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Báo cáo khoa học: Identification of domains involved in the allosteric regulation of cytosolic Arabidopsis thaliana NADP-malic enzymes

Báo cáo khoa học: Identification of domains involved in the allosteric regulation of cytosolic Arabidopsis thaliana NADP-malic enzymes

4 0 0
13 trang
Báo cáo khoa học: Identification of domains involved in the allosteric regulation of cytosolic Arabidopsis thaliana NADP-malic enzymes

Báo cáo khoa học: Identification of domains involved in the allosteric regulation of cytosolic Arabidopsis thaliana NADP-malic enzymes

4 0 0
13 trang
Báo cáo khoa học: Identification of domains involved in the allosteric regulation of cytosolic Arabidopsis thaliana NADP-malic enzymes

Báo cáo khoa học: Identification of domains involved in the allosteric regulation of cytosolic Arabidopsis thaliana NADP-malic enzymes

4 0 0
13 trang
Báo cáo khoa học: Identification of domains involved in the allosteric regulation of cytosolic Arabidopsis thaliana NADP-malic enzymes

Báo cáo khoa học: Identification of domains involved in the allosteric regulation of cytosolic Arabidopsis thaliana NADP-malic enzymes

4 0 0
13 trang
Báo cáo khoa học: Cytosolic phospholipase A2-a and cyclooxygenase-2 localize to intracellular membranes of EA.hy.926 endothelial cells that are distinct from the endoplasmic reticulum and the Golgi apparatus

Báo cáo khoa học: Cytosolic phospholipase A2-a and cyclooxygenase-2 localize to intracellular membranes of EA.hy.926 endothelial cells that are distinct from the endoplasmic reticulum and the Golgi apparatus

5 0 0
13 trang
Báo cáo khoa học: Cytosolic phospholipase A2-a and cyclooxygenase-2 localize to intracellular membranes of EA.hy.926 endothelial cells that are distinct from the endoplasmic reticulum and the Golgi apparatus

Báo cáo khoa học: Cytosolic phospholipase A2-a and cyclooxygenase-2 localize to intracellular membranes of EA.hy.926 endothelial cells that are distinct from the endoplasmic reticulum and the Golgi apparatus

5 0 0
13 trang
Báo cáo khoa học: Cytosolic phospholipase A2-a and cyclooxygenase-2 localize to intracellular membranes of EA.hy.926 endothelial cells that are distinct from the endoplasmic reticulum and the Golgi apparatus

Báo cáo khoa học: Cytosolic phospholipase A2-a and cyclooxygenase-2 localize to intracellular membranes of EA.hy.926 endothelial cells that are distinct from the endoplasmic reticulum and the Golgi apparatus

5 0 0
13 trang
Báo cáo khoa học: Cytosolic phospholipase A2-a and cyclooxygenase-2 localize to intracellular membranes of EA.hy.926 endothelial cells that are distinct from the endoplasmic reticulum and the Golgi apparatus

Báo cáo khoa học: Cytosolic phospholipase A2-a and cyclooxygenase-2 localize to intracellular membranes of EA.hy.926 endothelial cells that are distinct from the endoplasmic reticulum and the Golgi apparatus

5 0 0
13 trang
Báo cáo khoa học: Insulin-induced proliferation of bladder cancer cells is mediated through activation of the epidermal growth factor system

Báo cáo khoa học: Insulin-induced proliferation of bladder cancer cells is mediated through activation of the epidermal growth factor system

16 0 0
11 trang
Báo cáo khoa học: Insulin-induced proliferation of bladder cancer cells is mediated through activation of the epidermal growth factor system

Báo cáo khoa học: Insulin-induced proliferation of bladder cancer cells is mediated through activation of the epidermal growth factor system

16 0 0
11 trang
Báo cáo khoa học: Insulin-induced proliferation of bladder cancer cells is mediated through activation of the epidermal growth factor system

Báo cáo khoa học: Insulin-induced proliferation of bladder cancer cells is mediated through activation of the epidermal growth factor system

16 0 0
11 trang
Báo cáo khoa học: Insulin-induced proliferation of bladder cancer cells is mediated through activation of the epidermal growth factor system

Báo cáo khoa học: Insulin-induced proliferation of bladder cancer cells is mediated through activation of the epidermal growth factor system

16 0 0
11 trang
Báo cáo khoa hoc : Matrix metalloproteinase proteolysis of the mycobacterial HSP65 protein as a potential source of immunogenic peptides in human tuberculosis

Báo cáo khoa hoc : Matrix metalloproteinase proteolysis of the mycobacterial HSP65 protein as a potential source of immunogenic peptides in human tuberculosis

16 0 0
10 trang
Báo cáo khoa hoc : Matrix metalloproteinase proteolysis of the mycobacterial HSP65 protein as a potential source of immunogenic peptides in human tuberculosis

Báo cáo khoa hoc : Matrix metalloproteinase proteolysis of the mycobacterial HSP65 protein as a potential source of immunogenic peptides in human tuberculosis

16 0 0
10 trang
Báo cáo khoa hoc : Matrix metalloproteinase proteolysis of the mycobacterial HSP65 protein as a potential source of immunogenic peptides in human tuberculosis

Báo cáo khoa hoc : Matrix metalloproteinase proteolysis of the mycobacterial HSP65 protein as a potential source of immunogenic peptides in human tuberculosis

16 0 0
10 trang
Báo cáo khoa hoc : Matrix metalloproteinase proteolysis of the mycobacterial HSP65 protein as a potential source of immunogenic peptides in human tuberculosis

Báo cáo khoa hoc : Matrix metalloproteinase proteolysis of the mycobacterial HSP65 protein as a potential source of immunogenic peptides in human tuberculosis

16 0 0
10 trang
Báo cáo khoa hoc : Stage-specific excretory–secretory small heat shock proteins from the parasitic nematode Strongyloides ratti – putative links to host's intestinal mucosal defense system

Báo cáo khoa hoc : Stage-specific excretory–secretory small heat shock proteins from the parasitic nematode Strongyloides ratti – putative links to host's intestinal mucosal defense system

5 0 0
18 trang
Báo cáo khoa hoc : Stage-specific excretory–secretory small heat shock proteins from the parasitic nematode Strongyloides ratti – putative links to host's intestinal mucosal defense system

Báo cáo khoa hoc : Stage-specific excretory–secretory small heat shock proteins from the parasitic nematode Strongyloides ratti – putative links to host's intestinal mucosal defense system

5 0 0
18 trang