Add to ORKGWe screened 685 subjects from Southern Italy for a promoter polymorphism of the UDP-glucuronosyltransferase (UGTA1) gene tightly linked to Gilbert’s syndrome (GS), consisting in the insertion of a TA repeat in the TATA box. The frequency of the polymorphism was 0.387 which is similar to the frequencies reported for other investigated populations of different ethnic backgrounds and is consistent with the antiquity of this polymorphism
We describe 4 jaundiced neonates with acute pyelonephritis of whom family history was positive for o...
BACKGROUND: The basis of Gilbert's syndrome is a 70% reduction in bilirubin glucuronidation which, i...
Relevance. Gilbert’s syndrome (GS) is a disease with an autosomal recessive type of inheritance caus...
Gilbert syndrome (GS) is a hereditary relatively common benign unconjugated hyperbilirubinaemia. The...
Abstract Background Gilbert syndrome is caused by defects in bilirubin UDP-glucuronosyltransferase (...
Background and Objective. Gilbert's syndrome, a chronic non-hemolytic unconjugated hyperbilirubinemi...
BACKGROUND AND OBJECTIVE: Gilbert's syndrome, a chronic non-hemolytic unconjugated hyperbilirubinem...
Gilbert syndrome (GS) is a hereditary relatively common benign unconjugated hyperbilirubinaemia. Th...
[[abstract]]Gilbert's syndrome is mainly diagnosed through genetic analysis and is primarily detecte...
Variation of a short (TA)(n) repeat sequence (rs8175347) covering the TATA box of UGT1A1 (UDP-glucur...
Background Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubi...
Gilbert’s syndrome is mainly diagnosed through genetic analysis and is primarily detected through a ...
Objective To assess whether UGT1A1 promoter polymorphisms associated with Gilbert Syndrome (GS) occu...
BACKGROUND/AIMS: UDP-glucuronosyltransferases (UGTs) are important enzymes involved in glucuronidati...
The UGT1A1 enzyme is involved in the metabolism of bilirubin and numerous medications. Unconjugated ...
We describe 4 jaundiced neonates with acute pyelonephritis of whom family history was positive for o...
BACKGROUND: The basis of Gilbert's syndrome is a 70% reduction in bilirubin glucuronidation which, i...
Relevance. Gilbert’s syndrome (GS) is a disease with an autosomal recessive type of inheritance caus...
Gilbert syndrome (GS) is a hereditary relatively common benign unconjugated hyperbilirubinaemia. The...
Abstract Background Gilbert syndrome is caused by defects in bilirubin UDP-glucuronosyltransferase (...
Background and Objective. Gilbert's syndrome, a chronic non-hemolytic unconjugated hyperbilirubinemi...
BACKGROUND AND OBJECTIVE: Gilbert's syndrome, a chronic non-hemolytic unconjugated hyperbilirubinem...
Gilbert syndrome (GS) is a hereditary relatively common benign unconjugated hyperbilirubinaemia. Th...
[[abstract]]Gilbert's syndrome is mainly diagnosed through genetic analysis and is primarily detecte...
Variation of a short (TA)(n) repeat sequence (rs8175347) covering the TATA box of UGT1A1 (UDP-glucur...
Background Gilbert syndrome is an inherited disease characterised by mild unconjugated hyperbilirubi...
Gilbert’s syndrome is mainly diagnosed through genetic analysis and is primarily detected through a ...
Objective To assess whether UGT1A1 promoter polymorphisms associated with Gilbert Syndrome (GS) occu...
BACKGROUND/AIMS: UDP-glucuronosyltransferases (UGTs) are important enzymes involved in glucuronidati...
The UGT1A1 enzyme is involved in the metabolism of bilirubin and numerous medications. Unconjugated ...
We describe 4 jaundiced neonates with acute pyelonephritis of whom family history was positive for o...
BACKGROUND: The basis of Gilbert's syndrome is a 70% reduction in bilirubin glucuronidation which, i...
Relevance. Gilbert’s syndrome (GS) is a disease with an autosomal recessive type of inheritance caus...