C. Slater

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Safety factor at the neuromuscular junction

S. J. Wood, C. Slater, Clarke R. Slater, 2001, Progress in Neurobiology.

An improved method for the simultaneous demonstration of mRNA and esterase activity at the human neuromuscular junction

R. Vater, S. Lindsay, C. Young, 2004, The Histochemical Journal.

Diverse aspects of vulnerability at the neuromuscular junction.

C. Slater, 2012, Brain : a journal of neurology.

β-Spectrin Is Colocalized with Both Voltage-gated Sodium Channels and AnkyrinG at the Adult Rat Neuromuscular Junction

S. J. Wood, C. Slater, Clarke R. Slater, 1998, The Journal of cell biology.

Spatial distribution of acetylcholine receptors at developing chick neuromuscular junctions

M. Smith, C. Slater, M. Smith, 1983, Journal of neurocytology.

Salbutamol modifies the neuromuscular junction in a mouse model of ColQ myasthenic syndrome

R. Whittaker, H. Lochmüller, R. Horvath, 2019, Human molecular genetics.

Neuromuscular Junction (NMJ): Postsynaptic Events in Neuromuscular Transmission

C. Slater, 2009 .

Accumulation of NaV1 mRNAs at differentiating postsynaptic sites in rat soleus muscles

R. Lightowlers, C. Young, C. Slater, 2005, Molecular and Cellular Neuroscience.

Voltage-Gated Sodium Channels and AnkyrinG Occupy a Different Postsynaptic Domain from Acetylcholine Receptors from an Early Stage of Neuromuscular Junction Maturation in Rats

C. Young, C. Slater, Mark A. Stocksley, 2003, The Journal of Neuroscience.

Sodium Channel mRNAs at the Neuromuscular Junction: Distinct Patterns of Accumulation and Effects of Muscle Activity

T. Lømo, Z. Chrzanowska-Lightowlers, R. Lightowlers, 2001, The Journal of Neuroscience.

An early stage in sodium channel clustering at developing rat neuromuscular junctions

C. Young, S. J. Wood, C. Slater, 1998, Neuroreport.

Glutamatergic modulation of synaptic-like vesicle recycling in mechanosensory lanceolate nerve terminals of mammalian hair follicles

R. W. Banks, Anna B. Graca, P. Cahusac, 2013, The Journal of physiology.

Innervation of Regenerating Muscle

S. Schiaffino, C. Slater, 2008 .

Electron-microscopic structure of denervated skeletal muscle

R. Miledi, C. Slater, 1969, Proceedings of the Royal Society of London. Series B. Biological Sciences.

Control of myogenesis in vitro by chick embryo extract.

C. Slater, 1976, Developmental biology.

Plasticity of the Mammalian Neuromuscular Junction and the Response to Botulinum Toxins

C. Slater, 2016 .

Neuromuscular Junction Plasticity in Mammals and Botulinum Toxins

C. Slater, 2009 .

Utrophin mRNA Expression in Muscle Is Not Restricted to the Neuromuscular Junction

K. Davies, R. Vater, S. Lindsay, 1998, Molecular and Cellular Neuroscience.

The effect of age on motor neurone death following axotomy in the mouse.

C. Slater, S. McHanwell, M. Pollin, 1991, Development.

Double agents and breakdown of integrity at the neuromuscular junction in Miller-Fisher syndrome.

C. Slater, 2001, Brain : a journal of neurology.

Synapse-specific expression of acetylcholine receptor genes and their products at original synaptic sites in rat soleus muscle fibres regenerating in the absence of innervation.

A. Herczeg, C. Slater, H. Brenner, 1992, Development.

Dok-7 Mutations Underlie a Neuromuscular Junction Synaptopathy

J. Palace, Hanns Lochmüller, A. Vincent, 2006, Science.

Time Course of Failure of Neuromuscular Transmission after Motor Nerve Section

C. Slater, 1966, Nature.

Different distributions of dystrophin and related proteins at nerve-muscle junctions.

C. Young, G. Bewick, C. Slater, 1992, Neuroreport.

Spatial relationships of utrophin, dystrophin, beta-dystroglycan and beta-spectrin to acetylcholine receptor clusters during postnatal maturation of the rat neuromuscular junction.

C. Young, G. Bewick, C. Slater, 1996, Journal of neurocytology.

Control of acetylcholine sensitivity and synapse formation by muscle activity.

T. Lømo, C. Slater, 1978, The Journal of physiology.

C. Slater, S. Willadt, Mark S. Nash, 2016, Scientific Reports.

Modulation of the Acetylcholine Receptor Clustering Pathway Improves Neuromuscular Junction Structure and Muscle Strength in a Mouse Model of Congenital Myasthenic Syndrome

H. Lochmüller, R. Horvath, Kaitlyn Quinlan, 2020, Frontiers in Molecular Neuroscience.

Action potential generation in rat slow‐ and fast‐twitch muscles.

C. Slater, S. J. Wood, 1995, The Journal of physiology.

Control of junctional acetylcholinesterase by neural and muscular influences in the rat.

T. Lømo, C. Slater, 1980, The Journal of physiology.

The influence of basal lamina on the accumulation of acetylcholine receptors at synaptic sites in regenerating muscle

U J McMahan, C. Slater, U. J. McMahan, 1984, The Journal of cell biology.

Electrophysiology and electron-microscopy of rat neuromuscular junctions after nerve degeneration

R. Miledi, C. Slater, Ricardo Miledi, 1968, Proceedings of the Royal Society of London. Series B. Biological Sciences.

Reliability of neuromuscular transmission and how it is maintained.

C. Slater, Clarke R Slater, 2008, Handbook of clinical neurology.

Structural determinants of the reliability of synaptic transmission at the vertebrate neuromuscular junction

C. Slater, 2003, Journal of neurocytology.

Utrophin abundance is reduced at neuromuscular junctions of patients with both inherited and acquired acetylcholine receptor deficiencies.

A. Vincent, J. Newsom-Davis, C. Young, 1997, Brain : a journal of neurology.

The contribution of postsynaptic folds to the safety factor for neuromuscular transmission in rat fast‐ and slow‐twitch muscles.

S. J. Wood, C. Slater, C R Slater, 1997, The Journal of physiology.

Dystrophin in skeletal muscle II. Immunoreactivity in patients with Xp21 muscular dystrophy

Margaret A. Johnson, S. Bhattacharya, C. Young, 1989, Journal of the Neurological Sciences.

Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates.

Jacqueline A Palace, S. Twigg, S. McGowan, 2012, American journal of human genetics.

Ricardo Miledi. 15 September 1927—18 December 2017

S. Cull-Candy, I. Parker, C. Slater, 2021, BIOGRAPHICAL MEMOIRS OF FELLOWS OF THE ROYAL SOCIETY.

On the degeneration of rat neuromuscular junctions after nerve section

R. Miledi, C. Slater, 1970, The Journal of physiology.

Ectopic Expression of NCAM in Skeletal Muscle of Transgenic Mice Results in Terminal Sprouting at the Neuromuscular Junction and Altered Structure But Not Function

F. Walsh, C. Hobbs, D. Wells, 2000, Molecular and Cellular Neuroscience.

Some mitochondrial changes in denervated muscle.

R. Miledi, C. Slater, 1968, Journal of cell science.

Synaptic Vesicle Dynamics in Rat Fast and Slow Motor Nerve Terminals

G. Bewick, C. Slater, B. Reid, 1999, The Journal of Neuroscience.

Structure and function of the neuromuscular junction in young adultmdx mice

C. Slater, P. Lyons, 1991, Journal of neurocytology.

Differential Localization of Voltage-Dependent Calcium Channel α1 Subunits at the Human and Rat Neuromuscular Junction

P. Ince, P. Shaw, W. Smith, 1997, The Journal of Neuroscience.

Dystrophin in skeletal muscle I. Western blot analysis using a monoclonal antibody

C. Harwood, G. Falkous, J. Harris, 1989, Journal of the Neurological Sciences.

Neural influence on the postnatal changes in acetylcholine receptor distribution at nerve-muscle junctions in the mouse.

C. Slater, 1982, Developmental biology.

Postnatal maturation of nerve-muscle junctions in hindlimb muscles of the mouse.

C. Slater, 1982, Developmental biology.

The basal lamina and stability of the mammalian neuromuscular junction.

C. Slater, 1990, Progress in brain research.

Loss of motor neurons from the median nerve motor nucleus of the mutant mouse ‘wobbler’

C. Slater, S. McHanwell, M. Pollin, 1990, Journal of neurocytology.

The functional organization of motor nerve terminals

C. Slater, Clarke R. Slater, 2015, Progress in Neurobiology.

Animal models: what is their relevance to the pathogenesis of human muscular dystrophy?

J. Harris, C. Slater, 1980, British medical bulletin.

Release and synthesis of acetylcholine at ectopic neuromuscular junctions in the rat.

P. Molenaar, C. Slater, G. T. V. van Kempen, 1994, The Journal of physiology.

Postsynaptic Abnormalities at the Neuromuscular Junctions of Utrophin-deficient Mice

K. Davies, R. Vater, A. Vincent, 1997, The Journal of cell biology.

Pre- and post-synaptic abnormalities associated with impaired neuromuscular transmission in a group of patients with 'limb-girdle myasthenia'.

D. Beeson, C. Young, P. Fawcett, 2006, Brain : a journal of neurology.

Relationship of a dystrophin-associated glycoprotein to junctional acetylcholine receptor clusters in rat skeletal muscle

C. Young, G. Bewick, C. Slater, 1993, Neuromuscular Disorders.

Recovery of mouse neuromuscular junctions from single and repeated injections of botulinum neurotoxin A

C. Young, C. Slater, A. Rogozhin, 2008, The Journal of physiology.

Muscle proteins and muscular dystrophy.

C. Slater, 1989, Current opinion in cell biology.

Is dystrophin labelling always discontinuous in Becker muscular dystrophy?

C. Slater, L. Nicholson, 1991, Journal of the Neurological Sciences.

Structural Factors Influencing the Efficacy of Neuromuscular Transmission

C. Slater, 2008, Annals of the New York Academy of Sciences.

The action of calcium on neuronal synapses in the squid

R. Miledi, C. Slater, 1966, The Journal of physiology.

The Structure of Human Neuromuscular Junctions: Some Unanswered Molecular Questions

C. Slater, 2017, International journal of molecular sciences.

GFPT1 deficiency in muscle leads to myasthenia and myopathy in mice

Hanns Lochmüller, J. Weis, R. Rudolf, 2018, Human molecular genetics.

C. Slater, S. Willadt, Mark S. Nash, 2018, Annals of the New York Academy of Sciences.

Confocal Endomicroscopy of Neuromuscular Junctions Stained with Physiologically Inert Protein Fragments of Tetanus Toxin

R. Ribchester, T. Gillingwater, P. Skehel, 2021, Biomolecules.

Myasthenic Syndrome with Tubular Aggregates

Jacqueline A Palace, S. McGowan, J. Cossins, 2012 .

Structural Abnormalities of the AChR Caused by Mutations Underlying Congenital Myasthenic Syndromes

D. Colquhoun, A. Vincent, D. Beeson, 2003, Annals of the New York Academy of Sciences.

Acetylcholine sensitivity of developing ectopic nerve‐muscle junctions in adult rat soleus muscles.

T. Lømo, C. Slater, 1980, The Journal of physiology.

End-plate gamma- and epsilon-subunit mRNA levels in AChR deficiency syndrome due to epsilon-subunit null mutations.

A. Vincent, D. Beeson, C. Young, 2001, Brain : a journal of neurology.

Neuromuscular Connections: Vertebrate Patterns of

C. Slater, 2009 .

Congenital Myasthenic Syndromes or Inherited Disorders of Neuromuscular Transmission: Recent Discoveries and Open Questions

Hanns Lochmüller, B. Eymard, S. Nicole, 2017, Journal of neuromuscular diseases.

‘Fragmentation’ of NMJs: a sign of degeneration or regeneration? A long journey with many junctions

C. Slater, 2020, Neuroscience.

Structure and function of neuromuscular junctions in the vastus lateralis of man. A motor point biopsy study of two groups of patients.

C. Young, P. Fawcett, T. Walls, 1992, Brain : a journal of neurology.

Modulation of Agrin and RhoA Pathways Ameliorates Movement Defects and Synapse Morphology in MYO9A-Depleted Zebrafish

H. Lochmüller, R. Horvath, S. Hettwer, 2019, Cells.

Congenital Myasthenic Syndromes and the Formation of the Neuromuscular Junction

Jacqueline Palace, A. Vincent, J. Cossins, 2008, Annals of the New York Academy of Sciences.

Neuromuscular Junction (NMJ): Mammalian Development

C. Slater, 2009 .

Rapid retrograde regulation of transmitter release at the NMJ

R. Ribchester, C. Slater, 2018, Current Opinion in Physiology.

Agrin signals at the junction

C. Slater, 1996, Nature.