Αποτελέσματα αναζήτησης - Lizhu Yang
- Εμφανίζονται 1 - 8 Αποτελέσματα από 8
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Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning Techniques από Yu Fujinami‐Yokokawa, Nikolas Pontikos, Lizhu Yang, Kazushige Tsunoda, Kazutoshi Yoshitake, Takeshi Iwata, Hiroaki Miyata, Kaoru Fujinami, on behalf of Japan Eye Genetics Consortium
Έκδοση 2019Artigo -
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Enhanced Strength for Double Network Hydrogel Adhesive Through Cohesion‐Adhesion Balance από 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
Έκδοση 2024Artigo -
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Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies από 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
Έκδοση 2017Artigo
Εργαλεία αναζήτησης:
Σχετικά θέματα
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