Results
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761.
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762.
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763.
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A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey. [electronic resource] by
- Dinçer, P
- Leturcq, F
- Richard, I
- Piccolo, F
- Yalnizoglu, D
- de Toma, C
- Akçören, Z
- Broux, O
- Deburgrave, N
- Brenguier, L
- Roudaut, C
- Urtizberea, J A
- Jung, D
- Tan, E
- Jeanpierre, M
- Campbell, K P
- Kaplan, J C
- Beckmann, J S
- Topaloglu, H
Producer: 19970905
In:
Annals of neurology vol. 42
Availability: No items available.
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764.
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765.
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766.
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767.
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768.
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769.
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770.
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Complete repair of dystrophic skeletal muscle by mesoangioblasts with enhanced migration ability. [electronic resource] by
- Galvez, Beatriz G
- Sampaolesi, Maurilio
- Brunelli, Silvia
- Covarello, Diego
- Gavina, Manuela
- Rossi, Barbara
- Constantin, Gabriela
- Costantin, Gabriela
- Torrente, Yvan
- Cossu, Giulio
Producer: 20060816
In:
The Journal of cell biology vol. 174
Availability: No items available.
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771.
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Marine n3 polyunsaturated fatty acids enhance resistance to mitochondrial permeability transition in heart failure but do not improve survival. [electronic resource] by
- Galvao, Tatiana F
- Khairallah, Ramzi J
- Dabkowski, Erinne R
- Brown, Bethany H
- Hecker, Peter A
- O'Connell, Kelly A
- O'Shea, Karen M
- Sabbah, Hani N
- Rastogi, Sharad
- Daneault, Caroline
- Des Rosiers, Christine
- Stanley, William C
Producer: 20130220
In:
American journal of physiology. Heart and circulatory physiology vol. 304
Availability: No items available.
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772.
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773.
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774.
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Long-term miR-669a therapy alleviates chronic dilated cardiomyopathy in dystrophic mice. [electronic resource] by
- Quattrocelli, Mattia
- Crippa, Stefania
- Montecchiani, Celeste
- Camps, Jordi
- Cornaglia, Antonia Icaro
- Boldrin, Luisa
- Morgan, Jennifer
- Calligaro, Alberto
- Casasco, Andrea
- Orlacchio, Aldo
- Gijsbers, Rik
- D'Hooge, Jan
- Toelen, Jaan
- Janssens, Stefan
- Sampaolesi, Maurilio
Producer: 20140502
In:
Journal of the American Heart Association vol. 2
Availability: No items available.
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775.
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776.
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777.
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778.
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779.
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Reengineering a transmembrane protein to treat muscular dystrophy using exon skipping. [electronic resource] by
- Gao, Quan Q
- Wyatt, Eugene
- Goldstein, Jeff A
- LoPresti, Peter
- Castillo, Lisa M
- Gazda, Alec
- Petrossian, Natalie
- Earley, Judy U
- Hadhazy, Michele
- Barefield, David Y
- Demonbreun, Alexis R
- Bönnemann, Carsten
- Wolf, Matthew
- McNally, Elizabeth M
Producer: 20160222
In:
The Journal of clinical investigation vol. 125
Availability: No items available.
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780.
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A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy. [electronic resource] by
- Bueno, M R
- Moreira, E S
- Vainzof, M
- Chamberlain, J
- Marie, S K
- Pereira, L
- Akiyama, J
- Roberds, S L
- Campbell, K P
- Zatz, M
Producer: 19960126
In:
Human molecular genetics vol. 4
Availability: No items available.
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