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	341.	Presence of translatable mRNA for pro alpha 2(I) chains in fibroblasts from a patient with osteogenesis imperfecta whose type I collagen does not contain alpha 2(I) chains. [electronic resource] by Chu, M L Rowe, D Nicholls, A C Pope, F M Prockop, D J Producer: 19850204 In: Collagen and related research vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	342.	Use of R-loop mapping for the assessment of human collagen mutations. [electronic resource] by de Wett, W Sippola, M Tromp, G Prockop, D Chu, M L Ramirez, F Producer: 19860416 In: The Journal of biological chemistry vol. 261 Availability: No items available. Save to lists Add to cart (remove)
	343.	Mutations in type 1 procollagen that cause osteogenesis imperfecta: effects of the mutations on the assembly of collagen into fibrils, the basis of phenotypic variations, and potential antisense therapies. [electronic resource] by Prockop, D J Colige, A Helminen, H Khillan, J S Pereira, R Vandenberg, P Producer: 19940407 In: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 8 Suppl 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	344.	A recombinant homotrimer of type I procollagen that lacks the central two D-periods. The thermal stability of the triple helix is decreased by 2 to 4 degrees C. [electronic resource] by Zafarullah, K Sieron, A L Fertala, A Tromp, G Kuivaniemi, H Prockop, D J Producer: 19980504 In: Matrix biology : journal of the International Society for Matrix Biology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	345.	Donor variation in the growth properties and osteogenic potential of human marrow stromal cells. [electronic resource] by Phinney, D G Kopen, G Righter, W Webster, S Tremain, N Prockop, D J Producer: 20000124 In: Journal of cellular biochemistry vol. 75 Availability: No items available. Save to lists Add to cart (remove)
	346.	Substitution of aspartate for glycine 1018 in the type III procollagen (COL3A1) gene causes type IV Ehlers-Danlos syndrome: the mutated allele is present in most blood leukocytes of the asymptomatic and mosaic mother. [electronic resource] by Kontusaari, S Tromp, G Kuivaniemi, H Stolle, C Pope, F M Prockop, D J Producer: 19920910 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	347.	Transgenic mice expressing a partially deleted gene for type I procollagen (COL1A1). A breeding line with a phenotype of spontaneous fractures and decreased bone collagen and mineral. [electronic resource] by Pereira, R Khillan, J S Helminen, H J Hume, E L Prockop, D J Producer: 19930312 In: The Journal of clinical investigation vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	348.	Evidence for a structural mutation of procollagen type I in a patient with the Ehlers-Danlos syndrome type VII. [electronic resource] by Steinmann, B Tuderman, L Peltonen, L Martin, G R McKusick, V A Prockop, D J Producer: 19801124 In: The Journal of biological chemistry vol. 255 Availability: No items available. Save to lists Add to cart (remove)
	349.	Complete structure of the human COL11A2 gene: the exon sizes and other features indicate the gene has not evolved with genes for other fibriller collagens. [electronic resource] by Vuoristo, M M Pihlajamaa, T Vandenberg, P Körkkö, J Prockop, D J Ala-Kokko, L Producer: 19960903 In: Annals of the New York Academy of Sciences vol. 785 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	350.	PvuII polymorphism at the COL1A2 locus. [electronic resource] by Constantinou, C D Spotila, L D Zhuang, J Sereda, L Hanning, C Prockop, D J Producer: 19901105 In: Nucleic acids research vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	351.	Potential use of marrow stromal cells as therapeutic vectors for diseases of the central nervous system. [electronic resource] by Prockop, D J Azizi, S A Phinney, D G Kopen, G C Schwarz, E J Producer: 20010104 In: Progress in brain research vol. 128 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	352.	Expression of a partially deleted gene of human type II procollagen (COL2A1) in transgenic mice produces a chondrodysplasia. [electronic resource] by Vandenberg, P Khillan, J S Prockop, D J Helminen, H Kontusaari, S Ala-Kokko, L Producer: 19911003 In: Proceedings of the National Academy of Sciences of the United States of America vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	353.	Comparison of the NH2-Terminal sequences of chick Type I preprocollagen chains synthesized in an nRNA-dependent reticulocyte lysate. [electronic resource] by Graves, P N Olsen, B R Fietzek, P P Prockop, D J Monson, J M Producer: 19811222 In: European journal of biochemistry vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	354.	Human COL9A1 and COL9A2 genes. Two genes of 90 and 15 kb code for similar polypeptides of the same collagen molecule. [electronic resource] by Pihlajamaa, T Vuoristo, M M Annunen, S Perälä, M Prockop, D J Ala-Kokko, L Producer: 19981103 In: Matrix biology : journal of the International Society for Matrix Biology vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	355.	DNA polymorphisms in collagen genes: potential use in the study of disease. [electronic resource] by Børresen, A L Berg, K Tsipouras, P Dickson, L A Prockop, D J Ramirez, F Producer: 19850814 In: Progress in clinical and biological research vol. 177 Availability: No items available. Save to lists Add to cart (remove)
	356.	A fourth example suggests that premature termination codons in the COL2A1 gene are a common cause of the Stickler syndrome: analysis of the COL2A1 gene by denaturing gradient gel electrophoresis. [electronic resource] by Ritvaniemi, P Hyland, J Ignatius, J Kivirikko, K I Prockop, D J Ala-Kokko, L Producer: 19931022 In: Genomics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	357.	Analysis of the COL1A1 and COL1A2 genes by PCR amplification and scanning by conformation-sensitive gel electrophoresis identifies only COL1A1 mutations in 15 patients with osteogenesis imperfecta type I: identification of common sequences of null-allele mutations. [electronic resource] by Körkkö, J Ala-Kokko, L De Paepe, A Nuytinck, L Earley, J Prockop, D J Producer: 19980304 In: American journal of human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	358.	Propagation and senescence of human marrow stromal cells in culture: a simple colony-forming assay identifies samples with the greatest potential to propagate and differentiate. [electronic resource] by Digirolamo, C M Stokes, D Colter, D Phinney, D G Class, R Prockop, D J Producer: 20000104 In: British journal of haematology vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	359.	Potential use of stem cells from bone marrow to repair the extracellular matrix and the central nervous system. [electronic resource] by Prockop, D J Azizi, S A Colter, D Digirolamo, C Kopen, G Phinney, D G Producer: 20010215 In: Biochemical Society transactions vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	360.	Correction of a mineralization defect by overexpression of a wild-type cDNA for COL1A1 in marrow stromal cells (MSCs) from a patient with osteogenesis imperfecta: a strategy for rescuing mutations that produce dominant-negative protein defects. [electronic resource] by Pochampally, R R Horwitz, E M DiGirolamo, C M Stokes, D S Prockop, D J Producer: 20051114 In: Gene therapy vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 461 results.