Christine M. Finck
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Christine M. Finck has a total of 27 co-authors. Here are the top co-authors by number of shared publications:
Daniel J. Weiss
Department of Medicine, University of Vermont College of Medicine, 89 Beaumont Avenue Given Bldg. C317, Burlington, VT 05405, USA
2 shared publications- Eric D. Girard
Department of Surgery, UConn Health, Farmington, USA
2 shared publications - Todd Jensen
Department of Pediatrics, University of Connecticut School of Medicine, Farmington, CT, USA
2 shared publications - Adam P. Matson
Department of Pediatrics, UConn Health, Farmington, USA
1 shared publication Alex E. Blanchette
Department of Vascular Biology, University of Connecticut Health Center, 263 Farmington Avenue, MC3501, Farmington, CT 06030, USA
1 shared publicationAlex M. Dressler
Department of Critical Care, Connecticut Children's Medical Center, Hartford, CT 06106, USA
1 shared publication
Latest Publications
- 1 December 2013
- Published by Elsevier in Biomaterials
- Vol. 34 (38) , 10043-10055
Automated procedure for biomimetic de-cellularized lung scaffold supporting alveolar epithelial transdifferentiation
- 1 December 2013
- Published by Elsevier in Biomaterials
- Vol. 34 (38) , 10043-10055
Automated procedure for biomimetic de-cellularized lung scaffold supporting alveolar epithelial transdifferentiation
- Open Access
- 13 February 2013
- Published by Elsevier in Journal of Pediatric Surgery Case Reports
- Vol. 1 (2) , 20-22
A novel case of pediatric thoracic malignant ectomesenchymoma in an infant
- 13 February 2013
- Published by Elsevier in Journal of Pediatric Surgery Case Reports
- Vol. 1 (2) , 20-22
Open AccessA novel case of pediatric thoracic malignant ectomesenchymoma in an infant
- Open Access
- 12 April 2012
- Published by SAGE Publications in Tissue Engineering Part C: Methods
- Vol. 18 (8) , 632-646
A Rapid Lung De-cellularization Protocol Supports Embryonic Stem Cell Differentiation In Vitro and Following Implantation
Pulmonary diseases represent a large portion of neonatal and adult morbidity and mortality. Many of these have no cure, and new therapeutic approaches are desperately needed. De-cellularization of whole organs, which removes cellular elements but leaves intact important extracellular matrix (ECM) proteins and three-dimensional architecture, has recently been investigated for ex vivo generation of lung tissues. As specific cell culture surfaces, including ECM composition, profoundly affect cell differentiation, this approach offers a potential means of using de-cellularized lungs to direct differentiation of embryonic and other types of stem/progenitor cells into lung phenotypes. Several different methods of whole-lung de-cellularization have been reported, but the optimal method that will best support re-cellularization and generation of lung tissues from embryonic stem cells (ESCs) has not been determined. We present a 24-h approach for de-cellularizing mouse lungs utilizing a detergent-based (Triton-X100 and sodium deoxycholate) approach with maintenance of three-dimensional lung architecture and ECM protein composition. Predifferentiated murine ESCs (mESCs), with phenotypic characteristics of type II alveolar epithelial cells, were seeded into the de-cellularized lung scaffolds. Additionally, we evaluated the effect of coating the de-cellularized scaffold with either collagen or Matrigel to determine if this would enhance cell adhesion and affect mechanics of the scaffold. Finally, we subcutaneously implanted scaffolds in vivo after seeding them with mESCs that are predifferentiated to express pro-surfactant protein C (pro-SPC). The in vivo environment supported maintenance of the pro-SPC-expressing phenotype and further resulted in vascularization of the implant. We conclude that a rapid detergent-based de-cellularization approach results in a scaffold that can maintain phenotypic evidence of alveolar epithelial differentiation of ESCs and support neovascularization after in vivo implantation.
- 12 April 2012
- Published by SAGE Publications in Tissue Engineering Part C: Methods
- Vol. 18 (8) , 632-646
Open AccessA Rapid Lung De-cellularization Protocol Supports Embryonic Stem Cell Differentiation In Vitro and Following Implantation
Pulmonary diseases represent a large portion of neonatal and adult morbidity and mortality. Many of these have no cure, and new therapeutic approaches are desperately needed. De-cellularization of whole organs, which removes cellular elements but leaves intact important extracellular matrix (ECM) proteins and three-dimensional architecture, has recently been investigated for ex vivo generation of lung tissues. As specific cell culture surfaces, including ECM composition, profoundly affect cell differentiation, this approach offers a potential means of using de-cellularized lungs to direct differentiation of embryonic and other types of stem/progenitor cells into lung phenotypes. Several different methods of whole-lung de-cellularization have been reported, but the optimal method that will best support re-cellularization and generation of lung tissues from embryonic stem cells (ESCs) has not been determined. We present a 24-h approach for de-cellularizing mouse lungs utilizing a detergent-based (Triton-X100 and sodium deoxycholate) approach with maintenance of three-dimensional lung architecture and ECM protein composition. Predifferentiated murine ESCs (mESCs), with phenotypic characteristics of type II alveolar epithelial cells, were seeded into the de-cellularized lung scaffolds. Additionally, we evaluated the effect of coating the de-cellularized scaffold with either collagen or Matrigel to determine if this would enhance cell adhesion and affect mechanics of the scaffold. Finally, we subcutaneously implanted scaffolds in vivo after seeding them with mESCs that are predifferentiated to express pro-surfactant protein C (pro-SPC). The in vivo environment supported maintenance of the pro-SPC-expressing phenotype and further resulted in vascularization of the implant. We conclude that a rapid detergent-based de-cellularization approach results in a scaffold that can maintain phenotypic evidence of alveolar epithelial differentiation of ESCs and support neovascularization after in vivo implantation.
- 31 July 2010
- Published by Elsevier in Journal of Pediatric Surgery
- Vol. 45 (7) , 1530-1533
Use of a massive transfusion protocol with hemostatic resuscitation for severe intraoperative bleeding in a child
- 31 July 2010
- Published by Elsevier in Journal of Pediatric Surgery
- Vol. 45 (7) , 1530-1533
Use of a massive transfusion protocol with hemostatic resuscitation for severe intraoperative bleeding in a child
- 28 February 2010
- Published by Elsevier in Journal of Pediatric Surgery
- Vol. 45 (2) , 435-437
Congenital subcostal hernia with unusual contents
- 28 February 2010
- Published by Elsevier in Journal of Pediatric Surgery
- Vol. 45 (2) , 435-437
Congenital subcostal hernia with unusual contents