- A Novel APTX Variant and Ataxia with Oculomotor Apraxia Type 1
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Manzoor H, Bukhari I, Wajid M, Zhang Y, Zhang H, Brüggemann N, Klein C, Shi Q, Naz S
- KMID: 2391678
- J Clin Neurol.
- 2017 Jul;13(3):303-305.
- doi: 10.3988/jcn.2017.13.3.303
No abstract available. -
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- Intratracheal Transplantation of Amnion-Derived Mesenchymal Stem Cells Ameliorates Hyperoxia-Induced Neonatal Hyperoxic Lung Injury via Aminoacyl-Peptide Hydrolase
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Li Z, Gong X, Li D, Yang X, Shi Q, Ju X
- KMID: 2504335
- Int J Stem Cells.
- 2020 Jul;13(2):221-236.
- doi: 10.15283/ijsc19110
Background and Objectives: Bronchopulmonary dysplasia (BPD) has major effects in premature infants. Although previous literature has indicated that mesenchymal stem cells (MSCs) can alleviate lung pathology in BPD newborns and... -
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- Analysis of TRRAP as a Potential Molecular Marker and Therapeutic Target for Breast Cancer
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Wang J, Shan M, Liu T, Shi Q, Zhong Z, Wei W, Pang D
- KMID: 2176322
- J Breast Cancer.
- 2016 Mar;19(1):61-67.
- doi: 10.4048/jbc.2016.19.1.61
PURPOSE: This study was designed to assess the protein levels of transformation/transcription domain-associated protein (TRRAP) in invasive ductal breast carcinomas, and investigated the association between TRRAP and the clinicopathological features... -
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- Analysis of 12 Chinese Patients with Proline-to-Leucine Mutation at Codon 102-Associated Gerstmann-Sträussler-Scheinker Disease
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Wang J, Xiao K, Zhou W, Shi Q, Dong XP
- KMID: 2467732
- J Clin Neurol.
- 2019 Apr;15(2):184-190.
- doi: 10.3988/jcn.2019.15.2.184
BACKGROUND AND PURPOSE: Gerstmann-Sträussler-Scheinker disease (GSS) with a proline-to-leucine mutation at codon 102 (P102L) in the PRNP gene is the most frequently reported GSS subtype worldwide. This study aimed to... -
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