×
Entrez Id:
348
Gene Symbol:
APOE
APOE
0.020
GeneticVariation
disease
BEFREE
Our data suggest that in iodine-deficient areas, the APOE epsilon4 allele is a genetic risk factor for FIDD .
10889546
2000
×
Entrez Id:
7253
Gene Symbol:
TSHR
TSHR
0.510
Biomarker
disease
MGD
×
Entrez Id:
7253
Gene Symbol:
TSHR
TSHR
0.510
Biomarker
disease
BEFREE
In conclusion, our association results suggest that TSHR gene is not a susceptibility gene for FIDD in the iodine-deficient areas of China.
15911145
2005
×
Entrez Id:
7253
Gene Symbol:
TSHR
TSHR
0.510
Biomarker
disease
CTD_human
The W546X mutation of the thyrotropin receptor gene: potential major contributor to thyroid dysfunction in a Caucasian population.
12629076
2003
×
Entrez Id:
7173
Gene Symbol:
TPO
TPO
0.500
Biomarker
disease
CTD_human
Total iodide organification defect: clinical and molecular characterization of an Italian family.
16187919
2005
×
Entrez Id:
50506
Gene Symbol:
DUOX2
DUOX2
0.500
Biomarker
disease
MGD
×
Entrez Id:
7173
Gene Symbol:
TPO
TPO
0.500
Biomarker
disease
MGD
×
Entrez Id:
50506
Gene Symbol:
DUOX2
DUOX2
0.500
Biomarker
disease
CTD_human
Three mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A>C) in the dual oxidase 2 gene responsible for congenital goiter and iodide organification defect.
16322276
2006
×
Entrez Id:
7173
Gene Symbol:
TPO
TPO
0.500
Biomarker
disease
CTD_human
Congenital hypothyroidism with goiter in toy fox terriers.
12564727
2003
×
Entrez Id:
7173
Gene Symbol:
TPO
TPO
0.500
Biomarker
disease
CTD_human
Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect.
14751036
2003
×
Entrez Id:
7173
Gene Symbol:
TPO
TPO
0.500
Biomarker
disease
CTD_human
Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis.
17381485
2007
×
Entrez Id:
50506
Gene Symbol:
DUOX2
DUOX2
0.500
Biomarker
disease
CTD_human
Persistent mild hypothyroidism associated with novel sequence variants of the DUOX2 gene in two siblings.
16134168
2005
×
Entrez Id:
3547
Gene Symbol:
IGSF1
IGSF1
0.300
Biomarker
disease
CTD_human
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement.
23143598
2012
×
Entrez Id:
4741
Gene Symbol:
NEFM
NEFM
0.200
Biomarker
disease
RGD
Congenital hypothyroidism is associated with intermediate filament misregulation, glutamate transporters down-regulation and MAPK activation in developing rat brain.
18845185
2008
×
Entrez Id:
10092
Gene Symbol:
ARPC5
ARPC5
0.200
Biomarker
disease
RGD
Effects of hypothyroidism on expression of CRMP2B and ARPC5 during development of the rat frontal cortex.
23459330
2013
×
Entrez Id:
1958
Gene Symbol:
EGR1
EGR1
0.200
Biomarker
disease
RGD
Developmentally-induced hypothyroidism alters the expression of Egr-1 and Arc genes and the sensitivity to cannabinoid agonists in the hippocampus. Possible implications for memory and learning.
23079472
2013
×
Entrez Id:
7201
Gene Symbol:
TRHR
TRHR
0.200
Biomarker
disease
MGD
×
Entrez Id:
3479
Gene Symbol:
IGF1
IGF1
0.200
Biomarker
disease
RGD
The effects of thyroid hormone on insulin-like growth factor (IGF) and IGF-binding protein (IGFBP) expression in the neonatal rat: prolonged high expression of IGFBP-2 in methimazole-induced congenital hypothyroidism.
1718729
1991
×
Entrez Id:
7849
Gene Symbol:
PAX8
PAX8
0.200
Biomarker
disease
MGD
×
Entrez Id:
632
Gene Symbol:
BGLAP
BGLAP
0.200
Biomarker
disease
RGD
Studies on gene expression in calvaria and serum levels of insulin-like growth factor-I and bone Gla protein in the methimazole-induced congenital hypothyroid rat.
7920889
1993
×
Entrez Id:
3625
Gene Symbol:
INHBB
INHBB
0.200
Biomarker
disease
RGD
Developmental expression of testis messenger ribonucleic acids in the rat following propylthiouracil-induced neonatal hypothyroidism.
7819453
1994
×
Entrez Id:
2539
Gene Symbol:
G6PD
G6PD
0.200
Biomarker
disease
RGD
Congenital hypothyroidism alters the oxidative status, enzyme activities and morphological parameters in the hippocampus of developing rats.
23693027
2013
×
Entrez Id:
860
Gene Symbol:
RUNX2
RUNX2
0.200
Biomarker
disease
MGD
×
Entrez Id:
4744
Gene Symbol:
NEFH
NEFH
0.200
Biomarker
disease
RGD
Congenital hypothyroidism is associated with intermediate filament misregulation, glutamate transporters down-regulation and MAPK activation in developing rat brain.
18845185
2008
×
Entrez Id:
2304
Gene Symbol:
FOXE1
FOXE1
0.200
Biomarker
disease
MGD