Results
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441.
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Molecular cloning, expression and chromosomal localization of a human gene encoding a 33 kDa putative metallopeptidase (PRSM1). [electronic resource] by
- Scott, I C
- Halila, R
- Jenkins, J M
- Mehan, S
- Apostolou, S
- Winqvist, R
- Callen, D F
- Prockop, D J
- Peltonen, L
- Kadler, K E
Producer: 19961121
In:
Gene vol. 174
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442.
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Sequencing of cDNA from 50 unrelated patients reveals that mutations in the triple-helical domain of type III procollagen are an infrequent cause of aortic aneurysms. [electronic resource] by
- Tromp, G
- Wu, Y
- Prockop, D J
- Madhatheri, S L
- Kleinert, C
- Earley, J J
- Zhuang, J
- Norrgård, O
- Darling, R C
- Abbott, W M
Producer: 19930721
In:
The Journal of clinical investigation vol. 91
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443.
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A potential role for Dkk-1 in the pathogenesis of osteosarcoma predicts novel diagnostic and treatment strategies. [electronic resource] by
- Lee, N
- Smolarz, A J
- Olson, S
- David, O
- Reiser, J
- Kutner, R
- Daw, N C
- Prockop, D J
- Horwitz, E M
- Gregory, C A
Producer: 20080124
In:
British journal of cancer vol. 97
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444.
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Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridization. [electronic resource] by
- Junien, C
- Weil, D
- Myers, J C
- Van Cong, N
- Chu, M L
- Foubert, C
- Gross, M S
- Prockop, D J
- Kaplan, J C
- Ramirez, F
Producer: 19820722
In:
American journal of human genetics vol. 34
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445.
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The clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfecta. [electronic resource] by
- Nicholls, A C
- Osse, G
- Schloon, H G
- Lenard, H G
- Deak, S
- Myers, J C
- Prockop, D J
- Weigel, W R
- Fryer, P
- Pope, F M
Producer: 19841206
In:
Journal of medical genetics vol. 21
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446.
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Characterization of type I procollagen N-proteinase from fetal bovine tendon and skin. Purification of the 500-kilodalton form of the enzyme from bovine tendon. [electronic resource] by
- Hojima, Y
- Mörgelin, M M
- Engel, J
- Boutillon, M M
- van der Rest, M
- McKenzie, J
- Chen, G C
- Rafi, N
- Romanic, A M
- Prockop, D J
Producer: 19940519
In:
The Journal of biological chemistry vol. 269
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447.
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Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen gene. [electronic resource] by
- Knowlton, R G
- Weaver, E J
- Struyk, A F
- Knobloch, W H
- King, R A
- Norris, K
- Shamban, A
- Uitto, J
- Jimenez, S A
- Prockop, D J
Producer: 19891208
In:
American journal of human genetics vol. 45
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448.
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Clinical responses to bone marrow transplantation in children with severe osteogenesis imperfecta. [electronic resource] by
- Horwitz, E M
- Prockop, D J
- Gordon, P L
- Koo, W W
- Fitzpatrick, L A
- Neel, M D
- McCarville, M E
- Orchard, P J
- Pyeritz, R E
- Brenner, M K
Producer: 20010419
In:
Blood vol. 97
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449.
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Transplantability and therapeutic effects of bone marrow-derived mesenchymal cells in children with osteogenesis imperfecta. [electronic resource] by
- Horwitz, E M
- Prockop, D J
- Fitzpatrick, L A
- Koo, W W
- Gordon, P L
- Neel, M
- Sussman, M
- Orchard, P
- Marx, J C
- Pyeritz, R E
- Brenner, M K
Producer: 19990413
In:
Nature medicine vol. 5
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450.
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Complete sequence of the 23-kilobase human COL9A3 gene. Detection of Gly-X-Y triplet deletions that represent neutral variants. [electronic resource] by
- Paassilta, P
- Pihlajamaa, T
- Annunen, S
- Brewton, R G
- Wood, B M
- Johnson, C C
- Liu, J
- Gong, Y
- Warman, M L
- Prockop, D J
- Mayne, R
- Ala-Kokko, L
Producer: 19990902
In:
The Journal of biological chemistry vol. 274
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451.
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Premature vertebral endplate ossification and mild disc degeneration in mice after inactivation of one allele belonging to the Col2a1 gene for Type II collagen. [electronic resource] by
- Sahlman, J
- Inkinen, R
- Hirvonen, T
- Lammi, M J
- Lammi, P E
- Nieminen, J
- Lapveteläinen, T
- Prockop, D J
- Arita, M
- Li, S W
- Hyttinen, M M
- Helminen, H J
- Puustjärvi, K
Producer: 20020318
In:
Spine vol. 26
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452.
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An allele of COL9A2 associated with intervertebral disc disease. [electronic resource] by
- Annunen, S
- Paassilta, P
- Lohiniva, J
- Perälä, M
- Pihlajamaa, T
- Karppinen, J
- Tervonen, O
- Kröger, H
- Lähde, S
- Vanharanta, H
- Ryhänen, L
- Göring, H H
- Ott, J
- Prockop, D J
- Ala-Kokko, L
Producer: 19990804
In:
Science (New York, N.Y.) vol. 285
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453.
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Abnormal response to physical activity in femurs after heterozygous inactivation of one allele of the Col2a1 gene for type II collagen in mice. [electronic resource] by
- Nieminen, J
- Sahlman, J
- Hirvonen, T
- Jämsä, T
- Tuukkanen, J
- Kovanen, V
- Kröger, H
- Jurvelin, J
- Arita, M
- Li, S W
- Prockop, D J
- Hyttinen, M M
- Helminen, H J
- Lapveteläinen, T
- Puustjärvi, K
Producer: 20051108
In:
Calcified tissue international vol. 77
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454.
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Papilin in development; a pericellular protein with a homology to the ADAMTS metalloproteinases. [electronic resource] by
- Kramerova, I A
- Kawaguchi, N
- Fessler, L I
- Nelson, R E
- Chen, Y
- Kramerov, A A
- Kusche-Gullberg, M
- Kramer, J M
- Ackley, B D
- Sieron, A L
- Prockop, D J
- Fessler, J H
Producer: 20010202
In:
Development (Cambridge, England) vol. 127
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455.
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First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q. [electronic resource] by
- Devoto, M
- Shimoya, K
- Caminis, J
- Ott, J
- Tenenhouse, A
- Whyte, M P
- Sereda, L
- Hall, S
- Considine, E
- Williams, C J
- Tromp, G
- Kuivaniemi, H
- Ala-Kokko, L
- Prockop, D J
- Spotila, L D
Producer: 19981027
In:
European journal of human genetics : EJHG vol. 6
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456.
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Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene. [electronic resource] by
- Colige, A
- Sieron, A L
- Li, S W
- Schwarze, U
- Petty, E
- Wertelecki, W
- Wilcox, W
- Krakow, D
- Cohn, D H
- Reardon, W
- Byers, P H
- Lapière, C M
- Prockop, D J
- Nusgens, B V
Producer: 19990820
In:
American journal of human genetics vol. 65
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457.
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Human type I procollagen genes are located on different chromosomes. [electronic resource] by
- Huerre, C
- Junien, C
- Weil, D
- Chu, M L
- Morabito, M
- Van Cong, N
- Myers, J C
- Foubert, C
- Gross, M S
- Prockop, D J
- Boué, A
- Kaplan, J C
- de la Chapelle, A
- Ramirez, F
Producer: 19830127
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 79
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458.
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Characterization of recombinant type II collagen: arthritogenicity and tolerogenicity in DBA/1 mice. [electronic resource] by
- Myers, L K
- Brand, D D
- Ye, X J
- Cremer, M A
- Rosloniec, E F
- Bodo, M
- Myllyharju, J
- Helaakoski, T
- Nokelainen, M
- Pihlajaniemi, T
- Kivirikko, K
- Yang, C L
- Ala-Kokko, L
- Prockop, D J
- Notbohm, H
- Fietzek, P
- Stuart, J M
- Kang, A H
Producer: 19990205
In:
Immunology vol. 95
Availability: No items available.
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459.
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Refinement of the chromosome 5p locus for familial calcium pyrophosphate dihydrate deposition disease. [electronic resource] by
- Andrew, L J
- Brancolini, V
- de la Pena, L S
- Devoto, M
- Caeiro, F
- Marchegiani, R
- Reginato, A
- Gaucher, A
- Netter, P
- Gillet, P
- Loeuille, D
- Prockop, D J
- Carr, A
- Wordsworth, B F
- Lathrop, M
- Butcher, S
- Considine, E
- Everts, K
- Nicod, A
- Walsh, S
- Williams, C J
Producer: 19990310
In:
American journal of human genetics vol. 64
Availability: No items available.
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460.
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Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). [electronic resource] by
- McGuirt, W T
- Prasad, S D
- Griffith, A J
- Kunst, H P
- Green, G E
- Shpargel, K B
- Runge, C
- Huybrechts, C
- Mueller, R F
- Lynch, E
- King, M C
- Brunner, H G
- Cremers, C W
- Takanosu, M
- Li, S W
- Arita, M
- Mayne, R
- Prockop, D J
- Van Camp, G
- Smith, R J
Producer: 19991220
In:
Nature genetics vol. 23
Availability: No items available.
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