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Ehlers-Danlos Syndrome Type VI with Normal Lysyl Hydroxylase Activity cannot be Explained by a Defect in Cellular Uptake of Ascorbic Acid

✍ Scribed by Royce, P.M.; Moser, U.; Steinmann, B.

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Lysyl hydroxylase exhibits reduced stimu

✍ Yeowell, H.; Marshall, M.; Walker, L.; Ha, V.; Murad, S.; Pinnell, S. 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 58 KB

A Common Duplication in the Lysyl Hydrox

✍ Heather N. Yeowell; Linda C. Walker; Saood Murad; Sheldon R. Pinnell 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 247 KB

The mRNA and the Activity of Lysyl Hydro

✍ H.N. Yeowell; L.C. Walker; M.K. Marshall; S. Murad; S.R. Pinnell 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 659 KB

Transcriptional Activation of Type I Col

✍ Shun-Ichi Kurata; Haruki Senoo; Ryu-Ichiro Hata 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 829 KB