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Published in IEEE electron device letters (01.09.2021)
Published in IEEE electron device letters (01.09.2021)
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Recessive CHRM5 variant as a potential cause of neurogenic bladder
Schneider, Sophia, Schierbaum, Luca, Burger, Wessel A. C., Seltzsam, Steve, Wang, Chunyan, Zheng, Bixia, Wu, Chen‐Han Wilfred, Nakayama, Makiko, Connaughton, Dervla M., Mann, Nina, Shalaby, Mohamed A., Kari, Jameela A., ElDesoky, Sherif, Tasic, Velibor, Eid, Loai A., Shril, Shirlee, Thal, David M., Hildebrandt, Friedhelm
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Published in American journal of medical genetics. Part A (01.08.2023)
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Gaze Tracking and Point Estimation Using Low-Cost Head-Mounted Devices
Lee, Ko-Feng, Chen, Yen-Lin, Yu, Chao-Wei, Chin, Kai-Yi, Wu, Chen-Han
Published in Sensors (Basel, Switzerland) (30.03.2020)
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A systematic review and in silico study of potential genetic markers implicated in cases of overactive bladder
Isali, Ilaha, McClellan, Phillip, Wong, Thomas R., Sun, Clara, Stout, Amber Catherine, Schumacher, Fredrick R., Markt, Sarah, Wilfred Wu, Chen-Han, Penney, Kathryn L., El-Nashar, Sherif, Hijaz, Adonis, Sheyn, David
Published in American journal of obstetrics and gynecology (01.01.2023)
Published in American journal of obstetrics and gynecology (01.01.2023)
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ASC-J9 Blocks Cell Proliferation and Extracellular Matrix Production of Keloid Fibroblasts through Inhibiting STAT3 Signaling
Hong, Yi-Kai, Wu, Chen-Han, Lin, Yu-Chen, Huang, Yu-Lun, Hung, Kuo-Shu, Pai, Tsung-Pin, Liu, Yen-Ting, Chen, Tzu-Chi, Chan, Hardy, Hsu, Chao-Kai
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Published in International journal of molecular sciences (16.05.2022)
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TEM1/endosialin/CD248 promotes pathologic scarring and TGF-β activity through its receptor stability in dermal fibroblasts
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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Published in Journal of biomedical science (23.01.2024)
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Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs
Klämbt, Verena, Buerger, Florian, Wang, Chunyan, Naert, Thomas, Richter, Karin, Nauth, Theresa, Weiss, Anna-Carina, Sieckmann, Tobias, Lai, Ethan, Connaughton, Dervla M, Seltzsam, Steve, Mann, Nina, Majmundar, Amar J, Wu, Chen-Han W, Onuchic-Whitford, Ana C, Shril, Shirlee, Schneider, Sophia, Schierbaum, Luca, Dai, Rufeng, Bekheirnia, Mir Reza, Joosten, Marieke, Shlomovitz, Omer, Vivante, Asaf, Banne, Ehud, Mane, Shrikant, Lifton, Richard P, Kirschner, Karin M, Kispert, Andreas, Rosenberger, Georg, Fischer, Klaus-Dieter, Lienkamp, Soeren S, Zegers, Mirjam M P, Hildebrandt, Friedhelm
Published in Journal of the American Society of Nephrology (01.02.2023)
Published in Journal of the American Society of Nephrology (01.02.2023)
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CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor Mutations
Mann, Nina, Kause, Franziska, Henze, Erik K., Gharpure, Anant, Shril, Shirlee, Connaughton, Dervla M., Nakayama, Makiko, Klämbt, Verena, Majmundar, Amar J., Wu, Chen-Han W., Kolvenbach, Caroline M., Dai, Rufeng, Chen, Jing, van der Ven, Amelie T., Ityel, Hadas, Tooley, Madeleine J., Kari, Jameela A., Bownass, Lucy, El Desoky, Sherif, De Franco, Elisa, Shalaby, Mohamed, Tasic, Velibor, Bauer, Stuart B., Lee, Richard S., Beckel, Jonathan M., Yu, Weiqun, Mane, Shrikant M., Lifton, Richard P., Reutter, Heiko, Ellard, Sian, Hibbs, Ryan E., Kawate, Toshimitsu, Hildebrandt, Friedhelm
Published in American journal of human genetics (05.12.2019)
Published in American journal of human genetics (05.12.2019)
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Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)
Wu, Chen-Han Wilfred, Mann, Nina, Nakayama, Makiko, Connaughton, Dervla M., Dai, Rufeng, Kolvenbach, Caroline M., Kause, Franziska, Ottlewski, Isabel, Wang, Chunyan, Klämbt, Verena, Seltzsam, Steve, Lai, Ethan W., Selvin, Aravind, Senguttuva, Prabha, Bodamer, Olaf, Stein, Deborah R., El Desoky, Sherif, Kari, Jameela A., Tasic, Velibor, Bauer, Stuart B., Shril, Shirlee, Hildebrandt, Friedhelm
Published in Genetics in medicine (01.10.2020)
Published in Genetics in medicine (01.10.2020)
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Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models
Wang, Chunyan, Seltzsam, Steve, Zheng, Bixia, Wu, Chen‐Han Wilfred, Nicolas‐Frank, Camille, Yousef, Kirollos, Au, Kit Sing, Mann, Nina, Pantel, Dalia, Schneider, Sophia, Schierbaum, Luca, Kitzler, Thomas M., Connaughton, Dervla M., Mao, Youying, Dai, Rufeng, Nakayama, Makiko, Kari, Jameela A., El Desoky, Sherif, Shalaby, Mohammed, Eid, Loai A., Awad, Hazem S., Tasic, Velibor, Mane, Shrikant M., Lifton, Richard P., Baum, Michelle A., Shril, Shirlee, Estrada, Carlos R., Hildebrandt, Friedhelm
Published in American journal of medical genetics. Part A (01.05.2022)
Published in American journal of medical genetics. Part A (01.05.2022)
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COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans
Kitzler, Thomas M., Schneider, Ronen, Kohl, Stefan, Kolvenbach, Caroline M., Connaughton, Dervla M., Dai, Rufeng, Mann, Nina, Nakayama, Makiko, Majmundar, Amar J., Wu, Chen-Han W., Kari, Jameela A., El Desoky, Sherif M., Senguttuvan, Prabha, Bogdanovic, Radovan, Stajic, Natasa, Valivullah, Zaheer, Lek, Monkol, Mane, Shrikant, Lifton, Richard P., Tasic, Velibor, Shril, Shirlee, Hildebrandt, Friedhelm
Published in Human genetics (01.10.2019)
Published in Human genetics (01.10.2019)
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