-
1
المؤلفون: Yuanying Miao, Huaichao Luo, Zimeng Ye, Xueping Zhang, Ying Lin, Ping Shuai
المصدر: Journal of Genetics. 96:985-992
مصطلحات موضوعية: Male, 0301 basic medicine, Genotype, Blood lipids, Single-nucleotide polymorphism, Genome-wide association study, 030204 cardiovascular system & hematology, Biology, Logistic regression, Polymorphism, Single Nucleotide, 03 medical and health sciences, Apolipoproteins E, 0302 clinical medicine, Genetics, Genetic predisposition, medicine, Humans, Genetic Predisposition to Disease, Genetic Association Studies, Triglycerides, Dyslipidemias, PCSK9, Cholesterol, HDL, Hypertriglyceridemia, nutritional and metabolic diseases, Cholesterol, LDL, Middle Aged, medicine.disease, Lipids, 030104 developmental biology, Female, Hydroxymethylglutaryl CoA Reductases, lipids (amino acids, peptides, and proteins), Proprotein Convertase 9, Microtubule-Associated Proteins, Dyslipidemia
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45fc52b938c797bf7631f16a9eb10b4cTest
https://doi.org/10.1007/s12041-017-0864-xTest -
2
المؤلفون: Zhenglin Yang, Chang Tan, Xiaoxin Guo, Yilin Yin, Yi Shi, Chao Qu, Bo Gong, Xiaoqi Liu, Jing Li, Ying Lin, Zimeng Ye, Yilian Cheng, Ping Shuai
المصدر: Ophthalmic Genetics. 39:35-40
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, China, medicine.medical_specialty, Linkage disequilibrium, Intraocular pressure, Genotype, genetic structures, Open angle glaucoma, Glaucoma, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Linkage Disequilibrium, 03 medical and health sciences, Asian People, Gene Frequency, Ophthalmology, medicine, Humans, Allele frequency, Intraocular Pressure, Genetics (clinical), Aged, Aged, 80 and over, business.industry, Haplotype, Case-control study, Middle Aged, Catalase, medicine.disease, eye diseases, 030104 developmental biology, Haplotypes, Case-Control Studies, Pediatrics, Perinatology and Child Health, Female, sense organs, business, Glaucoma, Open-Angle
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11939ffd3bc6043fb631fc1293ede7bdTest
https://doi.org/10.1080/13816810.2017.1342132Test -
3
المؤلفون: Dongyan Luo, Rui Zheng, Tingting Wang, Yi Shi, Xiaoqi Liu, Yaru Zhai, Lingxi Jiang, Chao Qu, Bo Gong, Zimeng Ye
المصدر: Ophthalmic genetics. 40(3)
مصطلحات موضوعية: Adult, Male, China, Genotype, Population, Genome-wide association study, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Asian People, Myopia, SNP, Humans, Genetic Predisposition to Disease, Allele, education, Gene, Genetics (clinical), Genetics, education.field_of_study, Tankyrases, Haplotype, Middle Aged, Prognosis, Ophthalmology, Haplotypes, Case-Control Studies, Pediatrics, Perinatology and Child Health, Female, Follow-Up Studies
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a7fef74c9ec13b7bcf18c0c394f007bTest
https://pubmed.ncbi.nlm.nih.gov/31134845Test -
4
المؤلفون: Xiaolin Hou, Xuelai He, Zimeng Ye, Bo Gong, Luo Liang, Peixi Liu, Nengyi Hou, Jialiang Yang, Yijun Liu, Junwen Fu, Kang Wang, Minghui Pang
المصدر: Molecular Medicine Reports
مصطلحات موضوعية: Male, Models, Molecular, 0301 basic medicine, Cancer Research, Gene Expression, Biochemistry, Protein Structure, Secondary, 0302 clinical medicine, Frameshift Mutation, Sanger sequencing, Genetics, biology, High-Throughput Nucleotide Sequencing, Autosomal dominant trait, Exons, Articles, Middle Aged, Pedigree, Adenomatous Polyposis Coli, Oncology, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), symbols, Molecular Medicine, Female, Adult, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Adenomatous polyposis coli, Genetic counseling, Adenomatous Polyposis Coli Protein, Steatocystoma Multiplex, Frameshift mutation, Familial adenomatous polyposis, 03 medical and health sciences, symbols.namesake, Germline mutation, Asian People, familial adenomatous polyposis, medicine, Humans, Genetic Predisposition to Disease, neoplasms, Molecular Biology, Genetic Association Studies, Aged, Base Sequence, heterozygous mutation, medicine.disease, digestive system diseases, 030104 developmental biology, Case-Control Studies, biology.protein, next-generation sequencing
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9d161e861e65167815b4ca68c868426Test
https://doi.org/10.3892/mmr.2018.9130Test -
5
المؤلفون: Zhengzheng Wu, Yaru Zhai, Zhenglin Yang, Bo Gong, Fang Li, Yi Shi, Haiyan Wu, Lingxi Jiang, Ying Lin, Zimeng Ye, Ling Wan
المصدر: Ophthalmic genetics. 38(4)
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Han chinese, China, genetic structures, Genotype, Single-nucleotide polymorphism, Biology, Genome, Polymorphism, Single Nucleotide, 03 medical and health sciences, Sex Factors, Asian People, Gene Frequency, Humans, Genetic Predisposition to Disease, Genetics (clinical), Alleles, Genetic association, Aged, Genetics, Case-control study, High myopia, RNA-Binding Proteins, Middle Aged, eye diseases, Ophthalmology, 030104 developmental biology, Pediatrics, Perinatology and Child Health, Myopia, Degenerative, Susceptibility locus, RBFOX1 Gene, Female, RNA Splicing Factors, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a285a42257e89e9e378af4c0e8951c2Test
https://pubmed.ncbi.nlm.nih.gov/28085524Test -
6
المؤلفون: Yang Lan, Xiaoxin Guo, Yi Huang, Yi Shi, Fang Hao, Zhenglin Yang, Qu Chao, Chen Yang, Zimeng Ye, Qingwei Wang, Bo Gong
المصدر: Molecular Genetics & Genomic Medicine
مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, 0301 basic medicine, Marfan syndrome, China, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Fibrillin-1, 030105 genetics & heredity, Biology, medicine.disease_cause, fibrillin‐1 (FBN1), Marfan Syndrome, law.invention, Pathogenesis, targeted next‐generation sequencing (NGS), 03 medical and health sciences, symbols.namesake, law, Genetics, medicine, Humans, Child, Molecular Biology, Gene, Genetics (clinical), Polymerase chain reaction, Sanger sequencing, Mutation, Multiple sequence alignment, Genetic Carrier Screening, heterozygous mutation, Original Articles, Middle Aged, medicine.disease, Phenotype, Pedigree, 030104 developmental biology, Child, Preschool, symbols, Original Article, Female, Marfan syndrome (MFS)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8410a0e97c59180c87ceb1ddf75b32b3Test
https://doi.org/10.1002/mgg3.594Test -
7
المؤلفون: Yin Yang, Yuanfeng Li, Zhenglin Yang, Xuemei Wu, Hong Zheng, Zimeng Ye, Bo Gong, Dingding Zhang, Yi Shi, Xiaoqi Liu, Pu Wang
المصدر: Ophthalmic genetics. 38(2)
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Linkage disequilibrium, China, Genotyping Techniques, Haploview, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Linkage Disequilibrium, Receptor, IGF Type 1, 03 medical and health sciences, 0302 clinical medicine, Asian People, Gene Frequency, Humans, Genetic Predisposition to Disease, Allele, Insulin-Like Growth Factor I, Allele frequency, Genotyping, Genetics (clinical), Genetic association, Aged, Genetics, Receptors, Somatomedin, Middle Aged, body regions, Ophthalmology, Axial Length, Eye, 030104 developmental biology, Case-Control Studies, Pediatrics, Perinatology and Child Health, Myopia, Degenerative, 030221 ophthalmology & optometry, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75ebf997ad65f37e03c7f5c9fc2f490cTest
https://pubmed.ncbi.nlm.nih.gov/27044882Test -
8
المؤلفون: Zhenglin Yang, Houbin Zhang, Fang Lu, Fang Li, Xianjun Zhu, Zimeng Ye, Zhengzheng Wu, Feng Wen, Lingxi Jiang, Yaru Zhai, Xiaoqi Liu, Lulin Huang, Ping Shuai, Ying Lin, Huaichao Luo, Yi Shi, Bo Gong, Dingding Zhang
المصدر: Scientific Reports
مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, Linkage disequilibrium, genetic structures, Linkage Disequilibrium, Macular Degeneration, 0302 clinical medicine, Gene Frequency, Genotype, Receptor, Notch4, Aged, 80 and over, Multidisciplinary, Receptors, Notch, Tenascin, Middle Aged, Choroidal neovascularization, Chromosomes, Human, Pair 6, Female, medicine.symptom, medicine.medical_specialty, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Article, Tacrolimus Binding Proteins, 03 medical and health sciences, Proto-Oncogene Proteins, Internal medicine, medicine, Humans, Immunophilins, Allele frequency, Alleles, Genetic Association Studies, Aged, business.industry, Haplotype, DNA Helicases, Case-control study, Genetic Variation, Macular degeneration, medicine.disease, Choroidal Neovascularization, eye diseases, 030104 developmental biology, Genetic Loci, Case-Control Studies, 030221 ophthalmology & optometry, Optometry, sense organs, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91854a4db71ede8f6bdb5ba025056441Test
-
9
المؤلفون: Guangqun Zeng, Zhiwei Li, Zhenglin Yang, Fang Hao, Ying Xiao, Chao Qu, Xiaoqi Liu, Xiaoyun Feng, Guoying Mu, Yi Shi, Yuanfeng Li, Xiulan Li, Zimeng Ye, Bo Gong, Yu Meng Wang, Liping Liu
المصدر: Scientific Reports
مصطلحات موضوعية: Adult, China, Heterozygote, Adolescent, DNA Mutational Analysis, Molecular Sequence Data, Cystathionine beta-Synthase, Homocystinuria, Biology, medicine.disease_cause, Compound heterozygosity, Article, DNA sequencing, law.invention, Young Adult, Asian People, law, Gene Order, medicine, Humans, Missense mutation, Amino Acid Sequence, Age of Onset, Child, Gene, Genetic Association Studies, Polymerase chain reaction, Genetics, Mutation, Multidisciplinary, medicine.disease, Cystathionine beta synthase, Pedigree, Child, Preschool, biology.protein, Female, Sequence Alignment
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfcfef11cb1bdeaa7ef1e81233830501Test
-
10
المؤلفون: Qian Luo, Yi Shi, Zimeng Ye, Zhenglin Yang, Ping Shuai, Huaichao Luo, Xinghuai Sun, Xiaoqi Liu, Jiyun Yang, Yuhong Chen, Ying Lin, Yuanfeng Li, Kaijiong Zhang, Bo Gong, Yu Zhou, Chang Tan
المصدر: Investigative ophthalmologyvisual science. 56(11)
مصطلحات موضوعية: Adult, Male, Linkage disequilibrium, China, Genotype, Single-nucleotide polymorphism, Genome-wide association study, Biology, Gene Frequency, Ethnicity, Humans, Genetic Predisposition to Disease, Allele frequency, Genetic association, Retrospective Studies, Genetics, Polymorphism, Genetic, Incidence, Haplotype, DNA, Middle Aged, Chinese people, Female, Glaucoma, Angle-Closure, ATP Binding Cassette Transporter 1, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc78511bc861874e9cbca321f5e67da2Test
https://pubmed.ncbi.nlm.nih.gov/26431478Test