Neuromuscular junctions are pathological but not denervated in two mouse models of spinal bulbar muscular atrophy

Defects in Neuromuscular Transmission May Underlie Motor Dysfunction in Spinal and Bulbar Muscular Atrophy

(2016) Youfen Xu et al.   JOURNAL OF NEUROSCIENCE

Neuregulin1 displayed on motor axons regulates terminal Schwann cell-mediated synapse elimination at developing neuromuscular junctions

(2016) Young il Lee et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Selective Neuromuscular Denervation in Taiwanese Severe SMA Mouse Can Be Reversed by Morpholino Antisense Oligonucleotides

(2016) Te-Lin Lin et al.   PLoS One

Androgen-dependent loss of muscle BDNF mRNA in two mouse models of SBMA

(2015) Katherine Halievski et al.   EXPERIMENTAL NEUROLOGY

Contractile dysfunction in muscle may underlie androgen-dependent motor dysfunction in spinal bulbar muscular atrophy

(2015) Kentaro Oki et al.   JOURNAL OF APPLIED PHYSIOLOGY

Muscle Expression of Mutant Androgen Receptor Accounts for Systemic and Motor Neuron Disease Phenotypes in Spinal and Bulbar Muscular Atrophy

(2014) Constanza J. Cortes et al.   NEURON

Composition of isolated synaptic boutons reveals the amounts of vesicle trafficking proteins

(2014) B. G. Wilhelm et al.   SCIENCE

Effects ofin vivoinjury on the neuromuscular junction in healthy and dystrophic muscles

(2012) Stephen J.P. Pratt et al.   JOURNAL OF PHYSIOLOGY-LONDON

Fiji: an open-source platform for biological-image analysis

(2012) Johannes Schindelin et al.   NATURE METHODS

Destabilization of the neuromuscular junction by proteolytic cleavage of agrin results in precocious sarcopenia

(2011) Lukas Bütikofer et al.   FASEB JOURNAL

Impaired motoneuronal retrograde transport in two models of SBMA implicates two sites of androgen action

(2011) Michael Q. Kemp et al.   HUMAN MOLECULAR GENETICS

Severe neuromuscular denervation of clinically relevant muscles in a mouse model of spinal muscular atrophy

(2011) K. K. Y. Ling et al.   HUMAN MOLECULAR GENETICS

Reduced TrkB expression results in precocious age-like changes in neuromuscular structure, neurotransmission, and muscle function

(2011) Scott A. Kulakowski et al.   JOURNAL OF APPLIED PHYSIOLOGY

Changes in Aging Mouse Neuromuscular Junctions Are Explained by Degeneration and Regeneration of Muscle Fiber Segments at the Synapse

(2011) Y. Li et al.   JOURNAL OF NEUROSCIENCE

Prenatal Flutamide Enhances Survival in a Myogenic Mouse Model of Spinal Bulbar Muscular Atrophy

(2010) Jamie A. Johansen et al.   Neurodegenerative Diseases

Altered RNA splicing contributes to skeletal muscle pathology in Kennedy disease knock-in mice

(2009) Z. Yu et al.   Disease Models & Mechanisms

Truncated dystrophins can influence neuromuscular synapse structure

(2009) Glen B. Banks et al.   MOLECULAR AND CELLULAR NEUROSCIENCE

Recovery of function in a myogenic mouse model of spinal bulbar muscular atrophy

(2009) Jamie A. Johansen et al.   NEUROBIOLOGY OF DISEASE

Lysosomal proliferation and distal degeneration in motor neurons expressing the G59S mutation in the p150Glued subunit of dynactin

(2008) E. S. Chevalier-Larsen et al.   HUMAN MOLECULAR GENETICS

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

(2008) Shingo Kariya et al.   HUMAN MOLECULAR GENETICS

Synaptic Defects in a Drosophila Model of Congenital Muscular Dystrophy

(2008) Y. P. Wairkar et al.   JOURNAL OF NEUROSCIENCE

Administration of testosterone results in reversible deterioration in Kennedy's disease

(2006) P Kinirons et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY