Sökresultat - Wang, Fengxiang

Stratifying ferroptosis sensitivity in cells and mouse tissues by photochemical activation of lipid peroxidation and fluorescent imaging av Wang, Fengxiang, Naowarojna, Nathchar, Zou, Yilong

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Eomesodermin Requires Transforming Growth Factor-β/Activin Signaling and Binds Smad2 to Activate Mesodermal Genes av Picozzi, Paola, Wang, Fengxiang, Cronk, Kevin, Ryan, Kenneth

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A retrospective study of eyeball rupture in patients with or without orbital fracture av Chen, Xiang, Yao, Yi, Wang, Fengxiang, Liu, Tiecheng, Zhao, Xiao

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The Dark Side of Malleability: Incremental Theory Promotes Immoral Behaviors av Huang, Niwen, Zuo, Shijiang, Wang, Fang, Cai, Pan, Wang, Fengxiang

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Recognition and Classification of Ship Images Based on SMS-PCNN Model av Wang, Fengxiang, Liang, Huang, Zhang, Yalun, Xu, Qingxia, Zong, Ruirui

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Study of minimally invasive radiofrequency ablation of the ciliary body for the treatment of glaucoma in rabbits av Hou, Baoke, Wang, Fengxiang, Ye, Zi, Jin, Xin, Fu, Yu, Li, Zhaohui

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Construction and Validation of a Lung Cancer Diagnostic Model Based on 6-Gene Methylation Frequency in Blood, Clinical Features, and Serum Tumor Markers av Kang, Chunyan, Wang, Dandan, Zhang, Xiuzhi, Wang, Lingxiao, Wang, Fengxiang, Chen, Jie

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Clinical Study of Stellate Ganglion Block Combined with General Anesthesia on Hemodynamics, Cognitive Function, and Gastrointestinal Function in Elderly Patients Undergoing Partial... av Chen, Wen, Chen, Baohua, Wang, Fengxiang, Wu, Qingsong, Liu, Wenying, Wei, Hong, Li, Changke

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The IFN-induced expression of APOBEC3G in human blood brain barrier exerts a potent intrinsic immunity to block HIV-1 entry to central nervous system av Argyris, Elias G, Acheampong, Edward, Wang, Fengxiang, Huang, Jialing, Chen, Keyang, Mukhtar, Muhammad, Zhang, Hui

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Microduplications at the 15q11.2 BP1–BP2 locus are enriched in patients with anorexia nervosa av Chang, Xiao, qu, Huiqi, Liu, Yichuan, Glessner, Joseph, Hou, Cuiping, Wang, Fengxiang, Li, Jin, Sleiman, Patrick, Hakonarson, Hakon

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Early Infantile Epileptic Encephalopathy in an STXBP1 Patient with Lactic Acidemia and Normal Mitochondrial Respiratory Chain Function av Li, Dong, Bhoj, Elizabeth, McCormick, Elizabeth, Wang, Fengxiang, Snyder, James, Wang, Tiancheng, Zhao, Yan, Kim, Cecilia, Chiavacci, Rosetta, Tian, Lifeng, Falk, Marni J., Hakonarson, Hakon

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PALP: a rapid imaging technique for stratifying ferroptosis sensitivity in normal and tumor tissues in situ av Wang, Fengxiang, Graham, Emily T., Naowarojna, Nathchar, Shi, Zhennan, Wang, Yuqi, Xie, Guanglei, Zhou, Lili, Salmon, Wendy, Jia, Jie-Min, Wang, Xi, Huang, Yuwei, Schreiber, Stuart L., Zou, Yilong

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The effect of CD47 modified polymer surfaces on inflammatory cell attachment and activation av Stachelek, Stanley J., Finley, Matthew J., Alferiev, Ivan S., Wang, Fengxiang, Tsai, Richard, Eckells, Edward C., Tomczyk, Nancy, Connolly, Jeanne M., Discher, Dennis E., Eckmann, David M., Levy, Robert J.

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Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study av Cardinale, Christopher J., Li, Dong, Tian, Lifeng, Connolly, John J., March, Michael E., Hou, Cuiping, Wang, Fengxiang, Snyder, James, Kim, Cecilia E., Chiavacci, Rosetta M., Sleiman, Patrick M., Burnham, Jon M., Hakonarson, Hakon

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Genome-wide association identifies diverse causes of common variable immunodeficiency av Orange, Jordan S., Glessner, Joseph T., Resnick, Elena, Sullivan, Kathleen E., Lucas, Mary, Ferry, Berne, Kim, Cecilia E., Hou, Cuiping, Wang, Fengxiang, Chiavacci, Rosetta, Kugathasan, Subra, Sleasman, John W., Baldassano, Robert, Perez, Elena E., Chapel, Helen, Cunningham-Rundles, Charlotte, Hakonarson, Hakon

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Delayed diagnosis of congenital myasthenia due to associated mitochondrial enzyme defect av Guo, Yiran, Menezes, Minal, Menezes, Manoj, Liang, Jinlong, Li, Dong, Riley, Lisa G, Clarke, Nigel F, Ian Andrews, P., Tian, Lifeng, Webster, Richard, Wang, Fengxiang, Liu, Xuanzhu, Shen, Yulan, Thorburn, David R, Keating, Brendan J, Engel, Andrew, Hakonarson, Hakon, Christodoulou, John, Xu, Xun

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Copy Number Variations in Alternative Splicing Gene Networks Impact Lifespan av Glessner, Joseph T., Smith, Albert Vernon, Panossian, Saarene, Kim, Cecilia E., Takahashi, Nagahide, Thomas, Kelly A., Wang, Fengxiang, Seidler, Kallyn, Harris, Tamara B., Launer, Lenore J., Keating, Brendan, Connolly, John, Sleiman, Patrick M. A., Buxbaum, Joseph D., Grant, Struan F. A., Gudnason, Vilmundur, Hakonarson, Hakon

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Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population av Matsunami, Nori, Hensel, Charles H, Baird, Lisa, Stevens, Jeff, Otterud, Brith, Leppert, Tami, Varvil, Tena, Hadley, Dexter, Glessner, Joseph T, Pellegrino, Renata, Kim, Cecilia, Thomas, Kelly, Wang, Fengxiang, Otieno, Frederick G, Ho, Karen, Christensen, Gerald B, Li, Dongying, Prekeris, Rytis, Lambert, Christophe G, Hakonarson, Hakon, Leppert, Mark F

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Rare variants at 16p11.2 are associated with common variable immunodeficiency av Maggadottir, S. Melkorka, Li, Jin, Glessner, Joseph T., Li, Yun Rose, Wei, Zhi, Chang, Xiao, Mentch, Frank D, Thomas, Kelly A, Kim, Cecilia E., Zhao, Yan, Hou, Cuiping, Wang, Fengxiang, Jørgensen, Silje F., Perez, Elena E., Sullivan, Kathleen E., Orange, Jordan Scott, Karlsen, Tom H., Chapel, Helen, Cunningham-Rundles, Charlotte, Hakonarson, Hakon

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An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2 av Mancini, Cecilia, Orsi, Laura, Guo, Yiran, Li, Jiankang, Chen, Yulan, Wang, Fengxiang, Tian, Lifeng, Liu, Xuanzhu, Zhang, Jianguo, Jiang, Hui, Nmezi, Bruce Shike, Tatsuta, Takashi, Giorgio, Elisa, Di Gregorio, Eleonora, Cavalieri, Simona, Pozzi, Elisa, Mortara, Paolo, Caglio, Maria Marcella, Balducci, Alessandro, Pinessi, Lorenzo, Langer, Thomas, Padiath, Quasar S, Hakonarson, Hakon, Zhang, Xiuqing, Brusco, Alfredo

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