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Jiaxing Chen,Zhizhao Yang,Yongqiang Cui et al. Jiaxing Chen et al.
Background: Hepatocellular carcinoma (HCC) is the leading cause of cancer-related mortality worldwide owing to the lack of effective and early diagnostic tools and therapeutic approaches. DNAJC7, a member of the DnaJ heat...
Andrew C Fleming,Nalini R Rao,Matthew Wright et al. Andrew C Fleming et al.
The degeneration of neurons in patients with amyotrophic lateral sclerosis (ALS) is commonly associated with accumulation of misfolded, insoluble proteins. Heat shock proteins (HSPs) are central regulators of protein homeostasis as they fol...
Cheng-Lin Zhan,Dongjie Zhou,Ming-Hong Sun et al. Cheng-Lin Zhan et al.
Assisted reproduction technology (ART) procedures are often impacted by post-ovulatory aging (POA), which can lead to reduced fertilization rates and impaired embryo development. This study used RNA sequencing analysis and experimental vali...
Shichan Wang,Xiaoting Zheng,Qianqian Wei et al. Shichan Wang et al.
DnaJ heat shock protein family member C7 gene (DNAJC7) has been identified as a genetic risk factor for amyotrophic lateral sclerosis (ALS). In our study, we aimed to screen for rare variants in DNAJC7 in a large cohort of Chinese ALS patie...
Valerie Ann Perez,David W Sanders,Ayde Mendoza-Oliva et al. Valerie Ann Perez et al.
Neurodegenerative tauopathies are caused by accumulation of toxic tau protein assemblies. This appears to involve template-based seeding events, whereby tau monomer changes conformation and is recruited to a growing aggregate. Several large...
Valerie A Perez,David W Sanders,Ayde Mendoza-Oliva et al. Valerie A Perez et al.
Neurodegenerative tauopathies are caused by accumulation of toxic tau protein assemblies. This appears to involve template-based seeding events, whereby tau monomer changes conformation and is recruited to a growing aggregate. Several large...
Jie Cao,Shuhui Liu,Meng Liu et al. Jie Cao et al.
Fowl adenovirus serotype 4 (FAdV-4) infection results in serious hepatitis-hydropericardium syndrome (HHS) in broilers, which has caused great economic losses to the poultry industry; however, the specific host responses to FAdV-4 remain un...
Allison A Dilliott,Catherine M Andary,Meaghan Stoltz et al. Allison A Dilliott et al.
Protein misfolding is a common basis of many neurodegenerative diseases including amyotrophic lateral sclerosis (ALS). Misfolded proteins, such as TDP-43, FUS, Matrin3, and SOD1, mislocalize and form the hallmark cytoplasmic and nuclear inc...
Genki Tohnai,Ryoichi Nakamura,Naoki Atsuta et al. Genki Tohnai et al.
DNAJC7 has recently been identified as an amyotrophic lateral sclerosis (ALS) gene via large-scale exome analysis, and its involvement in ALS is still unclear in various populations. This study aimed to determine the frequencies and charact...
Zhiqiang Hou,Pawel M Wydorski,Valerie A Perez et al. Zhiqiang Hou et al.
Molecular chaperones, including Hsp70/J-domain protein (JDP) families, play central roles in binding substrates to prevent their aggregation. How JDPs select different conformations of substrates remains poorly understood. Here, we report a...
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