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Wu, Xingyao
Wu, Xingyao
Other namesXingyao Wu
Verified email at uiowa.edu
Title
Cited by
Cited by
Year
GDAP1, the protein causing Charcot–Marie–Tooth disease type 4A, is expressed in neurons and is associated with mitochondria
L Pedrola, A Espert, X Wu, R Claramunt, ME Shy, F Palau
Human molecular genetics 14 (8), 1087-1094, 2005
2312005
Calcineurin regulates bone formation by the osteoblast
L Sun, HC Blair, Y Peng, N Zaidi, OA Adebanjo, XB Wu, XY Wu, J Iqbal, ...
Proceedings of the National Academy of Sciences 102 (47), 17130-17135, 2005
1762005
High-dosage ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A: results of a randomized, double-masked, controlled trial
RA Lewis, MP McDermott, DN Herrmann, A Hoke, LL Clawson, C Siskind, ...
JAMA neurology 70 (8), 981-987, 2013
1552013
Skin biopsies in myelin-related neuropathies: bringing molecular pathology to the bedside
J Li, Y Bai, K Ghandour, P Qin, M Grandis, A Trostinskaia, E Ianakova, ...
Brain 128 (5), 1168-1177, 2005
1462005
Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice
A Patzko, Y Bai, MA Saporta, I Katona, XY Wu, D Vizzuso, ML Feltri, ...
Brain 135 (12), 3551-3566, 2012
1222012
A novel mechanism for coupling cellular intermediary metabolism to cytosolic Ca2+ signaling via CD38/ADP‐ribosyl cyclase, a putative intracellular NAD+ sensor
L Sun, OA Adebanjo, A Koval, HK Anandatheerthavarada, J Iqbal, XY Wu, ...
The FASEB journal 16 (3), 302-314, 2002
1062002
PMP22 expression in dermal nerve myelin from patients with CMT1A
I Katona, X Wu, SME Feely, S Sottile, CE Siskind, LJ Miller, ME Shy, J Li
Brain 132 (7), 1734-1740, 2009
922009
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot–Marie–Tooth disease type 1B
MAC Saporta, BR Shy, A Patzko, Y Bai, M Pennuto, C Ferri, E Tinelli, ...
Brain 135 (7), 2032-2047, 2012
692012
Skin biopsies demonstrate MPZ splicing abnormalities in Charcot-Marie-Tooth neuropathy 1B
A Sabet, J Li, K Ghandour, Q Pu, X Wu, J Kamholz, ME Shy, F Cambi
Neurology 67 (7), 1141-1146, 2006
462006
Myelin protein zero mutations and the unfolded protein response in Charcot Marie Tooth disease type 1B
Y Bai, X Wu, KM Brennan, DS Wang, M D'Antonio, J Moran, J Svaren, ...
Annals of clinical and translational neurology 5 (4), 445-455, 2018
442018
Transmembrane protease serine 5: a novel Schwann cell plasma marker for CMT1A
H Wang, M Davison, K Wang, TH Xia, M Kramer, K Call, J Luo, X Wu, ...
Annals of clinical and translational neurology 7 (1), 69-82, 2020
352020
Variation in SIPA1L2 is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A
F Tao, GW Beecham, AP Rebelo, J Svaren, SH Blanton, JJ Moran, ...
Annals of neurology 85 (3), 316-330, 2019
352019
Reduced neurofilament expression in cutaneous nerve fibers of patients with CMT2E
C Pisciotta, Y Bai, KM Brennan, X Wu, T Grider, S Feely, S Wang, S Moore, ...
Neurology 85 (3), 228-234, 2015
302015
Schwann cell transcript biomarkers for hereditary neuropathy skin biopsies
J Svaren, JJ Moran, X Wu, R Zuccarino, C Bacon, Y Bai, R Ramesh, ...
Annals of neurology 85 (6), 887-898, 2019
292019
Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease
J Huang, X Wu, G Montenegro, J Price, G Wang, JM Vance, ME Shy, ...
Journal of neurology 257 (5), 735-741, 2010
292010
Modifier gene candidates in Charcot-Marie-Tooth disease type 1A: a case-only genome-wide association study
F Tao, GW Beecham, AP Rebelo, SH Blanton, JJ Moran, C Lopez-Anido, ...
Journal of neuromuscular diseases 6 (2), 201-211, 2019
222019
Mitochondrial involvement in bladder function and dysfunction
RM Levin, N Haugaard, X Wu, AP Hudson
Molecular and cellular biochemistry 194 (1), 1-15, 1999
221999
MicroRNAs as biomarkers of Charcot-Marie-tooth disease type 1A
H Wang, M Davison, K Wang, T Xia, KM Call, J Luo, X Wu, R Zuccarino, ...
Neurology 97 (5), e489-e500, 2021
182021
PMP22 exon 4 deletion causes ER retention of PMP22 and a gain‐of‐function allele in CMT1E
DS Wang, X Wu, Y Bai, C Zaidman, T Grider, J Kamholz, JR Lupski, ...
Annals of clinical and translational neurology 4 (4), 236-245, 2017
92017
Loss of mitochondrial DNA in rabbit bladder smooth muscle following partial outlet obstruction results from lack of organellar DNA replication
Z Wang, X Wu, RM Levin, AP Hudson
Molecular Urology 5 (3), 99-104, 2001
82001
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