Distinct chaperone mechanisms can delay the formation of aggresomes by the myopathy-causing R120G αB-crystallin mutant

By Chávez Zobel A.T.   Loranger A.   Marceau N.   Thériault J.R.   Lambert H.   Landry J.  

Human Molecular Genetics, Vol. 12, Iss. 13, 2003-07 ,pp. : 1609-1620

Oxford University Press

Access to resources Recommend Favorite

Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice

By Wong Margaret   Martin Lee J.  

Human Molecular Genetics, Vol. 19, Iss. 11, 2010-06 ,pp. : 2284-2302

Oxford University Press

Access to resources Recommend Favorite

A novel mouse model with impaired dynein/dynactin function develops amyotrophic lateral sclerosis (ALS)-like features in motor neurons and improves lifespan in SOD1-ALS mice

By Teuling Eva   van Dis Vera   Wulf Phebe S.   Haasdijk Elize D.   Akhmanova Anna   Hoogenraad Casper C.   Jaarsma Dick  

Human Molecular Genetics, Vol. 17, Iss. 18, 2008-09 ,pp. : 2849-2862

Oxford University Press

Access to resources Recommend Favorite

An examination of wild-type SOD1 in modulating the toxicity and aggregation of ALS-associated mutant SOD1

By Prudencio Mercedes   Durazo Armando   Whitelegge Julian P.   Borchelt David R.  

Human Molecular Genetics, Vol. 19, Iss. 24, 2010-12 ,pp. : 4774-4789

Oxford University Press

Access to resources Recommend Favorite

Disruption of neurofilament network with aggregation of light neurofilament protein: a common pathway leading to motor neuron degeneration due to CharcotMarieTooth disease-linked mutations in NFL and HSPB1

By Zhai Jinbin   Lin Hong   Julien Jean-Pierre   Schlaepfer William W.  

Human Molecular Genetics, Vol. 16, Iss. 24, 2007-12 ,pp. : 3103-3116

Oxford University Press

Access to resources Recommend Favorite