|1.||Maruo, Yoshihiro: 4 articles (07/2014 - 11/2004)|
|2.||Sato, Hiroshi: 3 articles (07/2014 - 11/2004)|
|3.||Takeuchi, Yoshihiro: 3 articles (07/2014 - 11/2004)|
|4.||Mori, Asami: 2 articles (07/2014 - 11/2004)|
|5.||Matsui, Katsuyuki: 2 articles (07/2014 - 01/2010)|
|6.||Costa, Elísio: 2 articles (01/2006 - 11/2005)|
|7.||Yanagi, Takahide: 1 article (07/2014)|
|8.||Morioka, Yoriko: 1 article (07/2014)|
|9.||Nakahara, Sayuri: 1 article (07/2014)|
|10.||Fujito, Hiroshi: 1 article (07/2014)|
01/01/2010 - "Gilbert syndrome is caused by defects in bilirubin UDP-glucuronosyltransferase (UGT1A1). "
10/01/2007 - "Gilbert's syndrome (GS) is caused by a reduction in the activity of hepatic bilirubin UDP-glucuronosyltransferase (UGT). "
04/14/2006 - "Gilbert's syndrome: High frequency of the (TA)7 TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene."
05/01/2002 - "A patient suffering from Gilbert's syndrome may have hepatic activity of bilirubin-UDP-glucuronosyltransferase decreasing to levels around 30% of the normal. "
04/01/2001 - "Mutations in the promoter as well as in the coding region of the bilirubin UDP-glucuronosyltransferase gene (UGT1A1) have been found to be associated with Gilbert's syndrome. "
12/01/2001 - "Because the liver architecture is not disturbed in CN-1 and partial correction of bilirubin-UDP-glucuronosyltransferase (UGT1A1) activity is expected to be sufficient for protection against kernicterus, cell and gene therapies are being developed using the Gunn rat as an animal model of the disease. "
05/01/1995 - "Crigler-Najjar syndrome type I (CN-I) is a congenital hepatic metabolic deficiency in bilirubin UDP-glucuronosyltransferase activity which leads to profound jaundice and death from kernicterus. "
01/01/1984 - "For example, in Type I Crigler-Najjar syndrome, absence of hepatic bilirubin glucuronyl transferase activity causes severe unconjugated hyperbilirubinemia which invariably leads to death from kernicterus. "
02/01/1992 - "Thus, a deficiency in bilirubin UDP-glucuronosyltransferase, evidenced by jaundice, can be paralleled by a deficiency in glucuronidation of other compounds. "
04/01/1987 - "This jaundice trait occurs as the result of a deficiency of bilirubin glucuronyltransferase and appeared to transfer by simple Mendelian inheritance. "
12/15/1983 - "The genic transfer of the jaundice locus (jj) from the Gunn rat into the inbred RHA/++ rat produced congenic inbred homozygous RHA/jj rats which lacked detectable bilirubin UDP-glucuronosyltransferase activity. "
07/01/2014 - "To evaluate the role of bilirubin UDP-glucuronosyltransferase family 1, polypeptide A1 (UGT1A1) gene variations on prolonged unconjugated hyperbilirubinemia associated with breast milk feeding (breast milk jaundice [BMJ]). "
12/01/1981 - "A double blind controlled study of the therapeutic effect of clofibrate, an inductor of bilirubin glucuronyl transferase, was performed in neonates born at term and presenting with physiologic jaundice. "
04/01/1998 - "This study tested the hypothesis that a recently identified molecular marker for GS (a TA insertion in the promoter of UGT1A, the gene encoding bilirubin UDP-glucuronosyltransferase) is associated with neonatal jaundice. "
09/01/1999 - "A variant TATA box in the bilirubin UDP-glucuronosyltransferase 1 gene promoter does not contribute to neonatal jaundice in the Japanese population."
10/01/1995 - "A unique bilirubin-UDP-glucuronosyltransferase deficiency related to neonatal jaundice in mice."
|5.||Gallbladder Diseases (Gall Bladder Disease)
|2.||Aromatic Polycyclic Hydrocarbons (Polycyclic Aromatic Hydrocarbons)
|4.||Glucuronosyltransferase (UDP Glucuronosyltransferase)
|6.||DNA (Deoxyribonucleic Acid)
|8.||type 1 Crigler Najjar syndrome
|3.||Transplantation (Transplant Recipients)