-
1
المؤلفون: Lan Guo, Yiqun Wan, Hao Jiang, Aiping Yan, Fan Liu, Hai-Hua Xie
المصدر: Food Analytical Methods. 15:124-132
مصطلحات موضوعية: Detection limit, Correlation coefficient, Scattering, Sodium, Analytical chemistry, chemistry.chemical_element, Resonance, Mass spectrometry, Applied Microbiology and Biotechnology, Analytical Chemistry, Carboxymethyl cellulose, symbols.namesake, chemistry, medicine, symbols, Rayleigh scattering, Safety, Risk, Reliability and Quality, Safety Research, Food Science, medicine.drug
-
2
المؤلفون: Yiqun Wan, Fan Liu, Hai-Hua Xie, Aiping Yan, Lan Guo
المصدر: Journal of Liquid Chromatography & Related Technologies. 43:770-776
مصطلحات موضوعية: Chromatography, 010405 organic chemistry, 010401 analytical chemistry, Clinical Biochemistry, Ion chromatography, Pharmaceutical Science, 01 natural sciences, Biochemistry, Pyrophosphate, Quantitative determination, 0104 chemical sciences, Analytical Chemistry, chemistry.chemical_compound, chemistry
-
3
المؤلفون: Fa-Wen, Chen, Hai-Hua, Xie, Xiao-Jun, Yang, Jia-Feng, Sun, Li-Hong, Lin, Lu-Fei, Chen, Peng-Wei, Cai
المصدر: Zhongguo shi yan xue ye xue za zhi. 25(6)
مصطلحات موضوعية: Phenotype, Base Sequence, Genotype, Mutation, Humans, Exons, Fucosyltransferases, Alleles, ABO Blood-Group System
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::b0f0cb553f5932f60dd6894303b9ef2e
https://pubmed.ncbi.nlm.nih.gov/29262918 -
4
المؤلفون: Fenghua Lan, Hai-hua Xie, Zhongyong Zhu, Liang-hu Huang, Bo-sheng Yang, Zhihong Wang, Long-feng Ke
المصدر: Clinica Chimica Acta. 412:970-974
مصطلحات موضوعية: Male, China, Genetic counseling, DNA Mutational Analysis, Molecular Sequence Data, Clinical Biochemistry, Pedigree chart, Biology, medicine.disease_cause, ATP Binding Cassette Transporter, Subfamily D, Member 1, Biochemistry, Asymptomatic, medicine, Animals, Humans, Missense mutation, Amino Acid Sequence, Adrenoleukodystrophy, Adrenocortical Insufficiency, Genetics, Mutation, Biochemistry (medical), General Medicine, medicine.disease, Pedigree, Molecular Diagnostic Techniques, Mutation testing, ATP-Binding Cassette Transporters, Female, medicine.symptom, Laboratories
-
5
المؤلفون: Feng-hua Lan, Zhi-hong Wang, Bo-sheng Yang, Liang-hu Huang, Hai-hua Xie, Long-feng Ke, Zhong-yong Zhu
المصدر: Academic Journal of Second Military Medical University. 29:217-219
مصطلحات موضوعية: Genetics, Pseudogene, X-linked adrenoleukodystrophy, General Medicine, Biology, Interference (genetic)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::940713ab381883ca9b70935f94e87a9e
https://doi.org/10.3724/sp.j.1008.2009.00217 -
6
المؤلفون: Hai-hua Xie, Zhihong Wang, Yuxiang Lin, Aizhen Yan, Fenghua Lan, Chun-yan Zhou
المصدر: PLoS ONE, Vol 8, Iss 3, p e57977 (2013)
PLoS ONEمصطلحات موضوعية: Adult, Heterozygote, Heredity, DNA Mutational Analysis, Molecular Sequence Data, lcsh:Medicine, Biology, ATP Binding Cassette Transporter, Subfamily D, Member 1, X-inactivation, Chromosomal Inheritance, Asian People, X Chromosome Inactivation, Molecular Cell Biology, Genetics, medicine, Humans, Allele, Adrenoleukodystrophy, lcsh:Science, Skewed X-inactivation, Alleles, X chromosome, X-linked recessive inheritance, Aged, Clinical Genetics, Chromosomes, Human, X, Multidisciplinary, Base Sequence, Chromosome Biology, lcsh:R, Neurodegenerative Diseases, Genomics, medicine.disease, Pedigree, Neurology, Mutation, Medicine, ATP-Binding Cassette Transporters, Female, Epigenetics, XIST, lcsh:Q, Asymptomatic carrier, Research Article
-
7
المؤلفون: Hai-hua, Xie, Long-feng, Ke, Zhi-hong, Wang, Liang-hu, Huang, Feng-hua, Lan
المصدر: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 27(2)
مصطلحات موضوعية: Adult, Male, Heterozygote, Base Sequence, DNA Mutational Analysis, Molecular Sequence Data, Mutation, Missense, ATP Binding Cassette Transporter, Subfamily D, Member 1, Pedigree, Rats, Mice, Young Adult, Asian People, Animals, Humans, ATP-Binding Cassette Transporters, Cattle, Female, Amino Acid Sequence, Adrenoleukodystrophy, Sequence Alignment, Conserved Sequence, Aged
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::c528649e267185d5481bee86720174df
https://pubmed.ncbi.nlm.nih.gov/20376793 -
8
المؤلفون: Hai-hua Xie, Long-feng Ke, Fenghua Lan, Liang-hu Huang, Aizhen Yan, Zhihong Wang
المصدر: Neurological research. 32(7)
مصطلحات موضوعية: Proband, Male, congenital, hereditary, and neonatal diseases and abnormalities, Genotype, Pedigree chart, Biology, Asymptomatic, ATP Binding Cassette Transporter, Subfamily D, Member 1, Polymerase Chain Reaction, Denaturing high performance liquid chromatography, law.invention, Asian People, law, medicine, Humans, Adrenoleukodystrophy, Polymerase chain reaction, Chromatography, High Pressure Liquid, Genetics, General Medicine, Molecular biology, Pedigree, genomic DNA, Early Diagnosis, Neurology, Mutation (genetic algorithm), ATP-Binding Cassette Transporters, Neurology (clinical), medicine.symptom
-
9
المؤلفون: Long-feng, Ke, Lin-wen, Zheng, Hai-hua, Xie, Ai-zhen, Yan, Zhong-yong, Zhu, Feng-hua, Lan
المصدر: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 26(1)
مصطلحات موضوعية: Adult, Collagen Type I, alpha 1 Chain, Male, China, Asian People, Base Sequence, Mutation, Humans, Female, Sequence Analysis, DNA, Osteogenesis Imperfecta, Collagen Type I, Pedigree
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::aef5dfcd960b4ca4fe38bc30d3136e75
https://pubmed.ncbi.nlm.nih.gov/19199251 -
10
المؤلفون: Hai-Hua Xie, Qi-Cai Liu, Qi-Shui Ou, Ling Jiang, Bin Yang, Zu-Jian Cheng
المصدر: HEREDITAS. 29:433
مصطلحات موضوعية: Adult, Male, Mitochondrial DNA, Adolescent, DNA Mutational Analysis, Molecular Sequence Data, Biology, DNA, Mitochondrial, Polymerase Chain Reaction, Impaired glucose tolerance, Young Adult, Polymorphism (computer science), medicine, Humans, Point Mutation, Child, Aged, Aged, 80 and over, Genetics, Point mutation, Type 2 Diabetes Mellitus, NADH Dehydrogenase, Sequence Analysis, DNA, General Medicine, Middle Aged, medicine.disease, Molecular biology, Pedigree, Diabetes Mellitus, Type 2, Mutation (genetic algorithm), Female, Restriction fragment length polymorphism, TCF7L2, Polymorphism, Restriction Fragment Length
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::962a05611f82692085e320ee6e9b8ae1
https://doi.org/10.1360/yc-007-0433