Ingo
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A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa.
- Azam, Maleeha
- Khan, Muhammad Imran
- Gal, Andreas
- Hussain, Alamdar
- Shah, Syed Tahir Abbas
- Khan, Muhammad Shakil
- Sadeque, Ahmed
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Duplications of noncoding elements 5' of SOX9 are associated with brachydactyly-anonychia.
- Kurth, Ingo
- Klopocki, Eva
- Stricker, Sigmar
- van Oosterwijk, Jolieke
- Vanek, Sebastian
- Altmann, Jens
- Santos, Heliosa G
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