Structure and function of claudins.
By Gerd Krause, L. Winkler, S. Mueller, R. Haseloff, J. Piontek, I. Blasig. Biochimica et Biophysica Acta, 2008
849 citations recorded by the source corpus.
Subfields: Molecular Biology, Neurology
View Paper: https://www.semanticscholar.org/paper/2853849de7ca5a138526a53d975b524d7aba1cc7
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
- C. V. Van Itallie
- James M. Anderson
- Katherine R. Groschwitz
- S. Hogan
- Carola Förster
- Thomas K. Wood
- Takuya Suzuki
In Neurology
- C. V. Van Itallie
- James M. Anderson
- M. Deli
- Katherine R. Groschwitz
- S. Hogan
- Carola Förster
- Takuya Suzuki
Citations in the corpus
- The bacterial signal indole increases epithelial-cell tight-junction resistance and attenuates indicators of inflammation (2009, result): “The decrease in the expression of the pore-forming cldn2, which increases paracellular cation permeability (20), also further supports the theory that indole mediates an increase in paracellular resistance.”
- In vitro models of the blood–brain barrier: An overview of commonly used brain endothelial cell culture models and guidelines for their use (2016, background): “of claudins, gives the junctional complex its specific properties.(59,60) Claudin-5 has been established as a tightening claudin with high BBB expression, and loss of claudin-5 causes BBB leakage of small molecules.”
- Physiology and function of the tight junction. (2009, background): “…1981; Van Itallie and Anderson 2006), pathophysiology (Turner 2006; Schmitz et al. 1999; Nusrat et al. 2001), regulation (Tsukita et al. 2008; Gonzalez-Mariscal et al. 2008), and molecular components of the junction (Schneeberger and Lynch 2004; Krause et al. 2008; GonzalezMariscal et al. 2003).”
- A Genome-Wide CRISPR Screen in Toxoplasma Identifies Essential Apicomplexan Genes (2016, neutral): “Claudins are known to engage in homotypic and heterotypic interactions, as well as the formation of paracellular channels that restrict the flow of ions across the tight junction (Krause et al., 2008).”
- Cytokine regulation of tight junctions (2008, background): “A review of recent data groups claudins into two types, pore-forming claudins (2, 7, 10, 15, and 16) and sealing claudins (1, 4, 5, 8, 11, 14 and 19) [90].”
- Intestinal barrier function: molecular regulation and disease pathogenesis. (2009, background): “Claudin-claudin interactions between adjacent cells can be either homophilic or heterophilic.(86,87) Homophilic interactions have been demonstrated for claudin-1, claudin-2, claudin-3, claudin-5, claudin-6, claudin-9, claudin-11, claudin-14, and claudin19.”