المؤلفون: Xiao-Wen Liu, Su-Yang Wang, Zhan-Kui Xing, Yi-Ming Zhu, Wen-Juan Ding, Lei Duan, Xiao Cui, Bai-Cheng Xu, Shu-Juan Li, Yu-Fen Guo

المصدر: Journal of International Medical Research, Vol 48 (2020)

مصطلحات موضوعية: Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1473-2300

URL الوصول: https://doaj.org/article/8facfa741e7d447e92a255f7737696cf

المؤلفون: Zhe-wen Zhang, Xiao-wen Liu, Bai-cheng Xu, Su-yang Wang, Li Li, Ying-ying Kang, Yu-fen Guo

المصدر: PLoS ONE, Vol 8, Iss 1, p e53566 (2013)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23349719/?tool=EBI; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/ee090706b14e45f09c581104286829fb

المؤلفون: Yu-fen Guo, 郭毓芬

Thesis Advisors: Tzung-min Pai, 白宗民

وصف الملف: 28

الاتاحة: http://ndltd.ncl.edu.tw/handle/83517109451565952570

المؤلفون: Yu-Fen Guo, 郭宇芬

Thesis Advisors: Chui-Te Chiu, 邱垂德

وصف الملف: 130

الاتاحة: http://ndltd.ncl.edu.tw/handle/20464925482202589018

المؤلفون: Jialiang Guo, Yu-Fen Guo, Xiaolin Bao, Bai-Cheng Xu, Yuan Wang, Xiao-Wen Liu

المصدر: Minerva Surgery. 78

مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, business.industry, Medicine, Surgery, business, Gene

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6571aeb70db215857fe2a7c2e33e41a9
https://doi.org/10.23736/s2724-5691.21.09044-4

المؤلفون: Jing-Jing Wu, Zeng-Ping Liu, Chen-Yang Xu, Xue-Ling Zhang, Xiao-Wen Liu, Ju-Yuan Wang, Yu-Fen Guo

المصدر: Ear, nose,throat journal.

مصطلحات موضوعية: Otorhinolaryngology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c8899f83b7f94efe36fd54f91ad7061
https://pubmed.ncbi.nlm.nih.gov/35737853

المؤلفون: Chi Chen, Yu-Fen Guo, Pan-Pan Bian, Bei-Bei Liu, Bai-Cheng Xu

المصدر: Ear, Nose & Throat Journal. 100:NP354-NP356

مصطلحات موضوعية: Surgical approach, Ectopic thymus, business.industry, Infant, Newborn, Pharyngeal Diseases, Thymus Gland, Anatomy, Choristoma, medicine.disease, Diagnosis, Differential, 03 medical and health sciences, 0302 clinical medicine, Otorhinolaryngology, 030220 oncology & carcinogenesis, Medical Illustration, Humans, Pharynx, Medicine, Female, Differential diagnosis, 030223 otorhinolaryngology, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9fdc27bc6fb2680925bbdc472519992
https://doi.org/10.1177/0145561320918434

المؤلفون: Xing-Jian Chen, Yu-Fen Guo, Yong Li, Shihong Duan

المصدر: The Journal of International Medical Research
Journal of International Medical Research, Vol 49 (2021)

مصطلحات موضوعية: 0301 basic medicine, Han chinese, Medicine (General), China, mutation spectra, DNA Mutational Analysis, ethnic minority, Ethnic group, SNPscan, Deafness, Biochemistry, Connexins, Hearing impairment, 03 medical and health sciences, 0302 clinical medicine, R5-920, Chinese Han, variant frequency, Asian People, otorhinolaryngologic diseases, Ethnicity, Medicine, Humans, In patient, Case Series, Chinese han, Gene, Minority Groups, Genetics, Mutation Spectra, business.industry, 12s rrna, Biochemistry (medical), Cell Biology, General Medicine, 030104 developmental biology, 030220 oncology & carcinogenesis, Mutation, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac96f1068d2c395075072109689238b3
https://pubmed.ncbi.nlm.nih.gov/33827324

المؤلفون: Hui Jia, Xiao-wen Liu, Yong Li, Yu-fen Guo, Zeng-ping Liu

المصدر: Ear, Nose & Throat Journal. :014556132211163

مصطلحات موضوعية: Otorhinolaryngology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4f1b63de2efc44bac99fe0c72bedbcc
https://doi.org/10.1177/01455613221116337

المؤلفون: Shu-Juan Li, Xiao-Wen Liu, Wen-Juan Ding, Yu-Fen Guo, Yi-Ming Zhu, Jianchao Wang, Bai-Cheng Xu, Chen-Yang Xu, Lei Duan, Su-Yang Wang

المصدر: International journal of pediatric otorhinolaryngology. 136

مصطلحات موضوعية: Adult, Genetic Markers, Male, China, Adolescent, Hearing Loss, Sensorineural, DNA Mutational Analysis, MT-RNR1, medicine.disease_cause, Connexins, 03 medical and health sciences, symbols.namesake, Young Adult, 0302 clinical medicine, CDH23, Mutation Rate, 030225 pediatrics, otorhinolaryngologic diseases, Medicine, Humans, Genetic Testing, Allele, 030223 otorhinolaryngology, Child, Allele frequency, Gene, Genetics, Sanger sequencing, Mutation, business.industry, High-Throughput Nucleotide Sequencing, Infant, Genes, rRNA, General Medicine, medicine.disease, Connexin 26, Genes, Mitochondrial, Otorhinolaryngology, RNA, Ribosomal, Sulfate Transporters, Child, Preschool, Pediatrics, Perinatology and Child Health, symbols, Sensorineural hearing loss, Female, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33f1db6c6e82e7223c1003e2f5cb49f9
https://pubmed.ncbi.nlm.nih.gov/32645618

المؤلفون: Aishanjiang Maerhaba, Xiaowan Chen, Qianqian Li, Fang Wang, Yu-Fen Guo, Ye Chen, Jing Zheng, Xiao-Wen Liu, Jianchao Wang

المصدر: Gene. 652:59-65

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Proband, Mitochondrial DNA, Adolescent, Hearing loss, Biology, DNA, Mitochondrial, Genome, Hearing Loss, Bilateral, 03 medical and health sciences, Asian People, RNA, Transfer, RNA, Ribosomal, 16S, otorhinolaryngologic diseases, Genetics, medicine, Humans, Child, Gene, High-Throughput Nucleotide Sequencing, General Medicine, Middle Aged, Pathogenicity, Control subjects, Pedigree, Genes, Mitochondrial, 030104 developmental biology, RNA, Ribosomal, Case-Control Studies, Child, Preschool, Genome, Mitochondrial, Mutation, Female, medicine.symptom, Non syndromic

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08378606e89405e2e879c2daeacfe25c
https://doi.org/10.1016/j.gene.2018.01.098

المؤلفون: Wang, Qiu–ju, Shao–qi, Rao, Yu–fen, Guo, Qing–zhong, Li, Hui, Zhao, Li–dong, Zhao, Hu, Yuan, Liang, Zong, Qiong, Liu, Ya–li, Zhao, Da–yong, Wang, Ming–kun, Han, Yu–bin, Ji, Jian–qiang, Li, Lan, Lan, Wei–yan, Yang, Yan, Shen, Dong–yi, Han

المصدر: Journal of Otology ; volume 4, issue 2, page 98-105 ; ISSN 1672-2930

الاتاحة: http://dx.doi.org/10.1016/s1672-2930(09)50020-7
https://api.elsevier.com/content/article/PII:S1672293009500207?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1672293009500207?httpAccept=text/plain

المؤلفون: Ming-kun, Han, Dong-yi, Han, Yu-fen, Guo, Qing-zhong, Li, Ya-li, Zhao, Shao-qi, Rao, Hu, Yuan, Liang, Zong, Jing, Guan, Bai-cheng, Xu, Da-yong, Wang, lan, Lan, Qiu-ju, Wang

المصدر: Journal of Otology ; volume 2, issue 1, page 18-22 ; ISSN 1672-2930

الاتاحة: http://dx.doi.org/10.1016/s1672-2930(07)50004-8
https://api.elsevier.com/content/article/PII:S1672293007500048?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1672293007500048?httpAccept=text/plain

المؤلفون: Jian‑Li Ma, Xiao‑Long Yang, Yu‑Fen Guo, Shi‑Hong Duan

المصدر: Molecular Medicine Reports

مصطلحات موضوعية: Male, 0301 basic medicine, Cancer Research, Mutation rate, Deafness, Biochemistry, Connexins, 0302 clinical medicine, Medicine, Child, Genetics, Mutation Spectra, medicine.diagnostic_test, Articles, GJB2, Connexin 26, Oncology, Sulfate Transporters, Child, Preschool, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), Molecular Medicine, Female, Adult, minority patients, China, medicine.medical_specialty, Adolescent, Genotype, Single-nucleotide polymorphism, DNA, Mitochondrial, Polymorphism, Single Nucleotide, Young Adult, 03 medical and health sciences, Asian People, Internal medicine, SLC26A4, otorhinolaryngologic diseases, Humans, SNP, nonsyndromic hearing impairment, Molecular Biology, Allele frequency, Alleles, Genetic testing, business.industry, Membrane Transport Proteins, 030104 developmental biology, RNA, Ribosomal, mtDNA12SrRNA, Etiology, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e04776d0705c6e8a182a26d64de9a846
https://doi.org/10.3892/mmr.2017.7431

المؤلفون: Bai-Cheng Xu, Chi Chen, Yu-Fen Guo, Su-Yang Wang, Wen-Juan Ding, Xiao-Wen Liu, Pan-Pan Bian

المصدر: Acta oto-laryngologica. 139(3)

مصطلحات موضوعية: Male, Adolescent, Genotype, Hearing loss, Biology, Connexins, 03 medical and health sciences, 0302 clinical medicine, Inner ear malformation, medicine, Humans, 030223 otorhinolaryngology, Child, Infant, General Medicine, Anatomy, medicine.disease, Phenotype, Connexin 26, Otorhinolaryngology, Sulfate Transporters, 030220 oncology & carcinogenesis, Child, Preschool, Ear, Inner, Female, medicine.symptom, Enlarged vestibular aqueduct

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18c0b001043c6a417e9311ee70a0bc42
https://pubmed.ncbi.nlm.nih.gov/30762457

المؤلفون: Yu-Fen Guo, Yan-Li Wang, Shi-Hong Duan, Yi-Ming Zhu

المصدر: Acta Oto-Laryngologica. 135:586-591

مصطلحات موضوعية: Adult, Male, China, medicine.medical_specialty, Mitochondrial DNA, Adolescent, Hearing loss, DNA Mutational Analysis, Ethnic group, Deafness, Audiology, medicine.disease_cause, DNA, Mitochondrial, Connexins, Young Adult, otorhinolaryngologic diseases, medicine, Humans, Genetic Predisposition to Disease, Child, Genetics, Mutation, business.industry, Infant, Membrane Transport Proteins, General Medicine, Connexin 26, Otorhinolaryngology, Sulfate Transporters, Child, Preschool, Cohort, Etiology, Population study, Female, medicine.symptom, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8cecc5b38516432acbf90d25ee206c9
https://doi.org/10.3109/00016489.2015.1006334

المؤلفون: Liu Xiaowen, Bian Pan-Pan, Yi-Ming Zhu, Xiao-Long Yang, Xu Baicheng, Yu-Fen Guo, Du Wan, Ma Jian-Li, Xing-Jian Chen, Zhe-Wen Zhang

المصدر: Acta Oto-Laryngologica. 133:930-934

مصطلحات موضوعية: Adult, Male, Proband, Mitochondrial DNA, Adolescent, Hearing loss, Genetic counseling, Deafness, Tibet, Connexins, Young Adult, otorhinolaryngologic diseases, Humans, Medicine, Child, Gene, Aged, Genetics, Polymorphism, Genetic, business.industry, Membrane Transport Proteins, Mongolia, General Medicine, Middle Aged, Connexin 26, genomic DNA, Otorhinolaryngology, RNA, Ribosomal, Sulfate Transporters, Child, Preschool, Mutation, Etiology, Nationality, Female, medicine.symptom, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc31c96b9aa4b9d0482ca281c701a361
https://doi.org/10.3109/00016489.2013.795288

المؤلفون: Zhipeng Nie, Min-Xin Guan, Jianchao Wang, Xiao-Wen Liu, Yu-Fen Guo, Jing Zheng, Fang Wang, Xiaowan Chen

المصدر: Mitochondrion. 35

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Mitochondrial translation, Hearing loss, Late onset, Biology, Deafness, Haplogroup, Late Onset Disorders, 03 medical and health sciences, RNA, Transfer, Phe, Young Adult, 0302 clinical medicine, Adenosine Triphosphate, Asian People, medicine, Humans, Point Mutation, Child, Molecular Biology, Gene, Aged, Genetics, Aged, 80 and over, Family Health, Point mutation, Cell Biology, Middle Aged, medicine.disease, Mitochondria, 030104 developmental biology, Genes, Mitochondrial, Protein Biosynthesis, Transfer RNA, Molecular Medicine, Sensorineural hearing loss, Female, medicine.symptom, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::527f02adc10fcf526701a9a7a263a887
https://pubmed.ncbi.nlm.nih.gov/28579530

المؤلفون: Yao He, Yu Fen Guo, Yan Shen, Qiu Ju Wang, Wei Yan Yang, Dong Yi Han, Shao Qi Rao, Robert J. Ruben, Ya Li Zhao, Qing Yin Zheng, Lan Lan

المصدر: International Journal of Pediatric Otorhinolaryngology. 75:535-542

مصطلحات موضوعية: Male, China, Pediatrics, medicine.medical_specialty, Referral, Hearing loss, Population, Compound heterozygosity, Risk Assessment, Connexins, Cohort Studies, Hearing Loss, Bilateral, Neonatal Screening, otorhinolaryngologic diseases, Humans, Medicine, Genetic Predisposition to Disease, Genetic Testing, Allele, education, Gene screening, education.field_of_study, business.industry, Incidence, Infant, Newborn, General Medicine, Connexin 26, Otorhinolaryngology, RNA, Ribosomal, Mutation, Pediatrics, Perinatology and Child Health, Etiology, Female, medicine.symptom, business, Follow-Up Studies, Program Evaluation, Cohort study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1dcbf82f11a5d2e912e421c814ddd4f
https://doi.org/10.1016/j.ijporl.2011.01.016

المؤلفون: Yu-Fen Guo, Zong L, Guan J, Zhai Sq, Wang Dy, Ya-Li Zhao, Han Mk, Yuan H, Lan L, Xu Bc, Rao Sq, Yan Shen, Wang Qj

المصدر: Clinical Genetics. 72:245-254

مصطلحات موضوعية: Adult, Male, China, Vestibular aqueduct, Adolescent, Hearing loss, Hearing Loss, Sensorineural, Molecular Sequence Data, Biology, medicine.disease_cause, Vestibular Aqueduct, Asian People, otorhinolaryngologic diseases, Genetics, medicine, Humans, Allele, Child, Genetics (clinical), Mutation, Infant, Membrane Transport Proteins, medicine.disease, Pedigree, medicine.anatomical_structure, FOXI1, Sulfate Transporters, Child, Preschool, Mondini dysplasia, Female, Sensorineural hearing loss, sense organs, medicine.symptom, Enlarged vestibular aqueduct

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e72dcba1454da8a706ef2ef5eeddd6fb
https://doi.org/10.1111/j.1399-0004.2007.00862.x