Xueping Fan, Ph.D.

Affiliations: 
2002 McGill University, Montreal, QC, Canada 
Area:
Neurogenetics
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"Xueping Fan"
Mean distance: 19.61 (cluster 28)
 

Parents

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Guy A. Rouleau grad student 2002 McGill
 (Molecular characterization of the OPMD gene product, poly(A) binding protein nuclear 1 (PABPN1).)
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Publications

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Tumelty KE, Higginson-Scott N, Fan X, et al. (2018) Identification of direct negative crosstalk between the SLIT2 and Bone Morphogenetic Protein-Gremlin signaling pathways. The Journal of Biological Chemistry
Fan X, Yang H, Kumar S, et al. (2016) SLIT2/ROBO2 signaling pathway inhibits nonmuscle myosin IIA activity and destabilizes kidney podocyte adhesion. Jci Insight. 1: e86934
Zhang Y, Fan J, Ho JW, et al. (2015) Crim1 regulates integrin signaling in murine lens development. Development (Cambridge, England)
Hwang DY, Kohl S, Fan X, et al. (2015) Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract. Human Genetics. 134: 905-16
Quintero-Rivera F, Xi QJ, Keppler-Noreuil KM, et al. (2015) MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus. Human Molecular Genetics. 24: 2375-89
Fan X, Li Q, Pisarek-Horowitz A, et al. (2012) Inhibitory effects of Robo2 on nephrin: a crosstalk between positive and negative signals regulating podocyte structure. Cell Reports. 2: 52-61
Lu W, van Eerde AM, Fan X, et al. (2007) Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux. American Journal of Human Genetics. 80: 616-32
Lu W, Eerde Av, Fan X, et al. (2007) 128: Disruption of ROBO2 is Associated with Urinary Tract Anomalies and Confers Risk of Vesicoureteral Reflux American Journal of Kidney Diseases. 49
Abu-Baker A, Laganiere S, Fan X, et al. (2005) Cytoplasmic targeting of mutant poly(A)-binding protein nuclear 1 suppresses protein aggregation and toxicity in oculopharyngeal muscular dystrophy. Traffic (Copenhagen, Denmark). 6: 766-79
Fan X, Messaed C, Dion P, et al. (2003) HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 30: 244-51
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