Literature DB >> 4634741

Animal model of human disease. Crigler-Najjar Syndrome. Animal model: hereditary nonhemolytic unconjugated hyperbilirubinemia in Gunn rats.

C E Cornelius, I M Arias.   

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Year:  1972        PMID： 4634741      PMCID： PMC2032632     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN： 0002-9440            Impact factor:   4.307


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  3 in total

1.  Kernicterus in rats with an inherited deficiency of glucuronyl transferase.

Authors:  L JOHNSON; F SARMIENTO; W A BLANC; R DAY
Journal:  AMA J Dis Child       Date:  1959-05

2.  Congenital familial nonhemolytic jaundice with kernicterus.

Authors:  J F CRIGLER; V A NAJJAR
Journal:  Pediatrics       Date:  1952-08       Impact factor: 7.124

3.  HEREDITARY JAUNDICE IN THE RAT.

Authors:  H T Malloy; L Lowenstein
Journal:  Can Med Assoc J       Date:  1940-02       Impact factor: 8.262
  3 in total
  7 in total

1.  Animal model of human disease. Increased sensitivity to polychlorinated biphenyls. Animal model: gunn rats with hereditary hyperbilirubinemia.

Authors:  E J Calabrese
Journal:  Am J Pathol       Date:  1978-05       Impact factor: 4.307

2.  Stimulation of defective Gunn-rat liver uridine diphosphate glucuronyltransferase activity in vitro by alkyl ketones.

Authors:  E N Lalani; B Burchell
Journal:  Biochem J       Date:  1979-03-01       Impact factor: 3.857

3.  Postnatal development of uridine diphosphate glucuronyltransferase activity towards bilirubin and 2-aminophenol in human liver.

Authors:  S Onishi; N Kawade; S Itoh; K Isobe; S Sugiyama
Journal:  Biochem J       Date:  1979-12-15       Impact factor: 3.857

4.  The use of jejunal transplants to treat a genetic enzyme deficiency.

Authors:  B M Jaffe; A A Burgos; M Martinez-Noack
Journal:  Ann Surg       Date:  1996-06       Impact factor: 12.969

5.  Fine structural lesions and hormonal alterations in thyroid glands of perinatal rats exposed in utero and by the milk to polychlorinated biphenyls.

Authors:  W T Collins; C C Capen
Journal:  Am J Pathol       Date:  1980-04       Impact factor: 4.307

6.  A translationally optimized AAV-UGT1A1 vector drives safe and long-lasting correction of Crigler-Najjar syndrome.

Authors:  Giuseppe Ronzitti; Giulia Bortolussi; Remco van Dijk; Fanny Collaud; Severine Charles; Christian Leborgne; Patrice Vidal; Samia Martin; Bernard Gjata; Marcelo Simon Sola; Laetitia van Wittenberghe; Alban Vignaud; Philippe Veron; Piter J Bosma; Andres F Muro; Federico Mingozzi
Journal:  Mol Ther Methods Clin Dev       Date:  2016-07-20       Impact factor: 6.698

7.  Preclinical Development of an AAV8-hUGT1A1 Vector for the Treatment of Crigler-Najjar Syndrome.

Authors:  Fanny Collaud; Giulia Bortolussi; Laurence Guianvarc'h; Sem J Aronson; Thierry Bordet; Philippe Veron; Severine Charles; Patrice Vidal; Marcelo Simon Sola; Stephanie Rundwasser; Delphine G Dufour; Florence Lacoste; Cyril Luc; Laetitia V Wittenberghe; Samia Martin; Christine Le Bec; Piter J Bosma; Andres F Muro; Giuseppe Ronzitti; Matthias Hebben; Federico Mingozzi
Journal:  Mol Ther Methods Clin Dev       Date:  2018-12-31       Impact factor: 6.698
  7 in total

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