BACKGROUND: Juvenile idiopathic arthritis (JIA) is an autoimmune disease characterized by persistent chronic arthritis. Disease risk is believed to be influenced by both genetic and environmental factors. It is well established that the PTPN22 single nucleotide polymorphism (SNP) rs2476601 is associated with JIA susceptibility. It was recently reported in an Australian study that this association is restricted to females and is not observed in males. A significant source of inconsistency amongst the literature on autoimmune disease susceptibility genes stems from an inability to replicate genetic findings across different racial or ethnic groups. We therefore attempted to generate further evidence of the female-specific association of rs247...
Objectives. A missense SNP, C1858T, in PTPN22 has been identified as a genetic risk factor for rheum...
BACKGROUND: Our understanding of the genetic factors underlying juvenile idiopathic arthritis (JIA) ...
A functional single nucleotide polymorphism (SNP) C1858T in the protein tyrosine phosphatase nonrece...
Item does not contain fulltextOBJECTIVES: Juvenile idiopathic arthritis (JIA) is considered a comple...
Juvenile idiopathic arthritis (JIA) is a common autoimmune disease characterized by envi-ronmental i...
Juvenile idiopathic arthritis (JIA) is a common autoimmune disease characterized by environmental in...
Recent genetic studies have led to identification of numerous loci that are associated with suscepti...
© 2017 Dr. Rachel Carolyn Chiaroni-ClarkeJuvenile idiopathic arthritis (JIA) is a paediatric autoimm...
Objective. The PTPN22 rs2476601 genetic variant has been associated with rheumatoid arthritis (RA) a...
OBJECTIVES: Rheumatoid arthritis (RA) shares some similar clinical and pathological features with ju...
BACKGROUND: Over the last five years, there have been numerous reports of association of juvenile id...
ABSTRACT: Objectives: This study aimed to confirm whether 15 single nucleotide polymorphisms (SNPs) ...
INTRODUCTION: The purpose of the present study was to investigate the frequency of the PTPN22 +1858 ...
OBJECTIVE: Recently, a functional PTPN22 variant (R263Q; rs33996649) was found to be associated with...
The minor allele of the R620W missense single-nucleotide polymorphism (SNP) (rs2476601) in the hemat...
Objectives. A missense SNP, C1858T, in PTPN22 has been identified as a genetic risk factor for rheum...
BACKGROUND: Our understanding of the genetic factors underlying juvenile idiopathic arthritis (JIA) ...
A functional single nucleotide polymorphism (SNP) C1858T in the protein tyrosine phosphatase nonrece...
Item does not contain fulltextOBJECTIVES: Juvenile idiopathic arthritis (JIA) is considered a comple...
Juvenile idiopathic arthritis (JIA) is a common autoimmune disease characterized by envi-ronmental i...
Juvenile idiopathic arthritis (JIA) is a common autoimmune disease characterized by environmental in...
Recent genetic studies have led to identification of numerous loci that are associated with suscepti...
© 2017 Dr. Rachel Carolyn Chiaroni-ClarkeJuvenile idiopathic arthritis (JIA) is a paediatric autoimm...
Objective. The PTPN22 rs2476601 genetic variant has been associated with rheumatoid arthritis (RA) a...
OBJECTIVES: Rheumatoid arthritis (RA) shares some similar clinical and pathological features with ju...
BACKGROUND: Over the last five years, there have been numerous reports of association of juvenile id...
ABSTRACT: Objectives: This study aimed to confirm whether 15 single nucleotide polymorphisms (SNPs) ...
INTRODUCTION: The purpose of the present study was to investigate the frequency of the PTPN22 +1858 ...
OBJECTIVE: Recently, a functional PTPN22 variant (R263Q; rs33996649) was found to be associated with...
The minor allele of the R620W missense single-nucleotide polymorphism (SNP) (rs2476601) in the hemat...
Objectives. A missense SNP, C1858T, in PTPN22 has been identified as a genetic risk factor for rheum...
BACKGROUND: Our understanding of the genetic factors underlying juvenile idiopathic arthritis (JIA) ...
A functional single nucleotide polymorphism (SNP) C1858T in the protein tyrosine phosphatase nonrece...