Prospects for gene therapy in ornithine carbamoyltransferase deficiency and other urea cycle disorders-Reference-Cited by-同舟云学术

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Prospects for gene therapy in ornithine carbamoyltransferase deficiency and other urea cycle disorders

Published:1995 Issue:1 Volume:1 Page:62-70
ISSN:1080-4013
Container-title:Mental Retardation and Developmental Disabilities Research Reviews
language:en
Short-container-title:Ment. Retard. Dev. Disabil. Res. Rev.

Author:

Robinson Michael B.,Batshaw Mark L.,Ye Xuehai,Wilson James M.

Publisher

Wiley

Subject

Genetics(clinical),Neuropsychology and Physiological Psychology,Pediatrics, Perinatology, and Child Health

Reference59 articles.

1. Inborn errors of urea synthesis

2. Treatment of Carbamyl Phosphate Synthetase Deficiency with Keto Analogues of Essential Amino Acids

3. Treatment of Inborn Errors of Urea Synthesis

4. Increase of ornithine transcarbamylase protein in sparse-fur mice with ortnithine transcarbamylase deficiency

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A mechanobiological mathematical model of liver metabolism;Biotechnology and Bioengineering;2020-06-30

2. A Pilot Study ofIn VivoLiver-Directed Gene Transfer with an Adenoviral Vector in Partial Ornithine Transcarbamylase Deficiency;Human Gene Therapy;2002-01

3. Developing adenoviral-mediated in vivo gene therapy for ornithine transcarbamylase deficiency;Journal of Inherited Metabolic Disease;1998-06

4. In vivo measurement of ureagenesis with stable isotopes;Journal of Inherited Metabolic Disease;1998-06

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