A valid mouse model of AGRIN-associated congenital myasthenic syndrome

Induction of filopodia-like protrusions by transmembrane agrin: Role of agrin glycosaminoglycan chains and Rho-family GTPases

(2010) Lin Lin et al.   EXPERIMENTAL CELL RESEARCH

Specific proteolytic cleavage of agrin regulates maturation of the neuromuscular junction

(2010) M. F. Bolliger et al.   JOURNAL OF CELL SCIENCE

Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function

(2009) Caroline Huzé et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Jalview Version 2--a multiple sequence alignment editor and analysis workbench

(2009) A. M. Waterhouse et al.   BIOINFORMATICS

An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy

(2009) F. Achilli et al.   Disease Models & Mechanisms

A role for motoneuron subtype–selective ER stress in disease manifestations of FALS mice

(2009) Smita Saxena et al.   NATURE NEUROSCIENCE

Lrp4 Is a Receptor for Agrin and Forms a Complex with MuSK

(2008) Natalie Kim et al.   CELL

Neurotrypsin cleaves agrin locally at the synapse

(2008) Alexander Stephan et al.   FASEB JOURNAL

Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy

(2008) Shingo Kariya et al.   HUMAN MOLECULAR GENETICS

A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination

(2008) B. L. Patton et al.   JOURNAL OF CELL SCIENCE

LRP4 Serves as a Coreceptor of Agrin

(2008) Bin Zhang et al.   NEURON

The Jpred 3 secondary structure prediction server

(2008) C. Cole et al.   NUCLEIC ACIDS RESEARCH

SEA domain proteolysis determines the functional composition of dystroglycan

(2007) Armin Akhavan et al.   FASEB JOURNAL