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Collagens: molecular biology, diseases, and potentials for therapy.
Prockop DJ, Kivirikko KI. Prockop DJ, et al. Annu Rev Biochem. 1995;64:403-34. doi: 10.1146/ Annu Rev Biochem. 1995. PMID: 7574488 Review.
Inhibition of the self-assembly of collagen I into fibrils with synthetic peptides. Demonstration that assembly is driven by specific binding sites on the monomers.
Prockop DJ, Fertala A. Prockop DJ, et al. J Biol Chem. 1998 Jun 19;273(25):15598-604. doi: 10.1074/jbc.273.25.15598. J Biol Chem. 1998. PMID: 9624151
Assembly of type I collagen fibrils de novo by the specific enzymic cleavage of pC collagen. The fibrils formed at about 37 degrees C are similar in diameter, roundness, and apparent flexibility to the collagen fibrils seen in connective tissue.
Kadler KE, Hulmes DJ, Hojima Y, Prockop DJ. Kadler KE, et al. Among authors: prockop dj. Ann N Y Acad Sci. 1990;580:214-24. doi: 10.1111/j.1749-6632.1990.tb17930.x. Ann N Y Acad Sci. 1990. PMID: 2337298 No abstract available.
Molecular basis of osteogenesis imperfecta and related disorders of bone.
Prockop DJ, Kuivaniemi H, Tromp G. Prockop DJ, et al. Clin Plast Surg. 1994 Jul;21(3):407-13. Clin Plast Surg. 1994. PMID: 7924138 Review.
Osteogenesis imperfecta. A model for genetic causes of osteoporosis and perhaps several other common diseases of connective tissue.
Prockop DJ. Prockop DJ. Arthritis Rheum. 1988 Jan;31(1):1-8. doi: 10.1002/art.1780310101. Arthritis Rheum. 1988. PMID: 3345218 No abstract available.
Osteopenia in 37 members of seven families: analysis based on a model of dominant inheritance.
Spotila LD, Caminis J, Devoto M, Shimoya K, Sereda L, Ott J, Whyte MP, Tenenhouse A, Prockop DJ. Spotila LD, et al. Among authors: prockop dj. Mol Med. 1996 May;2(3):313-24. Mol Med. 1996. PMID: 8784784 Free PMC article.
Widely distributed mutations in the COL2A1 gene produce achondrogenesis type II/hypochondrogenesis.
Körkkö J, Cohn DH, Ala-Kokko L, Krakow D, Prockop DJ. Körkkö J, et al. Among authors: prockop dj. Am J Med Genet. 2000 May 15;92(2):95-100. doi: 10.1002/(sici)1096-8628(20000515)92:2<95::aid-ajmg3>;2-9. Am J Med Genet. 2000. PMID: 10797431
Recombinant procollagen II: Deletion of D period segments identifies sequences that are required for helix stabilization and generates a temperature-sensitive N-proteinase cleavage site.
Arnold WV, Fertala A, Sieron AL, Hattori H, Mechling D, Bächinger HP, Prockop DJ. Arnold WV, et al. Among authors: prockop dj. J Biol Chem. 1998 Nov 27;273(48):31822-8. doi: 10.1074/jbc.273.48.31822. J Biol Chem. 1998. PMID: 9822649
A point mutation in a type I procollagen gene converts glycine 748 of the alpha 1 chain to cysteine and destabilizes the triple helix in a lethal variant of osteogenesis imperfecta.
Vogel BE, Minor RR, Freund M, Prockop DJ. Vogel BE, et al. Among authors: prockop dj. J Biol Chem. 1987 Oct 25;262(30):14737-44. J Biol Chem. 1987. PMID: 3667599
Characterization of recombinant human collagen II with Arg519-to-Cys substitution.
Fertala A, Ala-Kokko L, Prockop DJ. Fertala A, et al. Among authors: prockop dj. Ann N Y Acad Sci. 1996 Jun 8;785:251-3. doi: 10.1111/j.1749-6632.1996.tb56275.x. Ann N Y Acad Sci. 1996. PMID: 8702144 No abstract available.
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