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Cytoskeletal protein kinases: titin and its relations in mechanosensing
Cytoskeletal protein kinases: titin and its relations in mechanosensing
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Cytoskeletal protein kinases: titin and its relations in mechanosensing

Gautel, Mathias

Pflügers Archiv, 2011-07, Vol.462 (1), p.119-134 [Periódico revisado por pares]

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2
Cardiac sodium channel Na(v)1.5 and interacting proteins: Physiology and pathophysiology
Cardiac sodium channel Na(v)1.5 and interacting proteins: Physiology and pathophysiology
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Cardiac sodium channel Na(v)1.5 and interacting proteins: Physiology and pathophysiology

Abriel, Hugues

Journal of molecular and cellular cardiology, 2010-01, Vol.48 (1), p.2-11 [Periódico revisado por pares]

England

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3
Telethonin-deficiency initially presenting as a congenital muscular dystrophy
Telethonin-deficiency initially presenting as a congenital muscular dystrophy
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Telethonin-deficiency initially presenting as a congenital muscular dystrophy

Ferreiro, Ana ; Mezmezian, Monica ; Olivé, Montse ; Herlicoviez, Danielle ; Fardeau, Michel ; Richard, Pascale ; Romero, Norma Beatriz

Neuromuscular disorders : NMD, 2011-06, Vol.21 (6), p.433-438 [Periódico revisado por pares]

England: Elsevier B.V

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4
A pilot study of muscle plasma protein changes after exercise
A pilot study of muscle plasma protein changes after exercise
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A pilot study of muscle plasma protein changes after exercise

Dahlqvist, Julia R. ; Voss, Line G. ; Lauridsen, Thomas ; Krag, Thomas O. ; Vissing, John

Muscle & nerve, 2014-02, Vol.49 (2), p.261-266 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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5
Muscle Phenotypic Variability in Limb Girdle Muscular Dystrophy 2 G
Muscle Phenotypic Variability in Limb Girdle Muscular Dystrophy 2 G
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Muscle Phenotypic Variability in Limb Girdle Muscular Dystrophy 2 G

Paim, Julia F. ; Cotta, Ana ; Vargas, Antonio P. ; Navarro, Monica M. ; Valicek, Jaquelin ; Carvalho, Elmano ; da-Cunha-Junior, Antonio L. ; Plentz, Estevão ; Braz, Shelida V. ; Takata, Reinaldo I. ; Almeida, Camila F. ; Vainzof, Mariz

Journal of molecular neuroscience, 2013-06, Vol.50 (2), p.339-344 [Periódico revisado por pares]

New York: Humana Press Inc

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6
Limb–Girdle and Congenital Muscular Dystrophies: Current Diagnostics, Management, and Emerging Technologies
Limb–Girdle and Congenital Muscular Dystrophies: Current Diagnostics, Management, and Emerging Technologies
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Limb–Girdle and Congenital Muscular Dystrophies: Current Diagnostics, Management, and Emerging Technologies

Tesi Rocha, Carolina ; Hoffman, Eric P.

Current neurology and neuroscience reports, 2010-07, Vol.10 (4), p.267-276 [Periódico revisado por pares]

New York: Current Science Inc

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7
A ZASP Missense Mutation, S196L, Leads to Cytoskeletal and Electrical Abnormalities in a Mouse Model of Cardiomyopathy
A ZASP Missense Mutation, S196L, Leads to Cytoskeletal and Electrical Abnormalities in a Mouse Model of Cardiomyopathy
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A ZASP Missense Mutation, S196L, Leads to Cytoskeletal and Electrical Abnormalities in a Mouse Model of Cardiomyopathy

Li, Zhaohui ; Ai, Tomohiko ; Samani, Kaveh ; Xi, Yutao ; Tzeng, Huei-Ping ; Xie, Mingxing ; Wu, Shan ; Ge, Shuping ; Taylor, Michael D ; Dong, Jian-Wen ; Cheng, Jie ; Ackerman, Michael J ; Kimura, Akinori ; Sinagra, Gianfranco ; Brunelli, Luca ; Faulkner, Georgine ; Vatta, Matteo

Circulation. Arrhythmia and electrophysiology, 2010-12, Vol.3 (6), p.646-656 [Periódico revisado por pares]

Hagerstown, MD: American Heart Association, Inc

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8
Distinct roles for telethonin N‐versus C‐terminus in sarcomere assembly and maintenance
Distinct roles for telethonin N‐versus C‐terminus in sarcomere assembly and maintenance
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Distinct roles for telethonin N‐versus C‐terminus in sarcomere assembly and maintenance

Sadikot, Takrima ; Hammond, Courtney R. ; Ferrari, Michael B.

Developmental dynamics, 2010-04, Vol.239 (4), p.1124-1135 [Periódico revisado por pares]

New York: Wiley‐Liss, Inc

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9
Limb-girdle muscular dystrophy in a Portuguese patient caused by a mutation in the telethonin gene
Limb-girdle muscular dystrophy in a Portuguese patient caused by a mutation in the telethonin gene
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Limb-girdle muscular dystrophy in a Portuguese patient caused by a mutation in the telethonin gene

Negrão, L ; Matos, A ; Geraldo, A ; Rebelo, O

Acta myologica, 2010-07, Vol.29 (1), p.21-24 [Periódico revisado por pares]

Italy: Pacini Editore SpA

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