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The enzymatic processing of α-dystroglycan by MMP-2 is controlled by two anchoring sites distinct from the active site. [electronic resource] by
- Gioia, Magda
- Fasciglione, Giovanni Francesco
- Sbardella, Diego
- Sciandra, Francesca
- Casella, MariaLuisa
- Camerini, Serena
- Crescenzi, Marco
- Gori, Alessandro
- Tarantino, Umberto
- Cozza, Paola
- Brancaccio, Andrea
- Coletta, Massimo
- Bozzi, Manuela
Producer: 20180402
In:
PloS one vol. 13
Availability: No items available.
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411.
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412.
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414.
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416.
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Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan. [electronic resource] by
- Longman, Cheryl
- Brockington, Martin
- Torelli, Silvia
- Jimenez-Mallebrera, Cecilia
- Kennedy, Colin
- Khalil, Nofal
- Feng, Lucy
- Saran, Ravindra K
- Voit, Thomas
- Merlini, Luciano
- Sewry, Caroline A
- Brown, Susan C
- Muntoni, Francesco
Producer: 20040622
In:
Human molecular genetics vol. 12
Availability: No items available.
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