|
Depression in children
|
0.310 |
GeneticVariation
|
disease |
BEFREE |
This study suggests that epigenetic changes in ID3, GRIN1, and TPPP genes, in combination with experiences of maltreatment, may confer risk for depression in children.
|
24655651 |
2014 |
|
Adenocarcinoma Of Esophagus
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis.
|
27527254 |
2016 |
|
Adenocarcinoma Of Esophagus
|
0.110 |
GeneticVariation
|
disease |
BEFREE |
We identified eight new risk loci associated with either Barrett's oesophagus or oesophageal adenocarcinoma, within or near the genes CFTR (rs17451754; p=4·8 × 10<sup>-10</sup>), MSRA (rs17749155; p=5·2 × 10<sup>-10</sup>), LINC00208 and BLK (rs10108511; p=2·1 × 10<sup>-9</sup>), KHDRBS2 (rs62423175; p=3·0 × 10<sup>-9</sup>), TPPP and CEP72 (rs9918259; p=3·2 × 10<sup>-9</sup>), TMOD1 (rs7852462; p=1·5 × 10<sup>-8</sup>), SATB2 (rs139606545; p=2·0 × 10<sup>-8</sup>), and HTR3C and ABCC5 (rs9823696; p=1·6 × 10<sup>-8</sup>).
|
27527254 |
2016 |
|
Barrett Esophagus
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis.
|
27527254 |
2016 |
|
Glomerular Filtration Rate
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program.
|
31451708 |
2019 |
|
Glomerular Filtration Rate
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
|
31152163 |
2019 |
|
HIV Infections
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Using an appropriate combination of C65690M and ANT-152 p24 antibodies capable of detecting all HIV types and highly sensitive TRF-based europium nano particle assay platform, we developed a sensitive p24 antigen assay that can detect HIV infection of all HIV subtypes and may be useful in early detection.
|
30411969 |
2019 |
|
HIV Infections
|
0.100 |
GeneticVariation
|
group |
BEFREE |
To investigate the association between human immunodeficiency virus (HIV) and Epstein-Barr virus (EBV), simultaneous determinations of HIV antigen (HIV Ag) p24 and EBV DNA were performed in lymphocyte culture supernatants from 63 individuals at risk of HIV infection.
|
1327786 |
1992 |
|
Immunologic Deficiency Syndromes
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Fourth-generation EIAs, especially those with a high sensitivity for HIV-1 p24 antigen, reduce the diagnostic window for primary HIV-1 subtype E infection in comparison with third-generation antibody-screening assays.
|
12925157 |
2003 |
|
HIV-1 infection
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In vitro HIV-1 infection assays with CCR5-using primary isolates demonstrated that thymocytes with the heterozygous CCR5 Delta 32 mutation produced less p24 than did CCR5 wild-type thymocytes.
|
10861047 |
2000 |
|
HIV-1 infection
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Viraemia and p24 antigenaemia are independent risk factors for the emergency of a zidovudine-resistant genotype in nucleoside analogue-treated HIV-1 infection.
|
11322281 |
1997 |
|
Human immunodeficiency virus (HIV) II infection category B1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Restriction fragment length polymorphism (RFLP) analysis was used to determine HIV-1 viral clades of nested polymerase chain reaction products from HIV-1 protease or p24 genes.
|
10669368 |
2000 |
|
Human immunodeficiency virus (HIV) II infection category B1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
This study examined the effect of antiretroviral therapy on human immunodeficiency virus (HIV-1) unintegrated DNA (uDNA), integrated DNA (iDNA), percent uDNA, immune complex dissociated (ICD) p24 antigenemia, and plasma viral titer.
|
7965634 |
1994 |
|
Human immunodeficiency virus (HIV) II infection category B1
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
A rapid method for identification of human immunodeficiency virus Type 1 (HIV-1) gag subtypes was developed based on restriction fragment length polymorphism (RFLP) analysis of 400 or 650 bp long polymerase chain reaction (PCR) fragments encompassing the start of the p17 (400 bp) and part of the p24 (650bp) regions.
|
10204696 |
1999 |
|
Amyotrophic Lateral Sclerosis
|
0.040 |
GeneticVariation
|
disease |
BEFREE |
After our recent report that a deregulation of Cdk5 activity by p25 may contribute to pathogenesis of amyotrophic lateral sclerosis (ALS), we further examined the possible involvement of other Cdks in mice expressing a mutant form of superoxide dismutase (SOD1(G37R)) linked to ALS.
|
12657672 |
2003 |
|
Acute HIV infection
|
0.040 |
GeneticVariation
|
disease |
BEFREE |
During acute HIV infection (AHI), detection depends on assay sensitivity for p24 Ag.
|
23485348 |
2013 |
|
Borna Disease
|
0.030 |
GeneticVariation
|
disease |
BEFREE |
RNA, extracted from peripheral blood mononuclear cells (PBMC) obtained from 81 Korean psychiatric patients (39 with schizophrenia, 33 with bipolar affective disorders and nine with major depression), was analyzed for a 391-nucleotide, highly conserved region of the p24 protein-encoding ORF II of Borna disease virus (BDV), using nested reverse transcription-polymerase chain reaction (RT-PCR).
|
10321984 |
1999 |
|
Renal Cell Carcinoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The majority of these markers clustered in three regions that have been suggested to be involved in the development of RCC, namely the p25 region, where the von Hippel Lindau (VHL) gene is located; the p21 region, which has been identified as a common region of overlap (SRO) of heterozygous deletions; and the p14 region, which is the location of the constitutional t(3;8) breakpoint occurring in an RCC family.
|
8824727 |
1996 |
|
Neuroblastoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Two regions of deletion in 9p22- p24 in neuroblastoma are frequently observed in favorable tumors.
|
12072202 |
2002 |
|
Superinfection
|
0.010 |
GeneticVariation
|
group |
BEFREE |
Plasma samples from HIV-infected FSWs in Kampala, Uganda were examined with next-generation sequencing of the p24 and gp41 HIV genomic regions for the occurrence of superinfection.
|
25265078 |
2014 |
|
Conventional (Clear Cell) Renal Cell Carcinoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The majority of these markers clustered in three regions that have been suggested to be involved in the development of RCC, namely the p25 region, where the von Hippel Lindau (VHL) gene is located; the p21 region, which has been identified as a common region of overlap (SRO) of heterozygous deletions; and the p14 region, which is the location of the constitutional t(3;8) breakpoint occurring in an RCC family.
|
8824727 |
1996 |
|
Frontotemporal dementia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The levels of CSF NF-L detected in p25 mice are about 4-fold higher than the CSF levels detected in patients with chronic neurodegenerative diseases, such as symptomatic FTD (bvFTD).
|
28392472 |
2017 |
|
Central neuroblastoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Two regions of deletion in 9p22- p24 in neuroblastoma are frequently observed in favorable tumors.
|
12072202 |
2002 |
|
Childhood Neuroblastoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Two regions of deletion in 9p22- p24 in neuroblastoma are frequently observed in favorable tumors.
|
12072202 |
2002 |
|
Depression in children
|
0.310 |
Biomarker
|
disease |
PSYGENET |
This study suggests that epigenetic changes in ID3, GRIN1, and TPPP genes, in combination with experiences of maltreatment, may confer risk for depression in children.
|
24655651 |
2014 |