Ngā hua rapu - Lizhu Yang
- E whakaatu ana i te 1 - 8 hua o te 8
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Selective Molecular Potassium Channel Blockade Prevents Atrial Fibrillation mā Guy Amit, Kan Kikuchi, Ian D. Greener, Lizhu Yang, Victor Novack, J. Kevin Donahue
I whakaputaina 2010Artigo -
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Alpha-Lipoic Acid Mediates Clearance of Iron Accumulation by Regulating Iron Metabolism in a Parkinson’s Disease Model Induced by 6-OHDA mā Shengyan Tai, Qian Zheng, Suzhen Zhai, Ting Cai, Li Xu, Lizhu Yang, Ling Jiao, Chunlin Zhang
I whakaputaina 2020Artigo -
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Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning Techniques mā Yu Fujinami‐Yokokawa, Nikolas Pontikos, Lizhu Yang, Kazushige Tsunoda, Kazutoshi Yoshitake, Takeshi Iwata, Hiroaki Miyata, Kaoru Fujinami, on behalf of Japan Eye Genetics Consortium
I whakaputaina 2019Artigo -
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Mutations in human IFT140 cause non-syndromic retinal degeneration mā Mingchu Xu, Lizhu Yang, Feng Wang, Huajin Li, Xia Wang, Weichen Wang, Zhongqi Ge, Keqing Wang, Li Zhao, Hui Li, Yumei Li, Ruifang Sui, Rui Chen
I whakaputaina 2015Artigo -
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Enhanced Strength for Double Network Hydrogel Adhesive Through Cohesion‐Adhesion Balance mā Rijian Song, Xiaoyu Wang, Melissa Johnson, Cameron Milne, Anna Lesniak‐Podsiadlo, Yinghao Li, Jing Lyu, Zishan Li, Chunyu Zhao, Lizhu Yang, Irene Lara‐Sáez, A Sigen, Wenxin Wang
I whakaputaina 2024Artigo -
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<i>CEP78</i>is mutated in a distinct type of Usher syndrome mā Qing Fu, Mingchu Xu, Chen Xue, Xunlun Sheng, Zhisheng Yuan, Yani Liu, Huajin Li, Zixi Sun, Huiping Li, Lizhu Yang, Keqing Wang, Fangxia Zhang, Yumei Li, Chen Zhao, Ruifang Sui, Rui Chen
I whakaputaina 2016Artigo -
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Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies mā Mingchu Xu, Ya‐Jing Xie, Hana Abouzeid, Christopher T. Gordon, Alessia Fiorentino, Zixi Sun, Anna Lehman, Ihab S. Osman, Rachayata Dharmat, Rosa Riveiro-Álvarez, Linda Bapst-Wicht, Darwin Babino, Gavin Arno, Virginia Busetto, Li Zhao, Hui Li, Miguel Ángel López-Martínez, Liliana F. Azevedo, Laurence Hubert, Nikolas Pontikos, Aiden Eblimit, Isabel Lorda‐Sánchez, Valeria Kheir, Vincent Plagnol, Myriam Oufadem, Zachry T. Soens, Lizhu Yang, Christine Bôle‐Feysot, Rolph Pfundt, Nathalie Allaman-Pillet, Patrick Nitschké, Michael E. Cheetham, Stanislas Lyonnet, Smriti A. Agrawal, Huajin Li, Gaëtan Pinton, Michel Michaelides, Claude Besmond, Yumei Li, Zhisheng Yuan, Johannes von Lintig, Andrew R. Webster, Hervé Le Hir, Peter Stoilov, Jeanne Amiel, Alison J. Hardcastle, Carmen Ayuso, Ruifang Sui, Rui Chen, Rando Allikmets, Daniel F. Schorderet, Graeme Black, Georgina Hall, Rachel Gillespie, Simon Ramsden, Forbes D.C. Manson, Panagiotis I. Sergouniotis, Chris F. Inglehearn, Carmel Toomes, Manir Ali, Martin McKibbin, James A. Poulter, Emma Lord, Andrea H. Németh, Stephanie Halford, Susan M. Downes, Jing Yu
I whakaputaina 2017Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Biology
Gene
Genetics
Medicine
Exome
Exome sequencing
Phenotype
Retinitis pigmentosa
Artificial intelligence
Biochemistry
Chemistry
Computer science
Disease gene identification
Genetic heterogeneity
Internal medicine
Mutation
Pharmacology
Retinal
Retinal degeneration
Sanger sequencing
Adhesion
Adhesive
Anterior cingulate cortex
Atrial fibrillation
Attentional control
Audiology
Bardet–Biedl syndrome
Blockade
Candidate gene
Cardiology