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1دورية أكاديمية
المؤلفون: Jing Chen, Gao-Bo Ye, Jin-Rong Huang, Min Peng, Wei-Yue Gu, Pin Xiong, Hong-min Zhu
المصدر: Frontiers in Molecular Neuroscience, Vol 16 (2023)
مصطلحات موضوعية: TP53RK gene, Galloway–Mowat syndrome, nephrotic syndrome, proteinuria, global developmental delays, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
وصف الملف: electronic resource
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2
المؤلفون: Min Xu, Jiao Jiang, Yan He, Wei-Yue Gu, Bo Jin
المصدر: World Journal of Clinical Cases. 10:9332-9339
مصطلحات موضوعية: General Medicine
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::86c13402e8d74b6355b4b35efc9de98b
https://doi.org/10.12998/wjcc.v10.i26.9332 -
3
المؤلفون: Qin Wang, Rui Gu, Fu‐wei Li, Wei‐yue Gu, Jian‐jiang Zhang
المصدر: Clinical Genetics.
مصطلحات موضوعية: Genetics, Genetics (clinical)
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4
المؤلفون: Meng Zhang, Jing Yang, Ling Jin, Wei-Yue Gu, Yonghong Zhang, Xisi Wang, Shuang Huang, Jun Li, Chunju Zhou, Yi Liu, Chao Gao, Huyong Zheng, Yan-long Duan
المصدر: World J Clin Cases
مصطلحات موضوعية: Alectinib, business.industry, Central nervous system, Case Report, General Medicine, medicine.disease, Lymphoma, 03 medical and health sciences, Pediatric Anaplastic Large Cell Lymphoma, 0302 clinical medicine, medicine.anatomical_structure, hemic and lymphatic diseases, 030220 oncology & carcinogenesis, Cancer research, Medicine, 030211 gastroenterology & hepatology, CLTC, business, ALK Translocation
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94bdf3b139774e4691683c2a977bb1a8
https://doi.org/10.12998/wjcc.v8.i9.1685 -
5
المؤلفون: Jing-Da Qiao, Wen-Jun Bian, Yan-Hui Chen, Rong-Na Ren, Na He, Mi Jiang, Jie Wang, Xiao-Rong Liu, Yi Wu, Si-Mei Lin, Yu-Xi Liu, Tao Su, Yan Sun, Bin Li, Zhen Mei, Wei-Ping Liao, Yi-Wu Shi, De-Tian Liu, Yu Jing, Wei-Yue Gu, Bing-Mei Li, Yong-Hong Yi, Han-Kui Liu
المصدر: Brain
مصطلحات موضوعية: Proband, Adult, Male, Adolescent, Hippocampus, Nerve Tissue Proteins, Biology, Compound heterozygosity, Bioinformatics, medicine.disease_cause, Drosophila knockdown model, Animals, Genetically Modified, Epilepsy, UNC13B, medicine, Missense mutation, Animals, Humans, Amino Acid Sequence, Child, Loss function, Mutation, AcademicSubjects/SCI01870, Genetic Variation, Original Articles, medicine.disease, electrophysiology, Treatment Outcome, loss of function, Child, Preschool, AcademicSubjects/MED00310, Drosophila, Female, Neurology (clinical), Epilepsies, Partial, partial epilepsy, Synaptic vesicle priming
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fa099bf8721febbc8c453830e38a8f0
https://pubmed.ncbi.nlm.nih.gov/34897376 -
6
المؤلفون: Rong, Liu, Tao, Hu, Jun-hui, Li, Chao, Liang, Wei-yue, Gu, Xiao-dong, Shi, Hong-xing, Wang
المصدر: Chinese medical journal. 126(23)
مصطلحات موضوعية: Male, Fanconi Anemia, Child, Preschool, Fanconi Anemia Complementation Group D2 Protein, Mutation, Ubiquitination, Humans, Female, Child
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::91fd75f948a30c932055be7982c80fe9
https://pubmed.ncbi.nlm.nih.gov/24286411