Congenital atransferrinemia
|
0.910 |
GeneticVariation
|
disease |
BEFREE |
A new case of human atransferrinemia with a previously undescribed mutation in the transferrin gene.
|
18097132 |
2007 |
Congenital atransferrinemia
|
0.910 |
GeneticVariation
|
disease |
CLINVAR |
Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia.
|
17768112 |
2007 |
Congenital atransferrinemia
|
0.910 |
GeneticVariation
|
disease |
UNIPROT |
Molecular characterization of a third case of human atransferrinemia.
|
15466165 |
2004 |
Congenital atransferrinemia
|
0.910 |
Biomarker
|
disease |
CTD_human |
Molecular analysis of the transferrin gene in a patient with hereditary hypotransferrinemia.
|
12111369 |
2002 |
Congenital atransferrinemia
|
0.910 |
GeneticVariation
|
disease |
CLINVAR |
Biochemical and genetic defects underlying human congenital hypotransferrinemia.
|
11920219 |
2000 |
Congenital atransferrinemia
|
0.910 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
The effect of transferrin polymorphisms on iron metabolism.
|
10660486 |
2000 |
Congenital atransferrinemia
|
0.910 |
GeneticVariation
|
disease |
UNIPROT |
Molecular characterization of a case of atransferrinemia.
|
11110675 |
2000 |
Congenital atransferrinemia
|
0.910 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Molecular characterization of a case of atransferrinemia.
|
11110675 |
2000 |
Congenital atransferrinemia
|
0.910 |
Biomarker
|
disease |
CTD_human |
Molecular characterization of a case of atransferrinemia.
|
11110675 |
2000 |
Congenital atransferrinemia
|
0.910 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Congenital atransferrinemia. A case report and review of the literature.
|
1862777 |
1991 |
Congenital atransferrinemia
|
0.910 |
Biomarker
|
disease |
MGD |
Hereditary hypotransferrinemia with hemosiderosis, a murine disorder resembling human atransferrinemia.
|
3681112 |
1987 |
Congenital atransferrinemia
|
0.910 |
Biomarker
|
disease |
HPO |
|
|
|
Congenital atransferrinemia
|
0.910 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
Congenital atransferrinemia
|
0.910 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
Obesity
|
0.500 |
Biomarker
|
disease |
CTD_human |
Orchestrated downregulation of genes involved in oxidative metabolic pathways in obese vs. lean high-fat young male consumers.
|
20882379 |
2011 |
Obesity
|
0.500 |
Biomarker
|
disease |
RGD |
Target identification of the novel antiobesity agent tungstate in adipose tissue from obese rats.
|
16267817 |
2005 |
Alzheimer's Disease
|
0.350 |
GeneticVariation
|
disease |
BEFREE |
Effects of hemochromatosis and transferrin gene mutations on iron dyshomeostasis, liver dysfunction and on the risk of Alzheimer's disease.
|
21514009 |
2012 |
Alzheimer's Disease
|
0.350 |
GeneticVariation
|
disease |
BEFREE |
(2004); J Med Genet 41:261-265] reported that epistatic interaction between rs1049296 (rs1049296" genes_norm="7018">P589S) in the transferrin gene (TF) and rs1800562 (C282Y) in the hemochromatosis gene (HFE) results in significant association with risk for AD.
|
20029940 |
2010 |
Alzheimer's Disease
|
0.350 |
Biomarker
|
disease |
LHGDN |
Sugar chains of cerebrospinal fluid transferrin as a new biological marker of Alzheimer's disease.
|
18654083 |
2008 |
Alzheimer's Disease
|
0.350 |
Biomarker
|
disease |
CTD_human |
Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database.
|
17192785 |
2007 |
Alzheimer's Disease
|
0.350 |
GeneticVariation
|
disease |
LHGDN |
Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.
|
15060098 |
2004 |
Alzheimer's Disease
|
0.350 |
Biomarker
|
disease |
CTD_human |
Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.
|
15060098 |
2004 |
Alzheimer's Disease
|
0.350 |
GeneticVariation
|
disease |
BEFREE |
As several lines of evidence indicate that oxidative stress and free radical damage occur in AD, the transferrin gene (TF) has been suggested as a candidate locus for AD since it is the major transport protein for iron, which itself is a major factor in free radical generation.
|
11750985 |
2002 |
Schizophrenia
|
0.340 |
Biomarker
|
disease |
PSYGENET |
The aim of this study was to investigate the possible influence of hemochromatosis gene mutations (HFE-C282Y and H63D) and transferrin gene C2 variant (TF-C2) on susceptibility to schizophrenia and schizoaffective disorder and/or age at first hospital admission.
|
21643746 |
2012 |
Schizophrenia
|
0.340 |
GeneticVariation
|
disease |
BEFREE |
The aim of this study was to investigate the possible influence of hemochromatosis gene mutations (HFE-C282Y and H63D) and transferrin gene C2 variant (TF-C2) on susceptibility to schizophrenia and schizoaffective disorder and/or age at first hospital admission.
|
21643746 |
2012 |