Results
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5441.
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5442.
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An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line. [electronic resource] by
- Zvaritch, Elena
- Depreux, Frederic
- Kraeva, Natasha
- Loy, Ryan E
- Goonasekera, Sanjeewa A
- Boncompagni, Simona
- Boncompagi, Simona
- Kraev, Alexander
- Gramolini, Anthony O
- Dirksen, Robert T
- Franzini-Armstrong, Clara
- Seidman, Christine E
- Seidman, J G
- Maclennan, David H
Producer: 20080102
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 104
Availability: No items available.
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5443.
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5444.
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5445.
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5446.
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5447.
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5448.
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5449.
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5450.
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5451.
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5452.
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5453.
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SRP-35, a newly identified protein of the skeletal muscle sarcoplasmic reticulum, is a retinol dehydrogenase. [electronic resource] by
- Treves, Susan
- Thurnheer, Raphael
- Mosca, Barbara
- Vukcevic, Mirko
- Bergamelli, Leda
- Voltan, Rebecca
- Oberhauser, Vitus
- Ronjat, Michel
- Csernoch, Laszlo
- Szentesi, Peter
- Zorzato, Francesco
Producer: 20120214
In:
The Biochemical journal vol. 441
Availability: No items available.
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5454.
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5455.
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5456.
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5457.
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5458.
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Muscle magnetic resonance imaging in congenital myopathies due to ryanodine receptor type 1 gene mutations. [electronic resource] by
- Klein, Andrea
- Jungbluth, Heinz
- Clement, Emma
- Lillis, Suzanne
- Abbs, Stephen
- Munot, Pinki
- Pane, Marika
- Wraige, Elizabeth
- Schara, Ulrike
- Straub, Volker
- Mercuri, Eugenio
- Muntoni, Francesco
Producer: 20111102
In:
Archives of neurology vol. 68
Availability: No items available.
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5459.
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5460.
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