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J Uitto

Showing results (461-470 of 693) with videos related to

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Journal of Dental Research|July 5, 2002
Matrilysin (matrix metalloproteinase-7) expression in human junctional epitheliumV-J Uitto, J I Salonen, J D Firth, et al.
The Journal of Investigative Dermatology|January 15, 2000
Compound heterozygosity for novel splice site mutations in the BPAG2/COL17A1 gene underlies generalized atrophic benign epidermolysis bullosaL Pulkkinen, M P Marinkovich, H T Tran, et al.
Transactions of the Association of American Physicians|January 1, 1992
Transcriptional activation of fibroblast stromelysin-1 and collagenase gene expression by a novel lymphokine, leukoregulinA Mauviel, V M Kähäri, Y Q Chen, et al.
American Journal of Human Genetics|February 1, 1997
Cloning of the human type XVII collagen gene (COL17A1), and detection of novel mutations in generalized atrophic benign epidermolysis bullosaB Gatalica, L Pulkkinen, K Li, et al.
The Journal of Investigative Dermatology|May 14, 1998
International Centennial Meeting on Pseudoxanthoma Elasticum: progress in PXE researchJ Uitto, C D Boyd, M G Lebwohl, et al.
Arthritis and Rheumatism|December 1, 1984
The production of collagenase by adherent mononuclear cells cultured from human peripheral bloodJ S Louie, J Weiss, L Ryhänen, et al.
Cutis|March 1, 1990
Dermatology daysJ W Burnett, W F Bergfeld, W P Jordan, et al.
The Journal of Clinical Investigation|February 1, 1985
Demonstration of elastin gene expression in human skin fibroblast cultures and reduced tropoelastin production by cells from a patient with atrophodermaM G Giro, A I Oikarinen, H Oikarinen, et al.
The Journal of Investigative Dermatology|August 22, 2000
Mutation report: complete paternal uniparental isodisomy of chromosome 1: a novel mechanism for Herlitz junctional epidermolysis bullosaY Takizawa, L Pulkkinen, S C Chao, et al.
The Journal of Clinical Investigation|April 1, 1994
Elevated expression of type VII collagen in the skin of patients with systemic sclerosis. Regulation by transforming growth factor-betaL Rudnicka, J Varga, A M Christiano, et al.
Pageof 70

Showing results (461-470 of 693) with videos related to

Sort By:
Pageof 70
Journal of Dental Research|July 5, 2002
Matrilysin (matrix metalloproteinase-7) expression in human junctional epitheliumV-J Uitto, J I Salonen, J D Firth, et al.
The Journal of Investigative Dermatology|January 15, 2000
Compound heterozygosity for novel splice site mutations in the BPAG2/COL17A1 gene underlies generalized atrophic benign epidermolysis bullosaL Pulkkinen, M P Marinkovich, H T Tran, et al.
Transactions of the Association of American Physicians|January 1, 1992
Transcriptional activation of fibroblast stromelysin-1 and collagenase gene expression by a novel lymphokine, leukoregulinA Mauviel, V M Kähäri, Y Q Chen, et al.
American Journal of Human Genetics|February 1, 1997
Cloning of the human type XVII collagen gene (COL17A1), and detection of novel mutations in generalized atrophic benign epidermolysis bullosaB Gatalica, L Pulkkinen, K Li, et al.
The Journal of Investigative Dermatology|May 14, 1998
International Centennial Meeting on Pseudoxanthoma Elasticum: progress in PXE researchJ Uitto, C D Boyd, M G Lebwohl, et al.
Arthritis and Rheumatism|December 1, 1984
The production of collagenase by adherent mononuclear cells cultured from human peripheral bloodJ S Louie, J Weiss, L Ryhänen, et al.
Cutis|March 1, 1990
Dermatology daysJ W Burnett, W F Bergfeld, W P Jordan, et al.
The Journal of Clinical Investigation|February 1, 1985
Demonstration of elastin gene expression in human skin fibroblast cultures and reduced tropoelastin production by cells from a patient with atrophodermaM G Giro, A I Oikarinen, H Oikarinen, et al.
The Journal of Investigative Dermatology|August 22, 2000
Mutation report: complete paternal uniparental isodisomy of chromosome 1: a novel mechanism for Herlitz junctional epidermolysis bullosaY Takizawa, L Pulkkinen, S C Chao, et al.
The Journal of Clinical Investigation|April 1, 1994
Elevated expression of type VII collagen in the skin of patients with systemic sclerosis. Regulation by transforming growth factor-betaL Rudnicka, J Varga, A M Christiano, et al.
Pageof 70