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Tianyou Li

Showing results (61-70 of 68) with videos related to

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Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|September 21, 2022
Inhibition of the dopamine transporter promotes lysosome biogenesis and ameliorates Alzheimer's disease-like symptoms in miceLimin Yin, Jianhui Zhou, Tianyou Li, et al.
Intractable & Rare Diseases Research|June 21, 2019
Splice receptor-site mutation c.697-2A>G of the <i>COL1A1</i> gene in a Chinese family with osteogenesis imperfectaNaixiang Zhai, Yanqin Lu, Yanzhou Wang, et al.
Bone|June 24, 2018
Novel WNT1 mutations in children with osteogenesis imperfecta: Clinical and functional characterizationYanqin Lu, Xiuzhi Ren, Yanzhou Wang, et al.
Clinical Endocrinology|October 24, 2013
Mutational and structural characteristics of four novel heterozygous C-propeptide mutations in the proα1(I) collagen gene in Chinese osteogenesis imperfecta patientsYanqin Lu, Xiuzhi Ren, Yanzhou Wang, et al.
Intractable & Rare Diseases Research|February 13, 2015
Heterozygous mutation of c.3521C>T in COL1A1 may cause mild osteogenesis imperfecta/Ehlers-Danlos syndrome in a Chinese familyXianlong Shi, Yanqin Lu, Yanzhou Wang, et al.
Life Sciences|July 22, 2025
Endoplasmic reticulum stress and autophagy as potential therapeutic targets in SERPINF1 mutation-induced type VI osteogenesis imperfectaYang Tian, Xinyu Chen, Shuoshuo Wei, et al.
Cancer Letters|November 10, 2025
KLF7 as a biomarker for the pre-metastatic state promotes colorectal cancer liver metastasis via TGFβ autocrine signalingXiaozhuang Fang, Hongyu Huang, Zize Zhao, et al.
The Journal of Clinical Endocrinology and Metabolism|March 5, 2024
Characterization of Novel PHEX Variants in X-linked Hypophosphatemic Rickets and Genotype-PHEX Activity CorrelationHuixiao Wu, Hui Ying, Wanyi Zhao, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|September 21, 2022
Inhibition of the dopamine transporter promotes lysosome biogenesis and ameliorates Alzheimer's disease-like symptoms in miceLimin Yin, Jianhui Zhou, Tianyou Li, et al.
Intractable & Rare Diseases Research|June 21, 2019
Splice receptor-site mutation c.697-2A>G of the <i>COL1A1</i> gene in a Chinese family with osteogenesis imperfectaNaixiang Zhai, Yanqin Lu, Yanzhou Wang, et al.
Bone|June 24, 2018
Novel WNT1 mutations in children with osteogenesis imperfecta: Clinical and functional characterizationYanqin Lu, Xiuzhi Ren, Yanzhou Wang, et al.
Clinical Endocrinology|October 24, 2013
Mutational and structural characteristics of four novel heterozygous C-propeptide mutations in the proα1(I) collagen gene in Chinese osteogenesis imperfecta patientsYanqin Lu, Xiuzhi Ren, Yanzhou Wang, et al.
Intractable & Rare Diseases Research|February 13, 2015
Heterozygous mutation of c.3521C>T in COL1A1 may cause mild osteogenesis imperfecta/Ehlers-Danlos syndrome in a Chinese familyXianlong Shi, Yanqin Lu, Yanzhou Wang, et al.
Life Sciences|July 22, 2025
Endoplasmic reticulum stress and autophagy as potential therapeutic targets in SERPINF1 mutation-induced type VI osteogenesis imperfectaYang Tian, Xinyu Chen, Shuoshuo Wei, et al.
Cancer Letters|November 10, 2025
KLF7 as a biomarker for the pre-metastatic state promotes colorectal cancer liver metastasis via TGFβ autocrine signalingXiaozhuang Fang, Hongyu Huang, Zize Zhao, et al.
The Journal of Clinical Endocrinology and Metabolism|March 5, 2024
Characterization of Novel PHEX Variants in X-linked Hypophosphatemic Rickets and Genotype-PHEX Activity CorrelationHuixiao Wu, Hui Ying, Wanyi Zhao, et al.
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