|1.||Prockop, D J: 1 article (04/2001)|
|2.||Hyttinen, M M: 1 article (04/2001)|
|3.||Helminen, H J: 1 article (04/2001)|
|4.||Arita, M: 1 article (04/2001)|
|5.||Kopen, G C: 1 article (04/2001)|
|6.||Långsjö, T K: 1 article (04/2001)|
|7.||Fertala, A: 1 article (04/2001)|
|8.||Bao, Y: 1 article (04/2001)|
|9.||Li, S W: 1 article (04/2001)|
|10.||Tang, B L: 1 article (01/2001)|
|1.||Ehlers-Danlos Syndrome (Syndrome, Ehlers-Danlos)
01/01/2001 - "ADAMTS2 is a procollagen N-proteinase, and the mutations of its gene are responsible for Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis. "
01/01/1973 - "Procollagen peptidase deficiency in a form of the Ehlers-Danlos syndrome."
04/15/1990 - "The cause of the Ehlers-Danlos syndrome Type VII (EDS VII) is considered to be defective removal of the amino-terminal propeptide (N-propeptide) of Type I procollagen due to deficiency of procollagen N-proteinase, the enzyme responsible for the normal proteolytic excision of this precursor-specific domain. "
02/01/1977 - "Of the many clinical forms of the Ehlers-Danlos syndrome, some are due to a deficiency of lysine oxidase, others to deficiency of lysine hydroxylase and still others to procollagen peptidase deficiency. "
|2.||Osteogenesis Imperfecta (Lobstein Disease)
|4.||Male Infertility (Male Sterility)
|5.||Connective Tissue Diseases (Connective Tissue Disease)
|1.||Collagen Type I (Type I Collagen)
|4.||2-Oxoglutarate 5-Dioxygenase Procollagen-Lysine (Lysyl Hydroxylase)
|6.||Glycine (Aminoacetic Acid)