Prenatal diagnosis of ornithine transcarbamylase deficiency: Results in SPFASH mice
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference18 articles.
1. Changes in ornithine transcarbamylase activity and protein level during perinatal period in rat liver. Effects of actinomycin D
2. . (1989). Urea cycle enzymes. In: , , (Eds). The Metabolic Basis of Inherited Metabolic Disease, New York: McGraw-Hill, 629–633.
3. Abnormal ornithine carbamoyltransferase in mice having the sparse-fur mutation
4. A new allele of the sparse fur gene in the mouse
Cited by 3 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. Comprehensive characterization of ureagenesis in the spf ash mouse, a model of human ornithine transcarbamylase deficiency, reveals age‐dependency of ammonia detoxification;Journal of Inherited Metabolic Disease;2019-03-13
2. Sparse-Fur (spf) Mouse as a Model of Hyperammonemia: Alterations in the Neurotransmitter Systems;Advances in Experimental Medicine and Biology;1997
3. In vivo retroviral-mediated transfer of a marker-gene in ornithine transcarbamylase-deficient Spfash mice;Journal of Pediatric Surgery;1996-11
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