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1دورية أكاديمية
المؤلفون: Jianfan Chen, Xueqing Xu, Song Chen, Ting Lu, Yingchun Zheng, Zhongzhi Gan, Zongrui Shen, Shunfei Ma, Duocai Wang, Leyi Su, Fei He, Xuan Shang, Huiyong Xu, Dong Chen, Leitao Zhang, Fu Xiong
المصدر: International Journal of Oral Science, Vol 15, Iss 1, Pp 1-13 (2023)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2049-3169
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2دورية أكاديمية
المؤلفون: Yushi Peng, Meize Pan, Yuchen Wang, Zongrui Shen, Jian Xu, Fu Xiong, Hongbo Xiao, Yun Miao
المصدر: Renal Failure, Vol 46, Iss 2 (2024)
مصطلحات موضوعية: Fabry disease, α-Gal A protein, mutation, enzymatic activity, subcellular localization, cell apoptosis, Diseases of the genitourinary system. Urology, RC870-923
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Qi Liu, Zongrui Shen, Hong Pan, Shunfei Ma, Fu Xiong, Fei He
المصدر: Frontiers in Pediatrics, Vol 11 (2023)
مصطلحات موضوعية: Gaucher disease, GBA1, c.1240G > C, c.1342G > C, cell experiment, Pediatrics, RJ1-570
وصف الملف: electronic resource
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4
المؤلفون: Zongrui Shen, Jinquan Lao, Wan Ying Lin, Xiang Qu, Qianqian Zhang, Jie Yang, Liuyuan Wei, Qi Wang, Xiangmin Xu, Yuhao Qiu
المصدر: International Journal of Laboratory Hematology. 43:1620-1627
مصطلحات موضوعية: Erythrocyte Indices, Proband, Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, Erythrocytes, Genotype, Clinical Biochemistry, beta-Globins, Biology, Compound heterozygosity, Frameshift mutation, Exon, hemic and lymphatic diseases, Humans, Genetic Predisposition to Disease, Genetic Testing, Globin, Frameshift Mutation, Alleles, Genetic Association Studies, Sequence Deletion, Inclusion Bodies, Genetics, beta-Thalassemia, Biochemistry (medical), Heterozygote advantage, Exons, Hematology, General Medicine, Phenotype, Stop codon, Amino Acid Substitution