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W N de Vries

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

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The Journal of Biological Chemistry|July 5, 1986
The molecular defect in an autosomal dominant form of osteogenesis imperfecta. Synthesis of type I procollagen containing cysteine in the triple-helical domain of pro-alpha 1(I) chainsW N de Vries, W J de Wet
Archives of Biochemistry and Biophysics|April 25, 2000
Characterization of a novel transcription factor binding to the regulatory regions of the human pro-alpha1(I) collagen geneM K Zhao, P J Pretorius, W N de Vries
Archives of Biochemistry and Biophysics|April 25, 2000
Interaction of Ap1, Ap2, and Sp1 with the regulatory regions of the human pro-alpha1(I) collagen geneW P Vergeer, J M Sogo, P J Pretorius, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Prenatal analysis in two suspected cases of glutathione synthetase deficiencyE Erasmus, L J Mienie, W N de Vries, et al.
Cold Spring Harbor Symposia on Quantitative Biology|November 22, 2008
Reprogramming and differentiation in mammals: motifs and mechanismsW N de Vries, A V Evsikov, L J Brogan, et al.
Connective Tissue Research|January 1, 1993
A cysteine for glycine substitution at position 175 in an alpha 1 (I) chain of type I collagen produces a clinically heterogeneous form of osteogenesis imperfectaM K Wirtz, V H Rao, R W Glanville, et al.
Cytogenetic and Genome Research|July 9, 2004
Systems biology of the 2-cell mouse embryoA V Evsikov, W N de Vries, A E Peaston, et al.
Pageof 1

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

Sort By:
Pageof 1
The Journal of Biological Chemistry|July 5, 1986
The molecular defect in an autosomal dominant form of osteogenesis imperfecta. Synthesis of type I procollagen containing cysteine in the triple-helical domain of pro-alpha 1(I) chainsW N de Vries, W J de Wet
Archives of Biochemistry and Biophysics|April 25, 2000
Characterization of a novel transcription factor binding to the regulatory regions of the human pro-alpha1(I) collagen geneM K Zhao, P J Pretorius, W N de Vries
Archives of Biochemistry and Biophysics|April 25, 2000
Interaction of Ap1, Ap2, and Sp1 with the regulatory regions of the human pro-alpha1(I) collagen geneW P Vergeer, J M Sogo, P J Pretorius, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Prenatal analysis in two suspected cases of glutathione synthetase deficiencyE Erasmus, L J Mienie, W N de Vries, et al.
Cold Spring Harbor Symposia on Quantitative Biology|November 22, 2008
Reprogramming and differentiation in mammals: motifs and mechanismsW N de Vries, A V Evsikov, L J Brogan, et al.
Connective Tissue Research|January 1, 1993
A cysteine for glycine substitution at position 175 in an alpha 1 (I) chain of type I collagen produces a clinically heterogeneous form of osteogenesis imperfectaM K Wirtz, V H Rao, R W Glanville, et al.
Cytogenetic and Genome Research|July 9, 2004
Systems biology of the 2-cell mouse embryoA V Evsikov, W N de Vries, A E Peaston, et al.
Pageof 1