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1دورية أكاديمية
المؤلفون: Minna Luo, Ruida He, Zaisheng Lin, Yue Shen, Guangyu Zhang, Zongfu Cao, Chao Lu, Dan Meng, Jing Zhang, Xu Ma, Muqing Cao
المصدر: Frontiers in Genetics, Vol 11 (2020)
مصطلحات موضوعية: cilia, ciliopathy, Joubert syndrome, B9 proteins, MKS1, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/article/10.3389/fgene.2020.576235/fullTest; https://doaj.org/toc/1664-8021Test
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2
المؤلفون: Min Huang, Xinlong Kong, Zaiming Tang, Zaisheng Lin, Ruida He, Muqing Cao, Xiujuan Zhang
المصدر: Journal of Cellular Physiology. 237:2703-2712
مصطلحات موضوعية: Centrosome, Physiology, Cell Cycle, Clinical Biochemistry, Cell Cycle Checkpoints, Cilia, Cell Biology, Centrioles, S Phase
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f41b7d0856753a6f315763526a200bacTest
https://doi.org/10.1002/jcp.30693Test -
3
المؤلفون: Muqing Cao, Dan Meng, Minjun Jin, Tian Zhu, Chao Lu, Yong Zhao, Xuan Zou, Huike Jiao, Gao Huafang, Chengtian Zhao, Zaisheng Lin, Yue Shen, Xueyan Wang, Li Cao, Min Huang, Hui Li, Cai Ruikun, Xu Ma, Minna Luo, Ruida He, Guanjun Luo, Cao Zongfu, Ruifang Sui, Shijing Wu
المصدر: Genetics in Medicine. 23:1041-1049
مصطلحات موضوعية: Genetics, Cilium, Kidney Diseases, Cystic, Biology, medicine.disease, Ciliopathies, Phosphoric Monoester Hydrolases, Retina, Joubert syndrome, Cytoskeletal Proteins, Ciliopathy, Intraflagellar transport, Cerebellum, Ciliogenesis, INPP5E, medicine, Animals, Humans, Abnormalities, Multiple, Hedgehog Proteins, Eye Abnormalities, sense organs, Ciliary membrane, Zebrafish, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::127ad44b0bfaf0e2964913f0402a42d6Test
https://doi.org/10.1038/s41436-021-01106-zTest -
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المؤلفون: Minna Luo, Ruida He, Zaisheng Lin, Yue Shen, Guangyu Zhang, Zongfu Cao, Chao Lu, Dan Meng, Jing Zhang, Xu Ma, Muqing Cao
مصطلحات موضوعية: Genetics, Genetic Engineering, Biomarkers, Developmental Genetics (incl. Sex Determination), Epigenetics (incl. Genome Methylation and Epigenomics), Gene Expression (incl. Microarray and other genome-wide approaches), Genome Structure and Regulation, Genomics, Genetically Modified Animals, Livestock Cloning, Gene and Molecular Therapy, cilia, ciliopathy, Joubert syndrome, B9 proteins, MKS1
الإتاحة: https://doi.org/10.3389/fgene.2020.576235.s001Test
https://figshare.com/articles/dataset/Table_1_Novel_Compound_Heterozygous_Variants_in_MKS1_Leading_to_Joubert_Syndrome_xlsx/13088612Test -
5
المؤلفون: Cao Zongfu, Chao Lu, Li Cao, Tian Zhu, Min Huang, Xu Ma, Muqing Cao, Gao Huafang, Minjun Jin, Shijing Wu, Dan Meng, Xuan Zou, Huike Jiao, Yong Zhao, Zaisheng Lin, Hui Li, Guanjun Luo, Ruida He, Chengtian Zhao, Yue Shen, Cai Ruikun, Xueyan Wang, Minna Luo, Ruifang Sui
المصدر: Genetics in Medicine. 23:1175
مصطلحات موضوعية: Genetics, Intraflagellar transport, medicine, Biology, medicine.disease, Genetics (clinical), Joubert syndrome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::9f64cc09012cea8a9197d03d966d26d5Test
https://doi.org/10.1038/s41436-021-01191-0Test