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Keyword [PITX2]
Result: 1 - 20 | Page: 1 of 2
1.
Association Studies On Susceptive Genes Of Atrial Fibrillation In The Chinese Han Population And Drug Screening For Prion-Related Disease In Vitro By Protein Misfolding Cyclic Amplification
2.
PITX
2
Gene Ploymorphism Associated With Congenital Heart Diesease
3.
BRCA2Silencing Associated Aberrant Pitx2Expression Promotes PanIN Malignant Transformation
4.
Screening Of Proteins Interacting With PITX2by Yeast Two-Hybrid System
5.
Genetic Variations Of PITX2and TBX5in Lone Atrial Fibrillation
6.
The Effect Of Transcription Factors Pitx2and Twist1on Stenrness Maintenance Of Induced Hepatic Stem Cells
7.
Expression And Significance Of PITX2 And β-catenin In Epithelial Ovarian Cancer
8.
Differential Regulation Of Human Keratinocytes Into Enamel-secreting Ameloblasts By PITX2 Isoforms
9.
Genetic Variants In NEURL And PITX2 Are Associated With The Risk Of Atrial Fibrillation
10.
The Expression Of PITX2 And Its Clinical Significance In ⅢA-N2 Non-Small Cell Lung Cancer
11.
Study On The Function And Mechanism Of Prrx1 In The Process Of Recurrence And Metastasis Of Hepatocellular Carcinoma
12.
The Study On The Influence Of Long Non-coding RNA FOXF1-AS1 On NSCLC Cell Migration And Its Potential Mechanism
13.
Association Of Rs17042171 At Chromosome 4q25 With Atrial Fibrillation In The Chinese Han Population From The Central Plains
14.
The Expression And Significance Of DACT2 And PITX2 In Colon Cancer And Colon Adenoma
15.
The Application Research Of PITX2 Gene Polymorphism And ABC Score In Risk Stratification Of Atrial Fibrillation
16.
Transcriptional regulation and functional characterization of FoxJ1 during oro-facial and pituitary morphogenesis
17.
The function of the homeobox transcription factor Pitx2 during mammalian skeletal muscle development
18.
Factors affecting tooth and B cell development
19.
Functional study of Pitx2 in tooth development and craniofacial myogenesis
20.
The molecular mechanisms of PITX2 in tooth development and enamel defects in Axenfeld-Rieger Syndrome
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