✦ LIBER ✦

Molecular analysis of a human liver mitochondrial ornithine transcarbamylase deficiency

✍ Scribed by J.-M. Berrez; O. Bardot; M.-C. Thiard; F. Alvarez; N. Latruffe

Publisher: Springer
Year: 1991
Tongue: English
Weight: 542 KB
Volume: 14
Category: Article
ISSN: 0141-8955
DOI: 10.1007/bf01804385

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Molecular basis of ornithine transcarbam

Molecular basis of ornithine transcarbamylase deficiency inspfandspf-ashmutant mice

✍ A. Ohtake; M. Takayanagi; S. Yamamoto; H. Kakinuma; H. Nakajima; M. Tatibana; M. 📂 Article 📅 1986 🏛 Springer 🌐 English ⚖ 237 KB

Molecular basis of ornithine transcarbam

Molecular basis of ornithine transcarbamylase deficiency lacking enzyme protein

✍ T. Saheki; Y. Imamura; I. Inoue; S. Miura; M. Mori; A. Ohtake; M. Tatibana; N. K 📂 Article 📅 1984 🏛 Springer 🌐 English ⚖ 1013 KB

Cultured fibroblasts as a tool for impro

Cultured fibroblasts as a tool for improvement of molecular analysis in ornithine transcarbamylase (OTC) deficiency

✍ Johannes Häberle; Hans Georg Koch 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 59 KB

The role of orthotopic liver transplanta

The role of orthotopic liver transplantation in the treatment of ornithine transcarbamylase deficiency

✍ Busuttil, Ashley A. ;Goss, John A. ;Seu, Philip ;Dulkanchainun, Tom S. ;Yanni, G 📂 Article 📅 1998 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 55 KB

The purpose of this study was to combine our clinical experience with a review of the literature to determine the value of orthotopic liver transplantation in the treatment of both boys and girls with ornithine transcarbamylase deficiency. Three boys younger than 1 year of age with symptomatic ornit

The R40H mutation in a late onset type o

The R40H mutation in a late onset type of human ornithine transcarbamylase deficiency in male patients

✍ Atsushi Nishiyori; M. Yoshino; Hirohisa Kato; Toshinobu Matsuura; Ryuuji Hoshide 📂 Article 📅 1997 🏛 Springer 🌐 English ⚖ 139 KB

Molecular cloning of cDNA for human mito

Molecular cloning of cDNA for human mitochondrial acetoacetyl-CoA thiolase and molecular analysis of 3-ketothiolase deficiency

✍ T. Fukao; S. Yamaguchi; H. Nagasawa; M. Kano; T. Orii; Y. Fujiki; T. Osumi; T. H 📂 Article 📅 1990 🏛 Springer 🌐 English ⚖ 493 KB