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

Yin-Hung Lin

Showing results (11-20 of 24) with videos related to

Pageof 3
Sort By:
Scientific Reports|August 10, 2017
A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing lossYin-Hung Lin, Yi-Hsin Lin, Ying-Chang Lu, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 15, 2019
P53 ICE CRIM mouse: a tool to generate mutant allelic series in somatic cells and germ lines for cancer studiesHsiang-Hsuan Fan, I-Shing Yu, Yin-Hung Lin, et al.
Scientific Reports|June 20, 2020
An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state responsePei-Hsuan Lin, Chuan-Jen Hsu, Yin-Hung Lin, et al.
Ear and Hearing|June 28, 2019
Prediction Model for Audiological Outcomes in Patients With GJB2 MutationsPey-Yu Chen, Yin-Hung Lin, Tien-Chen Liu, et al.
Plos One|June 12, 2013
Differences in the pathogenicity of the p.H723R mutation of the common deafness-associated SLC26A4 gene in humans and miceYing-Chang Lu, Chen-Chi Wu, Ting-Hua Yang, et al.
Nucleic Acids Research|May 10, 2022
pubmedKB: an interactive web server for exploring biomedical entity relations in the biomedical literaturePeng-Hsuan Li, Ting-Fu Chen, Jheng-Ying Yu, et al.
Plos One|December 22, 2018
Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populationsJargalkhuu Erdenechuluun, Yin-Hung Lin, Khongorzul Ganbat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2016
Newborn genetic screening for hearing impairment: a population-based longitudinal studyChen-Chi Wu, Ching-Hui Tsai, Chia-Cheng Hung, et al.
Parkinsonism & Related Disorders|September 16, 2016
Clinical heterogeneity of LRRK2 p.I2012T mutationTian-Sin Fan, Ruey-Meei Wu, Pei-Lung Chen, et al.
The Journal of Molecular Diagnostics : JMD|July 29, 2021
Hearing Impairment with Monoallelic GJB2 Variants: A GJB2 Cause or Non-GJB2 Cause?Yi-Hsin Lin, Ping-Che Wu, Cheng-Yu Tsai, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Scientific Reports|August 10, 2017
A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing lossYin-Hung Lin, Yi-Hsin Lin, Ying-Chang Lu, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 15, 2019
P53 ICE CRIM mouse: a tool to generate mutant allelic series in somatic cells and germ lines for cancer studiesHsiang-Hsuan Fan, I-Shing Yu, Yin-Hung Lin, et al.
Scientific Reports|June 20, 2020
An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state responsePei-Hsuan Lin, Chuan-Jen Hsu, Yin-Hung Lin, et al.
Ear and Hearing|June 28, 2019
Prediction Model for Audiological Outcomes in Patients With GJB2 MutationsPey-Yu Chen, Yin-Hung Lin, Tien-Chen Liu, et al.
Plos One|June 12, 2013
Differences in the pathogenicity of the p.H723R mutation of the common deafness-associated SLC26A4 gene in humans and miceYing-Chang Lu, Chen-Chi Wu, Ting-Hua Yang, et al.
Nucleic Acids Research|May 10, 2022
pubmedKB: an interactive web server for exploring biomedical entity relations in the biomedical literaturePeng-Hsuan Li, Ting-Fu Chen, Jheng-Ying Yu, et al.
Plos One|December 22, 2018
Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populationsJargalkhuu Erdenechuluun, Yin-Hung Lin, Khongorzul Ganbat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2016
Newborn genetic screening for hearing impairment: a population-based longitudinal studyChen-Chi Wu, Ching-Hui Tsai, Chia-Cheng Hung, et al.
Parkinsonism & Related Disorders|September 16, 2016
Clinical heterogeneity of LRRK2 p.I2012T mutationTian-Sin Fan, Ruey-Meei Wu, Pei-Lung Chen, et al.
The Journal of Molecular Diagnostics : JMD|July 29, 2021
Hearing Impairment with Monoallelic GJB2 Variants: A GJB2 Cause or Non-GJB2 Cause?Yi-Hsin Lin, Ping-Che Wu, Cheng-Yu Tsai, et al.
Pageof 3