No.	Author/year	Language	Type of study	Result/outcome
1.	Potdar PD, Deshpande S. (2013)	English	Review of article	MSCs transplantation promises to transform the traditional use of embryonic stem cells to modern therapeutic applications.
2.	Pravin D Potdar, Yogita D Jethmalani. (2015)	English	Review of article	Advancement in stem cell and scaffold technology, damaged or lost teeth can be replaced by the use of regenerative therapies.
3.	Potdar P, Sutar J. (2010)	English	Laboratory study	It has been shown for the first time that both VAST and SCAT cell types differ in their characteristics by morphology as well as at molecular level, indicating that both cell types play different roles in the adipogenesis process.
4.	Potdar PD, D’souza SB. (2011)	English	Review of article	Peripheral blood can be used as a source of MCs from diabetes mellitus patients for use in future regenerative stem cell therapy and that this particular model system may be useful to study the mechanism of diabetes mellitus involving downregulation of the SOX2 cascade.
5.	Potdar P, Subedi R. (2011)	English	Laboratory study	Isolated MSCs and HSCs can be used as a model system to study the mechanism of leukemia at stem cell level and their use in stem cell regeneration therapy for Acute Lymphocytic Leukemia.
6.	Potdar PD, Chougule S. (2011)	English	Laboratory study	hBCMSCs cell line may represent a suitable in vitro model to study the mechanism of breast cancer which further leads to an identification of molecular targets for future breast cancer targeted therapy.
7.	Marcella La Noce a, Francesca Paino a, et al. (2014)	English	Review of article	DPSCs are mesenchymal stem cells expressing mesenchymal, haematopoietic and stemness markers. These cells: 1) differentiate into different tissues of mesenchymal origin, but also into functional melanocytes and neurons; 2) maintain their characteristics after cryopreservation for years if stored as selected stem cells and not as part of whole pulp; 3) differentiate into bone-like tissues in animal models when loaded on scaffolds; 4) regenerate bone in human grafts; 5) are an excellent model for the study of bone formation on substrates appropriate for clinical bone remodelling applications.
8.	Byung-Chul Kim, Hojae Bae, et al. (2012)	English	Review of article	The multilineage differentiation capacity, especially into osteoblastic/ cementoblastic lineage and neural lineages of dental stem cells such as dental pulp stem cells (DPSC), dental follicle stem cells (DFSC), periodontal ligament stem cells (PDLSC), and dental papilla stem cells (DPPSC).
9.	Chiho Ikebe and Ken Suzuki. (2014)	English	Review of article	Feasibility and safety of the employment of BM-derived MSCs for a variety of therapeutic indications including regenerative therapy.
10.	Shihua Wang, Xuebin Qu, et al. (2012)	English	Review of article	Currently, more randomized, controlled, multicenter clinical trials are needed to find the optimal conditions for MSC therapy.
11.	Agnes Arthur, a, b, c Grigori Rychkov, d et al. (2008)	English	Laboratory study	Studies suggest that DPSCs are responsive to the surrounding microenvironment, surviving, migrating, and differentiating accordingly into the appropriate cell types within the avian host neural tissue.
12.	Maryam Raoof, Mohammad Mehdi Yaghoobi, et al. (2014)	English	Laboratory study	This study proposes a new method with high efficacy to obtain dental pulp stem cells in a short time.
13.	Daniele Lindemann Sefanie B. Werle Daniela Steffens Franklin Garcia- Godoy Patricia Pranke Luciano Casagrande. (2014)	English	Laboratory study	Isolation success rate was 61% and 30% for non-cryopreserved and cryopreserved groups respectively. There were no statistical differences between the groups for the tested surface markers. The cells in both groups were capable of differentiating into three mesenchymal lineages.
14.	Lin SL, Chang WJ, et al. (2015)	English	Laboratory study	SMF exposure improved DMSO-free cryopreservation. This phenomenon may be due to the improvement of membrane stability for resisting damage caused by ice crystals during the freezing procedure.
15.	Silvia Gioventu, Gabriella Andriolo, et al. (2012)	English	Laboratory study	DPSC isolated from laser pierced cryopreserved teeth show mesenchymal stem cells morphology, immunophenotype, viability and proliferation rate similar to those of cells isolated from fresh, non cryopreserved teeth, whereas significant loss of cell viability and proliferation rate was shown by cells isolated from teeth cryopreserved without laser piercing. These data support the use of this method for prospective whole tooth banking.