Literature DB >> 14051149

STUDIES ON THE INHERITANCE OF CRIGLER--NAJJAR'S SYNDROME BY THE MENTHOL TEST.

L SZABO, P EBREY.   

Abstract

Keywords:  GENETICS, HUMAN; GLUCURONATES; HYPERBILIRUBINEMIA; JAUNDICE, NEONATAL; MENTHOL; URINE

Mesh：

Substances：

Year:  1963        PMID： 14051149

Source DB:  PubMed          Journal:  Acta Paediatr Acad Sci Hung        ISSN： 0001-6527


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  3 in total

1.  Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler-Najjar type I patient.

Authors:  J K Ritter; M T Yeatman; P Ferreira; I S Owens
Journal:  J Clin Invest       Date:  1992-07       Impact factor: 14.808

Review 2.  Investigation of the molecular basis of the genetic deficiency of UDP-glucuronosyltransferase in Crigler-Najjar syndrome.

Authors:  K J Robertson; D Clarke; L Sutherland; R Wooster; M W Coughtrie; B Burchell
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

Review 3.  Genetic and environmental factors associated with variation of human xenobiotic glucuronidation and sulfation.

Authors:  B Burchell; M W Coughtrie
Journal:  Environ Health Perspect       Date:  1997-06       Impact factor: 9.031
  3 in total

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