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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) chains
W 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 gene
M 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 gene
W 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 deficiency
E 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 mechanisms
W 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 imperfecta
M K Wirtz, V H Rao, R W Glanville, et al.
Cytogenetic and Genome Research
|
July 9, 2004
Systems biology of the 2-cell mouse embryo
A V Evsikov, W N de Vries, A E Peaston, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 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) chains
W 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 gene
M 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 gene
W 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 deficiency
E 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 mechanisms
W 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 imperfecta
M K Wirtz, V H Rao, R W Glanville, et al.
Cytogenetic and Genome Research
|
July 9, 2004
Systems biology of the 2-cell mouse embryo
A V Evsikov, W N de Vries, A E Peaston, et al.
Page
of 1