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Author/Creator Hirano, Michio

2. A POGLUT1 mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss. Issue 11 (10th October 2016)

Authors:
Servián‐Morilla, Emilia; Takeuchi, Hideyuki; Lee, Tom V; Clarimon, Jordi; Mavillard, Fabiola; Area‐Gómez, Estela; Rivas, Eloy; Nieto‐González, Jose L; Rivero, Maria C; Cabrera‐Serrano, Macarena; Gómez‐Sánchez, Leonardo; Martínez‐López, Jose A; Estrada, Beatriz; Márquez, Celedonio; Morgado, Yoland...
Journal:
EMBO molecular medicine
Issue:
Volume 8:Issue 11(2016)
Page Start:
1289
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

6. Cardiomyopathy and altered integrin-actin signaling in Fhl1 mutant female mice. (26th September 2018)

Authors:
Kubota, Akatsuki; Juanola-Falgarona, Martí; Emmanuele, Valentina; Sanchez-Quintero, Maria Jose; Kariya, Shingo; Sera, Fusako; Homma, Shunichi; Tanji, Kurenai; Quinzii, Catarina M; Hirano, Michio
Journal:
Human molecular genetics
Issue:
Volume 28:Number 2(2019)
Page Start:
209
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

8. Deoxynucleoside Therapy for Thymidine Kinase 2–Deficient Myopathy. Issue 2 (17th June 2019)

Authors:
Domínguez‐González, Cristina; Madruga‐Garrido, Marcos; Mavillard, Fabiola; Garone, Caterina; Aguirre‐Rodríguez, Francisco Javier; Donati, M. Alice; Kleinsteuber, Karin; Martí, Itxaso; Martín‐Hernández, Elena; Morealejo‐Aycinena, Juan P.; Munell, Francina; Nascimento, Andrés; Kalko, Susana G.; Sar...
Journal:
Annals of neurology
Issue:
Volume 86:Issue 2(2019)
Page Start:
293
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗