𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Location and methylation pattern of a nuclear matrix associated region in the human proα2(I) collagen gene

✍ Scribed by G.C. Ellis; A.F. Grobler-Rabie; F.S. Hough; A.J. Bester

Book ID
117057868
Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
876 KB
Volume
157
Category
Article
ISSN
0006-291X

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Role of the pro-α2(I) COOH-terminal regi
Role of the pro-α2(I) COOH-terminal region in assembly of type I collagen: Disruption of two intramolecular disulfide bonds in pro-α2(I) blocks assembly of type I collagen
✍ Sharon A. Doyle; Barbara D. Smith 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 141 KB 👁 1 views

Collagen biosynthesis is a complex process that begins with the association of three procollagen chains. A series of conserved intra-and interchain disulfide bonds in the carboxyl-terminal region of the procollagen chains, or C-propeptide, has been hypothesized to play an important role in the nucle

Role of the pro-α2(I) COOH-terminal regi
Role of the pro-α2(I) COOH-terminal region in assembly of type I collagen: Truncation of the last 10 amino acid residues of pro-α2(I) chain prevents assembly of type I collagen heterotrimer
✍ Ai-lee Lim; Sharon A. Doyle; Gary Balian; Barbara D. Smith 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 325 KB 👁 1 views

Procollagen (Type I) contains a noncollagenous COOH-terminal propeptide (C-propeptide) hypothesized to be important in directing chain association and alignment during assembly. We previously expressed human pro-␣2(I) cDNA in rat liver epithelial cells, W8, that produce only pro-␣1(I) trimer collage

A 38 base pair insertion in the proα2(I)
A 38 base pair insertion in the proα2(I) collagen gene of a patient with Marfan syndrome
✍ Elizabeth Henke; Mark Leader; Shingo Tajima; Sheldon Pinnell; Russel Kaufman 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 English ⚖ 385 KB

Abnormalities in type I collagen have been recognized in a number of connective tissue disorders. In the Marfan syndrome, an autosomal dominant condition producing a generalized abnormality in connective tissue, no consistent abnormality has been identified, although one individual has been found to