Adhesion formation and interanimal variability in a laparoscopic mouse model varies with strains.

[1]  Jann Hau,et al.  Handbook of Laboratory Animal Science , 2004 .

[2]  P. Carmeliet,et al.  Role of vascular endothelial growth factor receptor 1 in basal adhesion formation and in carbon dioxide pneumoperitoneum-enhanced adhesion formation after laparoscopic surgery in mice. , 2004, Fertility and sterility.

[3]  M. Tjwa,et al.  Role of CO(2) pneumoperitoneum-induced acidosis in CO(2) pneumoperitoneum-enhanced adhesion formation in mice. , 2004, Fertility and sterility.

[4]  P. Carmeliet,et al.  Role of vascular endothelial growth factor and placental growth factor in basal adhesion formation and in carbon dioxide pneumoperitoneum-enhanced adhesion formation after laparoscopic surgery in transgenic mice. , 2003, Fertility and sterility.

[5]  P. Carmeliet,et al.  Role of hypoxia inducible factors 1alpha and 2alpha in basal adhesion formation and in carbon dioxide pneumoperitoneum-enhanced adhesion formation after laparoscopic surgery in transgenic mice. , 2003, Fertility and sterility.

[6]  A. Luttun,et al.  Role of the plasminogen system in basal adhesion formation and carbon dioxide pneumoperitoneum-enhanced adhesion formation after laparoscopic surgery in transgenic mice. , 2003, Fertility and sterility.

[7]  O. Mynbaev,et al.  Prevention of adhesions with crystalloids during laparoscopic surgery in mice. , 2002, The Journal of the American Association of Gynecologic Laparoscopists.

[8]  P. Novak,et al.  Peritoneal mesothelial hypoxia during pneumoperitoneum is a cofactor in adhesion formation in a laparoscopic mouse model. , 2001, Fertility and sterility.

[9]  D. Zwas,et al.  Heart regeneration in adult MRL mice , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[10]  S. Mohan,et al.  Genetic variation in bone-regenerative capacity among inbred strains of mice. , 2001, Bone.

[11]  A. Brody,et al.  Primary lung fibroblasts from the 129 mouse strain exhibit reduced growth factor responsiveness in vitro. , 2001, Experimental lung research.

[12]  S. Mohan,et al.  Differential protein profile in the ear-punched tissue of regeneration and non-regeneration strains of mice: a novel approach to explore the candidate genes for soft-tissue regeneration. , 2000, Biochimica et biophysica acta.

[13]  M. Skwarchuk,et al.  Changes in histology and fibrogenic cytokines in irradiated colorectum of two murine strains. , 1998, International journal of radiation oncology, biology, physics.

[14]  M. Skwarchuk,et al.  Murine strain differences in the volume effect and incidence of radiation-induced colorectal obstruction. , 1998, International journal of radiation oncology, biology, physics.

[15]  D. Rockey,et al.  Strain-specific differences in mouse hepatic wound healing are mediated by divergent T helper cytokine responses. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[16]  G. diZerega Biochemical events in peritoneal tissue repair. , 1997, The European journal of surgery. Supplement. : = Acta chirurgica. Supplement.

[17]  L. Holmdahl The role of fibrinolysis in adhesion formation. , 1997, The European journal of surgery. Supplement. : = Acta chirurgica. Supplement.

[18]  M. Diamond,et al.  Pathogenesis of adhesion formation/reformation: Application to reproductive pelvic surgery , 1987, Microsurgery.

[19]  G E JAY,et al.  Variation in Response of Various Mouse Strains to Hexobarbital (Evipal) , 1955, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.