Literature DB >> 3044330

Osteogenesis imperfecta.

W G Cole.   

Abstract

Major advances have occurred in the classification of OI and in the definition of underlying molecular defects. A clearer understanding of the pathogenesis of OI and of the relationships between the phenotypes and genotypes should emerge. The study of induced mutations in selected regions of the collagen genes with expression in cultured cells or transgenic mice should hasten this process. These advances will also provide a basis for studies into the large number of other genetically determined connective tissue disorders that are grouped together as the skeletal dysplasias. The results of recent studies in OI are providing a unique insight into many aspects of collagen and connective tissue biochemistry, physiology and pathology.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 3044330     DOI: 10.1016/s0950-351x(88)80014-4

Source DB:  PubMed          Journal:  Baillieres Clin Endocrinol Metab        ISSN: 0950-351X


  4 in total

1.  Lysyl hydroxylation in collagens from hyperplastic callus and embryonic bones.

Authors:  H W Lehmann; M Bodo; C Frohn; A Nerlich; D Rimek; H Notbohm; P K Müller
Journal:  Biochem J       Date:  1992-03-01       Impact factor: 3.857

2.  Osteogenesis imperfecta and other bone disorders in the differential diagnosis of unexplained fractures.

Authors:  C R Paterson
Journal:  J R Soc Med       Date:  1990-02       Impact factor: 5.344

3.  Single base pair alterations as the predominant category of mutation in type I osteogenesis imperfecta.

Authors:  A J Brookes; B Sykes; E Solomon
Journal:  J Med Genet       Date:  1989-06       Impact factor: 6.318

4.  Characterization of a type I collagen alpha 2(I) glycine-586 to valine substitution in osteogenesis imperfecta type IV. Detection of the mutation and prenatal diagnosis by a chemical cleavage method.

Authors:  J F Bateman; M Hannagan; D Chan; W G Cole
Journal:  Biochem J       Date:  1991-06-15       Impact factor: 3.857

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.