C. Young

发表

Developmental Modulation of Retinal Wave Dynamics: Shedding Light on the GABA Saga

S. Eglen, E. Sernagor, C. Young, 2003, The Journal of Neuroscience.

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.

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.

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

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

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.

GABA Type-A Activity Controls Its Own Developmental Polarity Switch in the Maturing Retina

Carol Young, Evelyne Sernagor, E. Sernagor, 2005, The Journal of Neuroscience.

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.

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.

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.

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.

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.