Xingyao Wu

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Schwann cell transcript biomarkers for hereditary neuropathy skin biopsies

J. Svaren, John J. Moran, Xingyao Wu, 2019, Annals of neurology.

PMP22 expression in dermal nerve myelin from patients with CMT1A.

I. Katona, Xingyao Wu, M. Shy, 2009, Brain : a journal of neurology.

High-dosage ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A: results of a randomized, double-masked, controlled trial.

R. Lewis, M. Mcdermott, D. Herrmann, 2013, JAMA neurology.

PMP22 exon 4 deletion causes ER retention of PMP22 and a gain‐of‐function allele in CMT1E

J. Lupski, C. Zaidman, A. Connolly, 2017, Annals of clinical and translational neurology.

PMP 22 exon 4 deletion causes ER retention of PMP 22 and a gain-of-function allele in CMT 1 E

J. Lupski, C. Zaidman, A. Connolly, 2017 .

Transmembrane protease serine 5: a novel Schwann cell plasma marker for CMT1A

J. Svaren, K. Call, John J. Moran, 2019, Annals of clinical and translational neurology.

Myelin protein zero mutations and the unfolded protein response in Charcot Marie Tooth disease type 1B

J. Svaren, John J. Moran, Xingyao Wu, 2018, Annals of clinical and translational neurology.

PMP 22 expression in dermal nerve myelin from patients with CMT 1 A

I. Katona, Xingyao Wu, M. Shy, 2009 .

MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B.

D. Kirschner, M. Pennuto, Xingyao Wu, 2012, Brain : a journal of neurology.

MpzR 98 C arrests Schwann cell development in a mouse model of early-onset Charcot – Marie – Tooth disease type 1 B

D. Kirschner, M. Pennuto, Xingyao Wu, 2012 .

Cloning of COX4 cDNA from the NZ white rabbit and expression of this gene in bladder smooth muscle following partial outlet obstruction

A. Hudson, Xingyao Wu, R. Levin, 2002, World Journal of Urology.

Mitochondrial involvement in bladder function and dysfunction

A. Hudson, Xingyao Wu, R. Levin, 1999, Molecular and Cellular Biochemistry.

Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease

Gaofeng Wang, S. Züchner, J. Vance, 2010, Journal of Neurology.

Variation in SIPA1L2 is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A

F. Baas, S. Züchner, G. Beecham, 2019, Annals of neurology.

GDAP1, the protein causing Charcot-Marie-Tooth disease type 4A, is expressed in neurons and is associated with mitochondria.

Xingyao Wu, M. Shy, L. Pedrola, 2005, Human molecular genetics.

Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice.

I. Katona, F. Sarkar, D. Kirschner, 2012, Brain : a journal of neurology.

MicroRNAs as Biomarkers of Charcot-Marie-Tooth Disease Type 1A

J. Svaren, K. Call, Xingyao Wu, 2021, Neurology.

Negative correlation between serum pyruvate kinase M2 and cognitive function in patients with cerebral small vessel disease

Xingyao Wu, Xiangyang Zhu, Yong Zhou, 2023, Clinical Neurology and Neurosurgery.

Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedside.

A. Schenone, Xingyao Wu, M. Shy, 2005, Brain : a journal of neurology.

Reduced neurofilament expression in cutaneous nerve fibers of patients with CMT2E

Michael A. Gonzalez, S. Zuchner, Xingyao Wu, 2015, Neurology.

Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study

F. Baas, S. Züchner, G. Beecham, 2019, Journal of neuromuscular diseases.

Detection of Copy Number Variation by SNP-Allelotyping

N. Schnetz-Boutaud, Xingyao Wu, M. Shy, 2015, Journal of neurogenetics.

Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice.

I. Katona, F. Sarkar, D. Kirschner, 2012, Brain : a journal of neurology.