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Morgagnian cataract resulting from a naturally occurring nonsense mutation elucidates a role of CPAMD8 in mammalian lens development. [electronic resource] by
- Hollmann, Anne K
- Dammann, Insa
- Wemheuer, Wiebke M
- Wemheuer, Wilhelm E
- Chilla, Almuth
- Tipold, Andrea
- Schulz-Schaeffer, Walter J
- Beck, Julia
- Schütz, Ekkehard
- Brenig, Bertram
Producer: 20171006
In:
PloS one vol. 12
Availability: No items available.
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9.
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Spongiform encephalopathy in siblings with no evidence of protease-resistant prion protein or a mutation in the prion protein gene. [electronic resource] by
- Varges, Daniela
- Schulz-Schaeffer, Walter J
- Wemheuer, Wiebke M
- Damman, Insa
- Schmitz, Matthias
- Cramm, Maria
- Kallenberg, Kai
- Shirneshan, Katayoon
- Elkenani, Manar
- Markwort, Susanne
- Faist, Michael
- Kohlhase, Jürgen
- Windl, Otto
- Zerr, Inga
Producer: 20140219
In:
Journal of neurology vol. 260
Availability: No items available.
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Similarities between forms of sheep scrapie and Creutzfeldt-Jakob disease are encoded by distinct prion types. [electronic resource] by
- Wemheuer, Wiebke M
- Benestad, Sylvie L
- Wrede, Arne
- Schulze-Sturm, Ulf
- Wemheuer, Wilhelm E
- Hahmann, Uwe
- Gawinecka, Joanna
- Schütz, Ekkehard
- Zerr, Inga
- Brenig, Bertram
- Bratberg, Bjørn
- Andréoletti, Olivier
- Schulz-Schaeffer, Walter J
Producer: 20100225
In:
The American journal of pathology vol. 175
Availability: No items available.
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