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The FABP3 is induced in the mesangial cells and likely a mediator to induce MCP-1 (show CPT1B Proteins) in the diabetic nephropathy.
The results confirmed the altered expression of HFABP, a key fatty acid transport protein (show CD36 Proteins), and of enolase and PGK1 (show PGK1 Proteins), the key enzymes in the glycolytic process
Increased placental FABP3 promotes fatty acid transport and contributes to excess lipid accumulation in the fetal liver in model of obesity in pregnancy.
The frameshift and missense mutations in FABP3, FABP5 (show FABP5 Proteins), and FABP7 (show FABP7 Proteins) genes have been identified in schizophrenia and autism spectrum disorder in humans and in mouse behavioral studies.
ABR thresholds of young and aged Fabp3 knockout mice were unchanged compared with those of wild-type mice. Suggests that Fabp3 deficiency alone does not adversely affect hearing function.
Collectively FABP3 regulates n-3 (omega-3) and n-6 (omega-6) polyunsaturated FA transport in trophoblasts and plays a pivotal role in fetal development.
Brown adipocyte-characteristic fatty acid oxidation proteins are induced in beige cells in a different pathway from UCP1 (show UCP1 Proteins).
FABP3 silencing promotes apoptosis and inhibits the proliferation of P19 cells.
FABP3 overexpression has a detrimental effect on mitochondrion function in embryonic cancer P19 cells.
Results indicated that FABP3 knockdown promoted apoptosis and caused mitochondrial dysfunction in P19 cells.
The higher interaction footprint of aptamer N53 incited synergistic conformational changes in both N53 and FABP3 during interaction, leading to a decline in binding affinity in comparison to aptamer N13 which corroborated to the calculated Kd values.
There was no significant correlation between H-FABP, free triiodothyronine (fT3), free thyroxine (fT4), and thyroid stimulating hormone (TSH) levels in hyperthyroid patients
For patients recruited = 6 h after trauma, the CT-positive group indicated significantly higher levels of both H-FABP and S100B (show S100B Proteins) than the CT-negative group.
HFABP expression is significantly elevated in in-stent coronary resteonisis . Overexpression of HFABP induces multiple pathway-related promotion of inflammation, growth and migration in vascular smooth muscle cells.
cardiac damage in patients with CO poisoning could be partially mediated by CO-induced oxidative stress, where H-FABP3 level was directly and strongly associated with MDA and ADMA levels
findings demonstrate the interobserver reliability of a qualitative point of care h-FABP assay
Neonatal phthalate ester exposure induced placental MTs (show TIMM8A Proteins), FATP1 and HFABP mRNA expression
FABP3 expression was significantly lower in the schizophrenia group than in the control group.
This study demonstrated that CSF (show CSF2 Proteins) FABP-3 may be an early marker for later development of dementia.
Bedside H-FABP measurements may contribute to correct early diagnoses, as its levels are elevated soon following myocardial infarction, and measurement is easy, with a rapid result.
SNPs in the FABP3 promoter may contribute to intramuscular fat without influencing carcass fatness traits in pigs
Expression of the FABP3 gene enhances adipogenesis in 3T3-L1 preadipocytes primarily by upregulating lipogenic genes.
Results indicate that fatty acid binding protein H-FABP and CoA ligase 4 ACSL4 (show ACSL4 Proteins) genes might serve as markers to improve fat (IMF (show MDFI Proteins)) content in the breeding system.
hFABP rises faster and correlates better with infarct size and no-reflow than hsTnI in myocardial infarction + reperfusion when measured early after reperfusion.
Linkage disequilibrium analysis among MC4R (show MC4R Proteins), LEP (show LEP Proteins) and H-FABP revealed that these genes were independent.
The FABP3 polymorphisms can be used as genetic markers in breeding programs for intramuscular fat content as well as carcass back fat thickness.
The H-FABP MspI RFLP genotype affected unsaturated fatty acid content, and the ratio of polyunsaturated fatty acid to saturated fatty acid (P<0.05), whereas the H-FABP HaeIII RFLP genotype had no effect on fatty acid characteristics.
The objective of this study was to investigate the effect of FABP3 and LEPR genetic variations as well as their mRNA expression on the intramuscular fat content trait in a three-generation of Korean native pig and Yorkshire crossed animals.
Results of associated analysis show that the polymorphism of H-FABP gene was associated traits of Intramuscular fat content (IMF (show MDFI Proteins)) and back fat thickness (BF).
In our study FABP3 genotypes were confirmed to be significantly associated with intramuscular fat in pigs.
Sequence analysis showed that many transcriptional factor binding sites including TATA-box and CCAAT-box were present on the 5'-flanking region of bovine FABP3, and four CpG islands were found on nucleotides from -891 to +118.
FABP3 has a role in milk fat synthesis signaling.
FABP3 gene frequency and SNP genotypes in Holstein-Friesian cows and its relationship with protein and fat content in milk
Thus, the results of our study suggest that the H-FABP and PSMC1 (show PSMC1 Proteins) gene polymorphisms could be used as genetic markers in marker-assisted selection for improving Qinchuan beef cattle
MRF4 (show MYF6 Proteins) and H-FABP genes are associated with growth traits in Qinchuan cattle and related hybrids
The results of this study suggest that suggest that SLC27A6, ACSL1 (show Acsl1 Proteins), FABP3, AGPAT6 (show AGPAT6 Proteins), and LPIN1 (show LPIN1 Proteins) coordinately regulate the channeling of fatty acids toward copious milk fat synthesis in bovine mammary.
The intracellular fatty acid-binding proteins (FABPs) belongs to a multigene family. FABPs are divided into at least three distinct types, namely the hepatic-, intestinal- and cardiac-type. They form 14-15 kDa proteins and are thought to participate in the uptake, intracellular metabolism and/or transport of long-chain fatty acids. They may also be responsible in the modulation of cell growth and proliferation. Fatty acid-binding protein 3 gene contains four exons and its function is to arrest growth of mammary epithelial cells. This gene is a candidate tumor suppressor gene for human breast cancer.
Fatty acid binding protein 3 heart
, fatty acid binding protein 3 heart
, fatty acid-binding protein 3
, fatty acid-binding protein, heart
, heart fatty acid binding protein
, heart-type fatty acid-binding protein
, fatty acid binding protein heart 1
, fatty acid binding protein heart 4
, mammary-derived growth inhibitor
, Fatty acid-binding protein 3, muscle
, fatty acid binding protein 11
, muscle fatty acid-binding protein
, heart fatty acid-binding protein
, heart-type fatty acid binding protein
, fatty acid binding protein ( heart ) like