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1دورية أكاديمية
المؤلفون: Hui Lin, Jian-Wu Qiu, Yaqub-Muhammad Rauf, Gui-Zhi Lin, Rui Liu, Li-Jing Deng, Mei Deng, Yuan-Zong Song
المصدر: Frontiers in Genetics, Vol 10 (2019)
مصطلحات موضوعية: cholestasis, citrin deficiency, sodium taurocholate cotransporting polypeptide deficiency, SLC25A13, SLC10A1, variant, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/article/10.3389/fgene.2019.01108/fullTest; https://doaj.org/toc/1664-8021Test
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2دورية أكاديمية
المؤلفون: Hui-Jun Tan, Mei Deng, Jian-Wu Qiu, Jun-Feng Wu, Yuan-Zong Song
المصدر: Frontiers in Pediatrics, Vol 6 (2018)
مصطلحات موضوعية: sodium taurocholate cotransporting polypeptide deficiency, SLC10A1, bile acid, hypercholanemia, cholestasis, Pediatrics, RJ1-570
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/article/10.3389/fped.2018.00354/fullTest; https://doaj.org/toc/2296-2360Test
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3دورية أكاديمية
المؤلفون: Gui-Zhi Lin, Jian-Wu Qiu, Mei Deng, Rong Chen, Shun-Ye Zhu, Xiao-Min Xiao, Yaqub-Muhammad Rauf, Yuan-Zong Song
المصدر: The Tohoku Journal of Experimental Medicine. 2019, 248(1):57
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المؤلفون: Jian Wu Qiu, Mei Chen Guo, Jun Hui Fan, Zhi Kun Li
المصدر: Key Engineering Materials. 904:401-406
مصطلحات موضوعية: Mechanics of Materials, Chemistry, Mechanical Engineering, Environmental chemistry, technology, industry, and agriculture, chemistry.chemical_element, Iron removal, General Materials Science, Sulfate-reducing bacteria, equipment and supplies, Acid mine drainage, complex mixtures, Copper
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::9d22a7b1da3688d32336a823f7126bf8Test
https://doi.org/10.4028/www.scientific.net/kem.904.401Test -
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المؤلفون: Gui-Zhi, Lin, Jian-Wu, Qiu, Mei, Deng, Wei-Xia, Lin, Li, Guo, Yuan-Zong, Song
المصدر: Zhongguo Dang Dai Er Ke Za Zhi
مصطلحات موضوعية: Male, Phosphotransferases (Alcohol Group Acceptor), Mitochondrial Diseases, Mutation, 论著·临床研究, Humans, Infant, DNA, Mitochondrial
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::579f0c8866e7e4e382aa24d10557f2b3Test
https://pubmed.ncbi.nlm.nih.gov/32204766Test -
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المؤلفون: Yue-Jun Huang, Xiao-Ling Huang, Mei Deng, Feng-Ping Chen, Yaqub-Muhammad Rauf, Li-Jing Deng, Xiao-Ling Long, Yu-Ge Huang, Jian-Wu Qiu, Yuan-Zong Song, Ying Ouyang, Wei-Xia Lin, Hua Li, Shuang-Jie Li, Rui Liu, Wen-Xian Ouyang, Li Guo, Raza-Muhammad Atif
المصدر: SSRN Electronic Journal.
مصطلحات موضوعية: Sanger sequencing, SLC10A1, medicine.medical_specialty, biology, business.industry, Case-control study, Disease, medicine.disease, symbols.namesake, Informed consent, Internal medicine, Genotype, medicine, symbols, biology.protein, business, Genotyping, Cholestasis of pregnancy
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::d262fd276db71d530b46d07419687e3dTest
https://doi.org/10.2139/ssrn.3714951Test -
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المؤلفون: Yuan-Zong Song, Wei-Xia Lin, Xiao-Ling Huang, Raza-Muhammad Atif, Hua Li, Li Guo, Li-Jing Deng, Shuang-Jie Li, Xiao-Ling Long, Rui Liu, Mei Deng, Yue-Jun Huang, Feng-Ping Chen, Jian-Wu Qiu, Ying Ouyang, Yu-Ge Huang, Wen-Xian Ouyang, Yaqub-Muhammad Rauf
المصدر: SSRN Electronic Journal.
مصطلحات موضوعية: Sanger sequencing, SLC10A1, medicine.medical_specialty, biology, business.industry, Case-control study, Disease, medicine.disease, symbols.namesake, Informed consent, Internal medicine, Genotype, symbols, biology.protein, Medicine, business, Genotyping, Cholestasis of pregnancy
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::9132f3dedbf1bbc852ae262cf0441498Test
https://doi.org/10.2139/ssrn.3680078Test -
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المؤلفون: Gui-Zhi Lin, Rui Liu, Li-Jing Deng, Hui Lin, Jian-Wu Qiu, Yuan-Zong Song, Yaqub-Muhammad Rauf, Mei Deng
المصدر: Frontiers in Genetics
Frontiers in Genetics, Vol 10 (2019)مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, lcsh:QH426-470, SLC25A13, Citrin deficiency, Case Report, Gastroenterology, digestive system, 03 medical and health sciences, 0302 clinical medicine, Cholestasis, Internal medicine, medicine, Genetics, Cholestatic Jaundice, citrin deficiency, Genetics (clinical), SLC10A1, child, biology, business.industry, Early infancy, medicine.disease, lcsh:Genetics, sodium taurocholate cotransporting polypeptide deficiency, 030104 developmental biology, medicine.anatomical_structure, variant, Carrier protein, 030220 oncology & carcinogenesis, Hepatocyte, biology.protein, Molecular Medicine, Sodium taurocholate cotransporting polypeptide, business, cholestasis
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a19407190bb9f03e198253b06399872Test
http://europepmc.org/articles/PMC6856633Test -
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المؤلفون: Yuan Zong Song, Xiao‑Min Xiao, Hua Li, Xiao‑Ling Long, Gui‑Zhi Lin, Mei Deng, Li Guo, Jian‑Wu Qiu
المصدر: Molecular Medicine Reports
مصطلحات موضوعية: Adult, Male, Models, Molecular, 0301 basic medicine, Cancer Research, Organic anion transporter 1, sodium taurocholate cotransporting polypeptide, Mutation, Missense, Organic Anion Transporters, Sodium-Dependent, Compound heterozygosity, Polymorphism, Single Nucleotide, digestive system, Biochemistry, Bile Acids and Salts, hypercholanemia, 03 medical and health sciences, Autosomal recessive trait, 0302 clinical medicine, c.595A>C (p.Ser199Arg), solute carrier family 10 member 1, Genetics, Humans, Point Mutation, Missense mutation, Molecular Biology, SLC10A1, Symporters, biology, Chemistry, Point mutation, Infant, Articles, Molecular biology, Pedigree, Solute carrier family, 030104 developmental biology, Oncology, Genetic marker, Child, Preschool, 030220 oncology & carcinogenesis, biology.protein, Molecular Medicine, Female, Metabolism, Inborn Errors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71967d5b66fec62c6eb4d42772ddbe14Test
https://doi.org/10.3892/mmr.2019.10763Test -
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المؤلفون: Wei-Xia Lin, Raza-Muhammad Atif, Jian-Wu Qiu, Hua Li, Yuan-Zong Song, Ying Cheng, Mei Deng, Li Guo
المصدر: Oncotarget. 8:106598-106607
مصطلحات موضوعية: 0301 basic medicine, chemistry.chemical_classification, SLC10A1, medicine.medical_specialty, Mutation, biology, business.industry, medicine.disease_cause, digestive system, Amino acid, 03 medical and health sciences, 030104 developmental biology, medicine.anatomical_structure, Endocrinology, Oncology, chemistry, Hepatocyte, Internal medicine, Genotype, medicine, biology.protein, Missense mutation, business, Allele frequency, Gene
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::e16bd440abd6da4405cd4aea54205dbdTest
https://doi.org/10.18632/oncotarget.22503Test