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741.
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Excess SMAD signaling contributes to heart and muscle dysfunction in muscular dystrophy. [electronic resource] by
- Goldstein, Jeffery A
- Bogdanovich, Sasha
- Beiriger, Anastasia
- Wren, Lisa M
- Rossi, Ann E
- Gao, Quan Q
- Gardner, Brandon B
- Earley, Judy U
- Molkentin, Jeffery D
- McNally, Elizabeth M
Producer: 20150713
In:
Human molecular genetics vol. 23
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742.
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Abnormal striatal plasticity in a DYT11/SGCE myoclonus dystonia mouse model is reversed by adenosine A2A receptor inhibition. [electronic resource] by
- Maltese, M
- Martella, G
- Imbriani, P
- Schuermans, Jeroen
- Billion, Karolien
- Sciamanna, G
- Farook, Febin
- Ponterio, G
- Tassone, A
- Santoro, M
- Bonsi, P
- Pisani, A
- Goodchild, Rose E
Producer: 20180723
In:
Neurobiology of disease vol. 108
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743.
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Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency. [electronic resource] by
- Kawai, H
- Akaike, M
- Endo, T
- Adachi, K
- Inui, T
- Mitsui, T
- Kashiwagi, S
- Fujiwara, T
- Okuno, S
- Shin, S
Producer: 19951004
In:
The Journal of clinical investigation vol. 96
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744.
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745.
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Skeletal muscle differentiation of embryonic mesoangioblasts requires pax3 activity. [electronic resource] by
- Messina, Graziella
- Sirabella, Dario
- Monteverde, Stefania
- Galvez, Beatriz G
- Tonlorenzi, Rossana
- Schnapp, Esther
- De Angelis, Luciana
- Brunelli, Silvia
- Relaix, Frederic
- Buckingham, Margaret
- Cossu, Giulio
Producer: 20090625
In:
Stem cells (Dayton, Ohio) vol. 27
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746.
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747.
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748.
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749.
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Oxidative stress preconditioning of mouse perivascular myogenic progenitors selects a subpopulation of cells with a distinct survival advantage in vitro and in vivo. [electronic resource] by
- Gargioli, Cesare
- Turturici, Giuseppina
- Barreca, Maria M
- Spinello, Walter
- Fuoco, Claudia
- Testa, Stefano
- Feo, Salvatore
- Cannata, Stefano M
- Cossu, Giulio
- Sconzo, Gabriella
- Geraci, Fabiana
Producer: 20190430
In:
Cell death & disease vol. 9
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750.
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751.
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752.
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753.
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754.
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Absence of T and B lymphocytes modulates dystrophic features in dysferlin deficient animal model. [electronic resource] by
- Farini, Andrea
- Sitzia, Clementina
- Navarro, Claire
- D'Antona, Giuseppe
- Belicchi, Marzia
- Parolini, Daniele
- Del Fraro, Giulia
- Razini, Paola
- Bottinelli, Roberto
- Meregalli, Mirella
- Torrente, Yvan
Producer: 20120625
In:
Experimental cell research vol. 318
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755.
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A Haplotype of Two Novel Polymorphisms in δ-Sarcoglycan Gene Increases Risk of Dilated Cardiomyopathy in Mongoloid Population. [electronic resource] by
- Chen, Jie
- Jin, Ye
- Wang, Hong
- Wei, Sisi
- Chen, Dan
- Ying, Li
- Zhou, Qing
- Li, Gang
- Li, Joyce
- Gao, Jimin
- Kato, Naoya
- Hu, Wei
- Li, Yigang
- Wang, Yuepeng
Producer: 20160626
In:
PloS one vol. 10
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756.
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757.
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Fibrosis and inflammation are greater in muscles of beta-sarcoglycan-null mouse than mdx mouse. [electronic resource] by
- Gibertini, Sara
- Zanotti, Simona
- Savadori, Paolo
- Curcio, Maurizio
- Saredi, Simona
- Salerno, Franco
- Andreetta, Francesca
- Bernasconi, Pia
- Mantegazza, Renato
- Mora, Marina
Producer: 20150112
In:
Cell and tissue research vol. 356
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758.
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Cell therapy of alpha-sarcoglycan null dystrophic mice through intra-arterial delivery of mesoangioblasts. [electronic resource] by
- Sampaolesi, Maurilio
- Torrente, Yvan
- Innocenzi, Anna
- Tonlorenzi, Rossana
- D'Antona, Giuseppe
- Pellegrino, M Antonietta
- Barresi, Rita
- Bresolin, Nereo
- De Angelis, M Gabriella Cusella
- Campbell, Kevin P
- Bottinelli, Roberto
- Cossu, Giulio
Producer: 20030804
In:
Science (New York, N.Y.) vol. 301
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759.
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760.
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