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G M Corson

Showing results (1-10 of 7) with videos related to

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Genomics|August 1, 1993
Fibrillin binds calcium and is coded by cDNAs that reveal a multidomain structure and alternatively spliced exons at the 5' endG M Corson, S C Chalberg, H C Dietz, et al.
Nature|July 25, 1991
Partial sequence of a candidate gene for the Marfan syndromeC L Maslen, G M Corson, B K Maddox, et al.
Journal of Molecular Biology|April 26, 1996
Fibrillin-1: organization in microfibrils and structural propertiesD P Reinhardt, D R Keene, G M Corson, et al.
Genomics|August 1, 1993
Four novel FBN1 mutations: significance for mutant transcript level and EGF-like domain calcium binding in the pathogenesis of Marfan syndromeH C Dietz, I McIntosh, L Y Sakai, et al.
The Journal of Clinical Investigation|May 11, 1992
Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin geneH C Dietz, R E Pyeritz, E G Puffenberger, et al.
Nature|July 25, 1991
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin geneH C Dietz, G R Cutting, R E Pyeritz, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|August 1, 1997
Fibrillin-1 in human cartilage: developmental expression and formation of special banded fibersD R Keene, C D Jordan, D P Reinhardt, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Genomics|August 1, 1993
Fibrillin binds calcium and is coded by cDNAs that reveal a multidomain structure and alternatively spliced exons at the 5' endG M Corson, S C Chalberg, H C Dietz, et al.
Nature|July 25, 1991
Partial sequence of a candidate gene for the Marfan syndromeC L Maslen, G M Corson, B K Maddox, et al.
Journal of Molecular Biology|April 26, 1996
Fibrillin-1: organization in microfibrils and structural propertiesD P Reinhardt, D R Keene, G M Corson, et al.
Genomics|August 1, 1993
Four novel FBN1 mutations: significance for mutant transcript level and EGF-like domain calcium binding in the pathogenesis of Marfan syndromeH C Dietz, I McIntosh, L Y Sakai, et al.
The Journal of Clinical Investigation|May 11, 1992
Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin geneH C Dietz, R E Pyeritz, E G Puffenberger, et al.
Nature|July 25, 1991
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin geneH C Dietz, G R Cutting, R E Pyeritz, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|August 1, 1997
Fibrillin-1 in human cartilage: developmental expression and formation of special banded fibersD R Keene, C D Jordan, D P Reinhardt, et al.
Pageof 1