Perceptual Changes in the Anterior Maxilla after Placement of Endosseous Implants by Jacobs, Reinhilde, Wu, Chen-Han, Goossens, Kitty, Van Loven, Karen, van Steenberghe, Daniel

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Type-2 Fuzzy Control of a Mobile Robot for Avoiding Moving Object by Juang, Jih Gau, Wu, Chen Han

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A case-control study on the psychophysical and psychological characteristics of the phantom tooth phenomenon by Jacobs, Reinhilde, Wu, Chen-Han, Goossens, Kitty, De Laat, Antoon, Van Loven, Karen, Antonis, Yasmine, Lambrechts, Paul, van Steenberghe, Daniel

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Mlkl knockout mice demonstrate the indispensable role of Mlkl in necroptosis by Wu, Jianfeng, Huang, Zhe, Ren, Junming, Zhang, Zhirong, He, Peng, Li, Yangxin, Ma, Jianhui, Chen, Wanze, Zhang, Yingying, Zhou, Xiaojuan, Yang, Zhentao, Wu, Su-Qin, Chen, Lanfen, Han, Jiahuai

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Polygenic and polyphenotypic dimensions of nephrolithiasis: Unveiling the genetic and metabolic interconnections by Huang, Yu-Ren, Su, Ethan, Bodner, Donald, Schumacher, Fredrick, Wu, Chen-Han Wilfred

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Efficient quantum secure direct communication with authentication by Wen jie Liu, Han-wu Chen, Zhi-giang Li, Zhi-hao Liu, Fang-ying Xiao

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Multilevel Cell Ferroelectric HfZrO2 FinFET with High Speed and Large Memory Window using AlON Interfacial Layer by Yan, Siao-Cheng, Wu, Chen-Han, Sun, Chong-Jhe, Zhong, Xin-Chan, Chang, Chih-Siang, Peng, Hao-Kai, Wu, Yung-Hsien, Wu, Yung-Chun

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The convex-concave characteristics of Gaussian channel capacity functions by Han Wu Chen, Yanagi, K.

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GENETIC PREVALENCE OF PRIMARY HYPEROXALURIA TYPE 1 by Eam, Euhun, Chang, Joshua, Lovrenert, Katreya, Baum, Michelle, Hildebrandt, Friedhelm, Bodner, Donald, Schumacher, Fredrick, Wu, Chen-han

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Additional Mutations in NRIP1 in Families with Congenital Anomalies of the Kidneys and Urinary Tract (CAKUT): PO1671 by Zheng, Bixia, Schneider, Sophia, Deutsch, Konstantin, Wang, Chunyan, Seltzsam, Steve, Nakayama, Makiko, Wu, Chen-Han W., Shril, Shirlee, Hildebrandt, Friedhelm

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Reverse Phenotyping Facilitates Disease Allele Calling in Whole-Exome Sequencing of Patients with Congenital Anomalies of Kidney and Urinary Tract (CAKUT): PO1348 by Seltzsam, Steve, Wang, Chunyan, Zheng, Bixia, Connaughton, Dervla M., Wu, Chen-Han W., Schneider, Sophia, Schierbaum, Luca M., Shril, Shirlee, Hildebrandt, Friedhelm

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TEM1/endosialin/CD248 promotes pathologic scarring and TGF-[beta] activity through its receptor stability in dermal fibroblasts by Hong, Yi-Kai, Lin, Yu-Chen, Cheng, Tsung-Lin, Lai, Chao-Han, Chang, Yi-Han, Huang, Yu-Lun, Hung, Chia-Yi, Wu, Chen-Han, Hung, Kuo-Shu, Ku, Ya-Chu, Ho, Yen-Ting, Tang, Ming-Jer, Lin, Shu-Wha, Shi, Guey-Yueh, McGrath, John A, Wu, Hua-Lin, Hsu, Chao-Kai

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Generating Monogenic CAKUT Candidate Genes from Existing Single-Cell Transcriptomics Data of Human Fetal Kidney: PO1634 by Schierbaum, Luca M., Schneider, Sophia, Buerger, Florian, Seltzsam, Steve, Wang, Chunyan, Zheng, Bixia, Wu, Chen-Han W., Nakayama, Makiko, Shril, Shirlee, Hildebrandt, Friedhelm

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CHRM5 Mutations as a Potential Cause of Neurogenic Bladder: PO1635 by Schneider, Sophia, Schierbaum, Luca M., Seltzsam, Steve, Wang, Chunyan, Zheng, Bixia, Wu, Chen-Han W., Nakayama, Makiko, Shril, Shirlee, Hildebrandt, Friedhelm

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Degenerate asymmetric quantum concatenated codes for correcting biased quantum errors Project supported by the National Natural Science Foundation of China (Grant Nos. 61802175, 61... by Fan, Ji-Hao, Li, Jun, Chen, Han-Wu, Liu, Wen-Jie

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Neferine attenuates development of testosterone-induced benign prostatic hyperplasia in mice by regulating androgen and TGF-β/Smad signaling pathways by Liu, Chi-Ming, Shao, ZiChen, Chen, XuZhou, Chen, HanWu, Su, MengQiao, Zhang, ZiWen, Wu, ZhengPing, Zhang, Peng, An, LiJie, Jiang, YinJie, Ouyang, Ai-Jun

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A Construction of Quantum Error-Locating Codes Supported by the National Natural Science Foundation of China under Grant No. 61170321, the Specialized Research Fund for the Doctora... by Fan, Ji-Hao, Chen, Han-Wu

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An efficient quantum secret sharing scheme based on orthogonal product states by Juan Xu, Han-wu Chen, Wen-jie Liu, Zhi-hao Liu

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Copy Number Variation Analysis Increases Diagnostic Yield of Exome Sequencing and Facilitates the Identification of Genetic Causation for Congenital Anomalies of the Kidneys and Ur... by Wu, Chen-Han W., Lim, Tze Yin, Wang, Chunyan, Seltzsam, Steve, Zheng, Bixia, Schierbaum, Luca M., Schneider, Sophia, Mann, Nina, Connaughton, Dervla M., Bauer, Stuart B., Sanna-Cherchi, Simone, Shril, Shirlee, Hildebrandt, Friedhelm

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Whole-Exome Sequencing Identifies Likely Causative Variants in Four Candidate Genes in 16 Families with Spina Bifida: PO1645 by Wang, Chunyan, Wu, Chen-Han W., Seltzsam, Steve, Zheng, Bixia, Schneider, Sophia, Schierbaum, Luca M., Mann, Nina, Nakayama, Makiko, Shril, Shirlee, Bauer, Stuart B., Baum, Michelle A., Estrada, Carlos R., Hildebrandt, Friedhelm

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