최소 단어 이상 선택하여야 합니다.
최대 10 단어까지만 선택 가능합니다.
다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기Stem cells and development, v.24 no.11, 2015년, pp.1309 - 1319
Hwang, Hyo-In (Department of Nanobiomedical Science, BK21 PLUS Global Research Center for Regenerative Medicine, Dankook University, Cheonan, Korea.) , Lee, Tae-Hyong (Department of Nanobiomedical Science, BK21 PLUS Global Research Center for Regenerative Medicine, Dankook University, Cheonan, Korea.) , Jang, Young-Joo (Department of Nanobiomedical Science, BK21 PLUS Global Research Center for Regenerative Medicine, Dankook University, Cheonan, Korea.)
Dental pulp is a soft tissue located inside the hard part of a tooth and it contains a stem cell population that can regenerate damaged dentin and/or pulp itself. Human dental pulp stem cells (hDPSCs) are multipotent adult stem cells that have the potential to be differentiated into a variety of cel...
Abdallah, B M, Kassem, M. Human mesenchymal stem cells: from basic biology to clinical applications. Gene therapy, vol.15, no.2, 109-116.
Meirelles, Lindolfo da Silva, Chagastelles, Pedro Cesar, Nardi, Nance Beyer. Mesenchymal stem cells reside in virtually all post-natal organs and tissues. Journal of cell science, vol.119, no.11, 2204-2213.
Gronthos, S., Mankani, M., Brahim, J., Robey, P. Gehron, Shi, S.. Postnatal human dental pulp stem cells (DPSCs) in vitro and invivo. Proceedings of the National Academy of Sciences of the United States of America, vol.97, no.25, 13625-13630.
Laino, Gregorio, Carinci, Francesco, Graziano, Antonio, d'Aquino, Riccardo, Lanza, Vladimiro, De Rosa, Alfredo, Gombos, Fernando, Caruso, Filippo, Guida, Luigi, Rullo, Rosario, Menditti, Dardo, Papaccio, Gianpaolo. In Vitro Bone Production Using Stem Cells Derived From Human Dental Pulp. The Journal of craniofacial surgery, vol.17, no.3, 511-515.
Min, Jin-Hee, Ko, Seon-Yle, Cho, Yong-Bum, Ryu, Chun-Jeih, Jang, Young-Joo. Dentinogenic potential of human adult dental pulp cells during the extended primary culture. Human cell, vol.24, no.1, 43-50.
Tandon, Shobha, Saha, Rooposhi, Rajendran, Ramesh, Nayak, Rashmi. Dental Pulp Stem Cells from Primary and Permanent Teeth: Quality Analysis. The Journal of clinical pediatric dentistry, vol.35, no.1, 53-58.
Zhang, Weibo, Walboomers, X. Frank, Shi, Songtao, Fan, Mingwen, Jansen, John A.. Multilineage Differentiation Potential of Stem Cells Derived from Human Dental Pulp after Cryopreservation. Tissue engineering, vol.12, no.10, 2813-2823.
Ferro, Federico, Spelat, Renza, D'Aurizio, Federica, Puppato, Elisa, Pandolfi, Maura, Beltrami, Antonio Paolo, Cesselli, Daniela, Falini, Giuseppe, Beltrami, Carlo Alberto, Curcio, Francesco. Dental Pulp Stem Cells Differentiation Reveals New Insights in Oct4A Dynamics. PloS one, vol.7, no.7, e41774-.
Dominici, M, Le Blanc, K, Mueller, I, Slaper-Cortenbach, I, Marini, Fc, Krause, Ds, Deans, Rj, Keating, A, Prockop, Dj, Horwitz, Em. Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement. Cytotherapy : official journal of the International Society for Hematotherapy and Graft Engineering, vol.8, no.4, 315-317.
Prockop, Darwin J.. Marrow Stromal Cells as Stem Cells for Nonhematopoietic Tissues. Science, vol.276, no.5309, 71-74.
Dennis, James E., Carbillet, Jean-Pierre, Caplan, Arnold I., Charbord, Pierre. The STRO-1+ Marrow Cell Population Is Multipotential. Cells, tissues, organs, vol.170, no.2, 73-82.
Lab Invest Encina NR 449 79 1999
Blood Gronthos S 4164 84 1994 10.1182/blood.V84.12.4164.bloodjournal84124164
Oyajobi, Babatunde O., Lomri, Abderrahim, Hott, Monique, Dr. Marie, Pierre J.. Isolation and Characterization of Human Clonogenic Osteoblast Progenitors Immunoselected from Fetal Bone Marrow Stroma Using STRO-1 Monoclonal Antibody. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, vol.14, no.3, 351-361.
Karbanová, Jana, Soukup, Tomáš, Suchánek, Jakub, Pytlík, Robert, Corbeil, Denis, Mokrý, Jaroslav. Characterization of Dental Pulp Stem Cells from Impacted Third Molars Cultured in Low Serum-Containing Medium. Cells, tissues, organs, vol.193, no.6, 344-365.
Liu, L., Wei, X., Ling, J., Wu, L., Xiao, Y.. Expression Pattern of Oct-4, Sox2, and c-Myc in the Primary Culture of Human Dental Pulp Derived Cells. Journal of endodontics, vol.37, no.4, 466-472.
Morrison, Sean J., Spradling, Allan C.. Stem Cells and Niches: Mechanisms That Promote Stem Cell Maintenance throughout Life. Cell, vol.132, no.4, 598-611.
Bavister, Barry D.. The mitochondrial contribution to stem cell biology. Reproduction, fertility, and development, vol.18, no.8, 829-.
Nesti, Claudia, Pasquali, Livia, Vaglini, Francesca, Siciliano, Gabriele, Murri, Luigi. The Role of Mitochondria in Stem Cell Biology. Bioscience reports, vol.27, no.1, 165-171.
Chen, Chien-Tsun, Hsu, Shu-Han, Wei, Yau-Huei. Upregulation of mitochondrial function and antioxidant defense in the differentiation of stem cells. Biochimica et biophysica acta, General subjects, vol.1800, no.3, 257-263.
Kondoh, Hiroshi, Lleonart, Matilde E., Nakashima, Yasuhiro, Yokode, Masayuki, Tanaka, Makoto, Bernard, David, Gil, Jesus, Beach, David. A High Glycolytic Flux Supports the Proliferative Potential of Murine Embryonic Stem Cells. Antioxidants & redox signaling, vol.9, no.3, 293-299.
Varum, S., Momcilovic, O., Castro, C., Ben-Yehudah, A., Ramalho-Santos, J., Navara, C.S.. Enhancement of human embryonic stem cell pluripotency through inhibition of the mitochondrial respiratory chain. Stem cell research, vol.3, no.2, 142-156.
Schieke, Stefan M., Ma, Mingchao, Cao, Liu, McCoy Jr., J. Philip, Liu, Chengyu, Hensel, Nancy F., Barrett, A. John, Boehm, Manfred, Finkel, Toren. Mitochondrial Metabolism Modulates Differentiation and Teratoma Formation Capacity in Mouse Embryonic Stem Cells. The Journal of biological chemistry, vol.283, no.42, 28506-28512.
Pattappa, Girish, Heywood, Hannah K., de Bruijn, Joost D., Lee, David A.. The metabolism of human mesenchymal stem cells during proliferation and differentiation. Journal of cellular physiology, vol.226, no.10, 2562-2570.
Pietilä, Mika, Lehtonen, Siri, Närhi, Marko, Hassinen, Ilmo E., Leskelä, Hannu-Ville, Aranko, Kari, Nordström, Katrina, Vepsäläinen, Ari, Lehenkari, Petri. Mitochondrial Function Determines the Viability and Osteogenic Potency of Human Mesenchymal Stem Cells. Tissue engineering. Part C, Methods, vol.16, no.3, 435-445.
Mandal, Sudip, Lindgren, Anne G., Srivastava, Anand S., Clark, Amander T., Banerjee, Utpal. Mitochondrial Function Controls Proliferation and Early Differentiation Potential of Embryonic Stem Cells. Stem cells®, vol.29, no.3, 486-495.
Chen, C.T., Hsu, S.H., Wei, Y.H.. Mitochondrial bioenergetic function and metabolic plasticity in stem cell differentiation and cellular reprogramming. Biochimica et biophysica acta, General subjects, vol.1820, no.5, 571-576.
Xu, X., Duan, S., Yi, F., Ocampo, A., Liu, G.H., Izpisua Belmonte, J.. Mitochondrial Regulation in Pluripotent Stem Cells. Cell metabolism, vol.18, no.3, 325-332.
Paumard, Patrick, Vaillier, Jacques, Coulary, Bénédicte, Schaeffer, Jacques, Soubannier, Vincent, Mueller, David M., Brèthes, Daniel, di Rago, Jean‐Paul, Velours, Jean. The ATP synthase is involved in generating mitochondrial cristae morphology. The EMBO journal, vol.21, no.3, 221-230.
Velours, J., Dautant, A., Salin, B., Sagot, I., Brethes, D.. Mitochondrial F1F0-ATP synthase and organellar internal architecture. The international journal of biochemistry & cell biology, vol.41, no.10, 1783-1789.
Saddar, Sonika, Stuart, Rosemary A.. The Yeast F1F0-ATP Synthase. The Journal of biological chemistry, vol.280, no.26, 24435-24442.
Arselin, Geneviève, Vaillier, Jacques, Salin, Bénédicte, Schaeffer, Jacques, Giraud, Marie-France, Dautant, Alain, Brèthes, Daniel, Velours, Jean. The Modulation in Subunits e and g Amounts of Yeast ATP Synthase Modifies Mitochondrial Cristae Morphology. The Journal of biological chemistry, vol.279, no.39, 40392-40399.
Rabl, Regina, Soubannier, Vincent, Scholz, Roland, Vogel, Frank, Mendl, Nadine, Vasiljev-Neumeyer, Andreja, Körner, Christian, Jagasia, Ravi, Keil, Thomas, Baumeister, Wolfgang, Cyrklaff, Marek, Neupert, Walter, Reichert, Andreas S.. Formation of cristae and crista junctions in mitochondria depends on antagonism between Fcj1 and Su e / g. The Journal of cell biology, vol.185, no.6, 1047-1063.
Gieffers, Christian, Korioth, Frank, Heimann, Peter, Ungermann, Christian, Frey, Jürgen. Mitofilin Is a Transmembrane Protein of the Inner Mitochondrial Membrane Expressed as Two Isoforms. Experimental cell research, vol.232, no.2, 395-399.
Yu, Jinhua, He, Huixia, Tang, Chunbo, Zhang, Guangdong, Li, Yuanfei, Wang, Ruoning, Shi, Junnan, Jin, Yan. Differentiation potential of STRO-1 + dental pulp stem cells changes during cell passaging. Bmc cell biology, vol.11, 32-32.
Laino, Gregorio, D'Aquino, Riccardo, Graziano, Antonio, Lanza, Vladimiro, Carinci, Francesco, Naro, Fabio, Pirozzi, Giuseppe, Papaccio, Gianpaolo. A New Population of Human Adult Dental Pulp Stem Cells: A Useful Source of Living Autologous Fibrous Bone Tissue (LAB). Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, vol.20, no.8, 1394-1402.
Ma, Zhan, Cao, Manlin, Liu, Yiwen, He, Yiqing, Wang, Yingzhi, Yang, Cuixia, Wang, Wenjuan, Du, Yan, Zhou, Muqing, Gao, Feng. Mitochondrial F1Fo-ATP synthase translocates to cell surface in hepatocytes and has high activity in tumor-like acidic and hypoxic environment. Acta biochimica et biophysica Sinica, vol.42, no.8, 530-537.
Chi, Sulene L., Pizzo, Salvatore V.. Cell surface F1Fo ATP synthase: A new paradigm?. Annals of medicine, vol.38, no.6, 429-438.
La Noce, M., Paino, F., Spina, A., Naddeo, P., Montella, R., Desiderio, V., De Rosa, A., Papaccio, G., Tirino, V., Laino, L.. Dental pulp stem cells: State of the art and suggestions for a true translation of research into therapy. Journal of dentistry, vol.42, no.7, 761-768.
d'Aquino, R, Graziano, A, Sampaolesi, M, Laino, G, Pirozzi, G, De Rosa, A, Papaccio, G. Human postnatal dental pulp cells co-differentiate into osteoblasts and endotheliocytes: a pivotal synergy leading to adult bone tissue formation. Cell death and differentiation, vol.14, no.6, 1162-1171.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.