Clostridium perfringens enterotoxin and intestinal tight junctions

[1] Claudin-1 and -2: Novel integral membrane proteins localizing at tight junctions with no sequence similarity to occludin [J]. JOURNAL OF CELL BIOLOGY, 1998, 141 (07) : 1539 - 1550

[2] Cationic currents induced by Clostridium perfringens type A enterotoxin in human intestinal CaCO-2 cells [J]. JOURNAL OF MEDICAL MICROBIOLOGY, 1999, 48 (03) : 235 - 243

[3] Clostridium perfringens enterotoxin utilizes two structurally related membrane proteins as functional receptors in vivo [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (42) : 26652 - 26658

[4] Molecular cloning and functional characterization of the receptor for Clostridium perfringens enterotoxin [J]. JOURNAL OF CELL BIOLOGY, 1997, 136 (06) : 1239 - 1247

[5] Identification of a Clostridium perfringens enterotoxin region required for large complex formation and cytotoxicity by random mutagenesis [J]. INFECTION AND IMMUNITY, 1999, 67 (11) : 5634 - 5641

[6] McClane BA, 2000, GRAM-POSITIVE PATHOGENS, P551

[7] Claudin multigene family encoding four-transmembrane domain protein components of tight junction strands [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (02) : 511 - 516

[8] Rahner C, 1999, HEPATOLOGY, V30, p326A

[9] Inactivation of the gene (cpe) encoding Clostridium perfringens enterotoxin eliminates the ability of two cpe-positive C-perfringens type A human gastrointestinal disease isolates to affect rabbit ileal loops [J]. MOLECULAR MICROBIOLOGY, 1999, 33 (05) : 946 - 958

[10] SARKER MR, IN PRESS J NATURAL T

[1] Claudin-1 and -2: Novel integral membrane proteins localizing at tight junctions with no sequence similarity to occludin [J]. JOURNAL OF CELL BIOLOGY, 1998, 141 (07) : 1539 - 1550

[2] Cationic currents induced by Clostridium perfringens type A enterotoxin in human intestinal CaCO-2 cells [J]. JOURNAL OF MEDICAL MICROBIOLOGY, 1999, 48 (03) : 235 - 243

[3] Clostridium perfringens enterotoxin utilizes two structurally related membrane proteins as functional receptors in vivo [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (42) : 26652 - 26658

[4] Molecular cloning and functional characterization of the receptor for Clostridium perfringens enterotoxin [J]. JOURNAL OF CELL BIOLOGY, 1997, 136 (06) : 1239 - 1247

[5] Identification of a Clostridium perfringens enterotoxin region required for large complex formation and cytotoxicity by random mutagenesis [J]. INFECTION AND IMMUNITY, 1999, 67 (11) : 5634 - 5641

[6] McClane BA, 2000, GRAM-POSITIVE PATHOGENS, P551

[7] Claudin multigene family encoding four-transmembrane domain protein components of tight junction strands [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (02) : 511 - 516

[8] Rahner C, 1999, HEPATOLOGY, V30, p326A

[9] Inactivation of the gene (cpe) encoding Clostridium perfringens enterotoxin eliminates the ability of two cpe-positive C-perfringens type A human gastrointestinal disease isolates to affect rabbit ileal loops [J]. MOLECULAR MICROBIOLOGY, 1999, 33 (05) : 946 - 958

[10] SARKER MR, IN PRESS J NATURAL T