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

Feng-Yao Wu

Showing results (21-30 of 31) with videos related to

Pageof 4
Sort By:
Molecular Biology Reports|January 9, 2014
Identification and functional analysis of the cathepsin D gene promoter of Bombyx moriJie Yu, Feng-Yao Wu, Feng-Ming Zou, et al.
Nature Communications|April 11, 2024
Deficiency of the HGF/Met pathway leads to thyroid dysgenesis by impeding late thyroid expansionYa Fang, Jia-Ping Wan, Zheng Wang, et al.
Frontiers in Endocrinology|February 24, 2023
The <i>isl2a</i> transcription factor regulates pituitary development in zebrafishChen-Yan Yan, Feng-Yao Wu, Feng Sun, et al.
Nature Communications|December 6, 2023
Myeloid cells interact with a subset of thyrocytes to promote their migration and follicle formation through NF-κBRui-Meng Yang, Shi-Yang Song, Feng-Yao Wu, et al.
Hormone Research in Paediatrics|September 13, 2023
Genetic Screening and Functional Analysis of Thyroid Peroxidase Variants in Chinese Patients with Congenital HypothyroidismHai-Yang Zhang, Feng-Yao Wu, Xue-Song Li, et al.
Thyroid : Official Journal of the American Thyroid Association|September 8, 2025
Clinical Outcomes of Congenital Hypothyroidism Due to <i>DUOX2</i> Biallelic Mutations after Levothyroxine WithdrawalFeng Sun, Jia-Ping Wan, Na-Na Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 1, 2021
Upregulation of GBP1 in thyroid primordium is required for developmental thyroid morphogenesisRui-Meng Yang, Ming Zhan, Qin-Yi Zhou, et al.
Journal of Medical Genetics|March 10, 2023
Pathogenic variations in <i>MAML2</i> and <i>MAMLD1</i> contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathwayFeng-Yao Wu, Rui-Meng Yang, Hai-Yang Zhang, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2026
First large-scale screening of Notch biallelic variants implicates novel candidate genes in congenital hypothyroidismFeng-Yao Wu, Chen-Yang Wu, Zheng Wang, et al.
The Journal of Experimental Medicine|September 4, 2020
Anti-IFN-γ autoantibodies underlie disseminated Talaromyces marneffei infectionsJing Guo, Xin-Qiang Ning, Jing-Ya Ding, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Molecular Biology Reports|January 9, 2014
Identification and functional analysis of the cathepsin D gene promoter of Bombyx moriJie Yu, Feng-Yao Wu, Feng-Ming Zou, et al.
Nature Communications|April 11, 2024
Deficiency of the HGF/Met pathway leads to thyroid dysgenesis by impeding late thyroid expansionYa Fang, Jia-Ping Wan, Zheng Wang, et al.
Frontiers in Endocrinology|February 24, 2023
The <i>isl2a</i> transcription factor regulates pituitary development in zebrafishChen-Yan Yan, Feng-Yao Wu, Feng Sun, et al.
Nature Communications|December 6, 2023
Myeloid cells interact with a subset of thyrocytes to promote their migration and follicle formation through NF-κBRui-Meng Yang, Shi-Yang Song, Feng-Yao Wu, et al.
Hormone Research in Paediatrics|September 13, 2023
Genetic Screening and Functional Analysis of Thyroid Peroxidase Variants in Chinese Patients with Congenital HypothyroidismHai-Yang Zhang, Feng-Yao Wu, Xue-Song Li, et al.
Thyroid : Official Journal of the American Thyroid Association|September 8, 2025
Clinical Outcomes of Congenital Hypothyroidism Due to <i>DUOX2</i> Biallelic Mutations after Levothyroxine WithdrawalFeng Sun, Jia-Ping Wan, Na-Na Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 1, 2021
Upregulation of GBP1 in thyroid primordium is required for developmental thyroid morphogenesisRui-Meng Yang, Ming Zhan, Qin-Yi Zhou, et al.
Journal of Medical Genetics|March 10, 2023
Pathogenic variations in <i>MAML2</i> and <i>MAMLD1</i> contribute to congenital hypothyroidism due to dyshormonogenesis by regulating the Notch signalling pathwayFeng-Yao Wu, Rui-Meng Yang, Hai-Yang Zhang, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2026
First large-scale screening of Notch biallelic variants implicates novel candidate genes in congenital hypothyroidismFeng-Yao Wu, Chen-Yang Wu, Zheng Wang, et al.
The Journal of Experimental Medicine|September 4, 2020
Anti-IFN-γ autoantibodies underlie disseminated Talaromyces marneffei infectionsJing Guo, Xin-Qiang Ning, Jing-Ya Ding, et al.
Pageof 4