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Keyword [PTPRO]
Result: 1 - 20 | Page: 1 of 2
1.
Regulation Of PTPRO On LPS / TLR4 - Mediated Liver Injury
2.
Study On The Molecular Mechanism Of PTPRO-a Candidate Tumor Suppressor
3.
Transcriptional Regulation Of PTPRO Gene By E2F1 During PC12 Differentiation After NGF Stimulation
4.
Expression And Clinical Significance Of STAT5,SOCS1 And PTPRO In Leukemia
5.
Molecular Prognosis To Adjuvant Chemotherapy In Resected Patients With Advanced Gastric Carcinoma
6.
Expression And Clinical Significance Of PTPRO In Patients With Hepatocellular Carcinoma
7.
PTPRO Negatively Regulates Cell Cycle Progression By Targeting E2F1 Through C-Abl
8.
Estrogen Sensitive Protein Tyrosine Phosphatase Receptor Type-O Expressed In Hepatocellular Carcinoma
9.
Methylation Analysis In Breast Cancer Based On High-density Genomic DNA Methyaltion Chips And Clinical Verification Of Important Functional Genes
10.
Research Of The Relationship Between PTPRO Methylation And Colorectal Cancer
11.
Estrogen Sensitive PTPRO Expression Represses Hepatocellular Carcinoma Progression
12.
PTPRO-associated Hepatic Stellate Cell Activation Plays A Critical Role In Liver Fibrosis
13.
Mechanistic Study Of The Role Of Protein Tyrosine Phosphatase Receptor-type O Involved In The Inflammatory Microenvironment Of Hepatocellular Carcinoma
14.
PTPRO Promotes Ox-LDL Induced Oxidative Stress And Cell Apoptosis Through TLR4/NF-κB Pathway&Diagnostic Value Of TCM Tongue Diagnosis In Coronary Heart Disease Patients With Clopidogrel Resistance After PCI
15.
The Expression Of PTPRO In Colorectal Carcinoma And Its Relationship With Clinical Pathological Factors
16.
A Meta Analysis Of Multiple Genes Methylation And Susceptibility To Lung Cancer And Its Value In The Diagnosis Of Lung Cancer
17.
PTPRO Overexpression In Human Hepatoma Cells Regulate The Epithelial-mesenchymal Transition
18.
PTPRO-mediated Autophagy Inhibits Liver Steatosis And Tumor Formation
19.
Protein tyrosine phosphatase signaling in axon growth
20.
IL-6 Promotes PD-L1 Expression In Monocytes And Macrophages By Decreasing Protein Tyrosine Phosphatase Receptor Type O Expression In Human Hepatocellular Carcinoma
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