W. Yee

发表

Meiotic stability and genotype – phenotype correlation of the trinucleotide repeat in X–linked spinal and bulbar muscular atrophy

C. L. Warner, K. Fischbeck, A. Spada, 1992, Nature Genetics.

Correction of dystrophia myotonica type 1 pre-mRNA transcripts by artificial trans-splicing

P. Lai, W. Yee, H. Y. Chen, 2009, Gene Therapy.

Myopathy and paraproteinemia with serum igm binding to a high‐ molecular‐weight muscle fiber surface protein

A. Pestronk, W. Yee, M. Al-Lozi, 1995, Annals of neurology.

N lines in a myopathy with myosin loss

A. Pestronk, W. Yee, G. Lopate, 1998, Muscle & nerve.

Rapidly evolving myopathy with myosin‐deficient muscle fibers

A. Pestronk, W. Yee, S. Louis, 1994, Annals of neurology.

Serum IgM Monoclonal Autoantibody Binding to the 301 to 314 Amino Acid Epitope of Beta-tubulin

A. Pestronk, R. Olney, A. Connolly, 1997, Neurology.

Silver cholinesterase immunocytochemistry: A new neuromuscular junction stain

A. Pestronk, W. Yee, D. Drachman, 1989, Muscle & nerve.

Distal lower motor neuron syndrome with high‐titer serum IgM anti‐GM1 antibodies

A. Pestronk, L. Goodnough, W. Yee, 1994, Neurology.

Lower motor neuron syndromes defined by patterns of weakness, nerve conduction abnormalities, and high titers of antiglycolipid antibodies

A. Pestronk, R. Olney, E. Feldman, 1990, Annals of neurology.

Effect of ketoleucine treatment on atrophy of skeletal muscle

A. Pestronk, M. Walser, W. Yee, 1988, Experimental Neurology.

Mechanisms of postsynaptic plasticity: remodeling of the junctional acetylcholine receptor cluster induced by motor nerve terminal outgrowth

A. Pestronk, W. Yee, 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

Recurrent and founder mutations in the Netherlands: the cardiac phenotype of DES founder mutations p.S13F and p.N342D

M. P. van den Berg, P. Doevendans, E. Ippel, 2012, Netherlands Heart Journal.

Childhood chronic inflammatory demyelinating neuropathies

A. Pestronk, A. Kornberg, A. Connolly, 1996, Neurology.

Serum antibodies to heparan sulfate glycosaminoglycans in Guillain–Barré syndrome and other demyelinating polyneuropathies

A. Pestronk, A. Kornberg, R. Choksi, 1998, Journal of Neuroimmunology.

Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q.

J. Ivanovich, P. Goodfellow, J. Kwon, 1995, American Journal of Human Genetics.

Anti‐MAG antibodies

A. Pestronk, A. Kornberg, R. Choksi, 1994, Neurology.

Polyneuropathy syndromes associated with serum antibodies to sulfatide and myelin‐associated glycoprotein

B. Winslow, A. Pestronk, E. Feldman, 1991, Neurology.

Polyneuropathies associated with high titre antisulphatide antibodies: characteristics of patients with and without serum monoclonal proteins.

A. Pestronk, J. Goldstein, W. Yee, 1997, Journal of neurology, neurosurgery, and psychiatry.

Hereditary Motor and Sensory Neuropathy IIB

P. Goodfellow, J. Kwon, W. Yee, 1997, Neurology.

Characterization of cDNA and genomic DNA encoding SERCA1, the Ca(2+)-ATPase of human fast-twitch skeletal muscle sarcoplasmic reticulum, and its elimination as a candidate gene for Brody disease.

M. Phillips, J. Fujii, D. Cornblath, 1995, Genomics.

Two eminently treatable genetic metabolic myopathies.

W. Yee, 2008, Neurology India.

Reorganization of intrinsic components in the distal motor axon during outgrowth

A. Pestronk, W. Yee, K. Alderson, 1989, Journal of neurocytology.

Identification and characterisation of human dysferlin transcript variants: implications for dysferlin mutational screening and isoforms

P. Lai, W. Yee, Z. Pramono, 2009, Human Genetics.

G.P.8.15 Limb girdle muscular dystrophy 2G and novel TCAP mutations in ethnic Chinese

P. Lai, W. Yee, Z. Pramono, 2007, Neuromuscular Disorders.

Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody disease.

S. Scherer, P. Taschner, A. Odermatt, 1997, Genomics.

Dual Masking of Specific Negative Splicing Regulatory Elements Resulted in Maximal Exon 7 Inclusion of SMN2 Gene.

K. Wee, W. Yee, P. Pao, 2014, Molecular therapy : the journal of the American Society of Gene Therapy.

Identification and characterization of a novel human dysferlin transcript: dysferlin_v1

S. Takeda, P. Lai, W. Yee, 2006, Human Genetics.

A prospective study in the rational design of efficient antisense oligonucleotides for exon skipping in the DMD gene.

K. Wee, P. Lai, W. Yee, 2012, Human gene therapy.

Dynamics of Co-Transcriptional Pre-mRNA Folding Influences the Induction of Dystrophin Exon Skipping by Antisense Oligonucleotides

K. Wee, P. Lai, W. Yee, 2008, PloS one.

Phlebosclerotic colitis: imaging findings of a rare entity.

R. Cheifetz, W. Yee, J. Davis, 2005, AJR. American journal of roentgenology.

Fugu rubripes and human survival motor neuron genes: structural and functional similarities in comparative genome studies.

B. Venkatesh, P. Lai, W. Yee, 2008, Gene.

Serial diffusion-weighted magnetic resonance imaging in adult-onset citrullinaemia

Tchoyoson C. C. Lim, W. Au, P. Koh, 2003, Journal of Neurological Sciences.

Neuropathy in IgM lambda paraproteinemia. Immunoreactivity to neural proteins and chondroitin sulfate.

A. Hahn, W. Yee, S. Hearn, 1989, Acta neuropathologica.

Neuropathy in igMλ paraproteinemia

A. Hahn, W. Yee, S. Hearn, 2004, Acta Neuropathologica.

Characterization of a novel S13F desmin mutation associated with desmin myopathy and heart block in a Chinese family

P. Lai, W. Yee, P. Kathirvel, 2008, Neuromuscular Disorders.

Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy

D. Belsham, C. Greenberg, W. Yee, 1992, Journal of the Neurological Sciences.

Reply to Vance et al.

P. Goodfellow, J. Kwon, W. Yee, 1996 .

Regional heterogeneity in the distal motor axon: three zones with distinctive intrinsic components

A. Pestronk, W. Yee, K. Alderson, 1988, Journal of neurocytology.

Central sleep apnoea in congenital muscular dystrophy.

M. Mahowald, M. Kryger, W. Yee, 1991, Journal of neurology, neurosurgery, and psychiatry.

C.P.1.15 Myosin storage myopathy with a novel slow-skeletal myosin (MYH7) mutation in a Chinese patient

P. Lai, W. Yee, J. Chai, 2007, Neuromuscular Disorders.

Elevated Total Plasma Homocysteine and 677 C-T Mutation of the 5 , 1 0-Methylenetetrahydrofolate Reductase Gene in Thrombotic Vascular Disease

P. Goodfellow, J. Kwon, W. Yee, 2007 .