Výsledky vyhledávání - "Prockop, D J"

Akademický článek

Cultured Adherent Cells from Marrow can Serve as Long-Lasting Precursor Cells for Bone, Cartilage, and Lung in Irradiated Mice

Autor: Pereira, R. F., Halford, K. W., O'Hara, M. D., Leeper, D. B., Sokolov, B. P., Pollard, M. D., Bagasra, O., Prockop, D. J.

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America, 1995 May . 92(11), 4857-4861.

Externí odkaz: https://www.jstor.org/stable/2367629

Zobrazit plný text záznamu

Akademický článek

Growing Tips of Type I Collagen Fibrils Formed in vitro are Near- Paraboloidal in Shape, Implying a Reciprocal Relationship Between Accretion and Diameter

Autor: Holmes, D. F., Chapman, J. A., Prockop, D. J., Kadler, K. E.

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America, 1992 Oct . 89(20), 9855-9859.

Externí odkaz: https://www.jstor.org/stable/2360501

Zobrazit plný text záznamu

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Somatic cell mosaicism: Another source of phenotypic heterogeneity in nuclear families with osteogenesis imperfecta

Autor: Constantinou-Deltas, Constantinos D., Ladda, R. L., Prockop, D. J.

Publikováno v: American Journal of Medical Genetics
Am.J.Med.Genet.

Mutations in the genes coding for the proα1 and proα2 chains of type I procollagen have been found in many patients with osteogenesis imperfecta (OI), a heritable disorder of connective tissue. The severity of the disease varies between families an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::420ed2cefe2e09d4a405685e9e935f40
https://doi.org/10.1002/ajmg.1320450218

Zobrazit plný text záznamu

Mutation in a gene for type I procollagen (COL1A2) in a woman with postmenopausal osteoporosis: evidence for phenotypic and genotypic overlap with mild osteogenesis imperfecta

Autor: Spotila, L. D., Constantinou-Deltas, Constantinos D., Sereda, L., Ganguly, A., Riggs, B. L., Prockop, D. J.

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America
Proc.Natl.Acad.Sci.U.S.A.

Mutations in the two genes for type I collagen (COL1A1 or COL1A2) cause osteogenesis imperfecta (OI), a heritable disease characterized by moderate to extreme brittleness of bone early in life. Here we show that a 52-year-old postmenopausal woman wit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaf14342538bb564f38e13dfe475a43d
https://doi.org/10.1073/pnas.88.12.5423

Zobrazit plný text záznamu

Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COL1A2 locus

Autor: Spotila, L D, Sereda, L, Prockop, D J

Uniparental disomy for chromosome 7 has been described previously in two individuals with cystic fibrosis. Here, we describe a third case that was discovered because the proband was homozygous for a mutation in the COL1A2 gene for type I procollagen,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fe7f315718bdc4f1f2d50701faf809c3
https://europepmc.org/articles/PMC1682915/

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání