✦ LIBER ✦

Histopathologic and electron-microscopic futures of corneal and scleral collagen fibers in osteogenesis imperfecta type III

✍ Scribed by Holger Mietz; Louis Kasner; W. Richard Green

Publisher: Springer-Verlag
Year: 1997
Tongue: English
Weight: 706 KB
Volume: 235
Category: Article
ISSN: 0065-6100
DOI: 10.1007/bf00947058

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A novel G1006A substitution in the α2(I)

A novel G1006A substitution in the α2(I) chain of type I collagen produces osteogenesis imperfecta type III

✍ Jian Lu; Teresa Costa; William G. Cole 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 608 KB

Substitution of glycine-172 by arginine

Substitution of glycine-172 by arginine in the α1 chain of type I collagen in a patient with osteogenesis imperfecta, type III

✍ Katrina Mackay; Anne De Paepe; Lieve Nuytinck; Raymond Dalgleish 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 194 KB

A Gly859Ser substitution in the triple h

A Gly859Ser substitution in the triple helical domain of the α2 chain of type I collagen resulting in osteogenesis imperfecta type III in two unrelated individuals

✍ Nicola J. Rose; Katrina Mackay; Peter H. Byers; Raymond Dalgleish 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 624 KB

## Clinical Data on Patients KO was 35 years of age at the time her cell strain was sent to us. She was born to healthy unrelated parents and has two healthy siblings, both of whom have unaffected children, and no other individuals with 0 1 were identified in the family. She had many fractures at

Distribution of collagen types I and III

Distribution of collagen types I and III and basal lamina in human gastric carcinoma: An immunohistochemical and electron microscopic study

✍ Yamamoto, Masami ;Sumiyoshi, Hiromichi ;Nakagami, Kazuhiko ;Taniyama, Kiyomi ;Ta 📂 Article 📅 1984 🏛 Springer-Verlag 🌐 English ⚖ 807 KB

Mutation in the carboxy-terminal propept

Mutation in the carboxy-terminal propeptide of the proα1 (I) chain of type I collagen in a child with severe osteogenesis imperfecta (OI type III): Possible implications for protein folding

✍ Jane E. Oliver; Elizabeth M. Thompson; F. Michael Pope; Alan C. Nicholls 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 845 KB

A young girl presented with severe type 111 osteogenesis imperfecta; her otherwise healthy mother also had a mild connective tissue disorder with blue sclerae and recurrent joint dislocations. Skin fibroblast cultures from the child produced both normal and post-translationally overmodified type I c