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Journal of Medical Internet Research
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August 3, 2022
A Questionnaire-Based Ensemble Learning Model to Predict the Diagnosis of Vertigo: Model Development and Validation Study
Fangzhou Yu, Peixia Wu, Haowen Deng, et al.
Biorxiv : the Preprint Server for Biology
|
August 6, 2025
Rag GTPases Suppress Renal Cystic Disease by Inhibiting TFEB Independently of mTORC1
Flaviane de Fatima Silva, Alexander R Boucher, Huawei Li, et al.
Cell Stem Cell
|
August 21, 2018
Hoxc-Dependent Mesenchymal Niche Heterogeneity Drives Regional Hair Follicle Regeneration
Zhou Yu, Kaiju Jiang, Zijian Xu, et al.
American Journal of Human Genetics
|
July 5, 2011
Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64
Jing Cheng, Yuhua Zhu, Sudan He, et al.
Nature Biomedical Engineering
|
August 12, 2024
A base editor for the long-term restoration of auditory function in mice with recessive profound deafness
Chong Cui, Shengyi Wang, Daqi Wang, et al.
Journal of Medical Genetics
|
September 21, 2011
Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene
Xukun Yan, Xinjian Wang, Zhengmin Wang, et al.
Cell Reports
|
October 7, 2020
The Lipid Handling Capacity of Subcutaneous Fat Is Programmed by mTORC2 during Development
Wen-Yu Hsiao, Su Myung Jung, Yuefeng Tang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 26, 2021
Gene editing in a Myo6 semi-dominant mouse model rescues auditory function
Yuanyuan Xue, Xinde Hu, Daqi Wang, et al.
Molecular Cell
|
August 24, 2019
Non-canonical mTORC2 Signaling Regulates Brown Adipocyte Lipid Catabolism through SIRT6-FoxO1
Su Myung Jung, Chien-Min Hung, Samuel R Hildebrand, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
January 8, 2024
AAV-Mediated Gene Therapy Restores Hearing in Patients with DFNB9 Deafness
Jieyu Qi, Fangzhi Tan, Liyan Zhang, et al.
Page
of 41
Search research articles
Search
Showing results (381-390 of 401) with videos related to
Sort By:
Page
of 41
Journal of Medical Internet Research
|
August 3, 2022
A Questionnaire-Based Ensemble Learning Model to Predict the Diagnosis of Vertigo: Model Development and Validation Study
Fangzhou Yu, Peixia Wu, Haowen Deng, et al.
Biorxiv : the Preprint Server for Biology
|
August 6, 2025
Rag GTPases Suppress Renal Cystic Disease by Inhibiting TFEB Independently of mTORC1
Flaviane de Fatima Silva, Alexander R Boucher, Huawei Li, et al.
Cell Stem Cell
|
August 21, 2018
Hoxc-Dependent Mesenchymal Niche Heterogeneity Drives Regional Hair Follicle Regeneration
Zhou Yu, Kaiju Jiang, Zijian Xu, et al.
American Journal of Human Genetics
|
July 5, 2011
Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64
Jing Cheng, Yuhua Zhu, Sudan He, et al.
Nature Biomedical Engineering
|
August 12, 2024
A base editor for the long-term restoration of auditory function in mice with recessive profound deafness
Chong Cui, Shengyi Wang, Daqi Wang, et al.
Journal of Medical Genetics
|
September 21, 2011
Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene
Xukun Yan, Xinjian Wang, Zhengmin Wang, et al.
Cell Reports
|
October 7, 2020
The Lipid Handling Capacity of Subcutaneous Fat Is Programmed by mTORC2 during Development
Wen-Yu Hsiao, Su Myung Jung, Yuefeng Tang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 26, 2021
Gene editing in a Myo6 semi-dominant mouse model rescues auditory function
Yuanyuan Xue, Xinde Hu, Daqi Wang, et al.
Molecular Cell
|
August 24, 2019
Non-canonical mTORC2 Signaling Regulates Brown Adipocyte Lipid Catabolism through SIRT6-FoxO1
Su Myung Jung, Chien-Min Hung, Samuel R Hildebrand, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
January 8, 2024
AAV-Mediated Gene Therapy Restores Hearing in Patients with DFNB9 Deafness
Jieyu Qi, Fangzhi Tan, Liyan Zhang, et al.
Page
of 41