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DNA damage_ATM/ATR regulation of G1/S checkpoint [score: 1 (0%)]

DNA damage checkpoints are biochemical pathways that delay or arrest the cell cycle progression in response to the DNA damage. All eukaryotic cells have four phases within the cell cycle, G1, S, G2, and M, and one outside, G0 [1].

The G1/S checkpoint prevents cells ...

Immune response_IL-4 signaling pathway [score: 1 (0%)]

Interleukin-4 (IL-4) is a T cell derived multifunctional cytokine that plays a critical role in the regulation of immune responses. IL-4 induces Th2 (T helper 2) differentiation, causes macrophage suppression, and stimulates B cell production of Immunoglobulins E, G1 and G4 (IgE, ...

Development_TGF-beta receptor signaling [score: 1 (0%)]

Transforming growth factor beta (TGF-beta) signaling controls diverse cellular processes, including cell proliferation, differentiation, adhesion and migration [1], [2], [3].

TGF-beta 1 initiates ...

Development_Prolactin receptor signaling [score: 1 (0%)]

Prolactin is a polypeptide hormone secreted by the pituitary gland and to a lesser extent by numerous extrapituitary tissues. This hormone affects a great amount of physiological processes [1]. Numerous biological functions have been attributed to this hormone's ...

Cytokine production by Th17 cells in CF [score: 1 (0%)]

Cystic Fibrosis (CF) is a potentially lethal genetic disease that typically results in the development of bronchial inflammation, bronchiectasis, the progressive loss of lung function and, ultimately, death [1].

CF is caused by genetic defects in Cystic Fibrosis ...

Bacterial infections in CF airways [score: 1 (0%)]

The upper airways represent a primary site for the introduction of pathogenic microorganisms from inspired air. The ciliated epithelium features several powerful mechanisms for prevention of colonization by inhaled bacteria, thus the lower respiratory tract usually remains sterile [1].

Defective ...

Mucin expression in CF via TLRs, EGFR signaling pathways [score: 1 (0%)]

Cystic Fibrosis (CF) is a potentially lethal genetic disease that typically results in the development of bronchial inflammation, bronchiectasis, the progressive loss of lung function and ultimately death [1].

CF was initially called "mucoviscidosis" because of ...

Immune response_Bacterial infections in normal airways [score: 1 (0%)]

The upper airways represent a primary site for the introduction of pathogenic microorganisms from inspired air. The ciliated epithelium features several powerful mechanisms for prevention of colonization by inhaled bacteria, thus the lower respiratory tract usually remains sterile. Toll-like receptors ...

Cytokine production by Th17 cells in CF (Mouse model) [score: 1 (0%)]

Cystic Fibrosis (CF) is a potentially lethal genetic disease that typically results in the development of bronchial inflammation, bronchiectasis, the progressive loss of lung function and, ultimately, death [1].

CF is caused by genetic defects in Cystic Fibrosis ...

Result pages:   1 
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