Increased orosomucoid-like 3 (ORMDL3) expression levels, due to single nucleotide polymorphisms (SNPs), have been associated with several inflammatory diseases, including asthma and inflammatory bowel diseases. ORMDL proteins inhibit serine palmitoyltransferase (SPT), the first rate-limiting enzyme in de novo sphingolipid synthesis and alter cellular calcium homeostasis. Both processes are essential for immune response. The present study addresses ORMDL3 protein involvement in macrophage physiology using an overexpressing knock-in mouse model. Ceramide content was notably different in the bone-marrow-derived macrophages (BMDM) from the transgenic mouse model compared with the wild type (WT) macrophages. Our data revealed an alteration of de...
ORMDL proteins are regulators of serine palmitoyltransferase (SPT) enzyme, which catalyzes the first...
Abstract Introduction The chromosomal region 17q21 harbors the human orosomucoid‐like 3 (ORMDL3) gen...
Rationale: Polymorphisms on chromosome 17q21 confer the major genetic susceptibility to childhood-on...
Increased orosomucoid-like 3 (ORMDL3) expression levels, due to single nucleotide polymorphisms (SNP...
Increased orosomucoid-like 3 (ORMDL3) expression levels, due to single nucleotide polymorphisms (SNP...
Genome-wide association studies linked increased ORMDL3 expression levels to several inflammatory di...
Genome-wide association studies linked increased ORMDL3 expression levels to several inflammatory di...
Genome-wide association studies linked increased ORMDL3 expression levels to several inflammatory di...
ORMDL proteins are believed to be negative regulators of serine palmitoyltransferase (SPT), which ca...
ORMDL proteins are believed to be negative regulators of serine palmitoyltransferase (SPT), which ca...
ORMDL proteins are believed to be negative regulators of serine palmitoyltransferase (SPT), which ca...
ORMDL proteins are believed to be negative regulators of serine palmitoyltransferase (SPT), which ca...
The severity of asthma, a chronic inflammatory disease of the airways, is influenced by a multitude ...
BACKGROUND: Genome-wide association studies in asthma have repeatedly identified single nucleotide p...
ORMDL proteins are believed to be negative regulators of serine palmitoyltransferase (SPT), which ca...
ORMDL proteins are regulators of serine palmitoyltransferase (SPT) enzyme, which catalyzes the first...
Abstract Introduction The chromosomal region 17q21 harbors the human orosomucoid‐like 3 (ORMDL3) gen...
Rationale: Polymorphisms on chromosome 17q21 confer the major genetic susceptibility to childhood-on...
Increased orosomucoid-like 3 (ORMDL3) expression levels, due to single nucleotide polymorphisms (SNP...
Increased orosomucoid-like 3 (ORMDL3) expression levels, due to single nucleotide polymorphisms (SNP...
Genome-wide association studies linked increased ORMDL3 expression levels to several inflammatory di...
Genome-wide association studies linked increased ORMDL3 expression levels to several inflammatory di...
Genome-wide association studies linked increased ORMDL3 expression levels to several inflammatory di...
ORMDL proteins are believed to be negative regulators of serine palmitoyltransferase (SPT), which ca...
ORMDL proteins are believed to be negative regulators of serine palmitoyltransferase (SPT), which ca...
ORMDL proteins are believed to be negative regulators of serine palmitoyltransferase (SPT), which ca...
ORMDL proteins are believed to be negative regulators of serine palmitoyltransferase (SPT), which ca...
The severity of asthma, a chronic inflammatory disease of the airways, is influenced by a multitude ...
BACKGROUND: Genome-wide association studies in asthma have repeatedly identified single nucleotide p...
ORMDL proteins are believed to be negative regulators of serine palmitoyltransferase (SPT), which ca...
ORMDL proteins are regulators of serine palmitoyltransferase (SPT) enzyme, which catalyzes the first...
Abstract Introduction The chromosomal region 17q21 harbors the human orosomucoid‐like 3 (ORMDL3) gen...
Rationale: Polymorphisms on chromosome 17q21 confer the major genetic susceptibility to childhood-on...