Xin Fan, Ph.D.

2010 Department of Physics and Astronomy University of Delaware, Newark, DE, United States 
Condensed Matter Physics, Nanotechnology
"Xin Fan"


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John Q. Xiao grad student 2010 University of Delaware
 (Magnetic dynamics in nanostructures.)
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Li W, Fan X, Zhang Y, et al. (2020) A novel pathogenic frameshift variant unmasked by a large de novo deletion at 13q21.33-q31.1 in a Chinese patient with neuronal ceroid lipofuscinosis type 5. Bmc Medical Genetics. 21: 100
Fang D, Li X, Liu H, et al. (2020) Author Correction: BiVO-rGO with a novel structure on steel fabric used as high-performance photocatalysts. Scientific Reports. 10: 5669
Zhang Q, Zhang Y, Xu X, et al. (2019) [Establishment of a system for rapid detection of JAK2 V617F mutation in myeloproliferative diseases]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 36: 980-984
Zhang L, Shi H, Chen H, et al. (2019) Dedifferentiation process driven by radiotherapy-induced HMGB1/TLR2/YAP/HIF-1α signaling enhances pancreatic cancer stemness. Cell Death & Disease. 10: 724
Wang W, Wang T, Amin VP, et al. (2019) Anomalous spin-orbit torques in magnetic single-layer films. Nature Nanotechnology
Fan X, Du J, Wang MH, et al. (2019) Irisin Contributes to the Hepatoprotection of Dexmedetomidine during Intestinal Ischemia/Reperfusion. Oxidative Medicine and Cellular Longevity. 2019: 7857082
Fan X, Duan Y, Cheng S, et al. (2019) Fast density-peaks clustering for registration-free pediatric white matter tract analysis. Artificial Intelligence in Medicine. 96: 1-11
Du J, Fan X, Yang B, et al. (2019) Irisin pretreatment ameliorates intestinal ischemia/reperfusion injury in mice through activation of the Nrf2 pathway. International Immunopharmacology. 73: 225-235
Chen X, Cheng F, Liu Y, et al. (2019) Toll-like receptor 2 and Toll-like receptor 4 exhibit distinct regulation of cancer cell stemness mediated by cell death-induced high-mobility group box 1. Ebiomedicine
Fu C, Luo S, Zhang Y, et al. (2018) Chromosomal microarray and whole exome sequencing identify genetic causes of congenital hypothyroidism with extra-thyroidal congenital malformations. Clinica Chimica Acta; International Journal of Clinical Chemistry
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