about
Twist: a molecular target in cancer therapeuticsThe TWIST/Mi2/NuRD protein complex and its essential role in cancer metastasisIdentification of a novel heterozygous missense mutation in the CACNA1F gene in a chinese family with retinitis pigmentosa by next generation sequencing.TWIST represses estrogen receptor-alpha expression by recruiting the NuRD protein complex in breast cancer cells.Steroid receptor coactivator 3 regulates autophagy in breast cancer cells through macrophage migration inhibitory factorDLX4 upregulates TWIST and enhances tumor migration, invasion and metastasisPrognostic Value of EMT-inducing Transcription Factors (EMT-TFs) in Metastatic Breast Cancer: A Systematic Review and Meta-analysis.Tripartite motif containing 28 (TRIM28) promotes breast cancer metastasis by stabilizing TWIST1 protein.Deleted in breast cancer 1, a novel androgen receptor (AR) coactivator that promotes AR DNA-binding activity.Nanoemulsion improves the oral bioavailability of baicalin in rats: in vitro and in vivo evaluationDifferential regulation of the REGγ-proteasome pathway by p53/TGF-β signalling and mutant p53 in cancer cells.Diagnosis for choroideremia in a large Chinese pedigree by next‑generation sequencing (NGS) and non‑invasive prenatal testing (NIPT).A review on Ipomoea carnea: pharmacology, toxicology and phytochemistry.Epithelial to mesenchymal transition inducing transcription factors and metastatic cancer.Establishment of stable cell line for inducing KAP1 protein expression.REGγ is critical for skin carcinogenesis by modulating the Wnt/β-catenin pathway.Correlation between HFE gene polymorphisms and increased risk of coronary artery disease among patients with type 2 diabetes in Iran.REGγ Contributes to Regulation of Hemoglobin and Hemoglobin δ Subunit.Genetic Authentication of Gardenia jasminoides Ellis var. grandiflora Nakai by Improved RAPD-Derived DNA Markers.Resveratrol enhances polyubiquitination-mediated ARV7 degradation in prostate cancer cells.Mutant p53 promotes cell spreading and migration via ARHGAP44.Genetic characterization and authentication of Lonicera japonica Thunb. by using improved RAPD analysis.Development of RAPD-SCAR markers for Lonicera japonica (Caprifolicaceae) variety authentication by improved RAPD and DNA cloning.Thymoquinone Inhibits the Migration and Invasive Characteristics of Cervical Cancer Cells SiHa and CaSki In Vitro by Targeting Epithelial to Mesenchymal Transition Associated Transcription Factors Twist1 and Zeb1.Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing.Genetic analysis of Canarium album in different areas of China by improved RAPD and ISSR.Th17/Treg-related cytokine imbalance in sulfur mustard exposed and stable chronic obstructive pulmonary (COPD) patients: correlation with disease activity.A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing.MicroRNA-34 family in breast cancer: from research to therapeutic potentialEvaluation genotypes of cancer cell lines HCC1954 and SiHa by short tandem repeat (STR) analysis and DNA sequencingA novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigreeNovel splicing variant c. 208+2T>C in segregates with Bardet-Biedl syndrome in an Iranian family by targeted exome sequencingRoles of MicroRNA-34a in Epithelial to Mesenchymal Transition, Competing Endogenous RNA Sponging and Its Therapeutic PotentialDevelopment of a HPLC method to determine 5-fluorouracil in plasma: application in pharmacokinetics and steady-state concentration monitoringCharacterization and molecular cloning of novel isoforms of human spermatogenesis associated gene SPATA3A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS-based genetic diagnosisIdentification of a novel germline BRCA2 variant in a Chinese breast cancer familyCorrection to: Characterization and molecular cloning of novel isoforms of human spermatogenesis associated gene SPATA3Expressions and significances of the angiotensin-converting enzyme 2 gene, the receptor of SARS-CoV-2 for COVID-19A case of Usher syndrome type IIA caused by a rare USH2A homozygous frameshift variant with maternal uniparental disomy (UPD) in a Chinese family
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Junjiang Fu
@ast
Junjiang Fu
@en
Junjiang Fu
@es
Junjiang Fu
@nl
Junjiang Fu
@sl
type
label
Junjiang Fu
@ast
Junjiang Fu
@en
Junjiang Fu
@es
Junjiang Fu
@nl
Junjiang Fu
@sl
prefLabel
Junjiang Fu
@ast
Junjiang Fu
@en
Junjiang Fu
@es
Junjiang Fu
@nl
Junjiang Fu
@sl
P106
P31
P496
0000-0002-0708-2200
P569
2000-01-01T00:00:00Z