Relevant bibliographies by topics / Dental tissue

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Dental tissue'

Author: Grafiati
Published: 20 February 2023
Last updated: 14 March 2023

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Journal articles on the topic "Dental tissue"

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Haugen, Håvard Jostein, Poulami Basu, Mousumi Sukul, João F. Mano, and Janne Elin Reseland. "Injectable Biomaterials for Dental Tissue Regeneration." International Journal of Molecular Sciences 21, no. 10 (May 13, 2020): 3442. http://dx.doi.org/10.3390/ijms21103442.

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Injectable biomaterials scaffolds play a pivotal role for dental tissue regeneration, as such materials are highly applicable in the dental field, particularly when compared to pre-formed scaffolds. The defects in the maxilla-oral area are normally small, confined and sometimes hard to access. This narrative review describes different types of biomaterials for dental tissue regeneration, and also discusses the potential use of nanofibers for dental tissues. Various studies suggest that tissue engineering approaches involving the use of injectable biomaterials have the potential of restoring not only dental tissue function but also their biological purposes.
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Malhi, Ravneet, Basavaraj Patthi, Ashish Singla, Shilpi Singh, Venisha Pandita, and Vaibhav Vashishtha. "Dental pluripotent cells - a promise for tissue regeneration." Asian Pacific Journal of Health Sciences 2, no. 2 (April 2015): 117–27. http://dx.doi.org/10.21276/apjhs.2015.2.2.19.

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Zhai, Qiming, Zhiwei Dong, Wei Wang, Bei Li, and Yan Jin. "Dental stem cell and dental tissue regeneration." Frontiers of Medicine 13, no. 2 (July 4, 2018): 152–59. http://dx.doi.org/10.1007/s11684-018-0628-x.

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Hamano, Sayuri, Risa Sugiura, Daiki Yamashita, Atsushi Tomokiyo, Daigaku Hasegawa, and Hidefumi Maeda. "Current Application of iPS Cells in the Dental Tissue Regeneration." Biomedicines 10, no. 12 (December 16, 2022): 3269. http://dx.doi.org/10.3390/biomedicines10123269.

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When teeth and periodontal tissues are severely damaged by severe caries, trauma, and periodontal disease, such cases may be subject to tooth extraction. As tooth loss leads to the deterioration of quality of life, the development of regenerative medicine for tooth and periodontal tissue is desired. Induced pluripotent stem cells (iPS cells) are promising cell resources for dental tissue regeneration because they offer high self-renewal and pluripotency, along with fewer ethical issues than embryonic stem cells. As iPS cells retain the epigenetic memory of donor cells, they have been established from various dental tissues for dental tissue regeneration. This review describes the regeneration of dental tissue using iPS cells. It is important to mimic the process of tooth development in dental tissue regeneration using iPS cells. Although iPS cells had safety issues in clinical applications, they have been overcome in recent years. Dental tissue regeneration using iPS cells has not yet been established, but it is expected in the future.
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Natarajan, Prabhu Manickam, Mohamed Said Hamed, Sura Ali Ahmed Fuoad Al-Bayati, Dusan Surdilovic, and Pooja Narain Adtani. "Soft tissue dental lasers." Indian Journal of Public Health Research & Development 9, no. 11 (2018): 571. http://dx.doi.org/10.5958/0976-5506.2018.01518.8.

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Demarco, Flávio Fernando, Marcus Cristian Muniz Conde, Bruno Neves Cavalcanti, Luciano Casagrande, Vivien Thiemy Sakai, and Jacques Eduardo Nör. "Dental pulp tissue engineering." Brazilian Dental Journal 22, no. 1 (2011): 3–13. http://dx.doi.org/10.1590/s0103-64402011000100001.

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Dental pulp is a highly specialized mesenchymal tissue that has a limited regeneration capacity due to anatomical arrangement and post-mitotic nature of odontoblastic cells. Entire pulp amputation followed by pulp space disinfection and filling with an artificial material cause loss of a significant amount of dentin leaving as life-lasting sequelae a non-vital and weakened tooth. However, regenerative endodontics is an emerging field of modern tissue engineering that has demonstrated promising results using stem cells associated with scaffolds and responsive molecules. Thereby, this article reviews the most recent endeavors to regenerate pulp tissue based on tissue engineering principles and provides insightful information to readers about the different aspects involved in tissue engineering. Here, we speculate that the search for the ideal combination of cells, scaffolds, and morphogenic factors for dental pulp tissue engineering may be extended over future years and result in significant advances in other areas of dental and craniofacial research. The findings collected in this literature review show that we are now at a stage in which engineering a complex tissue, such as the dental pulp, is no longer an unachievable goal and the next decade will certainly be an exciting time for dental and craniofacial research.
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Estrela, Carlos, Ana Helena Gonçalves de Alencar, Gregory Thomas Kitten, Eneida Franco Vencio, and Elisandra Gava. "Mesenchymal stem cells in the dental tissues: perspectives for tissue regeneration." Brazilian Dental Journal 22, no. 2 (2011): 91–98. http://dx.doi.org/10.1590/s0103-64402011000200001.

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In recent years, stem cell research has grown exponentially owing to the recognition that stem cell-based therapies have the potential to improve the life of patients with conditions that range from Alzheimer’s disease to cardiac ischemia and regenerative medicine, like bone or tooth loss. Based on their ability to rescue and/or repair injured tissue and partially restore organ function, multiple types of stem/progenitor cells have been speculated. Growing evidence demonstrates that stem cells are primarily found in niches and that certain tissues contain more stem cells than others. Among these tissues, the dental tissues are considered a rich source of mesenchymal stem cells that are suitable for tissue engineering applications. It is known that these stem cells have the potential to differentiate into several cell types, including odontoblasts, neural progenitors, osteoblasts, chondrocytes, and adipocytes. In dentistry, stem cell biology and tissue engineering are of great interest since may provide an innovative for generation of clinical material and/or tissue regeneration. Mesenchymal stem cells were demonstrated in dental tissues, including dental pulp, periodontal ligament, dental papilla, and dental follicle. These stem cells can be isolated and grown under defined tissue culture conditions, and are potential cells for use in tissue engineering, including, dental tissue, nerves and bone regeneration. More recently, another source of stem cell has been successfully generated from human somatic cells into a pluripotent stage, the induced pluripotent stem cells (iPS cells), allowing creation of patient- and disease-specific stem cells. Collectively, the multipotency, high proliferation rates, and accessibility make the dental stem cell an attractive source of mesenchymal stem cells for tissue regeneration. This review describes new findings in the field of dental stem cell research and on their potential use in the tissue regeneration.
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Tosiriwatanapong, Terawat, and Weerachai Singhatanadgit. "Zirconia-Based Biomaterials for Hard Tissue Reconstruction." Bone and Tissue Regeneration Insights 9 (January 1, 2018): 1179061X1876788. http://dx.doi.org/10.1177/1179061x18767886.

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Implantable biomaterials are increasingly important in the practice of modern medicine, including fixative, replacement, and regeneration therapies, for reconstruction of hard tissues in patients with pathologic osseous and dental conditions. A number of newly developed advanced biomaterials have been introduced as promising candidates for tissue reconstruction. Among these, zirconia-based biomaterials have gained attention as a biomaterial for hard tissue reconstruction due to superior mechanical properties and good chemical and biological compatibilities. This review summarizes the types of zirconia, advantages of zirconia-based biomaterials for hard tissue reconstruction including bone and dental tissues, responses of tissue and cells to zirconia, and surface modifications for enhanced bioactivity of zirconia. Current and future applications of zirconia-based biomaterials for bone and dental reconstruction, ie, medical implanted devices, dental prostheses, and biocompatible osteogenic scaffolds, are also discussed.
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Nakabayashi, Nobuo. "Dental biomaterials and the healing of dental tissue." Biomaterials 24, no. 13 (June 2003): 2437–39. http://dx.doi.org/10.1016/s0142-9612(03)00112-1.

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Ratajczak, Jessica, Annelies Bronckaers, Yörg Dillen, Pascal Gervois, Tim Vangansewinkel, Ronald B. Driesen, Esther Wolfs, Ivo Lambrichts, and Petra Hilkens. "The Neurovascular Properties of Dental Stem Cells and Their Importance in Dental Tissue Engineering." Stem Cells International 2016 (2016): 1–17. http://dx.doi.org/10.1155/2016/9762871.

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Within the field of tissue engineering, natural tissues are reconstructed by combining growth factors, stem cells, and different biomaterials to serve as a scaffold for novel tissue growth. As adequate vascularization and innervation are essential components for the viability of regenerated tissues, there is a high need for easily accessible stem cells that are capable of supporting these functions. Within the human tooth and its surrounding tissues, different stem cell populations can be distinguished, such as dental pulp stem cells, stem cells from human deciduous teeth, stem cells from the apical papilla, dental follicle stem cells, and periodontal ligament stem cells. Given their straightforward and relatively easy isolation from extracted third molars, dental stem cells (DSCs) have become an attractive source of mesenchymal-like stem cells. Over the past decade, there have been numerous studies supporting the angiogenic, neuroprotective, and neurotrophic effects of the DSC secretome. Together with their ability to differentiate into endothelial cells and neural cell types, this makes DSCs suitable candidates for dental tissue engineering and nerve injury repair.
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Dissertations / Theses on the topic "Dental tissue"

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Hultin, Margareta. "Factors affecting peri-implant tissue reactions /." Stockholm, 2001. http://diss.kib.ki.se/2001/91-628-4761-9/.

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Welander, Maria. "Soft tissue integration to dental implants /." Göteborg : Deptartment of Periodontology, Institute of Odontology, The Sahlgrenska Academy at University of Gothenburg, 2008. http://hdl.handle.net/2077/18196.

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Sopkova, J., E. Blahovcova, H. Škovierova, J. Strnadel, and E. Halašova. "Characterization of dental tissue derived stem cells." Thesis, Сумський державний університет, 2016. http://essuir.sumdu.edu.ua/handle/123456789/44951.

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Stem cells (SCs) are undifferentiated cells that are capable to differentiate into more specialized cells with specific functions. Oral tissues, which are easily accessible for dentists are a rich source of stem cells. The isolation of stem cells from these location may still not be convenient, because most of them requires surgical procedures, tooth or pulp extraction. Furthermore, these SCs are present in small quantities and can therefore be difficult to isolate, purify and homogenously expand them.
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El-Gendy, Reem Omar Othman Mostafa. "Bone tissue engineering using dental pulp stem cells." Thesis, University of Leeds, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.535682.

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Hassan, Muhammad. "Development of novel citrate-based dental tissue conditioners." Thesis, Queen Mary, University of London, 2016. http://qmro.qmul.ac.uk/xmlui/handle/123456789/12848.

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Dental tissue conditioners are compliant, viscoelastic gels used primarily to form a soft cushion between the oral mucosa and the hard denture base. Their uses include the treatment of inflamed mucosa resulting from ill-fitting dentures and in treatment of denture related stomatitis. They are presented in powder/liquid format where the powder is usually poly(ethyl methacrylate) (PEMA) and the liquid is a mix of an aromatic ester (plasticiser, usually a phthalate) with ethanol. In use, the ethanol and plasticiser leach out with time causing the material to harden. In recent years there has been concern about possible toxic effects of the leached phthalate. Preliminary work has shown citrate plasticisers to be acceptable replacements for phthalates. Another disadvantage of the powder/liquid format is the porosity produced on mixing which can lead to microbial ingress and contamination. One possible solution would be to use a pre-gelled material which would have the advantages of easy application and reduced porosity. Candidal infections are a common etiological factor in denture related stomatitis. Earlier studies have shown it possible to release chlorhexidine diacetate (a broad spectrum antibacterial/antifungal agent) from powder/liquid tissue conditioners to treat these infections The aim of this study is to develop citrate-based pre-gelled and powder/liquid tissue conditioners and explore its use as potential drug delivery vehicle for chlorhexidine diacetate. The experimental pre-gelled system (EPGS) containing PEMA and acetyl tributyl citrate (ATBC) only showed stable Shore A hardness values over an 18 month time Abstract 5 period when stored at 7oC. The Shore A hardness and creep compliance ratio (flow) of EPGS indicated that it could be used as both a tissue conditioner and a temporary denture lining material, whereas experimental powder liquid system (EPLS), which contained 16 hours ball-milled PEMA powder and ATBC plus 5% ethanol, had more suitable properties for use as a tissue conditioner. Addition of chlorhexidine diacetate alone or with sodium fluoride did have an effect on the hardness and creep compliance ratio of the materials but these were within acceptable range. Both EPGS and EPLS containing 1% chlorhexidine had a higher percent release than those containing 9% chlorhexidine. The addition of sodium fluoride increased the release of chlorhexidine in all formulations.
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Davies, Owen. "Adipose-derived stem cells for dental tissue engineering." Thesis, University of Birmingham, 2014. http://etheses.bham.ac.uk//id/eprint/5026/.

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Mesenchymal stem cells are valuable for regenerative dental research. However, the use of adipose-derived cells (ADCs) within regenerative dentistry remains relatively unexplored. This project aimed to determine an optimal method for the isolation of rat ADCs, to evaluate the influence of cell selection and cryo-storage on MSC phenotype, and compare the relative stemness and dentinogenic capacity of ADCs with bone marrow (BMDCs) and dental pulp-derived cells (DPDCs). Digestion with type-I collagenase for 30 minutes at 37ºC released the greatest number of viable and proliferative ADCs from inguinal adipose tissue. FACS and sqRT-PCR profiling indicated that ADCs shared similar levels of MSC markers (e.g. CD73, CD90, CD105) with BMDCS and DPDCs. The expression of MSC markers was also increased following cryo-storage for all cell types. Alizarin red staining, SEM and micro-CT analyses indicated that the osteogenic differentiation capacity of ADCs appeared lower than that of BMDCs and DPDCs. The FACS procedure reduced cell viability and CD29/CD90 cells had limited osteogenic differentiation capacity when compared to unsorted cell populations. Dentine matrix component (DMCs) supplementation (1 µg/mL) increased the volume of mineralised deposits in ADC, BMDC and DPDC cultures, as well as the expression of odontogenic markers (DMP1 and DSPP) in ADC and BMDC cultures. In conclusion ADCs have an odontogenic capacity, although this may be limited when compared with BMDCs and DPDCs. These findings indicate that when compared with BMDCs or DPDCs, ADCs may have a comparatively limited applicability for dental tissue engineering. However, ADCs can be isolated in comparatively large numbers with relatively little patient discomfort when compared with BMDCs and DPDCs, and these and previous studies have indicated that ADCs can be induced towards a dentinogenic phenotype.
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Smith, Michael James. "Utilising mesenchymal stem cells from adipose tissue and dental pulp for epithelial tissue engineering." Thesis, University of Birmingham, 2017. http://etheses.bham.ac.uk//id/eprint/7394/.

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Current treatment of epithelial wounds utilise biomimetic materials, cells or a combination of both. This project aimed to examine the feasibility of incorporating mesenchymal stem cells (MSCs), isolated from adipose tissue and dental pulp, and induced pluripotent stem cells (iPSC)-derived cells into 3D organotypic cultures, as reports suggest MSCs facilitate wound healing and can generate constituent cells. The effect collagen hydrogels containing MSCs on H400 epithelial cells seeded on its surface was assessed. Fixed H&E-stained sections of organotypic cultures were used to determine epithelial maturation and thickness using image analysis. iPSCs generated using the STEMCCA lentivirus were assessed by gene expression analysis and immunofluorescent staining for pluripotent capabilities and keratinocyte differentiation. MSCs incorporated into collagen hydrogels exerted no effect on epithelial thickness. iPSCs generated from mouse adipose-derived stem cells (mADSC- iPSCs) expressed pluripotency markers and were capable of differentiating down embryonic lineages. Keratinocytes generated from mADSC-iPSCs expressed cytokeratins, but were unable to be cultured in 3D organotypic cultures. This thesis highlighted the importance of characterising stem cells when investigating their therapeutic potential. Future work will involve characterising MSCs and evaluating their effects on epithelial cell growth. Furthermore, the effects of iPSC-derived keratinocytes must be determined to exploit them for regenerative therapies.
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Dhiman, Amarpreet Singh. "Formulation and characterisation of new dental tissue conditioner systems." Thesis, Queen Mary, University of London, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.412010.

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Al-Hazaimeh, Nawaf Ismail. "Revascularization of human dental pulp using tissue engineering approaches." Thesis, University of Leeds, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582741.

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Advancement in stem cell technology allows for many therapeutic opportunities, including the treatment of previously intractable conditions. Revascularization of dental pulp tissue, and specifically angiogenic differentiation of Human Dental Pulp Stem Cells, is of great interest due to the crucial role of this process not only in dental pulp regeneration, but also in wound healing and in regenerative medicine in general. One of the challenges of tissue engineering is the ability to provide sufficient blood supply for engineered tissue and organs in the first phase after transplantation. The present study investigated the potential use of HDPSCs in revascularization of dental pulp in vitro as well as in vivo using Matrigel basement membrane as 3D scaffold and compared this data to that of stem cells isolated from dental pulp tissue using the stem cell marker Stro-1. Initially these cells were cultured under angiogenic condition (EGM-2) for cell differentiation and treated with VEGF. The angiogenic potential of human dental pulp stromal/stem cells was investigated at gene and protein level by qRT-PCR and immunohistochemical analysis of appropriate angiogenic markers. Moreover we monitored the differentiation of these cells by confocal and light microscopy. In the second part of the present study we investigated the ability of these cells to differentiate and form vascular tissue in an appropriate animal model. Two in vivo models were used; HDPSCs or Stro-1 +CD45- cells were suspended in Matrigel and injected into the root canal space of human tooth sections and implanted subcutaneously into immunocompromised mice for 3 weeks. The other model was the Matrigel plug assay, which is widely used for angiogenesis studies. qRT-PCR and Immunohistochemistry studies indicated that CD31 and VEGFR-2 were upregulated in HDPSCs and stro-t- CD45- cells in monolayer cultures, and all angiogenic markers (CD31, CD34, vWF, and VEGFR-2) in Matrigel cultures were upregulated as well following treatment with VEGF in endothelial cells growth medium-2. In 3D Matrigel culture, cells were also able to form tube like network structures. These results were confirmed by in vivo study, in which we were able to regenerate vascular like tissue which contained red blood cells in both in vivo models. This data indicated that these vessels are functional when compared to normal vascular tissue in both human and mice. In conclusion, the present study confirmed that HDPSCs and Stro-1 +CD45- cells were induced to express angiogenic markers in vitro and can be recruited in the formation of vascular tissue in a tooth section as well as Matrigel plug constructs in immunocompromised mice. This technique can be used in the future to revascularize dental pulp which will enhance the survival rate of traumatized teeth.
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Chouaib, Batoul. "Dental pulp stem cell-conditioned medium for tissue regeneration." Thesis, Montpellier, 2020. http://www.theses.fr/2020MONTT039.

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Le sécrétome des cellules souches mésenchymateuses ou milieu conditionné (MSC-CM), est une combinaison de biomolécules et de facteurs de croissance sécrétés par les cellules souches mésenchymateuses (MSCs) dans un milieu de croissance cellulaire. Les MSC-CM apparaissent comme une alternative efficace à la thérapie cellulaire pour les applications de régénération tissulaire. Cependant, plusieurs questions telles que les protocoles de fabrication doivent être abordées avant l'application clinique de ces produits prometteurs. Dans cette thèse, nous nous sommes concentrés sur les cellules souches de la pulpe dentaire humaine (DPSCs). Après avoir évalué l'impact de plusieurs paramètres de fabrication sur les sécrétomes des DPSCs, nous avons étudié les potentiels des DPSC-CM pour la croissance neuronale, la régénération osseuse, l'angiogenèse et la thérapie contre le cancer. Ensemble, nos travaux ont permis d'identifier des conditions de culture standardisées fournissant des DPSC-CM riches en facteurs, et ont indiqué des pistes prometteuses pour l'application des DPSC-CM, afin de favoriser la régénération neuronale et la réparation des tissus osseux. Cette thèse contribue aux contrôles qualitatifs et quantitatifs des produits dérivés des DPSC-CM nécessaires à leur production selon les bonnes pratiques de fabrication, et à leur développement clinique en médecine régénérative
Mesenchymal stem cell secretome or conditioned medium (MSC-CM), is a combination of biomolecules and growth factors secreted by mesenchymal stem cells (MSCs) in the cell growth medium. MSC-CM emerge as an effective alternative to cell therapy for tissue regeneration applications. However, several issues such as manufacturing protocols must be addressed before the clinical application of these promising products. In this thesis, we focused on human dental pulp stem cells (DPSCs). After evaluating the impact of several manufacturing parameters on DPSC secretomes, we investigated DPSC-CM potentials for neuronal growth, bone regeneration, angiogenesis, and cancer therapy. Importantly, our work allowed the identification of standardized culture conditions providing factor-rich DPSC-CM and pointed towards promising avenues for the application of DPSC-CM to aide neuronal regeneration, and bone tissue repair. This thesis contributes to the qualitative and quantitative controls of DPSC-CM derived products necessary for their GMP-grade production, and their clinical translation in regenerative medicine
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Books on the topic "Dental tissue"

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Blayden, Jessica, and Angie Mott. Soft-Tissue Lasers in Dental Hygiene. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781119421474.

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Murata, Masaru, and In-Woong Um. Advances in oral tissue engineering. Chicago: Quintessence Publishing Co. Inc., 2014.

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Goldberg, Michel, and Pamela Den Besten, eds. Extracellular Matrix Biomineralization of Dental Tissue Structures. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-76283-4.

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Patrick, Palacci, ed. Optimal implant positioning & soft tissue management for the Brånemark system. Chicago: Quintessence Pub. Co., 1995.

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Raigrodski, Ariel J. Soft tissue management: The restorative perspective : putting concepts into practice. Chicago: Quintessence Publishing Co, Inc., 2015.

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Saadoun, Andre P. Esthetic soft tissue management of teeth and implants. Chichester, West Sussex: John Wiley & Sons, 2013.

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International, Congress on Tissue Integration in Oral and Maxillofacial Reconstruction (3rd 1996 Tokyo Japan). Third International Congress on Tissue Integration in Oral and Maxillofacial Reconstruction: Proceedings of the Third International Congress on Tissue Integration in Oral and Maxillofacial Reconstruction, November 1996, Tokyo. Tokyo: Quintessence Pub. Co., 1999.

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World Congress for Oral Implantology (5th 2001 Tokyo). Biomechanics and tissue engineering: Proceedings of 5th World Congress for Oral Implantology. Edited by Furumoto Keiichi. Tokyo: Proceedings Committee, 2001.

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World Congress for Oral Implantology (5th 2001 Tokyo, Japan). Proceedings of 5th World Congress for Oral Implantology: Biomechanics and tissue engineering. Edited by Furumoto Keiichi, To kyo Shika Daigaku, and Japanese Society of Oral Implantology. Chiba: Department of Removable Partial Prosthodontics, Tokyo Dental College, 2001.

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Surya, Mallapragada, ed. Biomaterials for drug delivery and tissue engineering. Warrendale, Pa: Materials Research Society, 2001.

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Book chapters on the topic "Dental tissue"

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Slootweg, Pieter J. "Developmental Disturbances in Tissue Structure." In Dental Pathology, 35–54. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36714-4_5.

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Cooper, Paul R. "Dental and Craniofacial Tissue Stem Cells: Sources and Tissue Engineering Applications." In Dental Stem Cells, 1–27. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-28947-2_1.

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Slootweg, Pieter J. "Chapter 4 Developmental Disturbances in Tissue Structure." In Dental Pathology, 19–26. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71691-4_4.

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Gawor, Jerzy. "Tooth Hard Tissue Diseases." In Practical Veterinary Dental Radiography, 156–73. Boca Raton : CRC Press, [2017]: CRC Press, 2017. http://dx.doi.org/10.1201/b20288-12.

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Silver, Frederick H. "Dental Implants." In Biomaterials, Medical Devices and Tissue Engineering: An Integrated Approach, 220–35. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0735-8_7.

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Fan, Zhipeng, and Xiao Lin. "Dental Stem Cells for Bone Tissue Engineering." In Dental Stem Cells, 197–216. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-28947-2_10.

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Yu, Jinhua, Mohamed Jamal, Franklin Garcia-Godoy, and George T. J. Huang. "Dental Pulp Stem Cell Niche." In Tissue-Specific Stem Cell Niche, 163–89. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-21705-5_8.

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Rezai Rad, Maryam, Sepanta Hosseinpour, Qingsong Ye, and Shaomian Yao. "Dental Tissues Originated Stem Cells for Tissue Regeneration." In Regenerative Approaches in Dentistry, 9–33. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-59809-9_2.

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Sloan, Alastair J., John Colombo, Jessica Roberts, Rachel J. Waddington, and Wayne Nishio Ayre. "Tissue culture models and approaches for dental tissue regeneration." In Tissue Engineering and Regeneration in Dentistry, 96–109. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119282181.ch5.

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Yildirim, Sibel. "Dental Pulp Is a Connective Tissue." In SpringerBriefs in Stem Cells, 17–24. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-5687-2_3.

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Conference papers on the topic "Dental tissue"

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Pick, Robert M. "Lasers in soft tissue dental surgery." In OE/LASE '90, 14-19 Jan., Los Angeles, CA, edited by Stephen N. Joffe and Kazuhiko Atsumi. SPIE, 1990. http://dx.doi.org/10.1117/12.17487.

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Ling-Ling, Cui. "Dental Tissue Engineering of EMPs on Human Dental Pulp Stem Cells." In 2016 Eighth International Conference on Measuring Technology and Mechatronics Automation (ICMTMA). IEEE, 2016. http://dx.doi.org/10.1109/icmtma.2016.53.

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Skenderović, H., M. Rakić, E. Klarić Sever, and S. Vdović. "Femtosecond Pulse Laser Ablation of Dental Tissue." In Advanced Solid State Lasers. Washington, D.C.: OSA, 2019. http://dx.doi.org/10.1364/assl.2019.jw2a.53.

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Wannop, Neil M., Mark R. Dickinson, and Terence A. King. "Erbium:YAG laser radiation interaction with dental tissue." In Europto Biomedical Optics '93, edited by Gregory B. Altshuler and Raimund Hibst. SPIE, 1993. http://dx.doi.org/10.1117/12.166186.

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Huang, Qicheng. "Research Progress of Dental Tissue Engineering Technology." In 2020 International Conference on Public Health and Data Science (ICPHDS). IEEE, 2020. http://dx.doi.org/10.1109/icphds51617.2020.00075.

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Rubenchik, Alexander M., Luiz B. Da Silva, Michael D. Feit, Stephen M. Lane, Richard A. London, Michael D. Perry, Brent C. Stuart, and Joseph Neev. "Dental tissue processing with ultrashort-pulse laser." In Photonics West '96, edited by Harvey A. Wigdor, John D. B. Featherstone, Joel M. White, and Joseph Neev. SPIE, 1996. http://dx.doi.org/10.1117/12.238771.

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Motamedi, Massoud, Sohi Rastegar, and Bahman Anvari. "Thermal stress distribution in laser-irradiated hard dental tissue: implications for dental applications." In OE/LASE '92, edited by Steven L. Jacques. SPIE, 1992. http://dx.doi.org/10.1117/12.137474.

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Ling-Ling, Cui. "Dental Tissue Engineering on Human Dental Pulp Stem Cells Based on Tooth Development." In 2017 9th International Conference on Measuring Technology and Mechatronics Automation (ICMTMA). IEEE, 2017. http://dx.doi.org/10.1109/icmtma.2017.0117.

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Crawley, David A., Christopher Longbottom, Vincent P. Wallace, Bryan E. Cole, Donald D. Arnone, and Michael Pepper. "Three-dimensional terahertz pulse imaging of dental tissue." In High-Power Lasers and Applications, edited by Glenn S. Edwards, Joseph Neev, Andreas Ostendorf, and John C. Sutherland. SPIE, 2002. http://dx.doi.org/10.1117/12.461366.

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Blodgett, David W., and Ward L. Massey. "Dental hard tissue characterization using laser-based ultrasonics." In Biomedical Optics 2003, edited by Steven L. Jacques, Donald D. Duncan, Sean J. Kirkpatrick, and Andres Kriete. SPIE, 2003. http://dx.doi.org/10.1117/12.488445.

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Reports on the topic "Dental tissue"

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MALDONADO, KARELYS, JUAN ESPINOZA, DANIELA ASTUDILLO, and WILSON BRAVO. Fatigue and fracture resistance and survival of occlusal veneers of composite resin and ceramics blocks in posterior teeth with occlusal wear: A protocol for a systematic review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, October 2021. http://dx.doi.org/10.37766/inplasy2021.10.0036.

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Review question / Objective: The aim of this systematic review is to synthesize the scientific evidence that evaluates fatigue and fracture resistance, survival, and stress distribution, of composite resin CAD/CAM and ceramic CAD/CAM occlusal veneers in posterior teeth with severe occlusal wear. Condition being studied: Currently there is an increase in cases of dental wear, due to several factors such as: excessive consumption of carbonated drinks, a diet high in acids, gastric diseases, anorexia, bulimia, dental grinding, use of highly abrasive toothpastes, or a combination of these(9) (10) (11) (12); which affect the patient in several aspects: loss of vertical dimension, sensitivity due to the exposure of dentin, esthetics, affectation of the neuromuscular system(11) (13) (14). With the advent of minimally invasive dentistry, occlusal veneers have been found to be a valid option to rehabilitate this type of cases and thus avoid greater wear of the dental structure with full coverage restorations. Sometimes when performing a tabletop it is not necessary to perform any preparation, thus preserving the maximum amount of dental tissue(3) (6) (15). Due to the masticatory load either in patients without parafunction where the maximum masticatory force is approximately 424 N for women and 630 N for men or in those who present parafunction where the maximum bite force can vary from 780 to 1120N(7), it is necessary that the occlusal veneers support that load which makes indispensable a compilation of studies investigating both fatigue and fracture resistance and the survival rate of occlusal veneers in different materials and thicknesses.
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Steegman, Ralph, Anne-Marie Renkema, Herman Verbeek, Adriaan Schoeman, Anne Marie Kuijpers-Jagtman, and Yijin Ren. Upper Airway Volumetric Changes on CBCT after Orthodontic Interventions: protocol for a systematic review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, April 2022. http://dx.doi.org/10.37766/inplasy2022.4.0017.

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Review question / Objective: Does the volume of the upper airway change after an orthodontic intervention? P: growing subjects, adults; I: orthodontic treatment, dentofacial orthopedics, extractions; C: untreated subjects and/or non-extractions; O: volumetric changes of the upper airway measured on CBCT scans. Condition being studied: The primary objective of orthodontic treatment is to establish optimal dental and/or skeletal relationship in harmony with the soft tissue morphology and functioning. In addition, un-impeding or facilitating airway growth and development is an important objective, especially in patients susceptible for airway obstruction or sleep apnea. It is therefore important to look into the effect of various orthodontic treatments on the 3D volumetric changes of the upper airway. Compared with the use of traditional 2D lateral cephalograms, CBCT scans provide the opportunity to perform measurements in more dimensions on the airway with demonstrated reliability. This systematic review therefore includes studies using CBCT scans for evaluation of the airway.
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