Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Bai-Cheng Xu

Showing results (11-20 of 19) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 19 results.
Translational Oncology|January 7, 2026
Adaptive therapy for perioperative non-small cell lung cancer: strategies guided by dynamic minimal residual disease adjustmentLi-Jin Xie, Li-Li Fu, Shu-Cen Liu, et al.
Acta Oto-Laryngologica|June 19, 2014
Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, ChinaBai-Cheng Xu, Pan-Pan Bian, Xiao-Wen Liu, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|March 26, 2014
Comparison of complications of the suprameatal approach and mastoidectomy with posterior tympanotomy approach in cochlear implantation: a meta-analysisBai-Cheng Xu, Su-Yang Wang, Xiao-Wen Liu, et al.
Acta Oto-Laryngologica|April 21, 2015
The deafness-causing mutation c.508_511dup in the GJB2 gene and a literature reviewYi-Ming Zhu, Yong Li, Yan-Li Wang, et al.
The Journal of International Medical Research|November 30, 2020
Targeted next-generation sequencing identified a novel variant of <i>SOX10</i> in a Chinese family with Waardenburg syndrome type 2Xiao-Wen Liu, Su-Yang Wang, Zhan-Kui Xing, et al.
International Journal of Pediatric Otorhinolaryngology|July 10, 2020
The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest ChinaXiao-Wen Liu, Jian-Chao Wang, Su-Yang Wang, et al.
Genetic Testing and Molecular Biomarkers|July 29, 2010
Analysis of a large-scale screening of mitochondrial DNA m.1555A>G mutation in 2417 deaf-mute students in northwest of ChinaYu-Fen Guo, Xiao-Wen Liu, Bai-Cheng Xu, et al.
Molecular Cancer|March 7, 2026
Calibrating the RT-cGAS-STING axis to drive cold-to-hot tumor transformation: mechanistic foundations and translational strategies for combination with immunotherapyYi-Fan Kang, Jin-Ming Chen, Bai-Cheng Xu, et al.
International Journal of Pediatric Otorhinolaryngology|May 21, 2010
Identification of two novel mutations, c.232T>C and c.2006A>T, in SLC26A4 in a Chinese family associated with enlarged vestibular aqueductYu-Fen Guo, Yan-Li Wang, Bai-Cheng Xu, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Translational Oncology|January 7, 2026
Adaptive therapy for perioperative non-small cell lung cancer: strategies guided by dynamic minimal residual disease adjustmentLi-Jin Xie, Li-Li Fu, Shu-Cen Liu, et al.
Acta Oto-Laryngologica|June 19, 2014
Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, ChinaBai-Cheng Xu, Pan-Pan Bian, Xiao-Wen Liu, et al.
ORL; Journal for Oto-Rhino-Laryngology and Its Related Specialties|March 26, 2014
Comparison of complications of the suprameatal approach and mastoidectomy with posterior tympanotomy approach in cochlear implantation: a meta-analysisBai-Cheng Xu, Su-Yang Wang, Xiao-Wen Liu, et al.
Acta Oto-Laryngologica|April 21, 2015
The deafness-causing mutation c.508_511dup in the GJB2 gene and a literature reviewYi-Ming Zhu, Yong Li, Yan-Li Wang, et al.
The Journal of International Medical Research|November 30, 2020
Targeted next-generation sequencing identified a novel variant of <i>SOX10</i> in a Chinese family with Waardenburg syndrome type 2Xiao-Wen Liu, Su-Yang Wang, Zhan-Kui Xing, et al.
International Journal of Pediatric Otorhinolaryngology|July 10, 2020
The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest ChinaXiao-Wen Liu, Jian-Chao Wang, Su-Yang Wang, et al.
Genetic Testing and Molecular Biomarkers|July 29, 2010
Analysis of a large-scale screening of mitochondrial DNA m.1555A>G mutation in 2417 deaf-mute students in northwest of ChinaYu-Fen Guo, Xiao-Wen Liu, Bai-Cheng Xu, et al.
Molecular Cancer|March 7, 2026
Calibrating the RT-cGAS-STING axis to drive cold-to-hot tumor transformation: mechanistic foundations and translational strategies for combination with immunotherapyYi-Fan Kang, Jin-Ming Chen, Bai-Cheng Xu, et al.
International Journal of Pediatric Otorhinolaryngology|May 21, 2010
Identification of two novel mutations, c.232T>C and c.2006A>T, in SLC26A4 in a Chinese family associated with enlarged vestibular aqueductYu-Fen Guo, Yan-Li Wang, Bai-Cheng Xu, et al.
Pageof 2