Malignant neoplasm of urinary bladder
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Analysis of TCGA data indicated that TEF mRNA was decreased in BC samples compared to that in normal bladder epithelial cells and correlated with the poor survival of BC patients.
|
30515906 |
2019 |
Bladder Neoplasm
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Analysis of TCGA data indicated that TEF mRNA was decreased in BC samples compared to that in normal bladder epithelial cells and correlated with the poor survival of BC patients.
|
30515906 |
2019 |
Hypothyroidism
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Hypothyroidism disrupted the circadian expression pattern of Bmal1 and period circadian regulator 2 (Per2) and decreased the mesor of Nr1d1 and Tef.
|
30747053 |
2019 |
Carcinogenesis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Our results suggest that TEF might play an important role in suppressing BC cells proliferation and tumorigenesis.
|
30515906 |
2019 |
Carcinoma of bladder
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Analysis of TCGA data indicated that TEF mRNA was decreased in BC samples compared to that in normal bladder epithelial cells and correlated with the poor survival of BC patients.
|
30515906 |
2019 |
Precursor B-lymphoblastic lymphoma/leukemia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Characterization of TCF3 rearrangements in pediatric B-lymphoblastic leukemia/lymphoma by mate-pair sequencing (MPseq) identifies complex genomic rearrangements and a novel TCF3/TEF gene fusion.
|
31575852 |
2019 |
Congenital heart disease
|
0.010 |
Biomarker
|
group |
BEFREE |
A majority of patients undergo EA/TEF repair prior to congenital heart disease surgery.(Surgery 2017;160:XXX-XXX.).
|
29325785 |
2018 |
Tracheal diverticulosis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Our surgical approach used complete separation of the airway and esophagus, which reliably revealed the TEF (without need for cannulation) and freed the tissues for primary closure of the trachea and frequently resection of the tracheal diverticulum.
|
27616617 |
2017 |
Multiple Chronic Conditions
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Based on single- and multi-locus (ITS, TEF, TUB2) phylogenies, as well as morphological characters, host associations and geographical distributions, they were classified into at least 19 species in three genera, i.e.
|
28408743 |
2017 |
Anus, Imperforate
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The frequency of each component was: vertebral defects (V), 77 %; anal atresia (A), 62 %; tracheo-esophageal fistula/esophageal atresia (TEF/EA), 58 %; renal anomalies (R), 58 %; limb abnormalities (L), 50 %, and cardiac malformations (C), 42 %.
|
25008186 |
2015 |
Deformity of limb
|
0.010 |
Biomarker
|
group |
BEFREE |
The frequency of each component was: vertebral defects (V), 77 %; anal atresia (A), 62 %; tracheo-esophageal fistula/esophageal atresia (TEF/EA), 58 %; renal anomalies (R), 58 %; limb abnormalities (L), 50 %, and cardiac malformations (C), 42 %.
|
25008186 |
2015 |
Congenital anomaly of the kidney
|
0.010 |
Biomarker
|
group |
BEFREE |
The frequency of each component was: vertebral defects (V), 77 %; anal atresia (A), 62 %; tracheo-esophageal fistula/esophageal atresia (TEF/EA), 58 %; renal anomalies (R), 58 %; limb abnormalities (L), 50 %, and cardiac malformations (C), 42 %.
|
25008186 |
2015 |
Rheumatoid Arthritis
|
0.010 |
Biomarker
|
disease |
BEFREE |
TNF-α modulates the expression of the Per2 gene through the D-box binding proteins DBP, HLF, TEF, and E4BP4, in rheumatoid synovial cells, and thereby may contribute to the pathogenesis of RA.
|
23496259 |
2013 |
Esophageal Fistula
|
0.010 |
Biomarker
|
disease |
BEFREE |
Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: no evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectrum.
|
24307608 |
2013 |
VATER/VACTERL ASSOCIATION
|
0.010 |
Biomarker
|
disease |
BEFREE |
The presence of EA/TEF and malformations of the VATER/VACTERL association spectrum in relatives was systematically assessed.
|
24307608 |
2013 |
Neoplasm Metastasis
|
0.010 |
AlteredExpression
|
phenotype |
BEFREE |
Using a Luminex-based approach to multiplex in vivo assays, we determined that the domain of YAP that interacts with the TEAD/TEF family of transcription factors but not the WW domains or PDZ-binding motif, is essential for YAP-mediated tumor growth and metastasis.
|
22891335 |
2012 |
Parkinson Disease
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
All of them completed the PD Sleep Scale (PDSS) and other clinical and demographic assessments. rs738499, a single nucleotide polymorphism of the Tef gene, was genotyped by polymerase chain reaction-restriction fragment length polymorphism.
|
22257907 |
2012 |
Thyroglossal Cyst
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
This case helps to further delineate the critical region for TEF/EA, which is likely confined to the chromosomal region proximal to 17q23.1, and suggests that genes in 17q23.1q23.2 may be associated with thyroglossal duct cysts.
|
21271665 |
2011 |
Malignant transformation
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
These findings demonstrate that there are markedly abnormal expressions of TIF3 and TEF-1delta genes during malignant transformation of human bronchial epithelial cell lines induced by crystalline NiS.
|
16673819 |
2006 |
Congenital malrotation of intestine
|
0.010 |
Biomarker
|
disease |
BEFREE |
These findings indicate that intestinal malrotation is more common in infants with EA/TEF than is generally perceived, and that intestinal malrotation in an infant with EA/TEF is associated with a higher burden of additional congenital anomalies, suggesting that this group of infants may have more pervasive developmental deficits and poorer prognosis than has previously been recognized.
|
10471893 |
1999 |
leukemia
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Thus, TEF and HLF share indistinguishable DNA-binding and transcriptional regulatory properties, whose alteration in leukemia may be pathogenetically important.
|
8639829 |
1996 |
Childhood Leukemia
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Thus, TEF and HLF share indistinguishable DNA-binding and transcriptional regulatory properties, whose alteration in leukemia may be pathogenetically important.
|
8639829 |
1996 |
Deformity
|
0.010 |
Biomarker
|
group |
BEFREE |
Esophageal atresia with or without tracheoesophageal fistula (EA +/- TEF) usually occurs sporadically either as an isolated malformation or in conjunction with other congenital anomalies.
|
6714984 |
1984 |
Tracheoesophageal Fistula
|
0.020 |
Biomarker
|
disease |
BEFREE |
A male infant with oesophageal atresia and distal tracheo-oesophageal fistula (TEF type C) underwent right thoracotomy and transpleural repair of TEF on day 4 of life.
|
30413439 |
2018 |
Tracheal Diseases
|
0.020 |
Biomarker
|
group |
BEFREE |
Our surgical approach used complete separation of the airway and esophagus, which reliably revealed the TEF (without need for cannulation) and freed the tissues for primary closure of the trachea and frequently resection of the tracheal diverticulum.
|
27616617 |
2017 |